Claims cover methods of treating a subject
presenting with fatigue from post-acute sequelae of COVID-19
(PASC), a/k/a Long COVID, with Candidate AXA1125
Axcella Therapeutics (Nasdaq: AXLA), a clinical-stage
biotechnology company focused on pioneering a new approach to
address the biology of complex diseases using compositions of
endogenous metabolic modulators (EMMs), today announced that the
U.S. Patent and Trademark Office (USPTO) has granted U.S. Patent
No. 11,737,999 with claims covering methods of use of Candidate
AXA1125, for treating a subject having post-acute sequelae of
COVID-19 (PASC), a/k/a Long COVID, particularly fatigue. The patent
was issued on August 29, 2023, with anticipated expiration in
2042.
“Today’s issuance expands our global patent portfolio and
Axcella’s protection of its lead candidate, AXA1125,” said Paul F.
Fehlner, J.D., Ph.D., Senior Vice President, Chief Legal Officer of
Axcella. “These patents and our entire portfolio are fully owned by
Axcella.”
AXA1125 is a novel composition of EMMs designed to
simultaneously support metabolic, inflammatory and fibrotic
pathways associated with fatigue. Axcella was previously granted
patents related to AXA1125 with claims covering methods of use and
compositions. In particular, Patents Nos. 10,201,513, 10,471,034,
11,129,804, and 11,602,511 cover the AXA1125 compositions,
including pharmaceuticals and nutritional supplements. These
previously granted patents have an anticipated expiration date in
2037.
“In addition to further strengthening Axcella’s global
intellectual property position regarding its proprietary
composition of amino acids in AXA1125, today’s patent issuance
further validates AXA1125’s formulation and its tie to treating
PASC or Long COVID, explicitly symptoms of fatigue,” said Bill
Hinshaw, President and Chief Executive Officer of Axcella. “We are
pleased to have this additional designation as we pursue options to
bring our investigational product forward for the benefit of the
millions of people who continue to suffer from Long COVID Fatigue.
The understanding of the disease continues to advance and show the
importance of mitochondrial function and how a mitochondrial
activator like AXA1125 has the potential to impact the issues these
patients face.”
About Endogenous Metabolic Modulators
Endogenous metabolic modulators, or EMMs, are a broad family of
molecules, including amino acids, which fundamentally impact and
regulate human metabolism. Our AXA candidates are anchored by EMMs
that have a history of safe use as food. We believe that, unlike
conventional targeted interventions currently used to address
dysregulated metabolism, EMM compositions have the potential to
directly and simultaneously support and modulate multiple metabolic
pathways implicated both in complex diseases and overall
health.
Internet Posting of Information
Axcella uses the “Investors and News” section of its website,
www.axcellatx.com, as a means of disclosing material nonpublic
information, to communicate with investors and the public, and for
complying with its disclosure obligations under Regulation FD. Such
disclosures include, but may not be limited to, investor
presentations and FAQs, Securities and Exchange Commission filings,
press releases, and public conference calls and webcasts. The
information that we post on our website could be deemed to be
material information. As a result, we encourage investors, the
media and others interested to review the information that we post
there on a regular basis. The contents of our website shall not be
deemed incorporated by reference in any filing under the Securities
Act of 1933, as amended.
About Axcella Therapeutics (Nasdaq: AXLA)
Axcella is a clinical-stage biotechnology company focused on
pioneering a new approach to address the biology of complex
diseases using compositions of endogenous metabolic modulators
(EMMs). The company’s unique model allows for the evaluation of its
EMM compositions through non-IND clinical studies or IND clinical
trials. For more information, please visit www.axcellatx.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, including, without limitation, statements
regarding the potential utility of AXA1125 as a treatment of Long
COVID and the Company’s anticipated regulatory pathway for AXA1125
and the timing and potential success thereof. The words “may,”
“will,” “could,” “would,” “should,” “expect,” “plan,” “anticipate,”
“intend,” “believe,” “estimate,” “predict,” “project,” “potential,”
“continue,” “target” and similar expressions are intended to
identify forward-looking statements, although not all
forward-looking statements contain these identifying words. Any
forward-looking statements in this press release are based on
management’s current expectations and beliefs and are subject to a
number of risks, uncertainties and important factors that may cause
actual events or results to differ materially from those expressed
or implied by any forward-looking statements contained in this
press release, including, without limitation, those related to the
potential impact of COVID-19 on the company’s ability to conduct
and complete its ongoing or planned clinical studies and clinical
trials in a timely manner or at all due to patient or principal
investigator recruitment or availability challenges, clinical trial
site shutdowns or other interruptions and potential limitations on
the quality, completeness and interpretability of data the company
is able to collect in its clinical trials of AXA1125, other
potential impacts of COVID-19 on the company’s business and
financial results, including with respect to its ability to raise
additional capital and operational disruptions or delays, changes
in law, regulations, or interpretations and enforcement of
regulatory guidance, whether data readouts support the company’s
clinical trial plans and timing, clinical trial design and target
indications for AXA1125, the clinical development and safety
profile of AXA1125 and its therapeutic potential, whether and when,
if at all, the company’s product candidates will receive approval
from the FDA or other comparable regulatory authorities, potential
competition from other biopharma companies in the company’s target
indications, and other risks identified in the company’s SEC
filings, including Axcella’s Annual Report on Form 10-K, Quarterly
Report on Form 10-Q and subsequent filings with the SEC. The
company cautions you not to place undue reliance on any
forward-looking statements, which speak only as of the date they
are made. Axcella disclaims any obligation to publicly update or
revise any such statements to reflect any change in expectations or
in events, conditions or circumstances on which any such statements
may be based, or that may affect the likelihood that actual results
will differ from those set forth in the forward-looking statements.
Any forward-looking statements contained in this press release
represent the company’s views only as of the date hereof and should
not be relied upon as representing its views as of any subsequent
date. The company explicitly disclaims any obligation to update any
forward-looking statements.
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