Shattuck Labs IncSTTK
Price$6.84

Qualitative Analysis

Business overview

Business Overview

Shattuck Labs, Inc. (NASDAQ: STTK) is a clinical-stage biotechnology company pioneering the development of potentially first-in-class monoclonal and bispecific antibodies targeting the tumor necrosis factor (TNF) receptor superfamily. The company's core scientific focus centers on the clinically validated DR3/TL1A pathway to treat patients with inflammatory and immune-mediated diseases, such as Inflammatory Bowel Disease (IBD). Shattuck's lead clinical candidate is SL-325, a potentially first-in-class DR3 antagonist antibody designed to achieve a complete and durable blockade of the TL1A/DR3 pathway. Shattuck is also developing SL-425, a half-life extended version of SL-325, alongside preclinical DR3-based bispecific antibodies and its oncology-focused TRIM7 program.

Research as of 20 Jun 2026

Strategic Initiatives

Growth programs, investments, and their expected impact

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Clinical Development of SL-325Innovation

Advancing SL-325, a potentially first-in-class Death Receptor 3 (DR3) blocking antibody designed to achieve a complete and durable blockade of the clinically validated DR3/TL1A pathway for inflammatory bowel disease (IBD). Following positive Phase 1 results in healthy volunteers, the company is preparing to launch a Phase 2b trial in Crohn's disease.

Expected impact: Establish clinical efficacy and a best-in-mechanism immunogenicity profile in patients with moderate-to-severe Crohn's disease.

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InvestmentSupported by existing cash reserves and recent warrant exercises totaling over $145 million in total liquidity.
TimelinePhase 2b initiation expected in Q3 2026; primary endpoint data expected in H1 2028.
Development of DR3-Based Bispecific Antibodies (SL-846)Innovation

Developing SL-846, a bispecific antibody candidate designed to inhibit both the DR3/TL1A axis and the IL-23 receptor (IL-23R) for the treatment of inflammatory and immune-mediated diseases.

Expected impact: Expand the pipeline with a next-generation bispecific candidate that could improve upon the efficacy of single-pathway TL1A inhibitors.

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InvestmentFunded through the company's clinical development budget.
TimelineIND-enabling toxicology studies are ongoing; IND submission and Phase 1 initiation are expected in the first half of 2027.

Mergers, Acquisitions & Partnerships

Recent deals and strategic collaborations

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Strategic Partnerships

AI-assisted, source-linked narrative; figures from company filings (SEC EDGAR) and market data. Dates shown per section. Not investment advice. Terms of Use.