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NOT YET RECRUITING
NCT07753850
PHASE2

A Phase 2 Study of SL-325 in Crohn's Disease Patients

Sponsor: Shattuck Labs, Inc.

View on ClinicalTrials.gov

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

DRUG

SL-325

SL-325 administered intravenously

DRUG

Placebo

Placebo administered intravenously