LivingGLP1
Study S003378

A Multicenter, Randomized, Double-blind, Placebo-controlled Phase 2 Study Evaluating the Safety, Tolerability, and Efficacy of RAY1225 in Participants With Obesity

Registration

Registration
NCT06254261
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
DOUBLE
Status
RECRUITING
Enrollment
270
Start
2024-02-21
Primary completion
2025-12-20
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

  • Change From Baseline in Body Weight [Baseline,Week26]

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