Mereo BioPharma to Participate in Fireside Chat at the 23rd Annual Needham Virtual Healthcare Conference
03 Aprile 2024 - 1:30PM
Mereo BioPharma Group plc (NASDAQ: MREO) (“Mereo” or the
“Company”), a clinical-stage biopharmaceutical company focused on
rare diseases, today announced that Dr. Denise Scots-Knight, Chief
Executive Officer, will participate in a Fireside Chat at the 23rd
Annual Needham Virtual Healthcare Conference on Tuesday, April 9,
2024, at 10:15am ET / 03:15pm BST.
A live audio webcast of the presentation can be
accessed through the Investors section of the Company’s website at
www.mereobiopharma.com/investors. An archived replay of the
webcast will be available on the Company’s website for two weeks
following the live event.
About Mereo BioPharma
Mereo BioPharma is a biopharmaceutical company
focused on the development of innovative therapeutics for rare
diseases. The Company has two rare disease product candidates,
setrusumab for the treatment of osteogenesis imperfecta (OI) and
alvelestat primarily for the treatment of severe
alpha-1-antitrypsin deficiency-associated lung disease (AATD-LD).
The Company’s partner, Ultragenyx Pharmaceutical, Inc., has
initiated the Phase 3 portion of a pivotal Phase 2/3 pediatric
study in young adults (5 to <26 years old) for setrusumab in OI
and a Phase 3 study in pediatric patients (2 to <7 years old) in
the first half of 2023. The partnership with Ultragenyx includes
potential milestone payments of up to $245 million (following the
recent $9 million milestone) and royalties to Mereo on commercial
sales in Ultragenyx territories. Mereo has retained EU and UK
commercial rights and will pay Ultragenyx royalties on commercial
sales in those territories. Setrusumab has received orphan
designation for osteogenesis imperfecta from the EMA and FDA, PRIME
designation from the EMA and has pediatric disease designation from
the FDA. Alvelestat has received U.S. Orphan Drug Designation for
the treatment of AATD, Fast Track designation from the FDA.
Following results from ASTRAEUS and ATALANTa in AATD-lung disease,
the Company has aligned with the FDA and the EMA on the primary
endpoints for a Phase 3 pivotal study which if successful could
enable full approval in both the US and Europe. In addition to the
rare disease programs, Mereo has two oncology product candidates in
clinical development. Etigilimab (anti-TIGIT) has completed a Phase
1b/2 basket study evaluating its safety and efficacy in combination
with an anti-PD-1 in a range of tumor types including three rare
tumors and three gynecological carcinomas – cervical, ovarian,
and endometrial and is an ongoing Phase 1b/2 investigator led study
at the MD Anderson Cancer Center in clear cell ovarian cancer;
Navicixizumab, for the treatment of late line ovarian cancer, has
completed a Phase 1 study and has been partnered with Feng
Biosciences Inc. in a global licensing agreement that includes
milestone payments of up to $300 million and royalties. Mereo has
entered into an exclusive global license agreement with ReproNovo
SA for the development and commercialization of leflutrozole, a
non-steroidal aromatase inhibitor. Under the terms of the
agreement, ReproNovo, a reproductive medicine company, is
responsible for all future development and commercialization of
leflutrozole and Mereo is eligible to receive milestone payments of
up to $64.3 million and royalties.
For more information on Mereo BioPharma, please
visit www.mereobiopharma.com.
Forward-Looking Statements
This press release contains “forward-looking
statements” that involve substantial risks and uncertainties. All
statements other than statements of historical fact contained
herein are forward-looking statements within the meaning of Section
27A of the United States Securities Act of 1933, as amended, and
Section 21E of the United States Securities Exchange Act of 1934,
as amended. Forward-looking statements usually relate to future
events and anticipated revenues, earnings, cash flows or other
aspects of our operations or operating results. Forward-looking
statements are often identified by the words “believe,” “expect,”
“anticipate,” “plan,” “intend,” “foresee,” “should,” “would,”
“could,” “may,” “estimate,” “outlook” and similar expressions,
including the negative thereof. The absence of these words,
however, does not mean that the statements are not forward-looking.
These forward-looking statements are based on the Company’s current
expectations, beliefs and assumptions concerning future
developments and business conditions and their potential effect on
the Company. While management believes that these forward-looking
statements are reasonable as and when made, there can be no
assurance that future developments affecting the Company will be
those that it anticipates.
All of the Company’s forward-looking statements
involve known and unknown risks and uncertainties some of which are
significant or beyond its control and assumptions that could cause
actual results to differ materially from the Company’s historical
experience and its present expectations or projections. Such risks
and uncertainties include, among others, the uncertainties inherent
in the clinical development process; the Company’s reliance on
third parties to conduct and provide funding for its clinical
trials; the Company’s dependence on enrollment of patients in its
clinical trials; and the Company’s dependence on its key
executives. You should carefully consider the foregoing factors and
the other risks and uncertainties that affect the Company’s
business, including those described in the “Risk Factors” section
of its Annual Report on Form 10-K, as well as discussions of
potential risks, uncertainties, and other important factors in the
Company’s subsequent filings with the Securities and Exchange
Commission. The Company wishes to caution you not to place undue
reliance on any forward-looking statements, which speak only as of
the date hereof. The Company undertakes no obligation to publicly
update or revise any of our forward-looking statements after the
date they are made, whether as a result of new information, future
events or otherwise, except to the extent required by law.
Mereo BioPharma Contacts: |
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Mereo |
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+44 (0)333 023 7300 |
Denise Scots-Knight, Chief Executive Officer |
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Christine Fox, Chief Financial Officer |
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Burns McClellan (Investor Relations Adviser to
Mereo) |
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+01 646 930 4406 |
Lee Roth |
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Investors |
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investors@mereobiopharma.com |
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