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Study identifier: NCT06562907 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Study of GS-4571 in Healthy Participants, Nondiabetic Obese Participants, and Nonobese Participants With Type 2 Diabetes Mellitus (T2DM)

Condition: Weight Management  ·  Sponsor: Gilead Sciences

PhasePhase 1
Planned participants134
Who can joinAll sexes, 18 Years to 55 Years
Healthy volunteersYes

About this study

The goal of this clinical study is to learn more about the study drug, GS-4571, and how safe it is in 3 groups, i) Healthy participants, ii) Healthy non-diabetic obese participants, and iii) Non-obese participants with Type 2 Diabetes Mellitus (T2DM). The primary objectives of this study are: * To characterize the pharmacokinetics (PK) of GS-4571 following single and multiple ascending oral doses of GS-4571. * To evaluate the effect of concomitant food intake and (if conducted) a representative acid-reducing agent (proton pump inhibitor (PPI), omeprazole) on the PK of GS-4571. * To evaluate the safety and tolerability of single and multiple ascending oral doses of GS-4571.

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 (3)

Qps-Mra, Llc.Miami, Florida, United StatesRecruiting
ICON Early Phase Services, LLCSan Antonio, Texas, United StatesRecruiting
ICONSalt Lake City, Utah, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06562907