Iterum Therapeutics plc (Nasdaq: ITRM), (Iterum) a clinical-stage
pharmaceutical company focused on developing next generation oral
and IV antibiotics to treat infections caused by multi-drug
resistant pathogens in both community and hospital settings, today
reported financial results for the first quarter ended March 31,
2024.
“We are pleased to have recently resubmitted our new drug
application (NDA) for oral sulopenem just three months after
reporting positive topline data from our REASSURE trial in January
2024,” said Corey Fishman, Iterum’s Chief Executive Officer. “We
continue to believe that the strong results from this trial, which
was conducted under a Special Protocol Assessment (SPA) agreement
with the U.S. Food and Drug Administration (FDA), addresses the
FDA’s recommendations for additional data to support approval of
oral sulopenem for the treatment of adult women with uncomplicated
urinary tract infections (uUTIs). The potential approval of oral
sulopenem would mark the first oral penem approved in the U.S., and
the second antibiotic approved for the treatment of uUTIs over the
past 25 years.”
Highlights and Recent Events
- NDA Review Underway: Iterum began enrollment
in its pivotal Phase 3 clinical trial, REASSURE
(REnewed ASsessment of
Sulopenem in uUTI caused by
Resistant Enterobacterales), for
the treatment of uUTIs in adult women in October 2022 and completed
enrollment in October 2023 enrolling 2,222 patients. Iterum
reported positive topline data in January 2024 and resubmitted its
NDA in April 2024. Provided the FDA is satisfied that the
resubmitted NDA addresses all of the deficiencies identified in the
Complete Response Letter (CRL) Iterum received from the FDA in July
2021, Iterum expects that the FDA will complete its review and take
action six months from the date the FDA received the resubmitted
NDA (or early in the fourth quarter of 2024).
- Extended Cash Runway: During the first quarter
of 2024, Iterum sold 3.0 million ordinary shares under an
at-the-market offering (ATM) agreement, at an average price of
$2.51 per share for net proceeds of $7.2 million, which has
extended its cash runway into 2025 based on its current operating
plan. As of April 30, 2024, Iterum had approximately 16.6 million
ordinary shares outstanding.
First Quarter 2024 Financial
Results
Cash, cash equivalents and short-term
investments were $18.2 million at March 31, 2024. Based on Iterum’s
current operating plan, Iterum expects that its current cash, cash
equivalents and short-term investments will be sufficient to fund
its operations into 2025, including through the expected
Prescription Drug User Fee Act (PDUFA) date early in the fourth
quarter of 2024.
Research and development (R&D) expenses for the first
quarter 2024 were $4.0 million compared to $6.4 million for the
same period in 2023. The decrease for the three-month period was
primarily due to higher costs incurred in 2023 to support our
REASSURE trial, which began enrollment in October 2022 and
completed enrollment in October 2023.
General and administrative (G&A) expenses for the first
quarter 2024 were $2.2 million compared to $2.1 million for the
same period in 2023. The increase for the three-month period was
primarily due to an increase in legal fees and an increase in
consultants used to support pre-commercial activities.
Net loss for the first quarter 2024 was $7.1 million compared to
a net loss of $9.9 million for the same period in 2023. Non-GAAP1
net loss for the first quarter 2024 was $5.8 million compared to a
non-GAAP1 net loss of $7.4 million in 2024.
Conference Call Details
- Iterum will host a conference call today, Monday, May 13, 2024
at 8:30 a.m. Eastern Time. The dial-in information for the call is
as follows: United States: 1 833 470 1428; International: 1 404 975
4839; Access code: 818440
About Iterum Therapeutics plc
Iterum Therapeutics plc is a clinical-stage pharmaceutical
company dedicated to developing differentiated anti-infectives
aimed at combatting the global crisis of multi-drug resistant
pathogens to significantly improve the lives of people affected by
serious and life-threatening diseases around the world. Iterum is
currently advancing its first compound, sulopenem, a novel penem
anti-infective compound, in Phase 3 clinical development with an
oral formulation.Sulopenem also has an IV formulation. Sulopenem
has demonstrated potent in vitro activity against a wide variety of
gram-negative, gram-positive and anaerobic bacteria resistant to
other antibiotics. Iterum has received Qualified Infectious Disease
Product (QIDP) and Fast Track designations for its oral and IV
formulations of sulopenem in seven indications. For more
information, please visit http://www.iterumtx.com.
