LivingGLP1
Study S003270

A Multicenter, Randomized, Double-blind, Placebo-controlled Phase 3 Study Evaluating the Safety, Tolerability, and Efficacy of RAY1225 in Participants Who Have Obesity or Are Overweight

Registration

Registration
NCT06893016
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
DOUBLE
Status
RECRUITING
Enrollment
640
Start
2025-06-15
Primary completion
2026-06-15
Lead sponsor
Guangdong Raynovent Biotech Co., Ltd
Conditions
Obesity
Interventions
DRUG:RAY1225; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
UNDECIDED

Registered primary outcomes

  • Percent Change From Baseline in Body Weight at Week 52 [Baseline and Week 52]
  • Number of Participants who Achieved a ≥ 5% Reduction in Body Weight from Baseline at Week 52 [Baseline and Week 52]

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