Study S001196

A Phase 3 Randomized, Double-Blind, Placebo-Controlled, 68-Week Efficacy and Safety Study of VK2735 Administered Orally for Weight Management in Participants Without Type 2 Diabetes Mellitus Who Are Obese, or Overweight With at Least One Weight-related Comorbid Condition

ClinicalTrials.gov record

Registration

Registration: NCT07868835
Study type: INTERVENTIONAL
Allocation: RANDOMIZED
Phase: PHASE3
Masking: DOUBLE
Status: NOT_YET_RECRUITING
Enrollment: 560
Start: 2026-10-15
Primary completion: 2028-07
Lead sponsor: Viking Therapeutics, Inc.
Conditions: Weight Loss
Interventions: DRUG:VK2735; DRUG:Placebo comparator
Results posted: FALSE
Individual participant data sharing: NO

Registered primary outcomes

Percentage change in body weight for participants receiving VK2735 orally once daily [68 weeks]

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