STTKShattuck Labs, Inc.
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Thesis

First DR3 blocker in the clinic posts best-in-class immunogenicity; Phase 2b in Crohn's disease will confirm or disprove whether that translates to efficacy

Updated 35d ago

Shattuck Labs is a clinical-stage company developing a targeted immunology drug to treat Crohn's disease, which is not yet approved.

SL-325, the first DR3-blocking antibody in human testing, posted a 3.7% ADA rate and complete receptor occupancy supporting quarterly dosing, differentiated early benchmarks in a crowded TL1A/DR3 field. The thesis resolves on whether the 232-patient RECEPTIVE-CD1 trial hits endoscopic response at Week 12, establishing that DR3 blockade drives clinical benefit in Crohn's disease. With $208M cash and a 2029 runway, survival is not the risk; the risk is that a single-mechanism Phase 2b without prior efficacy data fails to prove the concept.

Status
Intact
Conviction

Current Thesis Drivers

  • SL-325 Phase 1: 3.7% ADA, complete DR3 occupancy >3 months
  • $208M cash; runway to 2029, past H1 2028 readout
  • No human efficacy data yet; DR3 blockade unproven clinically
  • SL-846 pre-IND; no clinical data from second program

What could change the thesis?

  • RECEPTIVE-CD1 H1 2028 readout: hit validates DR3 blockade, miss ends program
  • SL-846 Phase 1 2027 data: clean safety opens bispecific path, signal failure stalls platform
  • Dilutive financing risk: further equity raises if burn accelerates beyond projections

Generated from public SEC filings and disclosures. For informational purposes only — not investment advice. Always conduct your own research before making investment decisions.

Thesis log

Tracked in real time as it happened — not reconstructed after the fact

Key value driver

The most decisive event ahead

Bull and bear case

Both sides of the thesis, argued

Pipeline

4 programs · 9 catalysts

Stress Test