LivingGLP1
Study S001413

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

Registration

Registration
NCT06828055
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
TRIPLE
Status
COMPLETED
Enrollment
280
Start
2024-12-18
Primary completion
2025-06-24
Lead sponsor
Viking Therapeutics, Inc.
Conditions
Weight Loss
Interventions
DRUG:Placebo; DRUG:VK2735
Results posted
FALSE

Registered primary outcomes

  • Percent (relative) change from baseline in body weight after 13 weeks of treatment [13 Weeks]

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