LivingGLP1
Study S001939

A Phase 3 Randomized, Double-Blind, Placebo-Controlled, 78-Week Efficacy and Safety Study of VK2735 Administered Subcutaneously for Weight Management in Participants Without Type 2 Diabetes Who Are Obese, or Overweight With at Least One Weight-related Comorbid Condition

Registration

Registration
NCT07104500
Acronym
VANQUISH 1
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
TRIPLE
Status
ACTIVE_NOT_RECRUITING
Enrollment
4500
Start
2025-06-23
Primary completion
2027-07-01
Lead sponsor
Viking Therapeutics, Inc.
Conditions
Weight Loss
Interventions
DRUG:VK2735
Results posted
FALSE

Registered primary outcomes

  • Percentage change in body weight from baseline for participants receiving VK2735 after 78 weeks of treatment [78 Weeks]

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