Inozyme Pharma, Inc. (Nasdaq: INZY) (“the Company” or
“Inozyme”), a clinical-stage biopharmaceutical company developing
innovative therapeutics for rare diseases that affect bone health
and blood vessel function, today announced the appointment of Erik
Harris to its Board of Directors, effective October 3, 2024. Mr.
Harris, who currently serves as Chief Commercial Officer and
Executive Vice President at Ultragenyx, brings to Inozyme over 20
years of commercial expertise within the biopharma industry.
“It is a privilege to welcome Erik to the
Inozyme Board of Directors at this exciting juncture for Inozyme as
we continue to lay the groundwork for our transition into a
commercial-stage company,” said Douglas A. Treco, Ph.D., CEO and
Chairman of Inozyme Pharma. “Erik’s track record of spearheading
successful launches for rare disease therapies, combined with his
deep commercial insights, will be invaluable as we advance INZ-701
through late-stage development and prepare to bring this important
program to patients.”
Mr. Harris added: “INZ-701 holds significant
promise as an important new therapy for a broad range of serious
rare diseases affecting bone health and blood vessel function. I
look forward to collaborating with Inozyme’s talented team as they
work toward unlocking the full potential of this innovative therapy
for patients who urgently need it.”
Prior to his appointment as Chief Commercial
Officer, Mr. Harris served as the Senior Vice President and Head of
North American Commercial Operations at Ultragenyx. Before joining
Ultragenyx, he spent six years at Crescendo Bioscience, most
recently as Vice President of Commercial. Earlier in his career,
Mr. Harris served as Vice President of Marketing at Intermune,
Inc., and held positions in the commercial organizations at Elan
Pharmaceuticals, Inc., Genentech, Inc., and Bristol-Myers Squibb
Company. He currently serves on the Board of Directors at Denali
Therapeutics.
At the start of his professional career, Mr.
Harris served as a Lieutenant Commander in Naval Aviation and
Congressional Fellow for the United States Navy. Mr. Harris
received his M.B.A. from the Wharton School of Business, and a B.S.
from the United States Naval Academy.
About Inozyme Pharma
Inozyme Pharma is a pioneering clinical-stage
biopharmaceutical company dedicated to developing innovative
therapeutics for rare diseases that affect bone health and blood
vessel function. We are experts in the PPi-Adenosine Pathway, where
the ENPP1 enzyme generates inorganic pyrophosphate (PPi), which
regulates mineralization, and adenosine, which controls intimal
proliferation (the overgrowth of smooth muscle cells inside blood
vessels). Disruptions in this pathway impact the levels of these
molecules, leading to severe musculoskeletal, cardiovascular, and
neurological conditions, including ENPP1 Deficiency, ABCC6
Deficiency, calciphylaxis, and ossification of the posterior
longitudinal ligament (OPLL).
Our lead candidate, INZ-701, is an ENPP1 Fc
fusion protein enzyme replacement therapy (ERT) designed to
increase PPi and adenosine, enabling the potential treatment of
multiple diseases caused by deficiencies in these molecules. It is
currently in clinical development for the treatment of ENPP1
Deficiency, ABCC6 Deficiency, and calciphylaxis. By targeting the
PPi-Adenosine Pathway, INZ-701 aims to correct pathological
mineralization and intimal proliferation, addressing the
significant morbidity and mortality in these devastating
diseases.
For more information, please
visit https://www.inozyme.com/ or follow Inozyme
on LinkedIn, X, and Facebook.
Cautionary Note Regarding Forward-Looking
Statements
Statements in this press release about future
expectations, plans, and prospects, as well as any other statements
regarding matters that are not historical facts, may constitute
"forward-looking statements" within the meaning of The Private
Securities Litigation Reform Act of 1995. These statements include,
but are not limited to, statements relating to the initiation,
timing, and design of our planned clinical trials, availability of
data from clinical trials, the potential benefits of INZ-701, our
regulatory strategy, including our planned pathway to approval for
the ABCC6 Deficiency program, and the period over which we believe
that our existing cash, cash equivalents, and short-term
investments will be sufficient to fund our cash flow requirements.
The words "anticipate," "believe," "continue," "could," "estimate,"
"expect," "intend," "may," "plan," "potential," "predict,"
"project," "should," "target," "will," "would," and similar
expressions are intended to identify forward-looking statements,
although not all forward-looking statements contain these
identifying words. Any forward-looking statements are based on
management's current expectations of future events and are subject
to a number of risks and uncertainties that could cause actual
results to differ materially and adversely from those set forth in,
or implied by, such forward-looking statements. These risks and
uncertainties include, but are not limited to, risks associated
with the Company's ability to conduct its ongoing clinical trials
of INZ-701 for ENPP1 Deficiency, ABCC6 Deficiency, and
calciphylaxis; enroll patients in ongoing and planned trials;
obtain and maintain necessary approvals from the FDA and other
regulatory authorities; continue to advance its product candidates
in preclinical studies and clinical trials; replicate in later
clinical trials positive results found in preclinical studies and
early-stage clinical trials of its product candidates; advance the
development of its product candidates under the timelines it
anticipates in planned and future clinical trials; obtain,
maintain, and protect intellectual property rights related to its
product candidates; manage expenses; comply with covenants under
its outstanding loan agreement; and raise the substantial
additional capital needed to achieve its business objectives. For a
discussion of other risks and uncertainties, and other important
factors, any of which could cause the Company's actual results to
differ from those contained in the forward-looking statements, see
the "Risk Factors" section in the Company's most recent Annual
Report on Form 10-K filed with the Securities and Exchange
Commission, as well as discussions of potential risks,
uncertainties, and other important factors, in the Company's most
recent filings with the Securities and Exchange Commission. In
addition, the forward-looking statements included in this press
release represent the Company's views as of the date hereof and
should not be relied upon as representing the Company's views as of
any date subsequent to the date hereof. The Company anticipates
that subsequent events and developments will cause the Company's
views to change. However, while the Company may elect to update
these forward-looking statements at some point in the future, the
Company specifically disclaims any obligation to do so.
Contacts
Investors:Inozyme PharmaStefan Riley, Senior Director of IR and
Corporate Communications(857) 330-8871stefan.riley@inozyme.com
Media:Biongage CommunicationsTodd Cooper(617)
840-1637Todd@biongage.com
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