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Study identifier: NCT06029972 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Study of Tilpisertib Fosmecarbil in Participants With Moderately to Severely Active Ulcerative Colitis

Condition: Ulcerative Colitis  ·  Sponsor: Gilead Sciences

PhasePhase 2
Planned participants176
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

The goal of this study is to learn if tilpisertib fosmecarbil (formerly known as GS-5290) is effective and safe in treating participants with moderate to severe ulcerative colitis. The study will compare participants in different treatment groups treated with tilpisertib fosmecarbil with participants treated with placebo. The primary objective of this study is to demonstrate the efficacy of tilpisertib fosmecarbil, compared to placebo control, in achieving Clinical Response at Week 12.

This description comes directly from the study's public registry record.

Talk to the study team

Gilead Clinical Study Information Center  ·  1-833-445-3230 (GILEAD-0)  ·  GileadClinicalTrials@gilead.com

Always discuss trial participation with your own doctor first.

Locations (129)

GI AllianceSun City, Arizona, United StatesRecruiting
GastroSb Weight Loss ClinicChula Vista, California, United StatesRecruiting
Southern California Research CentersCoronado, California, United StatesRecruiting
VVCRD ResearchGarden Grove, California, United StatesRecruiting
UC San Diego Health SystemLa Jolla, California, United StatesRecruiting
Gastro Care InstituteLancaster, California, United StatesRecruiting
Om Research LLCLancaster, California, United StatesRecruiting
United Medical DoctorsMurrieta, California, United StatesWithdrawn
University of California, DavisSacramento, California, United StatesRecruiting
University of California San FranciscoSan Francisco, California, United StatesRecruiting
Amicis Research CenterValencia, California, United StatesWithdrawn
Luna ResearchCoral Gables, Florida, United StatesRecruiting

+ 117 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT06029972