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Compass Therapeutics Presents Preclinical Data on CTX-10726, a Differentiated PD-1 x VEGF-A Bispecific Antibody, at the 40th Society for Immunotherapy of Cancer (SITC) Annual Meeting

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Compass Therapeutics (Nasdaq: CMPX) presented preclinical data on CTX-10726, a tetravalent bispecific antibody targeting PD-1 and VEGF-A, at the 40th SITC Annual Meeting on November 7, 2025.

Key findings: CTX-10726 showed high-affinity binding to human and cynomolgus VEGF-A and PD-1, dose-dependent blockade of VEGF-A/VEGFR2 and PD-1/PD-L1 interactions, and potent IFN-γ immunomodulatory activity in vitro. In vivo, CTX-10726 produced tumor elimination in multiple models and demonstrated superior anti-tumor activity versus comparator antibodies including ivonescimab and bevacizumab in xenograft and knock-in mouse models. The company said an IND submission is on track for Q4 2025. Presentation materials will be posted on the company website after the meeting.

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Positive

  • Preclinical tumor elimination in multiple in vivo studies
  • Superior anti-tumor activity versus ivonescimab in HCC827 and MC38hPD-L1 models
  • Superior tumor-size reduction versus bevacizumab in MC38hPD-L1/hVEGF-A model
  • High-affinity binding to human and cynomolgus VEGF-A and PD-1 in vitro
  • IND submission on track for Q4 2025

Negative

  • Results are limited to preclinical in vitro and animal models (no clinical efficacy yet)
  • No human safety or clinical data reported to support translational outcomes

News Market Reaction 8 Alerts

+1.34% News Effect
-2.8% Trough in 18 hr 8 min
+$9M Valuation Impact
$650M Market Cap
0.9x Rel. Volume

On the day this news was published, CMPX gained 1.34%, reflecting a mild positive market reaction. Argus tracked a trough of -2.8% from its starting point during tracking. Our momentum scanner triggered 8 alerts that day, indicating moderate trading interest and price volatility. This price movement added approximately $9M to the company's valuation, bringing the market cap to $650M at that time.

Data tracked by StockTitan Argus on the day of publication.

  • CTX-10726 demonstrated potent, simultaneous inhibition of tumor angiogenesis and PD-1-mediated immune suppression, and eliminated tumors in multiple preclinical studies.
  • In vivo, CTX-10726 outperformed select competitive antibodies in the class, including ivonescimab, in controlling tumor growth across multiple xenograft and syngeneic models.
  • IND submission is on track for Q4 2025.

BOSTON, Nov. 04, 2025 (GLOBE NEWSWIRE) -- Compass Therapeutics, Inc. (Nasdaq: CMPX), a clinical-stage, oncology-focused biopharmaceutical company developing proprietary antibody-based therapeutics, today announced its poster presentation at the 40th Society for Immunotherapy of Cancer (SITC) Annual Meeting, taking place November 5-9, 2025, in National Harbor, MD.

Details of the presentation are as follows:

Title: Preclinical Development of CTX-10726, a Tetravalent Bispecific Antibody Targeting PD-1 and VEGF-A for the Treatment of Patients with Cancer
Presenter: Diana Albu, PhD; Compass Therapeutics
Date & Time: November 7, 2025, from 12:15 PM-1:45 PM and 5:35-7:00 PM
Abstract number: 1151
Location: Gaylord National Resort & Convention Center – Exhibit Halls AB

Data highlights from the poster presentation include:

  • In vitro, CTX-10726:
    • Showed high-affinity binding to both human and cynomolgus monkey VEGF-A and PD-1;
    • Effectively blocked VEGF-A/VEGFR2 and PD-1/PD-L1 interactions in a dose-dependent manner; and
    • Demonstrated potent immunomodulatory activity as measured by IFN-γ production.
  • In vivo, CTX-10726:
    • Exhibited superior anti-tumor efficacy in a human lung cancer model in mice (HCC827 xenografts) compared to ivonescimab and an anti-VEGF-A antibody;
    • Showed stronger anti-tumor activity against a human-PD-L1 expressing colon cancer cell line (MC38hPD-L1) implanted in human PD-1/PD-L1 double knock-in mice, compared with ivonescimab; and
    • Demonstrated anti-tumor activity against human-PD-1 and VEGF-A expressing colon cancer cell line (MC38hPD-L1/hVEGF-A) implanted in human PD-1/PD-L1/VEGF-A triple knock-in mice, with significant reduction in tumor size compared with bevacizumab.

A copy of the presentation materials can be accessed on the Compass website at https://www.compasstherapeutics.com/pipeline/ once the presentation has concluded.

About CTX-10726
CTX-10726 is a bispecific, tetravalent antibody that simultaneously targets vascular endothelial growth factor (VEGF)-A and programmed cell death (PD)-1. CTX-10726 is being developed for the treatment of patients with metastatic or locally advanced tumor types where clinical checkpoint and angiogenesis signals are present. Checkpoint inhibitor antibody therapies targeting PD-1 and PD-L1 as well as agents targeting tumor angiogenesis have shown great success for the treatment of various malignancies. However, a substantial fraction of patients with PD-(L)1-positive tumors remain unresponsive to these therapies. CTX-10726 is believed to enhance anti-tumor response by both targeting immune checkpoints and tumor vasculature and has shown potent anti-tumor activity in preclinical mouse models. Currently, CTX-10726 is being tested in IND-enabling studies.

About Compass Therapeutics
Compass Therapeutics, Inc. is a clinical-stage oncology-focused biopharmaceutical company developing proprietary antibody-based therapeutics to treat multiple human diseases. The company’s scientific focus is on the relationship between angiogenesis, the immune system, and tumor growth. Compass has built a robust pipeline of novel product candidates 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. The company 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.

Forward-Looking Statements

This 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, statements regarding Compass’s product candidates, including the therapeutic potential of CTX-10726. 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 and subsequent filings with the SEC.

Investor Contact
ir@compasstherapeutics.com

Media Contact
Anna Gifford, Chief of Staff
media@compasstherapeutics.com
617-500-8099


FAQ

What did Compass Therapeutics announce about CTX-10726 at SITC on November 7, 2025?

Compass presented preclinical data showing CTX-10726 binds PD-1 and VEGF-A, drove IFN-γ production, eliminated tumors in multiple models, and outperformed comparators in mouse studies.

How does CTX-10726 (CMPX) compare to ivonescimab and bevacizumab in the presented preclinical data?

CTX-10726 showed superior anti-tumor efficacy versus ivonescimab in HCC827 and MC38hPD-L1 models and greater tumor-size reduction versus bevacizumab in the MC38hPD-L1/hVEGF-A model.

When is Compass planning an IND submission for CTX-10726 (CMPX)?

The company said the IND submission for CTX-10726 is on track for Q4 2025.

Did the SITC presentation include human clinical data for CTX-10726 (CMPX)?

No; the presentation reported only in vitro and in vivo preclinical results, not human clinical data.

Where can investors access Compass Therapeutics' CTX-10726 presentation materials after SITC 2025?

Presentation materials will be posted on the Compass Therapeutics pipeline page on the company website after the presentation concludes.
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Biotechnology
Biological Products, (no Disgnostic Substances)
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United States
BOSTON