As
filed with the Securities and Exchange Commission on March 17, 2023.
Registration No. 333-
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM S-3
REGISTRATION STATEMENT
UNDER
THE SECURITIES ACT OF 1933
NUVECTIS PHARMA, INC.
(Exact name of registrant as specified in its charter)
Delaware
(State or other jurisdiction of
incorporation or organization) |
|
86-2405608
(I.R.S. Employer
Identification Number) |
1 Bridge Plaza
Suite 275
Fort Lee, NJ 07024
(201) 614-3150
(Address,
including zip code, and telephone number, including area code, of registrant’s principal executive offices)
Ron Bentsur, M.B.A.
Chairman, President and Chief Executive Officer
Nuvectis Pharma, Inc.
Bridge Plaza
Suite 275
Fort Lee, NJ 07024
(201) 614-3150
(Name, address, including zip code, and telephone
number, including area code, of agent for service)
The Commission is requested to send copies of
all communications to:
Matthew W. Mamak, Esq.
Alston & Bird LLP
90 Park Avenue
New York, New York 10016
Telephone: (212) 210-9400
Approximate date of commencement of proposed
sale to the public:
From time to time after the effective date of
this Registration Statement.
If
the only securities being registered on this form are being offered pursuant to dividend or interest reinvestment plans, please check
the following box. ¨
If any of the securities being registered on this
form are to be offered on a delayed or continuous basis pursuant to Rule 415 under the Securities Act of 1933, other than securities
offered only in connection with dividend or interest reinvestment plans, check the following box. x
If
this form is filed to register additional securities for an offering pursuant to Rule 462(b) under the Securities Act, please
check the following box and list the Securities Act registration statement number of the earlier effective registration statement for
the same offering. ¨
If
this form is a post-effective amendment filed pursuant to Rule 462(c) under the Securities Act, check the following box
and list the Securities Act registration statement number of the earlier effective registration statement for the same offering. ¨
If
this form is a registration statement pursuant to General Instruction I.D. or a post-effective amendment thereto that shall
become effective upon filing with the Commission pursuant to Rule 462(e) under the Securities Act, check the following
box. ¨
If
this form is a post-effective amendment to a registration statement filed pursuant to General Instruction I.D. filed to register
additional securities or additional classes of securities pursuant to Rule 413(b) under the Securities Act, check the following
box. ¨
Indicate by check mark whether the registrant is
a large accelerated filer, an accelerated filer, a non-accelerated filer, a smaller reporting company or an emerging growth company. See
definitions of “large accelerated filer,” “accelerated filer,” “smaller reporting company,” and “emerging
growth company” in Rule 12b-2 of the Exchange Act:
Large
accelerated filer ¨ |
|
Accelerated
filer ¨ |
Non-accelerated filer x |
|
Smaller reporting company x |
|
|
Emerging growth company x |
If
an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for
complying with any new or revised financial accounting standards provided pursuant to Section 7(a)(2)(B) of the Securities
Act. ¨
The Registrant hereby amends this registration
statement on such date or dates as may be necessary to delay its effective date until the Registrant shall file a further amendment
which specifically states that this registration statement shall thereafter become effective in accordance with Section 8(a) of
the Securities Act of 1933 or until the registration statement shall become effective on such date as the Securities and Exchange Commission,
acting pursuant to said Section 8(a), may determine.
EXPLANATORY NOTE
This registration statement contains two prospectuses:
| • | a base prospectus which covers the offer, issuance and sale by the registrant of up to a maximum aggregate offering price of $150,000,000
of our common stock, preferred stock, warrants, debt securities, and/or units; and |
| • | an at-the-market offering prospectus which covers the offer, issuance and sale by the registrant from time to time of up to $40,000,000
of our common stock available under our sales agreement with H.C. Wainwright & Co., LLC as sales agent dated March 17, 2023. |
The base prospectus immediately
follows this explanatory note. The specific terms of any other securities to be offered pursuant to the base prospectus will be specified
in one or more prospectus supplements to the base prospectus. The at-the-market offering prospectus immediately follows the base
prospectus. The common stock that may be offered, issued and sold by us under the at-the-market offering prospectus is included in the
$150,000,000 of securities that may be offered, issued and sold by us under the base prospectus. Upon termination of the sales agreement
with H.C. Wainwright & Co., LLC, any portion of the $40,000,000 included in the at-the-market offering prospectus that remain
unsold will be available for sale in other offerings pursuant to the base prospectus, and if no shares are sold under the sales agreement,
the full amount of this registration statement may be sold in other offerings pursuant to the base prospectus and a corresponding prospectus
supplement.
The information in this prospectus
is not complete and may be changed. We may not sell these securities until the registration statement filed with the Securities and Exchange
Commission is effective. This prospectus is not an offer to sell these securities and we are not soliciting offers to buy these securities
in any jurisdiction where the offer or sale is not permitted.
Subject
to Completion— March 17, 2023
PROSPECTUS
$150,000,000
Nuvectis Pharma, Inc.
Common Stock
Preferred Stock
Warrants
Debt Securities
Units
The following are types of
securities that we may offer, issue and sell from time to time, together or separately:
| • | shares of our common stock; |
| • | shares of our preferred stock; |
| • | units consisting of any combination of our common stock, preferred stock, warrants or debt securities. |
We may, from time to time,
offer these securities in amounts, at prices, and on terms determined at the time of offering. We may sell these securities directly to
you through agents, underwriters, or dealers we select. If we use agents, underwriters or dealers to sell these securities, we will name
them and describe their compensation in a prospectus supplement. You should read this prospectus and any prospectus supplement carefully
before you invest.
This prospectus provides a
general description of the securities we may offer. Each time we sell securities, we will provide specific terms of the securities offered
in a supplement to this prospectus. The prospectus supplement may also add, update or change information contained in this prospectus.
You should read this prospectus and the applicable prospectus supplement carefully, together with additional information described under
the heading “Where You Can Find More Information,” before you invest in any securities. This prospectus may not be used to
consummate a sale of securities unless accompanied by the applicable prospectus supplement.
We are an “emerging
growth company” as defined under U.S. federal securities laws and, as such, have elected to comply with reduced public company reporting
requirements. This prospectus complies with the requirements that apply to an issuer that is an emerging growth company.
Our common stock is traded
on the Nasdaq Capital Market under the symbol “NVCT.” On March 7, 2023, the per share closing price of our common stock
as reported on the Nasdaq Capital Market was $11.34 per share.
Investing in our securities
involves certain risks. See “Risk Factors” in our Annual Report on Form 10-K for the year ended December 31, 2022,
which has been filed with the SEC and are incorporated by reference into this prospectus. You should read the entire prospectus carefully
before you make your investment decision.
Neither the Securities
and Exchange Commission nor any state securities commission has approved or disapproved of these securities or passed upon the adequacy
or accuracy of this prospectus. Any representation to the contrary is a criminal offense.
The date of this prospectus is , 2023.
Table of Contents
ABOUT THIS PROSPECTUS
This prospectus is part of
a “shelf” registration statement that we filed with the United States Securities and Exchange Commission (the “SEC”).
By using a shelf registration statement, we may offer and sell any combination of the securities described a in this prospectus, from
time to time, in one or more offerings. Each time we sell securities, we will provide a prospectus supplement to this prospectus that
contains specific information about the terms of such offering. The prospectus supplement may also add, update or change information contained
in this prospectus. Before purchasing any securities, you should carefully read both this prospectus and any supplement, together with
the additional information incorporated into this prospectus or described under the heading “Where You Can Find More Information.”
You should rely only on the
information contained or incorporated by reference in this prospectus and any prospectus supplement. We have not authorized any other
person to provide you with different information. If anyone provides you with different or inconsistent information, you should not rely
on it. We will not make an offer to sell securities in any jurisdiction where the offer or sale is not permitted. You should assume that
the information appearing in this prospectus, as well as information we previously filed with the SEC and have incorporated by reference,
is accurate as of the date on the front cover of this prospectus only, or when such document was filed with the SEC. Our business, financial
condition, results of operations and prospects may have changed since the relevant date.
We will not use this prospectus
to offer and sell securities unless it is accompanied by a prospectus supplement that more fully describes the terms of the offering.
When we refer to “Nuvectis,”
“we,” “our,” “us” and the “Company” in this prospectus, we mean Nuvectis Pharma, Inc.,
unless otherwise specified. When we refer to “you,” we mean the potential holders of the applicable series of securities.
Solely
for convenience, tradenames referred to in this prospectus, the accompanying prospectus and the documents incorporated by reference may
appear without the ® or TM symbol,
but those references are not intended to indicate, in any way, that we will not assert, to the fullest extent under applicable law, our
rights or that the applicable owner will not assert its rights, to these tradenames.
NUVECTIS PHARMA, INC.
Overview
We are a biopharmaceutical
company focused on the development of innovative precision medicines for the treatment of serious conditions of unmet medical need in
oncology. We seek to develop drug candidates in the precision medicine space, and our processes for selection and clinical development
of drug candidates is -based on scientific insights into cancer-promoting factors, as well as on our understanding of the clinical landscape
and regulatory requirements.
Products Under Development
NXP800 – Our Lead Product Candidate
In May 2021,
we licensed exclusive world-wide commercial rights to NXP800, a novel orally bioavailable small molecule that was discovered in a screen
for Heat Shock Factor 1 (“HSF1”) pathway inhibitors; NXP800 was discovered at the Institute for Cancer Research (“ICR”)
in London, England. Our license agreement with the ICR is subject to certain milestone and royalty payments. For additional information
see section “NXP800 License Agreement.” In December 2022, NXP800 received Fast Track Designation from the U.S. Food and
Drug Administration (“FDA”) for treatment of Platinum Resistant, AT-Rich Interaction Domain (“ARID1a”)-Mutated
Ovarian Carcinoma.
Scientific Background:
In preclinical studies,
treatment with NXP800 inhibited tumor growth in xenografts of ovarian cancer that harbored a loss of function mutation in the AT-Rich
Interaction Domain (“ARID1a”) gene. Based on this work, we plan to evaluate the safety and efficacy of NXP800 in ARID1a-mutated
ovarian carcinoma, which is a cancer type comprised primarily of two histologies: ovarian clear cell carcinoma (“OCCC”) and
endometrioid ovarian carcinoma (“EOC”), and to investigate the use of ARID1a mutations as a potential patient selection marker
for additional types of cancer. The genetic screening for mutations in the ARID1a gene is included in commercially available Next Generation
Sequencing (“NGS”) kits.
NXP800 Clinical Development Plan
A comprehensive
preclinical data package supported the approval of the Clinical Trial Application (“CTA”) by the Medicines and Healthcare
Regulatory Agency (“MHRA”) in the United Kingdom, and the Investigational New Drug (“IND”) Application submission
by the FDA. In December 2021, we announced the commencement of the Phase 1 study for NXP800. The Phase 1 study is comprised of two
parts: dose-escalation Phase 1a, and an expansion Phase 1b. In the ongoing Phase 1a, we have been evaluating the safety and tolerability
of NXP800 in patients with advanced solid tumors to identify potential a doses and dosing schedule for the Phase 1b. The Phase 1a is nearing
completion and the Phase 1b is expected to begin in 1H 2023. In the Phase 1b, the safety and preliminary anti-tumor activity of NXP800
will be initially evaluated in in women with platinum-resistant, ARID1a-mutated OCCC and EOC. In December 2022, we announced that
the FDA granted Fast Track Designation status to the NXP800 for the treatment of patients with platinum-resistant development program
in platinum resistant, ARID1a-mutated ovarian carcinoma. Moreover, we recently announced that the European Network of Gynecological Oncology
Trial Groups (“ENGOT”) and the GOG Foundation, Inc. (“GOG-F”), the world's premier gynecology oncology clinical
trials consortia, will lead the Phase 1b clinical trial in ARID1a-mutated ovarian carcinoma. Additional cohorts/trials in patients with
other types of solid tumors may also be explored based on emerging data.
Addressing an Unmet Need in Clear
Cell Ovarian Cancer and Advanced-stage Endometrioid Ovarian Carcinoma
We are investigating
plan to initially investigate NXP800 as treatment for platinum-resistant, ARID1a- mutated ovarian carcinoma, which is a cancer type comprised
primarily of two histologies: OCCC and EOC.
OCCC is highly malignant,
difficult to treat, and has a very poor survival rate due to frequent recurrence after surgery and first-line treatment. First-line treatment
consists of platinum-based chemotherapy (“PBC”), for which the reported response rate in relapse/refractory, platinum resistant
patients is 1%, demonstrating a clear and dire need for a new treatment option for women with OCCC. OCCC represents approximately 10%
of all ovarian cancer cases in the United States, with an annual incidence of approximately 2,200 patients.
EOC also represents
approximately 10% of all diagnosed ovarian cancer cases. If diagnosed at an early-stage, EOC can often be resected. However, if diagnosed
at later stages, these tumors have a substantially worse prognosis. Advanced, platinum-refractory, endometrioid cancer in the United States
represents approximately 30% of the endometrioid ovarian cancer segment. In this ovarian subset the progression-free survival at three
years for women diagnosed with stage III/IV disease is a dismal 20% for stage III and 0% for stage IV, representing a clear unmet medical
need.
OCCC and EOC are
subtypes of epithelial ovarian carcinoma whose clinical characteristics are distinct from those of high-grade serous ovarian carcinoma.
