Instil Bio Announces Clinical Progress in China for IMM2510/SYN-2510, a Clinical-Stage PD-L1xVEGF Bispecific Antibody
January 14 2025 - 7:00AM
Instil Bio, Inc. (Nasdaq: TIL, “Instil”), today announced clinical
progress of IMM2510/SYN-2510 in China by its collaborator,
ImmuneOnco Biopharmaceuticals (Shanghai) Inc. (HKEX Code: 1541.HK,
“ImmuneOnco”).
ImmuneOnco announced that the first patient has
been dosed in its phase 1b/2 clinical trial of IMM2510/SYN-2510 in
combination with chemotherapy in patients with advanced non-small
cell lung cancer (NSCLC) in China. ImmuneOnco announced it plans to
enroll first-line patients in this trial and anticipates presenting
initial clinical data, including data for first-line NSCLC
patients, from this trial as soon as the second half of 2025.
Additionally, Instil announced that for its
anticipated initial U.S. clinical trial of SYN-2510/IMM2510 in lung
cancer, it plans to target enrollment of first-line patients with
NSCLC in combination with chemotherapy with an expected initiation
in the second half of 2025, assuming the necessary regulatory
approvals are obtained.
“We anticipate that ImmuneOnco’s initial clinical
data of IMM2510/SYN-2510 in combination with chemotherapy in
patients with front-line NSCLC could be extremely valuable in
advancing our development of IMM2510/SYN-2510 in NSCLC,” said
Bronson Crouch, CEO of Instil. “The data generated, if positive,
could position us to open a potential global registrational study
in front-line NSCLC.”
About SYN-2510/IMM2510
SYN-2510/IMM2510 is a PD-L1xVEGF bispecific
antibody in development for the treatment of multiple solid tumor
cancers. SYN-2510/IMM2510 is differentiated from other PD-(L)1xVEGF
bispecific antibodies by its VEGF trap, which binds multiple VEGF
receptor ligands beyond VEGF-A, a bispecific structure which
leverages PD-L1 as an anchor in the tumor microenvironment (TME),
and enhanced antibody-dependent cellular cytotoxicity (ADCC) to
direct killing of PD-L1-positive tumor cells.
About Instil Bio
Instil Bio is a clinical-stage biopharmaceutical
company focused on developing a pipeline of novel therapies.
Instil's lead asset, SYN-2510, is a novel and differentiated
PD-L1xVEGF bispecific antibody in development for the treatment of
multiple solid tumor cancers. For more information,
visit www.instilbio.com.
Forward-Looking Statements
This press release contains forward-looking
statements within the meaning of the Private Securities Litigation
Reform Act of 1995. Words (and variations of words) such as
“anticipates,” “believes,” “could,” “expects,” “expected,”
“exploring,” “future,” “intends,” “may,” “plans,” “potential,”
“projects,” “will,” “target,” and similar expressions are intended
to identify forward-looking statements. Forward-looking statements
include express or implied statements regarding Instil's
expectations with respect to the therapeutic potential of
SYN-2510/IMM2510, the clinical development of SYN-2510/IMM2510,
including IND submissions and clearances, clinical trials and the
timing, scope and design thereof, the availability and timing of
data from clinical trials, regulatory approvals and interactions
and other statements that are not historical fact. Forward-looking
statements are based on Instil management's current expectations
and are subject to various risks and uncertainties that could cause
actual results to differ materially and adversely from those
expressed or implied by such forward-looking statements, including
risks and uncertainties associated with in-licensing product
candidates and clinical trial collaborations; the costly and
time-consuming product development process and the uncertainty of
clinical success; the risks inherent in relying on collaborators
and other third parties, including for manufacturing and clinical
trial operation; the risks and uncertainties related to
successfully initiating, enrolling, completing and reporting data
from clinical studies, as well as the risks that results obtained
in clinical trials to date may not be indicative of results
obtained in ongoing or future trials and that Instil's product
candidates may otherwise not be effective treatments in their
planned indications; risks related to macroeconomic conditions,
including as a result of international conflicts, U.S.-China trade
and political tensions, interest rates, inflation, and other
factors, which could materially and adversely affect Instil's
business and operations; the risks and uncertainties associated
with the time-consuming and uncertain regulatory approval process
for product candidates across multiple indications and multiple
regulatory authorities; the impact of product candidates that may
compete with those developed by Instil; the sufficiency of Instil's
cash resources; and other risks and uncertainties affecting Instil
and its plans and development programs, including those discussed
in the section titled “Risk Factors” in Instil's Quarterly
Report on Form 10-Q for the quarter ended September 30, 2024 filed
with the SEC, as well as Instil's other filings with the SEC.
Additional information will be made available in other filings that
Instil makes from time to time with the SEC. Accordingly, these
forward-looking statements do not constitute guarantees of future
performance, and you are cautioned not to place undue reliance on
these forward-looking statements. These forward-looking statements
speak only as the date hereof, and Instil disclaims any obligation
to update these statements except as may be required by law.
Contacts:Investor
Relations:1-972-499-3350investorrelations@instilbio.comwww.instilbio.com
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