Non-GAAP Financial Measures
To supplement Iterum’s financial results presented in accordance
with U.S. generally accepted accounting principles (“GAAP”), Iterum
presents non-GAAP net loss and non-GAAP net loss per share to
exclude from reported GAAP net loss and GAAP net loss per share,
share-based compensation expense ($0.1 million); the interest
expense associated with accrued interest on the Exchangeable Notes,
payable in cash, shares or a combination of both upon exchange,
redemption or at January 31, 2025 (“the Maturity Date”), whichever
is earlier ($0.2 million); the non-cash amortization of the
Exchangeable Notes ($0.6 million); and the non-cash adjustments to
the fair value of the Royalty-Linked Notes ($0.4 million) for the
three months ended March 31, 2024, and intangible asset
amortization ($0.4 million); share-based compensation expense ($0.4
million); the interest expense associated with accrued interest on
the Exchangeable Notes payable in cash, shares or a combination of
both upon exchange, redemption or at the Maturity Date, whichever
is earlier ($0.2 million); the non-cash amortization of the
Exchangeable Notes ($0.6 million); and the non-cash adjustments to
the fair value of derivatives and Royalty-Linked Notes ($0.9
million) for the three months ended March 31, 2023,
respectively.
Iterum believes that the presentation of non-GAAP net loss and
non-GAAP net loss per share, when viewed with its results under
GAAP and the accompanying reconciliation, provides useful
supplementary information to, and facilitates additional analysis
by, investors, analysts, and Iterum’s management in assessing
Iterum’s performance and results from period to period. These
non-GAAP financial measures closely align with the way management
measures and evaluates Iterum’s performance. These non-GAAP
financial measures should be considered in addition to, and not a
substitute for, or superior to, net (loss) / income or other
financial measures calculated in accordance with GAAP. Non-GAAP net
loss and non-GAAP net loss per share are not based on any
standardized methodology prescribed by GAAP and represents GAAP net
loss, which is the most directly comparable GAAP measure, adjusted
to exclude intangible asset amortization; share-based compensation
expense; the interest expense associated with accrued interest on
the Exchangeable Notes payable in cash, shares or a combination of
both upon exchange, redemption or at the Maturity Date, whichever
is earlier; the non-cash amortization of the Exchangeable Notes;
and the non-cash adjustments to the fair value of derivatives and
Royalty-Linked Notes for the three months ended March 31, 2024 and
March 31, 2023. Because of the non-standardized definitions of
non-GAAP financial measures, non-GAAP net loss and non-GAAP net
loss per share used by Iterum in this press release and
accompanying tables has limits in its usefulness to investors and
may be calculated differently from, and therefore may not be
directly comparable to, similarly titled measures used by other
companies. A reconciliation of non-GAAP net loss to GAAP net loss
and non-GAAP net loss per share to GAAP net loss per share have
been provided in the tables included in this press release.
Special Note Regarding Forward Looking
Statements
This press release contains forward-looking statements within
the meaning of The Private Securities Litigation Reform Act of
1995. These forward-looking statements include, without limitation,
statements regarding Iterum’s plans, strategies and prospects for
its business, including the development, therapeutic and market
potential of sulopenem, Iterum’s ability to address the
deficiencies set out in the CRL received in July 2021, the expected
timing of review of the resubmitted NDA by the FDA, potential
action by the FDA with respect to the resubmitted NDA, the
sufficiency of Iterum’s cash resources to fund its operating
expenses into 2025, and Iterum’s strategic process to sell,
license, or otherwise dispose of its rights to sulopenem. In some
cases, forward-looking statements can be identified by words such
as “may,” “believes,” “intends,” “seeks,” “anticipates,” “plans,”
“estimates,” “expects,” “should,” “assumes,” “continues,” “could,”
“would,” “will,” “future,” “potential” or the negative of these or
similar terms and phrases. Forward-looking statements involve known
and unknown risks, uncertainties and other factors that may cause
Iterum’s actual results, performance or achievements to be
materially different from any future results, performance or
achievements expressed or implied by the forward-looking
statements. Forward-looking statements include all matters that are
not historical facts. Actual future results may be materially
different from what is expected due to factors largely outside
Iterum’s control, including uncertainties inherent in the design,
initiation and conduct of clinical and non-clinical development,
changes in regulatory requirements or decisions of regulatory
authorities, the timing or likelihood of regulatory filings and
approvals, changes in public policy or legislation,
commercialization plans and timelines, if oral sulopenem is
approved, the actions of third-party clinical research
organizations, suppliers and manufacturers, the accuracy of
Iterum’s expectations regarding how far into the future Iterum’s
cash on hand will fund Iterum’s ongoing operations, the sufficiency
of Iterum’s cash resources and the Company’s ability to continue as
a going concern, Iterum’s ability to maintain its listing on the
Nasdaq Capital Market, risks and uncertainties concerning the
outcome, impact, effects and results of Iterum’s pursuit of
strategic alternatives, including the terms, timing, structure,
value, benefits and costs of any strategic process and Iterum’s
ability to complete one whether on attractive terms at all and
other factors discussed under the caption “Risk Factors” in its
Annual Report on Form 10-Q filed with the SEC on May 13, 2024, and
other documents filed with the SEC from time to time.
