PepGen Announces Upcoming Data Presentations at the 2023 American Academy of Neurology Annual Meeting
April 17 2023 - 7:00AM
PepGen Inc. (Nasdaq: PEPG), a clinical-stage biotechnology company
advancing the next generation of oligonucleotide therapies with the
goal of transforming the treatment of severe neuromuscular and
neurological diseases, today announced that it will present at the
2023 American Academy of Neurology (AAN) Annual Meeting, taking
place on April 22-27, 2023 in Boston, Massachusetts.
Oral Presentation:
Title: Preclinical Data Supporting the
Development of an Enhanced Delivery Oligonucleotide (EDO) for the
Treatment of Myotonic Dystrophy Type 1 (DM1)Program
Number: S48.001Session Topic:
Therapeutics for Muscle Disease Date & Time:
Thursday, April 27, 2023 at 3:30pm ETPresenter:
Ashling Holland, Ph.D., Director of Preclinical Development
Poster Presentation:
Title: Preclinical Data Supporting the
Development of an Enhanced Delivery Oligonucleotide (EDO) for the
Treatment of Duchenne Muscular Dystrophy (DMD)Program
Number: P3.002Session Topic:
Neuromuscular Disease: Inherited Muscle Disorders 1 Date
& Time: Sunday, April 23, at 5:30pm ET
Presenter: Ashling Holland, Ph.D., Director of
Preclinical Development
Title: PGN-EDO51, an Enhanced Delivery
Oligonucleotide (EDO) for the Treatment of Duchenne Muscular
Dystrophy (DMD): Results of a Phase 1 Study in Healthy
VolunteersProgram Number: P3.004Session
Topic: Neuromuscular Disease: Inherited Muscle Disorders 1
Date & Time: Sunday, April 23, at 5:30pm
ETPresenter: Michelle Mellion, M.D., Senior Vice
President, Head of Clinical Development
Title: Design of a Phase 1, Placebo-Controlled
Study to Assess the Safety, Tolerability, Pharmacokinetics, and
Pharmacodynamics of Single-Ascending Doses of PGN-EDODM1 in Adult
Participants with Myotonic Dystrophy Type 1 (DM1)Program
Number: P6.004Session Topic:
Neuromuscular Disease: Inherited Muscle Disorders 3 Date
& Time: Monday, April 24, at 5:30pm
ETPresenter: Michelle Mellion, M.D., Senior Vice
President, Head of Clinical Development
About PepGen
PepGen Inc. is a clinical-stage biotechnology company advancing
the next-generation of oligonucleotide therapies with the goal of
transforming the treatment of severe neuromuscular and neurological
diseases. PepGen’s Enhanced Delivery Oligonucleotide, or EDO,
platform is founded on over a decade of research and development
and leverages cell-penetrating peptides to improve the uptake and
activity of conjugated oligonucleotide therapeutics. Using these
EDO peptides, we are generating a pipeline of oligonucleotide
therapeutic candidates that target the root cause of serious
diseases.
Forward-Looking Statements
This press release contains forward-looking
statements within the meaning of the Private Securities Litigation
Reform Act of 1995, as amended. These statements may be identified
by words such as “aims,” “anticipates,” “believes,” “could,”
“estimates,” “expects,” “forecasts,” “goal,” “intends,” “may,”
“plans,” “possible,” “potential,” “seeks,” “will,” and variations
of these words or similar expressions that are intended to identify
forward-looking statements. Any such statements in this press
release that are not statements of historical fact may be deemed to
be forward-looking statements. These forward-looking statements
include, without limitation, statements regarding the potential
therapeutic benefits and safety profile of our candidates,
initiation of the Phase 2 studies in PGN-EDO51 and the Phase 1
study in PGN-EDODM1, our interpretation of clinical and preclinical
study results and how they may impact our programs, the filing of
an IND application for PGN-EDODM1, scheduled participation and
presentation of information in conferences and statements about our
clinical and preclinical programs, product candidates, expected
cash runway, achievement of milestones, and corporate and
clinical/preclinical strategies.
Any forward-looking statements in this press
release are based on current expectations, estimates and
projections only as of the date of this release 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 that we may fail to
successfully initiate or complete our planned clinical trials for
PGN-EDO51 and and PGN-EDODM1 and preclinical studies of other
product candidates or to obtain regulatory approval before
commercialization for marketing of such products; our
interpretation of clinical and preclinical study results may be
incorrect; our product candidates may not be safe and effective;
there may be delays in regulatory approval or changes in regulatory
framework that are out of our control; we may not be able to
nominate new drug candidates within the estimated timeframes; our
estimation of addressable markets of our product candidates may be
inaccurate; we may need additional funding before the end of our
expected cash runway and may fail to timely raise such additional
required funding; more efficient competitors or more effective
competing treatment may emerge; we may be involved in disputes
surrounding the use of our intellectual property crucial to our
success; we may not be able to take advantage of certain
accelerated regulatory pathways; we may not be able to attract and
retain key employees and qualified personnel; earlier study results
may not be predictive of later stage study outcomes; we may
encounter liquidity distress due to failure of financial
institutions with which we maintain relationship; and we are
dependent on third parties for some or all aspects of our product
manufacturing, research and preclinical and clinical testing.
Additional risks concerning PepGen’s programs and operations are
described in its registration statement on Form S-1, which is on
file with the SEC, and in its most recent annual report on Form
10-K to be filed with the SEC. PepGen explicitly disclaims any
obligation to update any forward-looking statements except to the
extent required by law.
Investor Contact
Laurence Watts
Gilmartin Group
Laurence@gilmartinir.com
Media Contact
Sarah Sutton
Argot Partners
pepgen@argotpartners.com
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