LivingGLP1
Study S001333

A Phase 3 Randomized, Double-Blind, Placebo-Controlled, 78-Week Efficacy and Safety Study of VK2735 Administered Subcutaneously for Weight Management in Participants With Type 2 Diabetes Who Are Obese, or Overweight

Registration

Registration
NCT07104383
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
TRIPLE
Status
ACTIVE_NOT_RECRUITING
Enrollment
1100
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

  • Percent change in body weight from baseline to Week 78 in body weight [78 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
R0056047Pre-registered mechanistic prediction: VK2735 in VANQUISH-2 (NCT07104383)
Natalija Karpichina, Zenodo (CERN European Organization for Nuclear Research)
2026Nonrandomized studyDOIcites ClinicalTrials.gov:NCT07104383