LivingGLP1
Study S003308

A Phase III, Multicenter, Randomized, Double-Blind, Placebo-Controlled Clinical Study to Evaluate the Efficacy and Safety of HDM1005 Injection in Subjects With Obstructive Sleep Apnea (OSA) and Obesity Not Receiving Positive Airway Pressure (PAP) Therapy

Registration

Registration
NCT07787260
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
QUADRUPLE
Status
NOT_YET_RECRUITING
Enrollment
200
Start
2026-08
Primary completion
2028-03
Lead sponsor
Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd.
Conditions
Obstructive Sleep Apnea (OSA) and Obesity
Interventions
DRUG:HDM1005; DRUG:Placebo
Results posted
FALSE

Registered primary outcomes

  • Percentage change in body weight from baseline at week 52 [52 week]
  • Change in AHI from baseline at week 52 [52 week]

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