They exhibit a unique biological profile that is markedly different from those of other histologic types. The relative prevalence of OCCC
and EOC among women with ovarian cancer is higher in East Asia (for example, approximately 25% and 19% in Japan for OCCC and EOC, respectively),
than in Europe and the United States (approximately 10% for each indication).
NXP900
In August 2021,
we licensed worldwide commercial rights to NXP900 from the University of Edinburgh in Scotland. NXP900 is a targeted-therapy, small molecule
drug candidate that inhibits the Proto-oncogene c-Src (“SRC”) and YES1 kinases. We have completed the IND-enabling studies
and plan to submit an IND application with the FDA, or an equivalent submission with a foreign agency, in order to begin a Phase 1a dose-escalation
study of NXP900 in solid tumors in 1H 2023. Subsequently, upon successful completion of the dose-escalation study, we plan to conduct
a Phase 1b clinical trial to investigate NXP900 in solid tumors where the SRC and/or YES1 pathways are overactivated and implicated in
the disease etiology.
Scientific Background
SRC as an Anti-Cancer Target
SRC is aberrantly
activated in many cancer types, including solid tumor cancers such as breast, colon, prostate, pancreatic and ovarian cancers, while remaining
predominantly inactive in non-cancerous cells. Increased SRC activity is generally associated with late-stage cancers, metastatic potential
and resistance to therapies, and correlates with poor clinical prognosis. To date no kinase inhibitor has been approved for the treatment
of SRC-active solid tumor malignancies.
YES1 as an Anti-Cancer Target
YES1
is a nonreceptor tyrosine kinase that belongs to the SRC family of kinases and controls multiple cancer signaling pathways. YES1 is
amplified and overexpressed in many tumor types, where it promotes cell proliferation, survival, and invasiveness. In addition,
YES1 directly phosphorylates and activates the Yes-associated protein, the main
effector of the Hippo pathway, which has been identified as a promoter of drug resistance, cancer progression, and metastasis in several
cancer types, including squamous cell, mesothelioma and papillary kidney cancers.
NXP900’s Novel Mechanism of
Action
SRC pathway activation
is regulated by a switch between inactive and active conformations. The inactive conformation of SRC family kinases is associated with
lack of membrane binding, lack of phosphorylation of the activation loop, and characterized by a “closed conformation.” The
active “open” conformation allows for the binding of SRC to signaling partners and enables full activation of the pathway
via SRC’s kinase catalytic activity and the scaffolding property.
NXP900 is a targeted-therapy
that inhibits the SRC and YES1 kinases. Unlike the approved and clinical-stage kinase inhibitors that inhibit only the catalytic (enzymatic)
activity of SRC, NXP900 induces and locks SRC in its native inactive conformation, by inhibiting both the catalytic and scaffolding functions
of the kinase, thus preventing phosphorylation and complex formation with its primary partners. NXP900 is also highly selective, a property
typically associated with an improved therapeutic window.
In vivo, single-agent treatment with
NXP900 inhibited primary and metastatic tumor growth in xenograft models of breast, cervical, esophageal, head and neck cancers and medulloblastoma,
and demonstrated on-target pharmacodynamic effects. NXP900’s unique mechanism of action translated into substantial single-agent
induced tumor regression in several in vivo xenograft models. Moreover, publications in the scientific literature outlined opportunities
to potentially reverse resistance to osimertinib (Tagrisso) in non-small cell lung cancer and enzalutamide (Xtandi) in metastatic, castration
resistant prostate cancer, in combination with these agents, validating the importance of NXP900’s key targets, YES1 and SRC kinases,
in these disease settings.
Gene amplification
of the site containing the YES1 gene has been reported in clinical samples in several tumors including lung, head and neck, bladder and
esophageal cancers. YES1-dependent oncogenic transformation has also been reported, suggesting that YES1 plays a key role in these solid
tumors. The transforming ability of YES1 has been demonstrated via several experimental methods, for example down-regulating YES1 by short
hairpin RNA (shRNA) significantly inhibited cell growth in several malignancies, including colon carcinoma, rhabdomyosarcoma, and basal-like
breast cancer suggesting YES1 may play a key role in these solid tumors. Furthermore, it has been found that YES1 gene amplification is
a key mechanism of resistance to Epidermal Growth Factor Receptor, Alk and Human Epidermal growth factor Receptor 2 inhibitors.
There are no YES1 inhibitors that are FDA approved or currently in
clinical development. We plan to conduct additional in vivo studies to better understand the effects of YES1 inhibition in solid tumors
driven by YES1 overexpression or gene amplification.
Our Company
We were incorporated under the laws of the State
of Delaware in July 2020. Our principal executive office is located at 1 Bridge Plaza, Suite 275, Fort Lee, NJ 07024 and our
telephone number is (201) 614-3150.
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THE OFFERING |
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|
Use of Proceeds |
We intend to use the net proceeds of any offering as set forth
in the applicable prospectus supplement. |
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Nasdaq Capital Market Symbol |
NVCT |
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RISK FACTORS
An investment in our securities involves a high
degree of risk. The prospectus supplement applicable to each offering of our securities will contain a discussion of the risks applicable
to an investment in our securities. Prior to making a decision about investing in our securities, you should carefully consider the specific
factors discussed under the heading “Risk Factors” in the applicable prospectus supplement, together with all of the other
information contained or incorporated by reference in the prospectus supplement or appearing or incorporated by reference in this prospectus.
You should also consider the risks, uncertainties and assumptions discussed in the “Risk Factors” section of our most recent
Annual Report on Form 10-K, which is incorporated herein by reference, and may be amended, supplemented or superseded from time to time
by other reports we file with the SEC in the future. Each of the referenced risks and uncertainties could adversely affect our business,
operating results and financial condition, as well as adversely affect the value of an investment in our securities.
FORWARD-LOOKING STATEMENTS
This prospectus includes statements
that are, or may be deemed, “forward-looking statements.” In some cases, these forward-looking statements can be identified
by the use of forward-looking terminology, including the terms “believes,” “estimates,” “anticipates,”
“expects,” “plans,” “intends,” “may,” “could,” “would,” “might,”
“will,” “should,” “approximately” or, in each case, their negative or other variations thereon or
comparable terminology, although not all forward-looking statements contain these words. They appear in a number of places throughout
this prospectus and include statements regarding our intentions, beliefs, projections, outlook, analyses or current expectations concerning,
among other things, our history of net operating losses and uncertainty regarding our ability to obtain capital and achieve profitability,
our ability to develop and commercialize our product candidates, our ability to advance our development programs, enroll our trials, and
achieve clinical endpoints, our ability to use or expand our technology to build a pipeline of product candidates, our ability to obtain
and maintain regulatory approval of our product candidates and comply with ongoing regulatory requirements, our ability to successfully
operate in a competitive industry and gain market acceptance by physician, provider, patient, and payor communities, our reliance on third
parties, unstable economic or market conditions, and our ability to obtain and adequately protect intellectual property rights for our
product candidates.
By their nature, forward-looking
statements involve risks and uncertainties because they relate to events, competitive dynamics, and healthcare, regulatory and scientific
developments and depend on the economic circumstances that may or may not occur in the future or may occur on longer or shorter timelines
than anticipated. Although we believe that we have a reasonable basis for each forward-looking statement contained in this prospectus,
we caution you that forward-looking statements are not guarantees of future performance and that our actual results of operations, financial
condition and liquidity, and the development of the industry in which we operate may differ materially from the forward-looking statements
contained in this prospectus. In addition, even if our results of operations, financial condition and liquidity, and the development of
the industry in which we operate are consistent with the forward-looking statements contained in this prospectus, they may not be predictive
of results or developments in future periods. The forward-looking statements contained in this prospectus reflect our views and assumptions
only as of the date of this prospectus. Except as required by law, we assume no responsibility for updating any forward-looking statements.
We qualify all of our forward-looking statements by these cautionary statements. In addition, with respect to all of our forward-looking
statements, we claim the protection of the safe harbor for forward-looking statements contained in the Private Securities Litigation Reform
Act of 1995.
WHERE YOU CAN FIND MORE INFORMATION
We
file reports with the SEC on an annual basis using Form 10-K, quarterly reports on Form 10-Q and current reports on Form 8-K.
The SEC maintains a website that contains annual, quarterly, and current reports, proxy statements, and other information that issuers
(including us) file electronically with the SEC. The SEC’s website address is http://www.sec.gov. You can also obtain copies
of materials we file with the SEC from our internet website found at www.nuvectis.com. Our stock is quoted on the Nasdaq Capital Market
under the symbol “NVCT”.
INCORPORATION OF CERTAIN INFORMATION BY REFERENCE
The SEC allows us to “incorporate
by reference” the information we file with them. This means that we can disclose important information to you by referring you to
those documents instead of having to repeat the information in this document. The information incorporated by reference is considered
to be part of this prospectus, and later information that we file with the SEC will automatically update and supersede this information.
We incorporate by reference the documents listed below and any future filings made with the SEC under Sections 13(a), 13(c), 14 or
15(d) of the Exchange Act (1) after the date of the initial registration statement, as amended, and prior to effectiveness of
the registration statement, and (2) after the date of this prospectus and prior to the termination of this offering. Such information
will automatically update and supersede the information contained in this prospectus and the documents listed below; provided, however,
that we are not, unless specifically indicated, incorporating any information furnished under Item 2.02 or Item 7.01 of any
current report on Form 8-K, whether listed below or filed in the future, or related exhibits furnished pursuant to Item 9.01
of Form 8-K:
We will provide to each person, including any beneficial
owner, to whom a copy of this prospectus is delivered, a copy of any or all of the information that we have incorporated by reference
into this prospectus. We will provide this information upon written or oral request at no cost to the requester. You may request this
information by contacting our corporate headquarters at the following address: 1 Bridge Plaza, Suite 275, Fort Lee, NJ 07024, Attn:
Ron Bentsur, or by calling (201) 614-3150.
DESCRIPTION OF SECURITIES WE MAY OFFER
This prospectus contains summary
descriptions of the securities we may offer from time to time. These summary descriptions are not meant to be complete descriptions of
each security. The particular terms of any security will be described in the related prospectus supplement.
DESCRIPTION OF CAPITAL STOCK
The
following descriptions are summaries of the material terms of our amended and restated certificate of incorporation, as amended (“certificate
of incorporation”), and our amended and restated bylaws (“bylaws”). The following summaries may not be complete
and are subject to, and qualified by reference to, the terms and provisions of our certificate of incorporation and our bylaws. You should
refer to, and read this summary together with, our certificate of incorporation, and our bylaws to review all of the terms of that may
be important to you.
Common Stock
We are authorized to issue
a total of 60,000,000 shares of common stock, par value $0.00001 per share. As of March 1, 2023, we had 14,752,403 actual shares
of our common stock issued and outstanding. All outstanding shares of our common stock are fully paid and nonassessable. Our common stock
is listed on The Nasdaq Capital Market and trades under the symbol “NVCT” and has been publicly traded since February 4,
2022. Prior to that time, there was no public market for our common stock.
Holders
The number of record holders of our 14,752,403 shares
of outstanding common stock as of March 1, 2023 was 40. This number does not include beneficial owners whose shares are held by nominees
in street name.
Dividends
We have never declared or
paid any cash dividends on our common stock and do not anticipate paying any cash dividends in the foreseeable future. Any future determination
to pay dividends will be at the sole discretion of our board of directors.
Voting Rights
Holders of our common stock
are entitled to one vote for each share held on all matters submitted to a vote of stockholders and do not have cumulative voting rights.
An election of directors by our stockholders will be determined by a plurality of the votes cast by the stockholders entitled to vote
on the election. Holders of common stock are entitled to receive proportionately any dividends as may be declared by our board of directors
in its sole discretion, subject to any preferential dividend rights or other rights of outstanding preferred stock, if any.
Liquidation and Dissolution
In the event of our liquidation
or dissolution, the holders of common stock are entitled to receive proportionately all assets available for distribution to stockholders
after the payment of all debts and other liabilities and subject to the prior rights of any outstanding preferred stock. Holders of common
stock have no preemptive, subscription, redemption or conversion rights. The rights, preferences and privileges of holders of common stock
are subject to, and may be adversely affected by, the rights of the holders of shares of any series of preferred stock that we may designate
and issue in the future.
Preferred Stock
We currently do not have any
shares of preferred stock outstanding, and we have no present plan to issue any shares of preferred stock. Our board of directors has
the authority, without further action by our stockholders, to issue up to 5,000,000 shares of preferred stock in one or more series and
to fix the rights, preferences, privileges and restrictions thereof. These rights, preferences and privileges could include dividend rights,
conversion rights, voting rights, terms of redemption, liquidation preferences, sinking fund terms and the number of shares constituting,
or the designation of, such series, any or all of which may be greater than the rights of common stock. The issuance of our preferred
stock could adversely affect the voting power of holders of common stock and the likelihood that such holders will receive dividend payments
and payments upon our liquidation. In addition, the issuance of preferred stock could have the effect of delaying, deferring or preventing
a change in control of our company or other corporate action.
Anti-Takeover Provisions
Our certificate of incorporation
and bylaws include a number of provisions that may have the effect of delaying, deferring or preventing another party from acquiring control
of us and encouraging persons considering unsolicited tender offers or other unilateral takeover proposals to negotiate with our board
of directors rather than pursue non-negotiated takeover attempts. These provisions include the items described below.
