drugset / Trial / NCT04130919
Study to Evaluate the Efficacy and Safety of Tilpisertib in Adults With Moderately to Severely Active Ulcerative Colitis
RandomizedParallel-groupDouble-blindTreatment
Summary
The primary objective of this study is to demonstrate the efficacy of tilpisertib (formerly GS-4875) compared with placebo control in achieving clinical remission per modified Mayo Clinic Score (MCS) in adults with moderately to severely active ulcerative colitis (UC).
Timeline
- Start
- 2019-12-20
- Primary completion
- 2021-02-25
- Completion
- 2021-12-14
Outcome
Outcome not reported
Stopped: “Sponsor terminated the study since a new molecular entity was able to achieve greater target coverage”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Tilpisertib | Small molecule | 100 mg | Oral |
| Subject | Tilpisertib | Small molecule | 300 mg | Oral |