BRANFORD, Conn., Dec. 20,
2024 /PRNewswire/ -- Azitra, Inc. (NYSE American:
AZTR), a clinical stage biopharmaceutical company focused on
developing innovative therapies for precision dermatology, today
announced the company will present at Biotech Showcase 2025 being
held January 13-15, 2025 in
San Francisco.
Details of the presentation are as follows:
Event:
|
Biotech Showcase
2025
|
Date and
Time:
|
January 13, 2025 at
3:00 p.m., PT
|
Location:
|
Hilton San Francisco
Union Square (Yosemite C)
|
Participant:
|
Travis Whitfill, Chief
Operating Officer
|
Registration:
|
Link
|
During the conference, members of Azitra's management team will
conduct one-on-one meetings with registered investors and potential
partners, showcasing the company's business and clinical
development strategy, recent corporate achievements, and
anticipated milestones.
Biotech Showcase, produced by Demy-Colton and EBD Group, is a
premier investor conference committed to creating a platform for
private and micro-mid-cap biotechnology companies. It offers
companies a unique opportunity to showcase their innovations and
engage directly with investors and other biopharmaceutical
executives.
About Azitra, Inc.
Azitra, Inc. is a clinical stage biopharmaceutical company
focused on developing innovative therapies for precision
dermatology. The Company's lead product, ATR-12, is an engineered
strain of S. epidermidis designed to treat Netherton
syndrome, a rare, chronic skin disease with no approved treatment
options. Netherton syndrome is often fatal in infancy with those
living beyond a year having profound lifelong challenges. ATR-12 is
being evaluated in a Phase 1b
clinical trial in adult Netherton syndrome patients. ATR-04,
Azitra's next most advanced product, is being developed for the
treatment of EGFR inhibitor ("EGFRi") associated rash. Azitra has
received Fast Track designation from the FDA for EGFRi associated
rash, which impacts approximately 150,000 people in the U.S. Azitra
has an open IND for a Phase 1/2 clinical trial with ATR-04 in
patients with EGFRi associated rash. ATR-12 and ATR-04 were
developed from Azitra's proprietary platform of engineered proteins
and topical live biotherapeutic products that includes a microbial
library comprised of approximately 1,500 bacterial strains. The
platform is augmented by artificial intelligence and machine
learning technology that analyzes, predicts, and helps screen the
library of strains for drug like molecules. For more information,
please visit https://azitrainc.com.
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 expected
timing of the presentation of data from the Phase 1b study of ATR-12, the filing of an IND
application, and the presentation of data from our Phase
1b for ATR-04, the IND filing for
ATR-01, the timing of having a signed license agreement with Bayer,
and statements about our clinical and pre-clinical programs, and
corporate and clinical/pre-clinical 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 complete
our Phase 1b trial for ATR-12; we may
experience delays in the initiation of our Phase 1/2 trial for
ATR-04; our product candidates may not be effective; there may be
delays in regulatory approval or changes in regulatory framework
that are out of our control; our estimation of addressable markets
of our product candidates may be inaccurate; we may fail to timely
raise 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 attract and retain
key employees and qualified personnel; earlier study results may
not be predictive of later stage study outcomes; 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 Azitra's programs and operations are
described or incorporated by reference in our prospectus dated
July 23, 2024 filed with the SEC on
July 25, 2024 in our most recent
quarterly report on Form 10-Q filed with the SEC on November 12, 2024. Azitra explicitly disclaims
any obligation to update any forward-looking statements except to
the extent required by law.
Contact
Norman Staskey
Chief Financial Officer
staskey@azitrainc.com
Investor Relations
Tiberend Strategic Advisors, Inc.
Jon Nugent
205-566-3026
jnugent@tiberend.com
Media Relations
Tiberend Strategic Advisors, Inc.
Casey McDonald
646-577-8520
cmcdonald@tiberend.com
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SOURCE Azitra, Inc.