Shattuck Labs (STTK) 12th Annual Cantor Fitzgerald Global Healthcare Conference summary
Event summary combining transcript, slides, and related documents.
12th Annual Cantor Fitzgerald Global Healthcare Conference summary
9 Sep, 2026Strategic 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.
Latest events from Shattuck Labs
- DR3 blockade targets durable, low-immunogenicity IBD therapy with pivotal data expected in 2028.STTK
Wells Fargo 21st Annual Healthcare Conference - SL-325, a first-in-class DR3 antagonist for IBD, shows superior preclinical efficacy and durability.STTK
Corporate presentation - SL-325, a first-in-class DR3 antagonist for IBD, shows superior preclinical efficacy and safety.STTK
Corporate presentation - SL-325 offers a first-in-class DR3 blockade with durable efficacy and low immunogenicity for IBD.STTK
Corporate presentation - SL-325 completed Phase 1 with strong safety; $208.3M cash funds operations into 2029.STTK
Q2 2026 - Lead DR3 antibody SL-325 shows promise for IBD with strong safety and low immunogenicity.STTK
Corporate presentation - SL-325 showed durable DR3 blockade, low immunogenicity, and is advancing to phase IIb in Crohn's.STTK
Study result - SL-325, a first-in-class DR3 antibody for IBD, advances with strong preclinical data and funding.STTK
Corporate presentation - DR3 blocking antibodies for IBD aim to surpass TL1A blockers in efficacy and safety, with key trials imminent.STTK
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