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Trials / Withdrawn

WithdrawnNCT04649710

A Study to Evaluate the Drug Levels and Safety of Pegbelfermin in Healthy Overweight and Obese Chinese and Korean Participants

A Double-Blind, Multicenter, Placebo-Controlled, Randomized, Parallel, Multiple-Dose Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Pegbelfermin in Healthy Overweight and Obese Chinese and Korean Participants

Status
Withdrawn
Phase
Phase 1
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Bristol-Myers Squibb · Industry
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to evaluate the safety, tolerability, and drug level of Pegbelfermin in healthy overweight and obese Chinese and Korean participants.

Conditions

Interventions

TypeNameDescription
BIOLOGICALBMS-986036Specified dose on specified days
OTHERPlaceboSpecified dose on specified days

Timeline

Start date
2021-06-21
Primary completion
2021-09-21
Completion
2021-09-22
First posted
2020-12-02
Last updated
2022-04-28

Locations

2 sites across 2 countries: China, South Korea

Regulatory

Source: ClinicalTrials.gov record NCT04649710. Inclusion in this directory is not an endorsement.

A Study to Evaluate the Drug Levels and Safety of Pegbelfermin in Healthy Overweight and Obese Chinese and Korean Partic (NCT04649710) · Clinical Trials Directory