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A 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
2026-10-21
Completion Date
2030-06
Last Updated
2026-11-03
Healthy Volunteers
No
Conditions
Interventions
SL-325
SL-325 administered intravenously
Placebo
Placebo administered intravenously
Locations (20)
Clinical Trial Site
Little Rock, Arkansas, United States
Clinical Trial Site
Oxnard, California, United States
Clinical Trial Site
Temple City, California, United States
Clinical Trial Site
West Hills, California, United States
Clinical Trial Site
Inverness, Florida, United States
Clinical Trial Site
Kissimmee, Florida, United States
Clinical Trial Site
Naples, Florida, United States
Clinical Trial Site
Orlando, Florida, United States
Clinical Trial Site
Tampa, Florida, United States
Clinical Trial Site
Kansas City, Kansas, United States
Clinical Trial Site
Houma, Louisiana, United States
Clinical Trial Site
Marrero, Louisiana, United States
Clinical Trial Site
Glen Burnie, Maryland, United States
Clinical Trial Site
Boston, Massachusetts, United States
Clinical Trial Site
Liberty, Missouri, United States
Clinical Trial Site
St Louis, Missouri, United States
Clinical Trial Site
Maspeth, New York, United States
Clinical Trial Site
Cincinnati, Ohio, United States
Clinical Trial Site
Columbus, Ohio, United States
Clinical Trial Site
Nashville, Tennessee, United States