12th Annual Cantor Fitzgerald Global Healthcare Conference
Logotype for Shattuck Labs Inc

Shattuck Labs (STTK) 12th Annual Cantor Fitzgerald Global Healthcare Conference summary

Event summary combining transcript, slides, and related documents.

Logotype for Shattuck Labs Inc

12th Annual Cantor Fitzgerald Global Healthcare Conference summary

9 Sep, 2026

Strategic focus and differentiation

  • Exclusively targets the DR3 receptor, offering potential efficacy advantages over TL1A antibodies due to DR3's stable expression and lower immunogenicity.

  • DR3 blockade is expected to outperform TL1A antibodies in all indications where TL1A is effective, with a more durable pharmacodynamic effect.

  • Phase I data for SL-325 showed pure DR3 antagonism, durable receptor occupancy at low doses, and a low ADA rate of 3.7%.

  • Subcutaneous and IV formulations are being developed, with ongoing studies to compare bioavailability and optimize dosing.

  • Bispecific antibody SL-846 targets both DR3 and IL-23R, aiming for enhanced efficacy in diseases where both pathways are relevant.

Clinical development and trial design

  • Initial focus is on Crohn's disease due to stronger genetic linkage and a less crowded clinical landscape compared to ulcerative colitis.

  • Phase II trial uses a three-arm, randomized, blinded design with treat-through from induction to maintenance, enabling robust ITT analysis.

  • Dosing strategy includes high, middle, and low doses to ensure full DR3 occupancy and inform future phase III schedules.

  • Subcutaneous formulation is feasible for all doses, with potential use of on-body devices for higher doses.

  • ADA impact is expected to be more pronounced in maintenance, with differentiation from TL1A antibodies anticipated over time.

Pipeline expansion and future indications

  • Plans to pursue hidradenitis suppurativa (HS) as a priority non-IBD indication, aiming to be among the lead developers.

  • Psoriatic arthritis is considered a high-probability target for both DR3 and bispecific approaches.

  • Chronic tox studies in NHPs for the bispecific SL-846 show no unexpected agonism and manageable ADA rates.

  • Additional bispecifics are in development, with future advancement dependent on immunogenicity data from ongoing studies.

  • Further updates on non-IBD indications and bispecific pipeline are expected soon.

Partial view of Summaries dataset, powered by Quartr API
AI can get things wrong. Verify important information.
All investor relations material. One API.
Learn more