Shattuck Labs (STTK) Q1 2026 earnings summary
Event summary combining transcript, slides, and related documents.
Q1 2026 earnings summary
7 May, 2026Executive summary
Clinical-stage biotech focused on DR3 blocking antibodies for inflammatory and immune-mediated diseases, with lead candidate SL-325 advancing through Phase 1 trials and Phase 2 initiation planned for Q3 2026.
Completed enrollment in Phase 1 clinical trial of SL-325; data expected in Q2 2026.
Lead bispecific DR3 antibody entered IND-enabling activities; targets and timelines to be disclosed in Q2 2026.
Net loss for Q1 2026 was $14.8 million, up from $13.7 million in Q1 2025, reflecting increased R&D investment as clinical programs advance.
Cash and cash equivalents totaled $90.4 million as of March 31, 2026, with management projecting sufficient liquidity into 2029, assuming full warrant exercise.
Financial highlights
Revenue for Q1 2026 was $0, consistent with the prior year.
Research and development expenses rose to $10.9 million in Q1 2026, up from $9.9 million in Q1 2025, driven by clinical advancement of SL-325 and higher personnel costs.
General and administrative expenses were $4.6 million in Q1 2026, relatively flat year-over-year.
Net cash used in operating activities was $13.4 million for Q1 2026, compared to $12.0 million in Q1 2025.
Financing activities provided $25.8 million, primarily from ATM equity sales and warrant exercises.
Outlook and guidance
Phase 1 trial for SL-325 expected to complete in Q2 2026, with Phase 2 in Crohn's Disease to begin in Q3 2026.
Cash runway projected into 2029, assuming full exercise of outstanding warrants.
Anticipates continued increase in R&D expenses as clinical programs progress and workforce expands.
No product revenue expected until regulatory approval and commercialization, which is several years away.
Guidance excludes potential additional capital from business development or new clinical activities.
Latest events from Shattuck Labs
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Proxy filing8 Apr 2026 - Shareholders will vote on director elections, auditor ratification, executive pay, and equity plan changes.STTK
Proxy filing8 Apr 2026 - SL-325 offers a novel, potent approach to IBD by targeting DR3, with Phase 2 trials planned.STTK
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Study Update3 Feb 2026 - SL-172154 discontinued for marginal benefit; SL-325 DR3 antibody advances to phase I in 2026.STTK
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