Compass Therapeutics Announces Publication of CTX-8371 Preclinical Data in OncoImmunology, its Bispecific Antibody Checkpoint Inhibitor, now Advancing to First-in-Human Clinical Trial
28 Fevereiro 2024 - 10:00AM
Compass Therapeutics, Inc. (Nasdaq: CMPX), a clinical-stage,
oncology-focused biopharmaceutical company developing proprietary
antibody-based therapeutics to treat multiple human diseases,
announced the publication of a peer-reviewed article titled, “A
bispecific anti-PD-1 and PD-L1 antibody induces PD-1 cleavage and
provides enhanced anti-tumor activity” in the journal
OncoImmunology. CTX-8371 is a fully-human, tetravalent bispecific
antibody, discovered and developed by Compass Therapeutics as a
next generation checkpoint blocker. The data highlighted the unique
mechanism-of-action of CTX-8371, inducing dual blockade of PD-1 and
PDL-1 and cleavage of cell surface PD-1. In addition, CTX-8371
demonstrates enhanced anti-tumor activity relative to approved
anti-PD-1 blockers and anti-PD-L1 blockers in a series of in vitro
and in vivo experimental settings.
“We are very pleased that our bispecific antibody, CTX-8371,
outperformed known checkpoint blockers in a series of in vitro and
in vivo experiments and, in particular, demonstrated enhanced in
vivo anti-tumor efficacy in a mouse tumor model. Moreover, the data
also suggested that the combination of checkpoint blockade with
CTX-8371 and CTX-471, the CD137 agonistic antibody was potentially
synergistic, suggesting a unique opportunity for proprietary
combination regimens using our Compass antibodies,” says Thomas
Schuetz, MD, PhD, Co-founder, President of R&D, and Vice
Chairman of the board at Compass. “These compelling data are a
testament to the functionality of our novel checkpoint inhibitor
and we are excited to continue evaluating its potential in clinical
studies. Our IND was cleared by the FDA at the end of 2023, and we
expect to dose a first patient before the end of this quarter.”
About Compass TherapeuticsCompass Therapeutics,
Inc. is a clinical-stage oncology-focused biopharmaceutical company
developing proprietary antibody-based therapeutics to treat
multiple human diseases. Compass’s scientific focus is on the
relationship between angiogenesis, the immune system, and tumor
growth. The company pipeline of novel product candidates is
designed to target multiple critical biological pathways required
for an effective anti-tumor response. These include modulation of
the microvasculature via angiogenesis-targeted agents, induction of
a potent immune response via activators on effector cells in the
tumor microenvironment, and alleviation of immunosuppressive
mechanisms used by tumors to evade immune surveillance. Compass
plans to advance its product candidates through clinical
development as both standalone therapies and in combination with
proprietary pipeline antibodies based on supportive clinical and
nonclinical data. The company was founded in 2014 and is
headquartered in Boston, Massachusetts. For more information, visit
the Compass Therapeutics website
at https://www.compasstherapeutics.com.
Forward-Looking StatementsThis press release
contains forward-looking statements. Statements in this press
release that are not purely historical are forward-looking
statements. Such forward-looking statements include, among other
things, references to Compass’s product candidates, including
CTX-8371, and its development and clinical trial milestones such as
the expected trial design, timing of enrollment, patient dosing and
data readouts, regulatory plans with respect to Compass’s product
candidates and the therapeutic potential thereof. Actual results
could differ from those projected in any forward-looking statements
due to numerous factors. Such factors include, among others,
Compass’s ability to raise the additional funding it will need to
continue to pursue its business and product development plans, the
inherent uncertainties associated with developing product
candidates and operating as a development stage company, Compass’s
ability to identify additional product candidates for development,
Compass’s ability to develop, complete clinical trials for, obtain
approvals for and commercialize any of its product candidates,
competition in the industry in which Compass operates and market
conditions. These forward-looking statements are made as of the
date of this press release, and Compass assumes no obligation to
update the forward-looking statements, or to update the reasons why
actual results could differ from those projected in the
forward-looking statements, except as required by law. Investors
should consult all of the information set forth herein and should
also refer to the risk factor disclosure set forth in the reports
and other documents Compass files with the U.S. Securities and
Exchange Commission (SEC) available at www.sec.gov, including
without limitation Compass’s latest Annual Report on Form 10-K,
Quarterly Report on Form 10-Q and subsequent filings with the
SEC.
Investor Contactir@compasstherapeutics.com
Media Contact Anna Gifford, Senior
Communications Manager
media@compasstherapeutics.com617-500-8099
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