Board composition and filling vacancies
Our certificate of incorporation
provides for the division of our board of directors into three classes serving staggered three-year terms, with one class being elected
each year. Our certificate of incorporation also provides that directors may be removed only for cause and then only by the affirmative
vote of the holders of two-thirds of the shares then entitled to vote at an election of directors. Furthermore, any vacancy on our board
of directors, however occurring, including a vacancy resulting from an increase in the size of our board, may only be filled by the affirmative
vote of a majority of our directors then in office even if less than a quorum. The classification of directors, together with the limitations
on removal of directors and treatment of vacancies, has the effect of making it more difficult for stockholders to change the composition
of our board of directors.
No written consent of stockholders
Our certificate of incorporation
provides that all stockholder actions are required to be taken by a vote of the stockholders at an annual or special meeting, and that
stockholders may not take any action by written consent in lieu of a meeting. This limit may lengthen the amount of time required to take
stockholder actions and would prevent the amendment of our bylaws or removal of directors by our stockholders without holding a meeting
of stockholders.
Meetings of stockholders
Our certificate of incorporation
and bylaws provide that only a majority of the members of our board of directors then in office may call special meetings of stockholders
and only those matters set forth in the notice of the special meeting may be considered or acted upon at a special meeting of stockholders.
Our bylaws limit the business that may be conducted at an annual meeting of stockholders to those matters properly brought before the
meeting.
Advance notice requirements
Our bylaws establish advance
notice procedures with regard to stockholder proposals relating to the nomination of candidates for election as directors or new business
to be brought before meetings of our stockholders. These procedures provide that notice of stockholder proposals must be timely given
in writing to our corporate secretary prior to the meeting at which the action is to be taken. Generally, to be timely, notice must be
received at our principal executive offices not less than 90 days nor more than 120 days prior to the first anniversary date
of the annual meeting for the preceding year. Our bylaws specify the requirements as to form and content of all stockholders’ notices.
These requirements may preclude stockholders from bringing matters before the stockholders at an annual or special meeting.
Amendment to certificate of incorporation and bylaws
Any amendment of our certificate
of incorporation must first be approved by a majority of our board of directors, and if required by law or our certificate of incorporation,
must thereafter be approved by two-thirds of the outstanding shares entitled to vote on the amendment and two-thirds of the outstanding
shares of each class entitled to vote thereon as a class. Our bylaws may be amended by the affirmative vote of a majority of the directors
then in office, subject to any limitations set forth in the bylaws; and may also be amended by the affirmative vote of two-thirds of the
outstanding shares entitled to vote on the amendment, or, if our board of directors recommends that the stockholders approve the amendment,
by the affirmative vote of two-thirds of the outstanding shares entitled to vote on the amendment, in each case voting together as a single
class.
Undesignated preferred stock
Our certificate of incorporation
provides for 5,000,000 authorized shares of preferred stock. The existence of authorized but unissued shares of preferred stock may enable
our board of directors to discourage an attempt to obtain control of us by means of a merger, tender offer, proxy contest or otherwise.
For example, if in the due exercise of its fiduciary obligations, our board of directors were to determine that a takeover proposal is
not in the best interests of our stockholders, our board of directors could cause shares of preferred stock to be issued without stockholder
approval in one or more private offerings or other transactions that might dilute the voting or other rights of the proposed acquirer
or insurgent stockholder or stockholder group. In this regard, our certificate of incorporation grants our board of directors broad power
to establish the rights and preferences of authorized and unissued shares of preferred stock. The issuance of shares of preferred stock
could decrease the amount of earnings and assets available for distribution to holders of shares of common stock. The issuance may also
adversely affect the rights and powers, including voting rights, of these holders and may have the effect of delaying, deterring or preventing
a change in control of us.
Delaware anti-takeover statute
We are subject to the provisions
of Section 203 of the Delaware General Corporation Law. In general, Section 203 prohibits a publicly held Delaware corporation
from engaging in a “business combination” with an “interested stockholder” for a three-year period following the
time that this stockholder becomes an interested stockholder, unless the business combination is approved in a prescribed manner. Under
Section 203, a business combination between a corporation and an interested stockholder is prohibited unless it satisfies one of
the following conditions:
| • | before the stockholder became interested, our board of directors approved either the business combination
or the transaction which resulted in the stockholder becoming an interested stockholder; |
| • | upon consummation of the transaction which resulted in the stockholder becoming an interested stockholder,
the interested stockholder owned at least 85% of the voting stock of the corporation outstanding at the time the transaction commenced,
excluding for purposes of determining the voting stock outstanding, shares owned by persons who are directors and also officers, and employee
stock plans, in some instances, but not the outstanding voting stock owned by the interested stockholder; or |
| • | at or after the time the stockholder became interested, the business combination was approved by our board
of directors and authorized at an annual or special meeting of the stockholders by the affirmative vote of a majority of the outstanding
voting stock which is not owned by the interested stockholder. |
Section 203 defines a business combination
to include:
| • | any merger or consolidation involving the corporation and the interested stockholder; |
| • | any sale, transfer, lease, pledge, exchange, mortgage or other disposition involving the interested stockholder
of 10% or more of the assets of the corporation; |
| • | subject to exceptions, any transaction that results in the issuance or transfer by the corporation of
any stock of the corporation to the interested stockholder; or |
| • | the receipt by the interested stockholder of the benefit of any loans, advances, guarantees, pledges or other financial benefits provided
by or through the corporation. |
In general, Section 203 defines an interested
stockholder as any entity or person beneficially owning 15% or more of the outstanding voting stock of the corporation and any entity
or person affiliated with or controlling or controlled by the entity or person.
Choice of forum
Our bylaws provide that the
Court of Chancery of the State of Delaware will be the exclusive forum for state law claims for (i) any derivative action or proceeding
brought on our behalf, (ii) any action asserting a breach of fiduciary duty by one or more of our directors, officers or employees,
(iii) any action asserting a claim against us arising pursuant to the Delaware General Corporation Law or (iv) any action asserting
a claim against us that is governed by the internal affairs doctrine, in each case subject to the Court of Chancery having personal jurisdiction
over the indispensable parties named as defendants therein (the “Delaware Forum Provision”); provided, however, that this
forum provision will not apply to any causes of action arising under the Exchange Act or the Securities Act which, unless we consent in
writing to the selection of an alternative forum, are required to be brought exclusively in federal district courts of the United States
of America in accordance with our certificate of incorporation. In addition, our bylaws provide that any person or entity purchasing or
otherwise acquiring any interest in shares of our common stock is deemed to have notice of and consented to the Delaware Forum Provision.
We recognize that the Delaware Forum Provision in our bylaws may impose additional litigation costs on stockholders in pursuing any such
claims, particularly if the stockholders do not reside in or near the State of Delaware. Additionally, the Delaware Forum Provision may
limit our stockholders’ ability to bring a claim in a judicial forum that they find favorable for disputes with us or our directors,
officers or employees, which may discourage such lawsuits against us and our directors, officers and employees. The Court of Chancery
of the State of Delaware may also reach different judgments or results than would other courts, including courts where a stockholder considering
an action may be located or would otherwise choose to bring the action, and such judgments may be more or less favorable to us than our
stockholders.
Transfer Agent
The transfer agent and registrar
for our common stock is American Stock Transfer & Trust Company, LLC.
Listing
Our common stock is listed
on the Nasdaq Capital Market under the symbol “NVCT”.
DESCRIPTION OF WARRANTS
We may issue warrants to purchase
shares of our common stock, preferred stock, or debt securities in one or more series together with other securities or separately, as
described in each applicable prospectus supplement. The prospectus supplement relating to any warrants we offer will include specific
terms relating to the offering. These terms will include some or all of the following:
| • | the title of the warrants; |
| • | the aggregate number of warrants offered; |
| • | the designation, amount and terms of the securities for which the warrants are exercisable and the procedures and conditions relating
to the exercise of such warrants; |
| • | the exercise price of the warrants; |
| • | the dates or periods during which the warrants are exercisable; |
| • | the designation and terms of other securities, if any, with which the warrants are to be issued and the number of warrants issued
with each such security; |
| • | if the warrants are issued as a unit with another security, the date on and after which the warrants and the other security will be
separately transferable; |
| • | any provisions for the adjustment of the number or amount of securities receivable upon the exercise of the warrants or the exercise
price of the warrants; |
| • | the price or prices at which the securities purchasable upon exercise of the warrants may be purchased; |
| • | the form of consideration that may be used to exercise the warrants; |
| • | the date on which the right to exercise the warrants shall commence and the date on which the right will expire; |
| • | if the exercise price is not payable in U.S. dollars, the foreign currency, currency unit or composite currency in which the exercise
price is denominated; |
| • | any minimum or maximum amount of warrants that may be exercised at any one time; |
| • | the terms of any mandatory or option call provisions; |
| • | any terms relating to the modification of the warrants; |
| • | any terms, procedures and limitations relating to the transferability, exchange or exercise of the warrants; and |
| • | any other specific terms of the warrants. |
DESCRIPTION OF DEBT SECURITIES
We may offer debt securities,
in one or more series, which may be senior, subordinated or junior subordinated and may be convertible. Unless otherwise specified in
the applicable prospectus supplement, our debt securities will be issued in one or more series under an indenture to be entered into between
us and a trustee. We will issue the debt securities offered by this prospectus and any accompanying prospectus supplement under an indenture
to be entered into between us and the trustee identified in the applicable prospectus supplement. The terms of the debt securities will
include those stated in the indenture and those made part of the indenture by reference to the Trust Indenture Act of 1939, as in effect
on the date of the indenture. We have filed a copy of the form of indenture as an exhibit to the registration statement in which this
prospectus is included. The indenture will be subject to and governed by the terms of the Trust Indenture Act of 1939.
The following description
briefly sets forth certain general terms and provisions of the debt securities that we may offer. The particular terms of the debt securities
offered by any prospectus supplement and the extent, if any, to which these general provisions may apply to the debt securities, will
be described in the related prospectus supplement. Accordingly, for a description of the terms of a particular issue of debt securities,
reference must be made to both the related prospectus supplement and to the following description.
Debt Securities
The aggregate principal amount
of debt securities that may be issued under the indenture is unlimited. The debt securities may be issued in one or more series as may
be authorized from time to time pursuant to a supplemental indenture entered into between us and the trustee or an order delivered by
us to the trustee. For each series of debt securities we offer, a prospectus supplement accompanying this prospectus will describe the
following terms and conditions of the series of debt securities that we are offering, to the extent applicable:
| • | title and aggregate principal amount; |
| • | whether the debt securities will be senior, subordinated or junior subordinated; |
| • | any limit on the amount that may be issued; |
| • | applicable subordination provisions, if any; |
| • | provisions regarding whether the debt securities will be convertible or exchangeable into other securities or property of the Company
or any other person; |
| • | percentage or percentages of principal amount at which the debt securities will be issued; |
| • | interest rate(s) or the method for determining the interest rate(s); |
| • | whether interest on the debt securities will be payable in cash or additional debt securities of the same series; |
| • | dates on which interest will accrue or the method for determining dates on which interest will accrue and dates on which interest
will be payable; |
| • | whether the amount of payment of principal of, premium, if any, or interest on the debt securities may be determined with reference
to an index, formula or other method; |
| • | redemption, repurchase or early repayment provisions, including our obligation or right to redeem, purchase or repay debt securities
under a sinking fund, amortization or analogous provision; |
| • | if other than the debt securities’ principal amount, the portion of the principal amount of the debt securities that will be
payable upon declaration of acceleration of the maturity; |
| • | a discussion of certain material U.S. federal income tax considerations applicable to the debt securities; |
| • | amount of discount or premium, if any, with which the debt securities will be issued, including whether the debt securities will be
issued as “original issue discount” securities; |
| • | the place or places where the principal of, premium, if any, and interest on the debt securities will be payable; |
| • | where the debt securities may be presented for registration of transfer, exchange or conversion; |
| • | the place or places where notices and demands to or upon the Company in respect of the debt securities may be made; |
| • | whether the debt securities will be issued in whole or in part in the form of one or more global securities; |
| • | if the debt securities will be issued in whole or in part in the form of a book-entry security, the depository or its nominee with
respect to the debt securities and the circumstances under which the book-entry security may be registered for transfer or exchange or
authenticated and delivered in the name of a person other than the depository or its nominee; |
| • | whether a temporary security is to be issued with respect to such series and whether any interest payable prior to the issuance of
definitive securities of the series will be credited to the account of the persons entitled thereto; |
| • | the terms upon which beneficial interests in a temporary global security may be exchanged in whole or in part for beneficial interests
in a definitive global security or for individual definitive securities; |
| • | the guarantors, if any, of the debt securities, and the extent of the guarantees and any additions or changes to permit or facilitate
guarantees of such debt securities; |
| • | any covenants applicable to the particular debt securities being issued; |
| • | any defaults and events of default applicable to the debt securities, including the remedies available in connection therewith; |
| • | currency, currencies or currency units in which the purchase price for, the principal of and any premium and any interest on, such
debt securities will be payable; |
| • | time period within which, the manner in which and the terms and conditions upon which the Company or the purchaser of the debt securities
can select the payment currency; |
| • | securities exchange(s) on which the debt securities will be listed, if any; |
| • | whether any underwriter(s) will act as market maker(s) for the debt securities; |
| • | extent to which a secondary market for the debt securities is expected to develop; |
| • | provisions relating to defeasance; |
| • | provisions relating to satisfaction and discharge of the indenture; |
| • | any restrictions or conditions on the transferability of the debt securities; |
| • | provisions relating to the modification of the indenture both with and without the consent of holders of debt securities issued under
the indenture; |
| • | any addition or change in the provisions related to compensation and reimbursement of the trustee; |
| • | provisions, if any, granting special rights to holders upon the occurrence of specified events; |
| • | whether the debt securities will be secured or unsecured, and, if secured, the terms upon which the debt securities will be secured
and any other additions or changes relating to such security; and |
| • | any other terms of the debt securities that are not inconsistent with the provisions of the Trust Indenture Act (but may modify, amend,
supplement or delete any of the terms of the indenture with respect to such series of debt securities). |
General
One or more series of debt
securities may be sold as “original issue discount” securities. These debt securities would be sold at a substantial discount
below their stated principal amount, bearing no interest or interest at a rate which at the time of issuance is below market rates. One
or more series of debt securities may be variable rate debt securities that may be exchanged for fixed rate debt securities.
