LivingGLP1
Study S000255

A Phase 3 Randomized, Double-Blind, Placebo-Controlled, 68-Week Efficacy and Safety Study of VK2735 Administered Orally for Weight Management in Participants With Type 2 Diabetes Mellitus Who Are Obese, or Overweight

Registration

Registration
NCT07868939
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
DOUBLE
Status
NOT_YET_RECRUITING
Enrollment
560
Start
2026-10-16
Primary completion
2028-10
Lead sponsor
Viking Therapeutics, Inc.
Conditions
Weight Loss
Interventions
DRUG:VK2735 Oral; DRUG:Placebo Comparator
Results posted
FALSE
Individual participant data sharing
NO

Registered primary outcomes

  • Percent change in body weight for participants with type 2 diabetes mellitus receiving VK2735 orally once daily [68 weeks]

Linked records (0)

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