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Study identifier: NCT07279194 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

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

Condition: Obesity & Overweight  ·  Sponsor: Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd.

PhasePhase 3
Planned participants825
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Hui Qiao  ·  +86 0571-89908523  ·  qiaohui@eastchinapharm.com

Always discuss trial participation with your own doctor first.

Locations (1)

Zhongshan HoapitalShanghai, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07279194