United States federal income
tax consequences and special considerations, if any, applicable to any such series will be described in the applicable prospectus supplement.
Debt securities may be issued
where the amount of principal and/or interest payable is determined by reference to one or more currency exchange rates, commodity prices,
equity indices or other factors. Holders of such debt securities may receive a principal amount or a payment of interest that is greater
than or less than the amount of principal or interest otherwise payable on such dates, depending upon the value of the applicable currencies,
commodities, equity indices or other factors. Information as to the methods for determining the amount of principal or interest, if any,
payable on any date, the currencies, commodities, equity indices or other factors to which the amount payable on such date is linked and
certain additional United States federal income tax considerations will be set forth in the applicable prospectus supplement.
The term “debt securities”
includes debt securities denominated in U.S. dollars or, if specified in the applicable prospectus supplement, in any other freely transferable
currency or units based on or relating to foreign currencies.
We expect most debt securities
to be issued in fully registered form without coupons and in denominations of $2,000 and any integral multiples thereof. Subject to the
limitations provided in the indenture and in the prospectus supplement, debt securities that are issued in registered form may be transferred
or exchanged at the principal corporate trust office of the trustee, without the payment of any service charge, other than any tax or
other governmental charge payable in connection therewith.
Global Securities
The debt securities of a series
may be issued in whole or in part in the form of one or more global securities that will be deposited with, or on behalf of, a depositary
identified in the prospectus supplement. Global securities will be issued in registered form and in either temporary or definitive form.
Unless and until it is exchanged in whole or in part for the individual debt securities, a global security may not be transferred except
as a whole by the depositary for such global security to a nominee of such depositary or by a nominee of such depositary to such depositary
or another nominee of such depositary or by such depositary or any such nominee to a successor of such depositary or a nominee of such
successor. The specific terms of the depositary arrangement with respect to any debt securities of a series and the rights of and limitations
upon owners of beneficial interests in a global security will be described in the applicable prospectus supplement.
Governing Law
The indenture and the debt
securities shall be construed in accordance with and governed by the laws of the State of New York.
DESCRIPTION OF UNITS
We may issue units comprised
of one or more of the other securities described in this prospectus in any combination, as described in the applicable prospectus supplement.
Each unit will be issued so that the holder of the unit is also the holder of each security included in the unit. Thus, the holder of
a unit will have the rights and obligations of a holder of each included security. The unit agreement under which a unit is issued may
provide that the securities included in the unit may not be held or transferred separately at any time or at any time before a specified
date.
We may evidence units by unit
certificates that we issue under a separate agreement. We may issue the units under a unit agreement between us and one or more unit agents.
If we elect to enter into a unit agreement with a unit agent, the unit agent will act solely as our agent in connection with the units
and will not assume any obligation or relationship of agency or trust for or with any registered holders of units or beneficial owners
of units. We will indicate the name and address and other information regarding the unit agent in the applicable prospectus supplement
relating to a particular series of units if we elect to use a unit agent.
We will describe in the applicable prospectus supplement
the terms of the series of units being offered, including:
| • | the designation and material terms of the units and of the securities comprising the units, including whether and under what circumstances
those securities may be held or transferred separately; |
| • | any material provisions of the governing unit agreement that differ from those described herein; and |
| • | any material provisions for the issuance, payment, settlement, transfer or exchange of the units or of the securities comprising the
units. |
The other provisions regarding
our common stock, preferred stock, warrants and debt securities as described in this section will apply to each unit to the extent such
unit consists of shares of our common stock, preferred stock, warrants and/or debt securities.
PLAN OF DISTRIBUTION
We may sell the securities covered in this prospectus
from time to time in one or more of the following ways:
| • | through underwriters or dealers; |
| • | in short or long transactions; |
| • | directly to one or more purchasers; |
| • | through registered direct offerings; |
| • | as part of a collaboration with a third party; |
| • | through at-the-market issuances; |
| • | in privately negotiated transactions; or |
| • | through a combination of any of these methods of sale. |
Each time that we use this
prospectus to sell securities, we will also provide a prospectus supplement that contains the specific terms of the offering. The prospectus
supplement will set forth the terms of the offering of the securities, including the following, as applicable:
| • | the name or names of any underwriters, dealers or agents and the amounts of any securities underwritten or purchased by each of them; |
| • | the purchase price of the securities being offered and the proceeds to us and any discounts, commissions or concessions allowed or
reallowed or paid to dealers; |
| • | any options under which underwriters may purchase additional securities from us; and |
| • | any security exchanges on which the securities may be listed. |
The purchase price and any discounts or concessions
allowed or reallowed or paid to dealers may be changed from time to time.
If
underwriters are used in the sale of any securities, the securities will be acquired by the underwriters for their own account and may
be resold from time to time in one or more transactions, including negotiated transactions, at a fixed public offering price or at varying
prices determined at the time of sale. The securities may be either offered to the public through underwriting syndicates represented
by managing underwriters, or directly by underwriters. Generally, the underwriters’ obligations to purchase the securities
will be subject to certain conditions precedent. The underwriters will be obligated to purchase all of the securities if they purchase
any of the securities.
We may sell the securities
through agents from time to time. The prospectus supplement will name any agent involved in the offer or sale of the securities and any
commissions we pay to them. Generally, any agent will be acting on a best efforts basis for the period of its appointment.
We may authorize underwriters,
dealers or agents to solicit offers by certain purchasers to purchase the securities from us at the public offering price set forth in
the prospectus supplement pursuant to delayed delivery contracts providing for payment and delivery on a specified date in the future.
The contracts will be subject only to those conditions set forth in the prospectus supplement, and the prospectus supplement will set
forth any commissions we pay for solicitation of these contracts.
Agents and underwriters may
be entitled to indemnification by us against certain civil liabilities, including liabilities under the Securities Act of 1933, as amended,
or to contribution with respect to payments which the agents or underwriters may be required to make in respect thereof. Agents and underwriters
may be customers of, engage in transactions with, or perform services for us in the ordinary course of business.
We may enter into derivative
transactions with third parties, or sell securities not covered by this prospectus to third parties in privately negotiated transactions.
If the applicable prospectus supplement indicates, in connection with those derivatives, the third parties may sell securities covered
by this prospectus and the applicable prospectus supplement, including in short sale transactions. If so, the third party may use securities
pledged by us or borrowed from us or others to settle those sales or to close out any related open borrowings of securities, and may use
securities received from us in settlement of those derivatives to close out any related open borrowings of securities. The third party
in such sale transactions will be an underwriter and will be identified in the applicable prospectus supplement (or a post-effective amendment).
We may also use underwriters or such other third parties with whom we have a material relationship. We will describe the nature of any
such relationship in the applicable prospectus supplement.
In compliance with the guidelines
of the Financial Industry Regulatory Authority, Inc., or FINRA, the maximum compensation to be received by a FINRA member or independent
broker-dealer may not exceed 8% of the offering proceeds. It is anticipated that the maximum compensation to be received in any particular
offering of securities will be less than this amount.
At-the-Market Offerings
Upon written instruction from
us, a sales agent party to a distribution agency agreement with us will use its commercially reasonable efforts to sell on our behalf,
as our agent, the shares of common stock offered as agreed upon by us and the sales agent. We will designate the maximum amount of shares
of common stock to be sold through the sales agent, on a daily basis or otherwise as we and the sales agent agree. Subject to the terms
and conditions of the applicable distribution agency agreement, the sales agent will use its commercially reasonable efforts to sell,
as our sales agent and on our behalf, all of the designated shares of common stock. We may instruct the sales agent not to sell shares
of common stock if the sales cannot be effected at or above the price designated by us in any such instruction. We may suspend the offering
of shares of common stock under any distribution agency agreement by notifying the sales agent. Likewise, the sales agent may suspend
the offering of shares of common stock under the applicable distribution agency agreement by notifying us of such suspension.
We also may sell shares to
the sales agent as principal for its own account at a price agreed upon at the time of sale. If we sell shares to the sales agent as principal,
we will enter into a separate agreement setting forth the terms of such transaction.
The offering of common stock
pursuant to a distribution agency agreement will terminate upon the earlier of (1) the sale of all shares of common stock subject
to the distribution agency agreement or (2) the termination of the distribution agency agreement by us or by the sales agent.
Sales agents under our distribution
agency agreements may make sales in privately negotiated transactions and/or any other method permitted by law, including sales deemed
to be an “at-the-market” offering as defined in Rule 415 promulgated under the Securities Act, sales made directly on
the Nasdaq Capital Market, the existing trading market for our common stock, or sales made to or through a market maker other than on
an exchange. The name of any such underwriter or agent involved in the offer and sale of our common stock, the amounts underwritten, and
the nature of its obligations to take our common stock will be described in the applicable prospectus supplement.
LEGAL MATTERS
The legality and validity of the securities offered
from time to time under this prospectus will be passed upon by Alston & Bird LLP, New York, New York.
EXPERTS
The financial statements incorporated
in this Prospectus by reference to the Annual Report on Form 10-K for the year ended December 31, 2022 have been so incorporated
in reliance on the report of Kesselman & Kesselman, Certified Public Accountants (Isr.), a member firm of PricewaterhouseCoopers
International Limited, an independent registered public accounting firm, given on the authority of such firm as experts in auditing and
accounting.
$150,000,000
Nuvectis Pharma, Inc.
Common Stock
Preferred Stock
Warrants
Debt Securities
Units
PROSPECTUS
, 2023
The information in this prospectus
is not complete and may be changed. We may not sell these securities until the registration statement filed with the Securities and Exchange
Commission is effective. This prospectus is not an offer to sell these securities and we are not soliciting offers to buy these securities
in any jurisdiction where the offer or sale is not permitted.
Subject
to Completion— dated March 17, 2023
PROSPECTUS SUPPLEMENT
Up to $40,000,000 of Common Stock
We
have entered into an At the Market Offering Agreement, dated March 17, 2023 (the “sales agreement”), with H.C.
Wainwright & Co., LLC (“Wainwright” or the “sales agent”), relating to shares of our common stock offered
by this prospectus. In accordance with the terms of the sales agreement, we may offer and sell shares of our common stock having an aggregate
offering price of up to $40,000,000 from time to time through the sales agent.
Our common stock is traded
on the Nasdaq Capital Market under the symbol “NVCT”. On March 7, 2023, the closing price of our common stock as reported
on the Nasdaq Capital Market was $11.34 per share.
Sales
of our common stock, if any, under this prospectus may be made in sales deemed to be an “at the market offering” as defined
in Rule 415(a)(4) promulgated under the Securities Act of 1933, as amended, or the Securities Act. If we and Wainwright
agree on any method of distribution other than sales of shares of our common stock on or through the Nasdaq Capital Market or another
existing trading market in the United States at market prices, we will file a further prospectus supplement providing all information
about such offering as required by Rule 424(b) under the Securities Act. Subject to the terms of the sales agreement, Wainwright
will act as the sales agent and use commercially reasonable efforts to sell on our behalf all of the shares of common stock requested
to be sold by us, consistent with their normal trading and sales practices, and on mutually agreed terms. There is no arrangement for
funds to be received in any escrow, trust or similar arrangement.
The sales agent will receive from us a commission of 3.0% based on
the gross sales price per share for any shares sold through the sales agent under the sales agreement. See “Plan of Distribution”
beginning on page S-11 for additional information regarding the compensation to be paid to Wainwright. In connection with the sale
of shares of our common stock on our behalf, the sales agent will be deemed to be an “underwriter” within the meaning of the
Securities Act and the compensation of the sales agent will be deemed to be underwriting commissions or discounts. We have also agreed
to provide indemnification and contribution to Wainwright with respect to certain liabilities, including liabilities under the Securities
Act.
Investing in our securities involves certain
risks. See “Risk Factors” beginning on page 18 and our “Risk Factors” in our Annual Report on Form 10-K
for the year ended December 31, 2022, which has been filed with the SEC and are incorporated by reference into this prospectus. You
should read the entire prospectus carefully before you make your investment decision.
Neither the Securities and Exchange Commission
nor any state securities commission has approved or disapproved of these securities or determined if this prospectus is truthful or complete.
Any representation to the contrary is a criminal offense.
H.C. Wainwright &
Co.
The date of this prospectus is , 2023.
