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A Phase 2 Study to Evaluate the Efficacy, Safety, and Tolerability of TERN-601 in Adults With Overweight or Obesity
This is a Phase 2a multicenter, randomized, double-blind, placebo-controlled clinical trial studying the efficacy, safety, and tolerability of orally administered TERN-601 in adults with overweight or obesity.
Age
18 - 75 years
Sex
ALL
Healthy Volunteers
No
FALCON Research Site
Birmingham, Alabama, United States
FALCON Research Site
Homewood, Alabama, United States
FALCON Research Site
Tucson, Arizona, United States
FALCON Research Site
Spring Valley, California, United States
FALCON Research Site
Port Orange, Florida, United States
FALCON Research Site
Louisville, Kentucky, United States
FALCON Research Site
Marrero, Louisiana, United States
FALCON Research Site
Boston, Massachusetts, United States
FALCON Research Site
Rochester, Minnesota, United States
FALCON Research Site
City of Saint Peters, Missouri, United States
Start Date
March 7, 2025
Primary Completion Date
August 19, 2025
Completion Date
September 19, 2025
Last Updated
November 6, 2025
167
ACTUAL participants
TERN-601
DRUG
Matching Placebo
OTHER
Lead Sponsor
Terns, Inc.
NCT07160400
NCT07150962
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT06499857