LivingGLP1
Study S003322

A Phase 2, Randomized, Double-blind, Placebo-controlled, Parallel Group Study to Evaluate Efficacy, Safety, and Tolerability of HM15275 for 36 Weeks in Obese or Overweight Subjects Without Diabetes Mellitus

Registration

Registration
NCT07205900
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
TRIPLE
Status
ACTIVE_NOT_RECRUITING
Enrollment
267
Start
2025-12-02
Primary completion
2027-01
Lead sponsor
Hanmi Pharmaceutical Company Limited
Conditions
Obese; Obesity
Interventions
DRUG:HM15275; DRUG:Placebo of HM15275
Results posted
FALSE
Individual participant data sharing
NO

Registered primary outcomes

  • Percent Change in Body Weight. [Up to 41 weeks]

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