LivingGLP1
Study S002590

A Phase 2 Study to Evaluate the Efficacy, Safety, and Tolerability of TERN-601 in Adults With Overweight or Obesity

Registration

Registration
NCT06854952
Acronym
FALCON
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
QUADRUPLE
Status
COMPLETED
Enrollment
167
Start
2025-03-07
Primary completion
2025-08-19
Lead sponsor
Terns, Inc., a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA)
Conditions
Overweight or Obesity
Interventions
DRUG:TERN-601; OTHER:Matching Placebo
Results posted
TRUE
Individual participant data sharing
NO

Registered primary outcomes

  • Percent Change in Body Weight [12 weeks]

Linked records (1)

Automatic links, confirmed or rejected during screening. A record citing this registration may be a secondary analysis, a commentary or a review that mentions the trial.
RecordTitleYearDesignIdentifiersLink basis
R0004304Oral GLP-1RA TERN-601 for Adults With Obesity/Overweight: Placebo-Controlled, Multiple-Ascending-Dose, Phase 1 and 2 Studies.
Garvey WT, Obesity (Silver Spring, Md.)
2026Randomized trialPMID 42528333DOIcites ClinicalTrials.gov:NCT06854952; registry reference DERIVED:42528333