TABLE OF CONTENTS
ABOUT THIS PROSPECTUS
This prospectus is part of
a “shelf” registration statement that we filed with the United States Securities and Exchange Commission (the “SEC”).
This prospectus relates to the offering of shares of our common stock having an aggregate offering price of up to $40,000,000 from time
to time at prices and on terms to be determined by market conditions at the time of offering.
You should rely only on the
information contained or incorporated by reference in this prospectus and any prospectus supplement. We have not, and the sales agent
has not, authorized anyone to provide you with different information. If anyone provides you with different or inconsistent information,
you should not rely on it. We are not, and the sales agent is not, making an offer to sell these securities in any jurisdiction where
the offer or sale is not permitted or in which the person making that offer or solicitation is not qualified to do so or to anyone to
whom it is unlawful to make an offer or solicitation.
You should assume that the
information appearing in this prospectus, as well as information we previously filed with the SEC and incorporated by reference in this
prospectus, and any free writing prospectus that we have authorized for use in connection with this offering is accurate as of the date
of those respective documents. Our business, financial condition, results of operations and prospects may have changed since those dates.
You should read this prospectus, the documents incorporated by reference in this prospectus, and any free writing prospectus that we have
authorized for use in connection with this offering, in their entirety before making an investment decision. You should also read and
consider the information in the documents to which we have referred you in the sections of this prospectus entitled “Where You Can
Find Additional Information About Us” and “Incorporation of Certain Documents by Reference.”
We will not use this prospectus
to offer and sell securities unless it is accompanied by a prospectus supplement that more fully describes the terms of the offering.
When we refer to “Nuvectis,”
“we,” “our,” “us” and the “Company” in this prospectus, we mean Nuvectis Pharma, Inc.,
unless otherwise specified. When we refer to “you,” we mean the potential holders of the applicable series of securities.
Solely
for convenience, tradenames referred to in this prospectus, the accompanying prospectus and the documents incorporated by reference may
appear without the ® or TM symbol,
but those references are not intended to indicate, in any way, that we will not assert, to the fullest extent under applicable law, our
rights or that the applicable owner will not assert its rights, to these tradenames.
FORWARD-LOOKING STATEMENTS
This prospectus includes statements
that are, or may be deemed, “forward-looking statements.” In some cases, these forward-looking statements can be identified
by the use of forward-looking terminology, including the terms “believes,” “estimates,” “anticipates,”
“expects,” “plans,” “intends,” “may,” “could,” “would,” “might,”
“will,” “should,” “approximately” or, in each case, their negative or other variations thereon or
comparable terminology, although not all forward-looking statements contain these words. They appear in a number of places throughout
this prospectus and include statements regarding our intentions, beliefs, projections, outlook, analyses or current expectations concerning,
among other things, our history of net operating losses and uncertainty regarding our ability to obtain capital and achieve profitability,
our ability to develop and commercialize our product candidates, our ability to advance our development programs, enroll our trials, and
achieve clinical endpoints, our ability to use or expand our technology to build a pipeline of product candidates, our ability to obtain
and maintain regulatory approval of our product candidates and comply with ongoing regulatory requirements, our ability to successfully
operate in a competitive industry and gain market acceptance by physician, provider, patient, and payor communities, our reliance on third
parties, unstable economic or market conditions, and our ability to obtain and adequately protect intellectual property rights for our
product candidates.
By their nature, forward-looking
statements involve risks and uncertainties because they relate to events, competitive dynamics, and healthcare, regulatory and scientific
developments and depend on the economic circumstances that may or may not occur in the future or may occur on longer or shorter timelines
than anticipated. Although we believe that we have a reasonable basis for each forward-looking statement contained in this prospectus,
we caution you that forward-looking statements are not guarantees of future performance and that our actual results of operations, financial
condition and liquidity, and the development of the industry in which we operate may differ materially from the forward-looking statements
contained in this prospectus. In addition, even if our results of operations, financial condition and liquidity, and the development of
the industry in which we operate are consistent with the forward-looking statements contained in this prospectus, they may not be predictive
of results or developments in future periods. The forward-looking statements contained in this prospectus reflect our views and assumptions
only as of the date of this prospectus. Except as required by law, we assume no responsibility for updating any forward-looking statements.
We qualify all of our forward-looking statements by these cautionary statements. In addition, with respect to all of our forward-looking
statements, we claim the protection of the safe harbor for forward-looking statements contained in the Private Securities Litigation Reform
Act of 1995.
PROSPECTUS SUMMARY
This summary highlights information
contained elsewhere or incorporated by reference in this prospectus and the accompanying prospectus and in the documents we incorporate
by reference. This summary does not contain all of the information that you should consider before deciding to invest in our common stock.
You should read this entire prospectus and the accompanying prospectus carefully, including the information referred to in the section
entitled “Risk Factors” beginning on page 6 of this prospectus, our “Risk Factors” beginning on page 18
of our Annual Report on Form 10-K for the year ended December 31, 2022, which are incorporated by reference herein, as well
as the other documents that we incorporate by reference into this prospectus and the accompanying base prospectus, including our financial
statements and the exhibits to the registration statement of which this prospectus and the accompanying base prospectus is a part.
Overview
We are a biopharmaceutical
company focused on the development of innovative precision medicines for the treatment of serious conditions of unmet medical need in
oncology. We seek to develop drug candidates in the precision medicine space, and our processes for selection and clinical development
of drug candidates is -based on scientific insights into cancer-promoting factors, as well as on our understanding of the clinical landscape
and regulatory requirements.
Products Under Development
NXP800 – Our Lead Product Candidate
In May 2021,
we licensed exclusive world-wide commercial rights to NXP800, a novel orally bioavailable small molecule that was discovered in a screen
for Heat Shock Factor 1 (“HSF1”) pathway inhibitors; NXP800 was discovered at the Institute for Cancer Research (“ICR”)
in London, England. Our license agreement with the ICR is subject to certain milestone and royalty payments. For additional information
see section “NXP800 License Agreement.” In December 2022, NXP800 received Fast Track Designation from the U.S. Food and
Drug Administration (“FDA”) for treatment of Platinum Resistant, AT-Rich Interaction Domain (“ARID1a”)-Mutated
Ovarian Carcinoma.
Scientific Background:
In preclinical studies,
treatment with NXP800 inhibited tumor growth in xenografts of ovarian cancer that harbored a loss of function mutation in the AT-Rich
Interaction Domain (“ARID1a”) gene. Based on this work, we plan to evaluate the safety and efficacy of NXP800 in ARID1a-mutated
ovarian carcinoma, which is a cancer type comprised primarily of two histologies: ovarian clear cell carcinoma (“OCCC”) and
endometrioid ovarian carcinoma (“EOC”), and to investigate the use of ARID1a mutations as a potential patient selection marker
for additional types of cancer. The genetic screening for mutations in the ARID1a gene is included in commercially available Next Generation
Sequencing (“NGS”) kits.
NXP800 Clinical Development Plan
A comprehensive
preclinical data package supported the approval of the Clinical Trial Application (“CTA”) by the Medicines and Healthcare
Regulatory Agency (“MHRA”) in the United Kingdom, and the Investigational New Drug (“IND”) Application submission
by the FDA. In December 2021, we announced the commencement of the Phase 1 study for NXP800. The Phase 1 study is comprised of two
parts: dose-escalation Phase 1a, and an expansion Phase 1b. In the ongoing Phase 1a, we have been evaluating the safety and tolerability
of NXP800 in patients with advanced solid tumors to identify potential a doses and dosing schedule for the Phase 1b. The Phase 1a is nearing
completion and the Phase 1b is expected to begin in 1H 2023. In the Phase 1b, the safety and preliminary anti-tumor activity of NXP800
will be initially evaluated in in women with platinum-resistant, ARID1a-mutated OCCC and EOC. In December 2022, we announced that
the FDA granted Fast Track Designation status to the NXP800 for the treatment of patients with platinum-resistant development program
in platinum resistant, ARID1a-mutated ovarian carcinoma. Moreover, we recently announced that the European Network of Gynecological Oncology
Trial Groups (“ENGOT”) and the GOG Foundation, Inc. (“GOG-F”), the world's premier gynecology oncology clinical
trials consortia, will lead the Phase 1b clinical trial in ARID1a-mutated ovarian carcinoma. Additional cohorts/trials in patients with
other types of solid tumors may also be explored based on emerging data.
Addressing an Unmet Need in Clear
Cell Ovarian Cancer and Advanced-stage Endometrioid Ovarian Carcinoma
We are investigating
plan to initially investigate NXP800 as treatment for platinum-resistant, ARID1a- mutated ovarian carcinoma, which is a cancer type comprised
primarily of two histologies: OCCC and EOC.
OCCC is highly malignant,
difficult to treat, and has a very poor survival rate due to frequent recurrence after surgery and first-line treatment. First-line treatment
consists of platinum-based chemotherapy (“PBC”), for which the reported response rate in relapse/refractory, platinum resistant
patients is 1%, demonstrating a clear and dire need for a new treatment option for women with OCCC. OCCC represents approximately 10%
of all ovarian cancer cases in the United States, with an annual incidence of approximately 2,200 patients.
EOC also represents
approximately 10% of all diagnosed ovarian cancer cases. If diagnosed at an early-stage, EOC can often be resected. However, if diagnosed
at later stages, these tumors have a substantially worse prognosis. Advanced, platinum-refractory, endometrioid cancer in the United States
represents approximately 30% of the endometrioid ovarian cancer segment. In this ovarian subset the progression-free survival at three
years for women diagnosed with stage III/IV disease is a dismal 20% for stage III and 0% for stage IV, representing a clear unmet medical
need.
OCCC and EOC are
subtypes of epithelial ovarian carcinoma whose clinical characteristics are distinct from those of high-grade serous ovarian carcinoma.
They exhibit a unique biological profile that is markedly different from those of other histologic types. The relative prevalence of OCCC
and EOC among women with ovarian cancer is higher in East Asia (for example, approximately 25% and 19% in Japan for OCCC and EOC, respectively),
than in Europe and the United States (approximately 10% for each indication).
NXP900
In August 2021,
we licensed worldwide commercial rights to NXP900 from the University of Edinburgh in Scotland. NXP900 is a targeted-therapy, small molecule
drug candidate that inhibits the Proto-oncogene c-Src (“SRC”) and YES1 kinases. We have completed the IND-enabling studies
and plan to submit an IND application with the FDA, or an equivalent submission with a foreign agency, in order to begin a Phase 1a dose-escalation
study of NXP900 in solid tumors in 1H 2023. Subsequently, upon successful completion of the dose-escalation study, we plan to conduct
a Phase 1b clinical trial to investigate NXP900 in solid tumors where the SRC and/or YES1 pathways are overactivated and implicated in
the disease etiology.
Scientific Background
SRC as an Anti-Cancer Target
SRC is aberrantly
activated in many cancer types, including solid tumor cancers such as breast, colon, prostate, pancreatic and ovarian cancers, while remaining
predominantly inactive in non-cancerous cells. Increased SRC activity is generally associated with late-stage cancers, metastatic potential
and resistance to therapies, and correlates with poor clinical prognosis. To date no kinase inhibitor has been approved for the treatment
of SRC-active solid tumor malignancies.
YES1 as an Anti-Cancer Target
YES1
is a nonreceptor tyrosine kinase that belongs to the SRC family of kinases and controls multiple cancer signaling pathways. YES1 is
amplified and overexpressed in many tumor types, where it promotes cell proliferation, survival, and invasiveness. In addition,
YES1 directly phosphorylates and activates the Yes-associated protein, the main
effector of the Hippo pathway, which has been identified as a promoter of drug resistance, cancer progression, and metastasis in several
cancer types, including squamous cell, mesothelioma and papillary kidney cancers.
NXP900’s Novel Mechanism of
Action
SRC pathway activation
is regulated by a switch between inactive and active conformations. The inactive conformation of SRC family kinases is associated with
lack of membrane binding, lack of phosphorylation of the activation loop, and characterized by a “closed conformation.” The
active “open” conformation allows for the binding of SRC to signaling partners and enables full activation of the pathway
via SRC’s kinase catalytic activity and the scaffolding property.
NXP900 is a targeted-therapy
that inhibits the SRC and YES1 kinases. Unlike the approved and clinical-stage kinase inhibitors that inhibit only the catalytic (enzymatic)
activity of SRC, NXP900 induces and locks SRC in its native inactive conformation, by inhibiting both the catalytic and scaffolding functions
of the kinase, thus preventing phosphorylation and complex formation with its primary partners. NXP900 is also highly selective, a property
typically associated with an improved therapeutic window.
In vivo, single-agent treatment with
NXP900 inhibited primary and metastatic tumor growth in xenograft models of breast, cervical, esophageal, head and neck cancers and medulloblastoma,
and demonstrated on-target pharmacodynamic effects. NXP900’s unique mechanism of action translated into substantial single-agent
induced tumor regression in several in vivo xenograft models. Moreover, publications in the scientific literature outlined opportunities
to potentially reverse resistance to osimertinib (Tagrisso) in non-small cell lung cancer and enzalutamide (Xtandi) in metastatic, castration
resistant prostate cancer, in combination with these agents, validating the importance of NXP900’s key targets, YES1 and SRC kinases,
in these disease settings.
