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A Phase 2 Study of SL-325 in Crohn's Disease Patients
Sponsor: Shattuck Labs, Inc.
Summary
The primary purpose of this study is to evaluate the efficacy of SL-325 in adult participants with moderate to severely active Crohn's disease. The study consists of a screening period of up to 6 weeks, a 12-week induction period, 38-week maintenance period, 52-week long-term extension period, and a 10-week follow-up period.
Official title: A Phase 2 Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of SL-325 in Participants With Moderately to Severely Active Crohn's Disease
Key Details
Gender
All
Age Range
18 Years - 80 Years
Study Type
INTERVENTIONAL
Enrollment
232
Start Date
2026-10
Completion Date
2030-06
Last Updated
2026-08-10
Healthy Volunteers
No
Conditions
Interventions
SL-325
SL-325 administered intravenously
Placebo
Placebo administered intravenously