Press Releases June 5, 2026 04:05 PM

Shattuck Labs to Host Investor Call and Webcast on Phase 1 Clinical Data of SL-325, a Potentially First-in-Class DR3 Blocking Antibody, and Pipeline Update on June 8

Shattuck Labs Announces Investor Call to Present Promising Phase 1 Data for SL-325, a Novel DR3 Blocking Antibody

By Nina Shah
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Shattuck Labs, a clinical-stage biotech company focusing on monoclonal and bispecific DR3-blocking antibodies, will hold an investor call on June 8 to present comprehensive Phase 1 clinical data for its lead candidate SL-325. The data includes safety, pharmacokinetics, and immunogenicity results. SL-325 is a potential first-in-class treatment targeting the DR3/TL1A pathway for inflammatory and immune-mediated diseases. The update highlights the company’s progress and pipeline developments.

Shattuck Labs to Host Investor Call and Webcast on Phase 1 Clinical Data of SL-325, a Potentially First-in-Class DR3 Blocking Antibody, and Pipeline Update on June 8
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Key Points

  • Shattuck Labs will release detailed Phase 1 clinical trial results for SL-325, showing safety and pharmacodynamics data.
  • SL-325 is designed as a first-in-class DR3 blocking antibody, aiming for durable blockade of the DR3/TL1A pathway relevant in inflammatory and immune diseases.
  • The investor call features presentations from key management and provides a company pipeline update, reinforcing their leadership in protein engineering targeting TNF receptor therapeutics.

AUSTIN, Texas and DURHAM, N.C., June 05, 2026 (GLOBE NEWSWIRE) -- Shattuck Labs, Inc. (Shattuck) (NASDAQ: STTK), a clinical-stage biotechnology company pioneering the development of potentially first-in-class monoclonal and bispecific DR3-blocking antibodies for the treatment of patients with inflammatory and immune-mediated diseases, today announced that it will host an investor call and webcast on Monday, June 8, 2026 at 8:00 a.m. ET to present comprehensive Phase 1 clinical data for SL-325, including safety, tolerability, pharmacokinetics, receptor occupancy, pharmacodynamic and immunogenicity results and provide a pipeline update.

The event will feature presentations by members of Shattuck’s management team, including Taylor Schreiber, M.D., Ph.D., Chief Executive Officer, Lini Pandite, M.D., M.B.A., Chief Medical Officer, Suresh De Silva, Ph.D., Chief Scientific Officer, Michael Choi, M.D., Vice President of Clinical Development, and Andrew Neill, M.B.A., Chief Financial Officer, followed by a question-and-answer session.

Conference Details

Title: Phase 1 Clinical Data of SL-325, a Potentially First-in-Class DR3 Blocking Antibody, and Pipeline Update
Date & Time: Monday, June 8, 2026 at 8:00 a.m. ET
Webcast Details: Click here

Interested parties can access the live webcast via the Events & Presentations section of the Company’s website at www.shattucklabs.com. A replay of the webcast will be available for approximately 30 days following the event.

About SL-325
SL-325 is a potential first-in-class Death Receptor 3 (DR3) blocking antibody designed to achieve a complete and durable blockade of the clinically validated DR3/TL1A pathway. Shattuck’s preclinical studies demonstrate high affinity binding and superior activity over TL1A antibodies, and offer a data-driven rationale for targeting the TNF receptor, DR3, versus its ligand, TL1A. SL-325 is a fully Fc-silenced, fully human immunoglobulin G monoclonal antibody with a favorable safety profile in non-human primates, currently being evaluated in a Phase 1 clinical trial.

About Shattuck Labs, Inc.
Shattuck Labs, Inc. is a clinical-stage biotechnology company pioneering the development of potentially first-in-class monoclonal and bispecific DR3 blocking antibodies for the treatment of patients with inflammatory and immune-mediated diseases. Shattuck’s expertise in protein engineering and the development of novel TNF receptor therapeutics come together in its lead program, SL-325, a potentially first-in-class DR3 antagonist antibody designed to achieve a more complete blockade of the clinically validated DR3/TL1A pathway. The Company has offices in both Austin, Texas and Durham, North Carolina. For more information, please visit: www.ShattuckLabs.com.

Investor & Media Contact:
Andrew R. Neill
Chief Financial Officer
Shattuck Labs, Inc.
[email protected]


Risks

  • SL-325 is still in early clinical development (Phase 1), and future trial phases may face efficacy, safety, or regulatory hurdles.
  • As a clinical-stage biotech, Shattuck Labs depends heavily on successful trial outcomes, and delays or failures could impact financial and market performance.
  • The competitive biotech sector focusing on inflammatory and immune-mediated disease treatments carries risks from emerging therapies and changing regulatory environments.

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