Gene amplification
of the site containing the YES1 gene has been reported in clinical samples in several tumors including lung, head and neck, bladder and
esophageal cancers. YES1-dependent oncogenic transformation has also been reported, suggesting that YES1 plays a key role in these solid
tumors. The transforming ability of YES1 has been demonstrated via several experimental methods, for example down-regulating YES1 by short
hairpin RNA (shRNA) significantly inhibited cell growth in several malignancies, including colon carcinoma, rhabdomyosarcoma, and basal-like
breast cancer suggesting YES1 may play a key role in these solid tumors. Furthermore, it has been found that YES1 gene amplification is
a key mechanism of resistance to Epidermal Growth Factor Receptor, Alk and Human Epidermal growth factor Receptor 2 inhibitors.
There
are no YES1 inhibitors that are FDA approved or currently in clinical development. We plan to conduct additional in vivo studies to better
understand the effects of YES1 inhibition in solid tumors driven by YES1 overexpression or gene amplification.
Our Company
We were incorporated under the laws
of the State of Delaware in July 2020. Our principal executive office is located at 1 Bridge Plaza, Suite 275, Fort Lee, NJ
07024 and our telephone number is (201) 614-3150.
Company information
Our website address is www.nuvectis.com.
We are not including the information on our website as a part of, nor incorporating it by reference into, this prospectus.
THE OFFERING |
|
|
Common stock offered by us |
Shares of our common stock, par value $0.00001, having an aggregate
offering price of up to $40,000,000. |
|
|
Common stock to be outstanding after the offering |
14,752,403 shares of our common stock
on the Nasdaq Capital Market were outstanding as of March 1, 2023. The actual number of shares issued in connection with this offering
will vary depending on how many shares of our common stock we choose to sell and the prices at which such sales occur. |
|
|
Plan of Distribution |
Sales of shares of our common stock under
this prospectus may be made by any method deemed to be an “at the market offering” as defined in Rule 415(a)(4) under
the Securities Act of 1933, as amended. Subject to the terms of the sales agreement, the sales agent will make all sales using commercially
reasonable efforts consistent with their normal trading and sales practices and applicable state and federal laws, rules and regulations
and the rules of The Nasdaq Capital Market, on mutually agreeable terms between the sales agent and us. See “Plan of Distribution”
beginning on page 11 of this prospectus. |
|
|
Commercially reasonable efforts |
The Sales Agent is not required to sell any
specific number or dollar amount of our common stock, but the sales agent has agreed to make all sales using commercially reasonable
efforts consistent with such sales agent’s normal trading and sales practices. See “Plan of Distribution” in this prospectus. |
|
|
Use of proceeds |
We intend to use the net proceeds from this offering (i) to fund the preclinical and clinical development of NXP800 and NXP900, (ii) to continue development and sponsored research related to our current product candidates or any future product candidate, (iii) to hire additional personnel, (iv) for capital expenditures, (v) to cover costs of operating as a public company and (vi) for other general corporate purposes. See “Use of Proceeds” on page 8 of this prospectus. |
|
|
Risk factors |
See “Risk Factors” beginning
on page 6 of this prospectus and our “Risk Factors” beginning on page 18 of our Annual Report on Form 10-K
for the year ended December 31, 2022, which are incorporated by reference herein, for a discussion of factors that you should consider
before investing in our common stock. |
|
|
Nasdaq Capital Market symbol |
NVCT |
The number of shares of our common stock
outstanding after this offering is based on 14,752,403 actual shares of our common stock outstanding as of March 1, 2023, and excludes
as of such date:
| Ø | 355,090 shares of Common Stock issuable upon exercise of options outstanding under our 2021 Global Equity Incentive Plan as amended
and restated (the “2021 Plan”), at a weighted average exercise price of $4.60 per share as of March 1, 2023; |
| | |
| Ø | 122,973 shares of Common Stock issuable upon the exercise of warrants under the 2021 Plan to purchase Common Stock and underwriter
warrants associated with the 2022 IPO at a weighted exercise price of $3.62 per share as of March 1, 2023; |
| | |
| Ø | 193,557 shares of restricted stock granted to the Company’s three founders on July 27, 2021; |
| | |
| Ø | 940,179 shares of restricted stock issued under the 2021 Plan; |
| | |
| Ø | 103,838 shares of Common Stock to be reserved for future issuance under the 2021 Plan; and |
| | |
| Ø | 2,036,170 shares of Common Stock issuable upon the exercise of the Investment Options. |
RISK FACTORS
An investment in our common
stock involves a high degree of risk. Before deciding whether to invest in our common stock, you should consider carefully the risks discussed
below, together with other information in this prospectus, the accompanying base prospectus, the information and documents incorporated
by reference including the section “Risk Factors” in our Annual Report on Form 10-K for the year ended December 31,
2022, and in any free writing prospectus that we have authorized for use in connection with this offering. The risks described below may
not be the only ones relating to our company. Additional risks that we currently believe are immaterial or risks not currently known to
us may also impair our business and operations. Our business, results of operation, financial condition, cash flow and prospects and the
trading price of our common stock could be harmed as a result of any of these risks, and investors may lose all or part of their investment.
Risks associated with this offering
Future sales of our common stock could lower
our stock price and dilute existing stockholders.
We may, in the future, sell
additional shares of common stock in subsequent public or private offerings. We cannot predict the size of future issuances of our common
stock or the effect, if any, that future sales and issuances of shares of our common stock will have on the market price of our common
stock. Sales of substantial amounts of our common stock, or the perception that such sales could occur, may adversely affect prevailing
market prices for our common stock. In addition, these sales may be dilutive to existing stockholders.
A large number of shares may be sold in
the market following this offering, which may depress the market price of our common stock.
All of our shares of common
stock sold in the offering will be freely tradable without restriction or further registration under the Securities Act. As a result,
a substantial number of our shares of common stock may be sold in the public market following this offering, which may cause the market
price of our common stock to decline. If there are more shares of common stock offered for sale than buyers are willing to purchase, then
the market price of our common stock may decline to a market price at which buyers are willing to purchase the offered shares of common
stock and sellers remain willing to sell the shares of common stock.
The
common stock offered hereby will be sold in “at the market offerings,” and investors
who buy shares at different times will likely pay different prices.
Investors who purchase shares
in this offering at different times will likely pay different prices, and so may experience different levels of dilution and different
outcomes in their investment results. We will have discretion, subject to market demand, to vary the timing, prices, and number of shares
sold in this offering. In addition, subject to the final determination by our board of directors, there is no minimum or maximum sales
price for shares to be sold in this offering. Investors may experience a decline in the value of the shares they purchase in this offering
as a result of sales made at prices lower than the prices they paid.
It is not possible to predict the actual
number of shares of common stock sold and the aggregate proceeds resulting from sales made under the sales agreement.
Subject to certain limitations
in the sales agreement and compliance with applicable law, we have the discretion to deliver a placement notice to the sales agent at
any time throughout the term of the sales agreement. The number of shares that are sold through the sales agent after delivering a placement
notice will fluctuate based on a number of factors, including the market price of our common stock during the sales period, the limits
we set with the sales agent in any applicable placement notice, and the demand for our common stock during the sales period. Because the
price per share of each share sold will fluctuate during the sales period, it is not currently possible to predict the number of shares
that will actually be issued by us under the sales agreement or the aggregate proceeds we will raise in connection with those sales.
Raising additional capital may cause dilution to our existing
stockholders, restrict our operations or require us to relinquish rights to our technologies or product candidates.
We will likely seek to raise
additional capital through a combination of private and public equity offerings, debt financings, strategic partnerships and alliances
and licensing arrangements. To the extent that we raise additional capital through the sale of equity or convertible debt securities,
the ownership interests of existing stockholders will be diluted, and the terms may include liquidation or other preferences that adversely
affect stockholder rights. Debt financing, if available, may involve agreements that include covenants limiting or restricting our ability
to take certain actions, such as incurring debt, making capital expenditures or declaring dividends. If we raise additional funds through
strategic partnerships and alliances and licensing arrangements with third-parties, we may have to relinquish valuable rights to our technologies
or product candidates, or grant licenses on terms that are not favorable to us. If we are unable to raise additional funds through equity
or debt financing when needed, we may be required to delay, limit, reduce or terminate our product development or commercialization efforts
or grant rights to develop and market product candidates that we would otherwise prefer to develop and market ourselves.
We have broad discretion over the use of the net proceeds we
receive in this offering, and may not use them effectively.
Our management has broad discretion
to use our cash, cash equivalents and marketable securities, including the net proceeds we receive in this offering, to fund our operations
and could spend these funds in ways that do not improve our results of operations or enhance the value of our common stock. The failure
by our management to apply these funds effectively could result in financial losses that could have a material adverse effect on our business,
cause the price of our common stock to decline and delay the development of our product candidates. Pending their use to fund operations,
we may invest our cash, cash equivalents and marketable securities in a manner that does not produce income or that loses value.
We do not expect to pay dividends on our capital stock in the
foreseeable future.
We have never declared or
paid cash dividends on our capital stock. We currently intend to retain all of our future earnings, if any, to finance the growth and
development of our business, and we do not anticipate paying any cash dividends on our capital stock in the foreseeable future. In addition,
the terms of any future debt agreements may preclude us from paying dividends. As a result, capital appreciation, if any, of our common
stock will be your sole source of gain for the foreseeable future.
The trading price of our common stock has been volatile and may
be volatile in the future.
The trading price of our common
stock is likely to be highly volatile and may be subject to wide fluctuations in response to various factors, some of which are beyond
our control. Broad market and industry factors may negatively affect the market price of our common stock, regardless of our actual operating
performance.
We will require substantial additional funding. Raising additional
capital may cause dilution to our existing stockholders, or require us to relinquish proprietary rights.
We expect our expenses to
increase in parallel with our ongoing activities, particularly as we continue our activities to identify new product candidates and initiate
clinical trials of, and seek marketing approval for, any of our current or future product candidates. In addition, if we obtain marketing
approval for any of our current or future product candidates, we expect to incur significant commercialization expenses related to product
sales, marketing, manufacturing, and distribution. Furthermore, we expect to incur significant additional costs associated with operating
as a public company. Accordingly, we will need to obtain substantial additional funding in connection with our continuing operations.
We cannot be certain that additional funding will be available on acceptable terms, or at all. Until such time, if ever, as we can generate
substantial product revenue, we expect to finance our operations through a combination of public or private equity offerings, debt financings,
governmental funding, collaborations, strategic partnerships and alliances or marketing, distribution or licensing arrangements with third
parties. To the extent that we raise additional capital through the sale of equity or convertible debt securities, your ownership interest
will be diluted, and the terms of these securities may include liquidation or other preferences that adversely affect your rights as a
stockholder. Debt financing and preferred equity financing, if available, may involve agreements that include covenants limiting or restricting
our ability to take specific actions, such as incurring additional debt, making capital expenditures or declaring dividends.
Purchasers of common stock in this offering
will experience immediate and substantial dilution in the book value of their investment. You may experience further dilution upon exercise
of options and warrants.
The price per share of our common stock being offered may be higher
than the net tangible book value per share of our outstanding common stock prior to this offering. Assuming that an aggregate of 3,527,337
shares of our common stock are sold at a price of $11.34 per share, the last reported sale price of our common stock on the Nasdaq Global
Select Market on March 7, 2023, for aggregate gross proceeds of approximately $40 million, and after deducting commissions and estimated
offering expenses payable by us, new investors in this offering will incur immediate dilution of $8.44 per share. For a more detailed
discussion of the foregoing see the section entitled “Dilution” below. To the extent outstanding stock options or warrants
are exercised, there will be further dilution to new investors. In addition, to the extent we need to raise additional capital in the
future and we issue additional shares of common stock or securities convertible or exchangeable for our common stock, our then existing
stockholders may experience dilution and the new securities may have rights senior to those of our common stock offered in this offering.
Unstable market and economic factors could
adversely affect our business, financial condition or results of operations.
Various macroeconomic factors could adversely
affect our business and financial condition, including, for example, changes in inflation, interest rates and foreign currency exchange
rates, crises involving banking and financial institutions, such as the recent failures at Silicon Valley Bank and other banks,
and overall economic conditions and uncertainties generally. The global banking and financial markets have experienced extreme volatility
and disruptions in the past several years, including severely diminished liquidity and credit availability, declines in consumer confidence,
declines in economic growth, and uncertainty about economic stability. We cannot assure you that further deterioration in the banking
system and financial markets and confidence in economic conditions will not occur. Our general business strategy and ability to raise
capital may be adversely affected by any such economic downturn, volatile business environment, or continued unpredictable and unstable
market conditions, including as a result of liquidity constraints and instability in U.S.
and international financial banking systems. Failure to secure any necessary financing in a timely manner and on favorable
terms could have a material adverse effect on our growth strategy, financial performance, and stock price and could require us to delay
or abandon clinical development plans.
USE OF PROCEEDS
We may issue and sell shares
of our common stock having aggregate sales proceeds of up to $40,000,000 from time to time. Because there is no minimum offering amount
required as a condition of this offering, the actual total public offering amount, commissions and proceeds to us, if any, are not determinable
at this time. There can be no assurance that we will be able to sell any shares under or fully utilize the sales agreement with Wainwright.
We
expect to use the net proceeds from this offering to fund the preclinical and clinical development of NXP800 and NXP900, to continue
development and sponsored research related to our current product candidates or any future product candidate, to hire additional personnel,
capital expenditures, costs of operating as a public company, and other general corporate purposes.
