Cancer Therapy Evaluation Program Announces Availability of Botensilimab for Clinical Studies
27 Junho 2024 - 8:30AM
Business Wire
Agenus Inc. (“Agenus”) (Nasdaq: AGEN), a leader in developing
novel immunological agents to treat various cancers, today
announced that the Cancer Therapy Evaluation Program (CTEP) is
accepting Letters of Intent (LOIs) to conduct clinical studies
using botensilimab (BOT), a human Fc enhanced next-generation
anti-cytotoxic T-lymphocyte associated protein 4 (CTLA-4) antibody,
which is being developed by CTEP as an anticancer agent in
collaboration with Agenus Inc. CTEP will also consider requests to
supply botensilimab for nonclinical studies. All clinical and
nonclinical researchers interested in working with the agent are
welcome to apply. All proposals approved by CTEP will be sent to
the industry collaborator for a commitment to supply drug for the
study.
In addition to its commitment to support clinical studies in
collaboration with CTEP, Agenus is also committed to supporting
nonclinical research by providing investigators with botensilimab
and its mouse surrogate. This initiative is designed to facilitate
extensive investigations into the drug's potential and identify new
potential clinical applications. For additional information on the
CTEP program, including a list of therapies approved for use by
CTEP, access their website here.
About Botensilimab
Botensilimab is a human Fc enhanced CTLA-4 blocking antibody
designed to boost both innate and adaptive anti-tumor immune
responses. Its novel design leverages mechanisms of action to
extend immunotherapy benefits to "cold" tumors which generally
respond poorly to standard of care or are refractory to
conventional PD-1/CTLA-4 therapies and investigational therapies.
Botensilimab augments immune responses across a wide range of tumor
types by priming and activating T cells, downregulating
intratumoral regulatory T cells, activating myeloid cells and
inducing long-term memory responses.
Approximately 900 patients have been treated with botensilimab
in phase 1 and phase 2 clinical trials. Botensilimab alone, or in
combination with Agenus’ investigational PD-1 antibody,
balstilimab, has shown clinical responses across nine metastatic,
late-line cancers. For more information about botensilimab trials,
visit www.clinicaltrials.gov with the identifiers NCT03860272,
NCT05608044, NCT05630183, and NCT05529316.
About Agenus
Agenus is a leading immuno-oncology company targeting cancer and
infectious diseases with a comprehensive pipeline of immunological
agents. The company’s mission is to expand patient populations
benefiting from cancer immunotherapy through combination
approaches, using a broad repertoire of antibody therapeutics,
adoptive cell therapies (through MiNK Therapeutics) and adjuvants
(through SaponiQx). Agenus is headquartered in Lexington, MA. For
more information, visit www.agenusbio.com or @agenus_bio.
Information that may be important to investors will be routinely
posted on our website and social media channels.
Forward-Looking
Statements
This press release contains forward-looking statements that are
made pursuant to the safe harbor provisions of the federal
securities laws, including statements regarding a its botensilimab
and balstilimab programs, expected regulatory timelines and
filings, and any other statements containing the words "may,"
"believes," "expects," "anticipates," "hopes," "intends," "plans,"
"forecasts," "estimates," "will," “establish,” “potential,”
“superiority,” “best in class,” and similar expressions are
intended to identify forward-looking statements. These
forward-looking statements are subject to risks and uncertainties
that could cause actual results to differ materially. These risks
and uncertainties include, among others, the factors described
under the Risk Factors section of our most recent Annual Report on
Form 10-K for 2023, and subsequent Quarterly Reports on Form 10-Q
filed with the Securities and Exchange Commission. Agenus cautions
investors not to place considerable reliance on the forward-looking
statements contained in this release. These statements speak only
as of the date of this press release, and Agenus undertakes no
obligation to update or revise the statements, other than to the
extent required by law. All forward-looking statements are
expressly qualified in their entirety by this cautionary
statement.
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