Botensilimab/Balstilimab Clinical Responses in Refractory Sarcomas Presented at ESMO 2024
September 13 2024 - 10:00AM
Business Wire
BOT/BAL Demonstrates Broad and Durable Activity
in Advanced Sarcoma Population
Agenus Inc. (“Agenus”) (Nasdaq: AGEN), a leader in developing
novel immunological agents to treat various cancers, presented data
today at the European Society for Medical Oncology (ESMO) Congress
held in Barcelona, Spain. The data from a Phase 1 study of
botensilimab (BOT), an investigational Fc-enhanced CTLA-4
inhibitor, in combination with balstilimab (BAL), an
investigational PD-1 antibody, showed clinical activity in patients
with refractory sarcomas, a population with limited treatment
options.
"The continued activity with additional patients and longer
follow-up of BOT/BAL in this study reinforces it's potential as an
important treatment option for patients with sarcomas," said Dr.
Breelyn A Wilky, University of Colorado Cancer Center. "The deep
and durable responses we are observing, particularly in late line
patients with poorly immunogenic or ‘cold’ sarcomas like visceral
angiosarcoma, leiomyosarcoma, and dedifferentiated liposarcoma, are
significant. These findings highlight the potential of BOT/BAL to
deliver extended survival and a meaningful clinical benefit for
patients who previously had very limited options."
Study Highlights
- 64 patients with relapsed/refractory sarcomas (median of 3
prior lines of therapy) were treated with 1 or 2 mg/kg BOT + 3
mg/kg BAL.
- 52 patients were efficacy evaluable with at least one
post-baseline 6-week imaging scan. ORR and DOR reporting will be
based on the unconfirmed response in this cohort.
- Majority of sarcoma subtypes included angiosarcoma (39%) and
leiomyosarcoma (34%).
Clinical Findings
- 23% overall response rate (ORR) was observed in the full
sarcoma cohort, with a median duration of response (DOR) of 21.7
months. 12-month overall survival (OS) was 69% and the median OS
was not reached.
- 39% ORR achieved in the angiosarcoma subtype (33% in cutaneous
and 44% in visceral), with a median DOR of 21.7 months. 12-month OS
was 64% and the median OS was not reached.
- A representative patient with visceral angiosarcoma achieved a
durable response, ongoing beyond 3 years, that has been maintained
off-therapy.
- The adverse event profile of BOT+ BAL was manageable and
reversible with no new safety signals identified.
"The updated sarcoma data presented at ESMO underscore the
transformative potential of botensilimab and balstilimab for
patients with refractory sarcomas who have exhausted other
treatment options," said Dr. Steven O’Day, Chief Medical Officer at
Agenus. "Seeing these metastatic sarcoma patients experience tumor
reduction, with significant and durable responses is incredibly
encouraging. BOT/BAL not only offers hope to patients with sarcoma
but also holds promise for redefining the standard of care across
other historically IO-resistant cancers."
The presentation is available on the Agenus website at
https://agenusbio.com/publications.
About Botensilimab
Botensilimab is an investigational 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 1,100 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
with a comprehensive pipeline of immunological agents. The company
was founded in 1994 with a 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 has robust end-to-end development
capabilities, across commercial and clinical cGMP manufacturing
facilities, research and discovery, and a global clinical
operations footprint. 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 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.
View source
version on businesswire.com: https://www.businesswire.com/news/home/20240913805710/en/
Investors 917-362-1370 investor@agenusbio.com
Media 612-839-6748 communications@agenusbio.com
Agenus (NASDAQ:AGEN)
Historical Stock Chart
From Oct 2024 to Nov 2024
Agenus (NASDAQ:AGEN)
Historical Stock Chart
From Nov 2023 to Nov 2024