LivingGLP1
Study S000714

A Phase 2 Randomized, Double-Blind, Placebo-Controlled, 13-week Study of VK2735 for Weight Management in Subjects Who Are Obese, or Overweight With at Least One Weight-related Comorbid Condition

Registration

Registration
NCT06068946
Acronym
VENTURE
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
TRIPLE
Status
COMPLETED
Enrollment
176
Start
2023-08-31
Primary completion
2024-02-27
Lead sponsor
Viking Therapeutics, Inc.
Conditions
Weight Loss
Interventions
BIOLOGICAL:VK2735; BIOLOGICAL:Placebo
Results posted
FALSE

Registered primary outcomes

  • Percent (relative) change from baseline to Week 13 in body weight [13 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
R0011224Weekly Subcutaneous VK2735, a GIP/GLP-1 Receptor DualĀ Agonist, for Weight Management: Phase 2, Randomized, 13-Week VENTURE Study.
Bays HE, Obesity (Silver Spring, Md.)
2026Randomized trialPMID 41508550DOIcites ClinicalTrials.gov:NCT06068946; registry reference DERIVED:41508550