Clinical Trial

Efficacy and Safety of HDM1005 in Chinese Obesity or Overweight Patients Without Diabetes

Recruiting Phase 3
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Summary
This is a 56-week randomized, double blinded, parallel-controlled study evaluating the efficacy andsafety of the HDM1005 in patients with obesity or overweight. Eligible participants will be screened and randomized to different dose group of HDM1005 or the placebo group at a ratio of 1:1:1 , HDM1005 or placebo will be given once weekly for 52 weeks, following by a safety follow up of 4 weeks. All participants received a lifestyle intervention that involved counselling on diet and physical activity.
Trial Details
NCT Number NCT07279194
Lead Sponsor Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd.
Conditions Obesity & Overweight
Enrollment 825 participants
Start Date 2025-10-14
Primary Completion 2026-09-20 (estimated)
Study Completion 2026-12-13 (estimated)
Updated on ClinicalTrials.gov 2025-12-12