We may also use a portion
of the net proceeds to acquire or invest in complementary businesses, products and technologies. Although we currently have no specific
agreements, commitments or understandings with respect to any acquisition or investment, we evaluate acquisition and investment opportunities
and may engage in related discussions with other companies from time to time.
The timing and amounts of
our actual expenditures will depend on several factors, including data results, progression of our clinical development programs as well
as our joint collaborators. As of the date of this prospectus, we cannot specify with certainty all of the particular uses for the net
proceeds to us from an offering. Accordingly, our management will have broad discretion in the application of proceeds. Pending the uses
described above, we will invest the net proceeds in short-term and long-term, investment grade, interest-bearing securities.
DIVIDEND POLICY
We have never declared or
paid any cash dividends on our capital stock. We currently intend to retain any future earnings to fund the development and expansion
of our business, and therefore we do not anticipate paying cash dividends on our common stock in the foreseeable future. Any future determination
to pay dividends will be at the discretion of our board of directors and will depend on our results of operations, financial condition,
capital requirements, contractual restrictions and other factors deemed relevant by our board of directors.
DILUTION
If you invest in the shares
of our common stock in this offering, your ownership interest will be immediately diluted. As of December 31, 2022, we had a net
tangible book value of approximately $14.2 million, or $0.97 per share of our common stock, based upon 14,642,483 shares of our common
stock outstanding as of December 31, 2022. Historical net tangible book value per share is equal to our total tangible assets, less
total liabilities, divided by the number of outstanding shares of our common stock. Dilution in net tangible book value per share represents
the difference between the amount per share paid by purchasers of shares of common stock in this offering and the net tangible book value
per share of our common stock immediately after this offering.
After giving effect to the
assumed sale by us of 3,527,337 shares of our common stock in the aggregate amount of $40.0 million in this offering at an assumed public
offering price of $11.34 per share, which was the last reported sale price of our common stock on The Nasdaq Global Market on March 7,
2023, and after deducting commissions and estimated aggregate offering expenses payable by us, our as adjusted net tangible book value
as of December 31, 2022 would have been approximately $52.7 million, or $2.90 per share of our common stock outstanding. This represents
an immediate increase in net tangible book value of $1.93 per share to our existing stockholders and an immediate dilution of $8.44 per
share to investors purchasing shares of common stock in this offering.
The following table illustrates this per share
dilution to new investors:
Assumed public offering price per share |
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|
|
|
$ |
11.34 |
|
Historical net tangible book value per share as of December 31, 2022 |
|
$ |
0.97 |
|
|
|
|
|
Increase in net tangible book value per share attributable to new investors |
|
|
1.93 |
|
|
|
|
|
As adjusted net tangible book value per share after giving effect to this offering |
|
|
|
|
|
|
2.90 |
|
Dilution per share to investors in this offering |
|
|
|
|
|
$ |
8.44 |
|
For illustrative purposes, the table above assumes that an aggregate
of 3,527,337 shares of our common stock are sold at an assumed price of $11.34 per share, the last reported sale price of our common stock
on The Nasdaq Global Market on March 7, 2023, for aggregate gross proceeds of $40.0 million. The shares sold in this offering,
if any, will be sold from time to time at various prices. An increase of $0.50 per share in the price at which the shares are sold from
the assumed offering price of $11.34 per share shown in the table above, assuming that all of our common stock in the aggregate amount
of $40.0 million during the term of the sales agreement with Wainwright is sold at that price, would result in an increase in the dilution
in net tangible book value per share to new investors in this offering to $8.91 per share, after deducting commissions and estimated aggregate
offering expenses payable by us. A decrease of $0.50 per share in the price at which the shares are sold from the assumed offering price
of $11.34 per share shown in the table above, assuming that all of our common stock in the aggregate amount of $40.0 million during the
term of the sales agreement with Wainwright is sold at that price, would result in a decrease in the dilution in net tangible book value
per share to new investors in this offering to $7.96 per share, after deducting commissions and estimated aggregate offering expenses
payable by us. This information is supplied for illustrative purposes only and may differ based on the actual offering price and the actual
number of shares offered.
PLAN OF DISTRIBUTION
We have entered into the sales
agreement with Wainwright, under which we may issue and sell from time to time shares of our common stock having an aggregate offering
price of not more than $40,000,000 through Wainwright as our sales agent. Sales of the common stock, if any, will be made by any method
permitted by law deemed to be an “at the market offering” as defined in Rule 415 promulgated under the Securities Act.
If we and Wainwright agree on any method of distribution other than sales of shares of our common stock on or through Nasdaq or another
existing trading market in the United States at market prices, we will file a further prospectus supplement providing all information
about such offering as required by Rule 424(b) under the Securities Act.
Wainwright will offer our
shares of common stock at prevailing market prices subject to the terms and conditions of the sales agreement as agreed upon by us and
Wainwright. We will designate the number of shares which we desire to sell, the time period during which sales are requested to be made,
any limitation on the number of shares that may be sold in one day and any minimum price below which sales may not be made. Subject to
the terms and conditions of the sales agreement, Wainwright will use its commercially reasonable efforts consistent with its normal trading
and sales practices and applicable law and regulations to sell on our behalf all of the shares of common stock requested to be sold by
us. We or Wainwright may suspend the offering of the shares of common stock being made through Wainwright under the sales agreement upon
proper notice to the other party.
Settlement for sales of shares
of common stock will occur on the second business day or such shorter settlement cycle as may be in effect under Exchange Act Rule 15c6-1
from time to time, following the date on which any sales are made, or on some other date that is agreed upon by us and Wainwright in connection
with a particular transaction, in return for payment of the net proceeds to us. Sales of our shares of common stock as contemplated in
this prospectus supplement will be settled through the facilities of The Depository Trust Company or by such other means as we and Wainwright
may agree upon. There is no arrangement for funds to be received in an escrow, trust or similar arrangement.
We will pay Wainwright, upon
each sale of our shares of common stock pursuant to the sales agreement, compensation in cash at a commission rate equal to 3.0% of the
gross sales price of the shares of our common stock sold through it. Because there is no minimum offering amount required as a condition
to this offering, the actual total public offering amount, commissions and proceeds to us, if any, are not determinable at this time.
Pursuant to the terms of the sales agreement, we agreed to reimburse Wainwright for the fees and costs of its legal counsel reasonably
incurred in connection with entering into the transactions contemplated by the sales agreement in an amount not to exceed $50,000 in the
aggregate, in addition to up to $2,500 per due diligence update session for Wainwright’s counsel’s fees and any incidental expenses
to be reimbursed by us. We will report at least quarterly the number of shares of common stock sold through Wainwright under the sales agreement, the
net proceeds to us and the compensation paid by us to Wainwright in connection with the sales of common stock.
In connection with the sale
of the common stock on our behalf, Wainwright may be deemed to be an “underwriter” within the meaning of the Securities Act
and the compensation of Wainwright may be deemed to be underwriting commissions or discounts. We have also agreed to provide indemnification
and contribution to the sales agent with respect to certain liabilities, including liabilities under the Securities Act.
The offering of our shares
of common stock pursuant to the sales agreement will terminate upon the earlier of the (i) sale of all of our shares of common stock
provided for in this prospectus supplement and (ii) termination of the sales agreement as permitted therein.
Wainwright and its affiliates
may in the future provide various investment banking and other financial services for us and our affiliates, for which services they may
in the future receive customary fees. To the extent required by Regulation M, Wainwright will not engage in any market making activities
involving our shares of common stock while the offering is ongoing under this prospectus supplement. This summary of the material provisions
of the sales agreement does not purport to be a complete statement of its terms and conditions.
This prospectus in electronic
format may be made available on a website maintained by Wainwright and Wainwright may distribute this prospectus electronically.
LEGAL MATTERS
The
validity of the common stock offered by this prospectus and the accompanying base prospectus will be passed upon for us by Alston &
Bird LLP, New York, New York. Certain legal matters in connection with the offering will be passed upon for the sales agent
by Ellenoff Grossman & Schole LLP, New York, New York.
EXPERTS
The financial statements incorporated
in this Prospectus by reference to the Annual Report on Form 10-K for the year ended December 31, 2022 have been so incorporated
in reliance on the report of Kesselman & Kesselman, Certified Public Accountants (Isr.), a member firm of PricewaterhouseCoopers
International Limited, an independent registered public accounting firm, given on the authority of such firm as experts in auditing and
accounting.
WHERE YOU CAN FIND MORE INFORMATION
We
file reports with the SEC on an annual basis using Form 10-K, quarterly reports on Form 10-Q and current reports on Form 8-K.
The SEC maintains a website that contains annual, quarterly, and current reports, proxy statements, and other information that issuers
(including us) file electronically with the SEC. The SEC’s website address is http://www.sec.gov. You can also obtain copies
of materials we file with the SEC from our internet website found at www.nuvectis.com. Our stock is quoted on the Nasdaq Capital Market
under the symbol “NVCT.”
INCORPORATION OF CERTAIN INFORMATION BY REFERENCE
The SEC allows us to “incorporate
by reference” the information we file with them. This means that we can disclose important information to you by referring you to
those documents instead of having to repeat the information in this document. The information incorporated by reference is considered
to be part of this prospectus, and later information that we file with the SEC will automatically update and supersede this information.
We incorporate by reference the documents listed below and any future filings made with the SEC under Sections 13(a), 13(c), 14 or
15(d) of the Exchange Act (1) after the date of the initial registration statement, as amended, and prior to effectiveness of
the registration statement, and (2) after the date of this prospectus and prior to the termination of this offering. Such information
will automatically update and supersede the information contained in this prospectus and the documents listed below; provided, however,
that we are not, unless specifically indicated, incorporating any information furnished under Item 2.02 or Item 7.01 of any
current report on Form 8-K, whether listed below or filed in the future, or related exhibits furnished pursuant to Item 9.01
of Form 8-K:
We will provide to each person,
including any beneficial owner, to whom a copy of this prospectus is delivered, a copy of any or all of the information that we have incorporated
by reference into this prospectus. We will provide this information upon written or oral request at no cost to the requester. You may
request this information by contacting our corporate headquarters at the following address: 1 Bridge Plaza, Suite 275, Fort Lee,
NJ 07024, Attn: Ron Bentsur, or by calling (201) 614-315.
You should rely only on information
contained in, or incorporated by reference into, this prospectus. We have not authorized anyone to provide you with information different
from that contained in this prospectus or incorporated by reference in this prospectus.
Up to $40,000,000
Common stock
Prospectus Supplement
The date of this prospectus is ,
2023
PART II
INFORMATION NOT REQUIRED IN THE PROSPECTUS
ITEM 14. OTHER EXPENSES OF ISSUANCE AND DISTRIBUTION.
The table below itemizes the
expenses payable by the Registrant in connection with the registration and issuance of the securities being registered hereunder, other
than underwriting discounts and commissions. All amounts except the Securities and Exchange Commission registration fee are estimated.
Securities and Exchange Commission Registration Fee |
|
$ |
16,530 |
|
Legal Fees and Expenses |
|
$ |
* |
|
Accountants’ Fees and Expenses |
|
$ |
* |
|
Printing and Duplicating Expenses |
|
$ |
* |
|
Trustee’s Fees and Expenses |
|
$ |
* |
|
Miscellaneous Expenses |
|
$ |
* |
|
Total |
|
$ |
* |
|
| * | To be filed by amendment, Form 8-K or Rule 424 filing. |
ITEM 15. INDEMNIFICATION OF DIRECTORS AND OFFICERS.
Section 102 of the Delaware
General Corporation Law permits a corporation to eliminate the personal liability of its officers or directors to the company or its stockholders
for monetary damages for a breach of fiduciary duty as a director, except where the director breached his or her duty of loyalty, failed
to act in good faith, engaged in intentional misconduct or knowingly violated a law, authorized the payment of a dividend or approved
a stock repurchase in violation of Delaware corporate law or obtained an improper benefit. Our certificate of incorporation provides that
no officer or director shall be personally liable to us or our stockholders for monetary damages for any breach of fiduciary duty as an
officer or director, notwithstanding any provision of law imposing such liability, except to the extent that the Delaware General Corporation
Law prohibits the elimination or limitation of liability of officers or directors for breaches of fiduciary duty as described in the previous
sentence.
Section 145
of the Delaware General Corporation Law provides that a corporation has the power to indemnify a director, officer, employee or agent
of the corporation and certain other persons serving at the request of the corporation in related capacities against expenses (including
attorneys’ fees), judgments, fines and amounts paid in settlements actually and reasonably incurred by the person in connection
with an action, suit or proceeding to which he or she is party or is threatened to be made a party by reason of such position, if such
person acted in good faith and in a manner he or she reasonably believed to be in or not opposed to the best interests of the corporation,
and, in any criminal action or proceeding, had no reasonable cause to believe his or her conduct was unlawful, except that, in the case
of actions brought by or in the right of the corporation, no indemnification shall be made with respect to any claim, issue or matter
as to which such person shall have been adjudged to be liable to the corporation unless and only to the extent that the Court of Chancery
or other adjudicating court determines that, despite the adjudication of liability but in view of all of the circumstances of the case,
such person is fairly and reasonably entitled to indemnification for such expenses which the Court of Chancery or such other court shall
deem proper.