Forward-looking statements represent Iterum’s beliefs and
assumptions only as of the date of this press release. Except as
required by law, Iterum assumes no obligation to update these
forward-looking statements publicly, or to update the reasons
actual results could differ materially from those anticipated in
the forward-looking statements, even if new information becomes
available in the future.
Investor Contact:Judy MatthewsChief Financial
Officer 312-778-6073IR@iterumtx.com
ITERUM
THERAPEUTICS PLC |
Condensed
Consolidated Statement of Operations |
(In
thousands except share and per share data) |
(Unaudited) |
|
|
|
|
|
Three Months
Ended March 31, |
|
|
|
2024 |
|
|
|
2023 |
|
Operating
expenses: |
|
|
|
|
Research and
development |
|
|
(3,977 |
) |
|
|
(6,432 |
) |
General and
administrative |
|
|
(2,186 |
) |
|
|
(2,098 |
) |
Total
operating expenses |
|
|
(6,163 |
) |
|
|
(8,530 |
) |
Operating
loss |
|
|
(6,163 |
) |
|
|
(8,530 |
) |
Interest
expense, net |
|
|
(487 |
) |
|
|
(399 |
) |
Adjustments
to fair value of derivatives |
|
|
(386 |
) |
|
|
(878 |
) |
Other
(expense) / income, net |
|
|
(17 |
) |
|
|
41 |
|
Income tax
expense |
|
|
(48 |
) |
|
|
(123 |
) |
Net
loss |
|
$ |
(7,101 |
) |
|
$ |
(9,889 |
) |
Net loss per
share – basic and diluted |
|
$ |
(0.46 |
) |
|
$ |
(0.78 |
) |
Weighted
average ordinary shares outstanding – basic and diluted |
|
|
15,432,693 |
|
|
|
12,681,900 |
|
|
|
|
|
|
Reconciliation of non-GAAP net loss to GAAP net loss |
|
|
|
|
Net loss -
GAAP |
|
$ |
(7,101 |
) |
|
$ |
(9,889 |
) |
Intangible
asset amortization |
|
|
— |
|
|
|
429 |
|
Share based
compensation |
|
|
138 |
|
|
|
393 |
|
Interest
expense - accrued interest and amortization on exchangeable
notes |
|
|
750 |
|
|
|
783 |
|
Adjustments
to fair value of derivatives |
|
|
386 |
|
|
|
878 |
|
Non-GAAP net
loss |
|
$ |
(5,827 |
) |
|
$ |
(7,406 |
) |
Net loss per
share - basic and diluted |
|
$ |
(0.46 |
) |
|
$ |
(0.78 |
) |
Non-GAAP net
loss per share - basic and diluted |
|
$ |
(0.38 |
) |
|
$ |
(0.58 |
) |
|
|
|
|
|
|
ITERUM
THERAPEUTICS PLC |
Condensed
Consolidated Balance Sheet Data |
(In
thousands) |
(Unaudited) |
|
|
|
|
|
|
|
As
of |
|
As
of |
|
|
March 31, |
|
December 31, |
|
|
|
2024 |
|
|
|
2023 |
|
Cash, cash
equivalents and short-term investments |
|
$ |
18,214 |
|
|
$ |
23,930 |
|
Other
assets |
|
|
1,411 |
|
|
|
2,329 |
|
Total assets |
|
$ |
19,625 |
|
|
$ |
26,259 |
|
Exchangeable
notes |
|
$ |
12,203 |
|
|
$ |
11,453 |
|
Royalty-linked notes |
|
|
7,889 |
|
|
|
7,503 |
|
Other
liabilities |
|
|
5,683 |
|
|
|
13,706 |
|
Total
liabilities |
|
|
25,775 |
|
|
|
32,662 |
|
Total
shareholders' deficit |
|
|
(6,150 |
) |
|
|
(6,403 |
) |
Total liabilities and shareholders' deficit |
|
$ |
19,625 |
|
|
$ |
26,259 |
|
|
|
|
|
|
1 Definition and reconciliations of applicable GAAP reported to
non-GAAP adjusted information are included at the end of this press
release
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