Our
certificate of incorporation provides that we will indemnify each person who was or is a party or threatened to be made a party to any
threatened, pending or completed action, suit or proceeding, whether civil, criminal, administrative or investigative (other than an action
by or in the right of us) by reason of the fact that he or she is or was, or has agreed to become, our director or officer, or is or was
serving, or has agreed to serve, at our request as a director, officer, partner, employee or trustee of, or in a similar capacity with,
another corporation, partnership, joint venture, trust or other enterprise (including any employee benefit plan) (all such persons being
referred to as an “Indemnitee”), or by reason of any action alleged to have been taken or omitted in such capacity, against
all expenses (including attorneys’ fees), liabilities, losses, judgments, fines, excise taxes and penalties arising under
the Employee Retirement Income Security Act of 1974, and amounts paid in settlement actually and reasonably incurred in connection with
such action, suit or proceeding and any appeal therefrom, if such Indemnitee acted in good faith and in a manner he or she reasonably
believed to be in, or not opposed to, our best interests, and, with respect to any criminal action or proceeding, he or she had no reasonable
cause to believe his or her conduct was unlawful.
Our
certificate of incorporation also provides that we will indemnify any Indemnitee who was or is a party to any threatened, pending or completed
action or suit by or in the right of us to procure a judgment in our favor by reason of the fact that the Indemnitee is or was, or has
agreed to become, our director or officer, or is or was serving, or has agreed to serve, at our request as a director, officer, partner,
employee or trustee of, or in a similar capacity with, another corporation, partnership, joint venture, trust or other enterprise (including
any employee benefit plan), or by reason of any action alleged to have been taken or omitted in such capacity, against all expenses (including
attorneys’ fees) and, to the extent permitted by law, amounts paid in settlement actually and reasonably incurred in connection
with such action, suit or proceeding, and any appeal therefrom, if the Indemnitee acted in good faith and in a manner he or she reasonably
believed to be in, or not opposed to, our best interests, except that no indemnification shall be made with respect to any claim, issue
or matter as to which such person shall have been adjudged to be liable to us, unless a court determines that, despite such adjudication
but in view of all of the circumstances, he or she is entitled to indemnification of such expenses. Notwithstanding the foregoing, to
the extent that any Indemnitee has been successful, on the merits or otherwise, he or she will be indemnified by us against all expenses
(including attorneys’ fees) actually and reasonably incurred by him or her or on his or her behalf in connection therewith. If we
don’t assume the defense, expenses must be advanced to an Indemnitee under certain circumstances.
We maintain a general liability
insurance policy which covers certain liabilities of our directors and officers arising out of claims based on acts or omissions in their
capacities as directors or officers.
ITEM 16. EXHIBITS.
| * | To be filed by amendment or as an exhibit to a document to be incorporated by reference herein in connection with an offering of our
securities to the extent applicable. |
| ** | To be filed, if necessary separately pursuant to Section 305(b)(2) of the Trust Indenture Act of 1939. |
ITEM 17. UNDERTAKINGS.
The undersigned registrant hereby undertakes:
(1) To
file, during any period in which offers or sales are being made, a post-effective amendment to this registration statement:
| (i) | To include any prospectus required by Section 10(a)(3) of the Securities Act of 1933; |
| (ii) | To reflect in the prospectus any facts or events arising after the effective date of the registration statement (or the most recent
post-effective amendment thereof) which, individually or in the aggregate, represent a fundamental change in the information set forth
in the registration statement. Notwithstanding the foregoing, any increase or decrease in volume of securities offered (if the total dollar
value of securities offered would not exceed that which was registered) and any deviation from the low or high end of the estimated maximum
offering range may be reflected in the form of prospectus filed with the Commission pursuant to Rule 424(b) if, in the aggregate,
the changes in volume and price represent no more than 20 percent change in the maximum aggregate offering price set forth in the “Calculation
of Registration Fee” table in the effective registration statement; |
| (iii) | To include any material information with respect to the plan of distribution not previously disclosed in the registration statement
or any material change to such information in the registration statement; |
Provided, however, That:
| (A) | Paragraphs (a)(1)(i) and (a)(1)(ii) of this section do not apply if the registration statement is on Form S-8
(§ 239.16b of this chapter), and the information required to be included in a post-effective amendment by those paragraphs is
contained in reports filed with or furnished to the Commission by the registrant pursuant to section 13 or section 15(d) of
the Securities Exchange Act of 1934 (15 U.S.C. 78m or 78o(d)) that are incorporated by reference in the registration statement; and |
| (B) | Paragraphs (a)(1)(i), (a)(1)(ii) and (a)(1)(iii) of this section do not apply if the registration statement is on Form S-3
(§ 239.13 of this chapter) or Form F-3 (§ 239.33 of this chapter) and the information required to be included
in a post-effective amendment by those paragraphs is contained in reports filed with or furnished to the Commission by the registrant
pursuant to section 13 or section 15(d) of the Securities Exchange Act of 1934 that are incorporated by reference in the
registration statement, or is contained in a form of prospectus filed pursuant to Rule 424(b) (§ 230.424(b) of
this chapter) that is part of the registration statement. |
| (C) | Provided further, however, that paragraphs (a)(1)(i) and (a)(1)(ii) do not apply if the registration statement is for
an offering of asset-backed securities on Form S-1 (§ 239.11 of this chapter) or Form S-3 (§ 239.13 of this
chapter), and the information required to be included in a post-effective amendment is provided pursuant to Item 1100(c) of
Regulation AB (§ 229.1100(c)). |
(2) That,
for the purpose of determining any liability under the Securities Act of 1933, each such post-effective amendment shall be deemed to be
a new registration statement relating to the securities offered therein, and the offering of such securities at that time shall be deemed
to be the initial bona fide offering thereof.
(3) To
remove from registration by means of a post-effective amendment any of the securities being registered which remain unsold at the termination
of the offering.
(5) That,
for the purpose of determining liability under the Securities Act of 1933 to any purchaser:
| (A) | Each prospectus filed by the registrant pursuant to Rule 424(b)(3) shall be deemed to be part of the Registration Statement
as of the date the filed prospectus was deemed part of and included in the Registration Statement; and |
| (B) | Each prospectus required to be filed pursuant to Rule 424(b)(2), (b)(5), or (b)(7) as part of a Registration Statement in
reliance on Rule 430B relating to an offering made pursuant to Rule 415(a)(1)(i), (vii), or (x) for the purpose of providing
the information required by Section 10(a) of the Securities Act of 1933 shall be deemed to be part of and included in the Registration
Statement as of the earlier of the date such form of prospectus is first used after effectiveness or the date of the first contract of
sale of securities in the offering described in the prospectus. As provided in Rule 430B, for liability purposes of the issuer and
any person that is at that date an underwriter, such date shall be deemed to be a new effective date of the Registration Statement relating
to the securities in the Registration Statement to which that prospectus relates, and the offering of such securities at that time shall
be deemed to be the initial bona fide offering thereof. Provided, however, that no statement made in a Registration Statement or prospectus
that is part of the Registration Statement or made in a document incorporated or deemed incorporated by reference into the Registration
Statement or prospectus that is part of the Registration Statement will, as to a purchaser with a time of contract of sale prior to such
effective date, supersede or modify any statement that was made in the Registration Statement or prospectus that was part of the Registration
Statement or made in any such document immediately prior to such effective date. |
(6) That,
for the purpose of determining liability of the registrant under the Securities Act of 1933 to any purchaser in the initial distribution
of the securities:
The undersigned registrant undertakes
that in a primary offering of securities of the undersigned registrant pursuant to this Registration Statement, regardless of the underwriting
method used to sell the securities to the purchaser, if the securities are offered or sold to such purchaser by means of any of the following
communications, the undersigned registrant will be a seller to the purchaser and will be considered to offer or sell such securities to
such purchaser:
| (i) | Any preliminary prospectus or prospectus of the undersigned registrant relating to the offering required to be filed pursuant to Rule 424; |
| (ii) | Any free writing prospectus relating to the offering prepared by or on behalf of the undersigned registrant or used or referred to
by the undersigned registrant; |
| (iii) | The portion of any other free writing prospectus relating to the offering containing material information about the undersigned registrant
or its securities provided by or on behalf of the undersigned registrant; and |
| (iv) | Any other communication that is an offer in the offering made by the undersigned registrant to the purchaser. |
B. Filings
Incorporating Subsequent Exchange Act Documents By Reference
The
undersigned registrant hereby undertakes that, for purposes of determining any liability under the Securities Act of 1933, each filing
of the registrant’s annual report pursuant to Section 13(a) or 15(d) of the Securities Exchange Act of 1934
(and, where applicable, each filing of an employee benefit plan’s annual report pursuant to Section 15(d) of the Securities
Exchange Act of 1934) that is incorporated by reference in the registration statement shall be deemed to be a new registration statement
relating to the securities offered therein, and the offering of such securities at that time shall be deemed to be the initial bona fide
offering thereof.
| H. | Request for Acceleration of Effective Date or Filing of Registration Statement Becoming Effective Upon Filing |
Insofar as indemnification for liabilities arising
under the Securities Act of 1933 may be permitted to directors, officers and controlling persons of the registrant pursuant to the foregoing
provisions, or otherwise, the registrant has been advised that in the opinion of the Securities and Exchange Commission such indemnification
is against public policy as expressed in the Act and is, therefore, unenforceable. In the event that a claim for indemnification against
such liabilities (other than the payment by the registrant of expenses incurred or paid by a director, officer or controlling person of
the registrant in the successful defense of any action, suit or proceeding) is asserted by such director, officer or controlling person
in connection with the securities being registered, the registrant will, unless in the opinion of its counsel the matter has been settled
by controlling precedent, submit to a court of appropriate jurisdiction the question whether such indemnification by it is against public
policy as expressed in the Securities Act of 1933 and will be governed by the final adjudication of such issue.
| I. | The undersigned registrant hereby undertakes that: |
| (1) | For purposes of determining any liability under the Securities Act of 1933, the information omitted from the form of prospectus filed
as part of this registration statement in reliance upon Rule 430A and contained in a form of prospectus filed by the registrant pursuant
to Rule 424(b)(1) or (4) or 497(h) under the Securities Act shall be deemed to be part of this registration statement
as of the time it was declared effective. |
| (2) | For the purpose of determining any liability under the Securities Act of 1933, each post-effective amendment that contains a form
of prospectus shall be deemed to be a new registration statement relating to the securities offered therein, and the offering of such
securities at that time shall be deemed to be the initial bona fide offering thereof. |
| J. | Qualification of Trust Indentures |
The undersigned registrant hereby undertakes to
file an application for the purpose of determining the eligibility of the trustee to act under subsection (a) of Section 310
of the Trust Indenture Act in accordance with the rules and regulations prescribed by the Commission under Section 305(b)(2) of
the Act.
SIGNATURES
Pursuant to the requirements of the Securities
Act of 1933, as amended, the registrant certifies that it has reasonable grounds to believe that it meets all of the requirements for
filing on Form S-3 and has duly caused this registration statement to be signed on its behalf by the undersigned, thereunto duly
authorized in the City of Fort Lee, State of New Jersey, on March 17, 2023.
|
NUVECTIS PHARMA, INC. |
|
|
|
|
|
|
Date: March 17, 2023 |
By: |
/s/ Ron Bentsur |
|
|
Ron Bentsur |
|
|
Chairman, Chief Executive Officer, and President |
|
|
(Principal Executive Officer) |
|
|
|
|
|
|
Date: March 17, 2023 |
By: |
/s/ Michael Carson |
|
|
Michael Carson |
|
|
Vice President of Finance |
|
|
(Principal Financial and Accounting Officer) |
POWER OF ATTORNEY
We,
the undersigned directors and/or executive officers of Nuvectis Pharma, Inc., hereby severally constitute and appoint Ron Bentsur,
acting singly, his true and lawful attorney-in-fact and agent, with full power of substitution and resubstitution, for him and his name,
for him in any and all capacities, to sign this report and to file the same, with all exhibits thereto and other documents in connection
therewith, and to sign any or all amendments (including pre-effective and post-effective amendments) to this registration statement, and
to file the same, with all exhibits thereto and other documents in connection therewith, including any Registration Statement filed pursuant
to Rule 462(b) under the Securities Act of 1933, with the United States Securities and Exchange Commission, granting
unto said attorney-in-fact and agent, full power and authority to do and perform each and every act and thing requisite and necessary
to be done in and about the premises, as fully to all intents and purposes as he might or could do in person, hereby ratifying and confirming
all that said attorney-in-fact and agent or any of his substitutes, may lawfully do or cause to be done by virtue hereof.
Pursuant to the requirements
of the Securities Act of 1933, as amended, this registration statement has been signed by the following persons in the capacities indicated
as of March 17, 2023.
Signatures |
|
Title |
|
|
|
/s/ Ron Bentsur |
|
Chairman, Chief Executive Officer, and President |
Ron Bentsur |
|
(Principal Executive Officer) |
|
|
|
/s/ Michael J. Carson |
|
Vice President of Finance |
Michael J. Carson |
|
(Principal Financial and Accounting Officer) |
|
|
|
/s/ Ron Bentsur |
|
Director |
Ron Bentsur |
|
|
|
|
|
/s/ Kenneth Hoberman |
|
Director |
Kenneth Hoberman |
|
|
|
|
|
/s/ James F. Olivero III |
|
Director |
James F. Olivero III |
|
|
|
|
|
/s/ Matthew L. Kaplan |
|
Director |
Matthew L. Kaplan |
|
|
|
|
|
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