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Study identifier: NCT07521631 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Efficacy and Safety of HDM1005 Compared to Tirzepatide in Obese Adults Without Diabetes

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

PhasePhase 2
Planned participants372
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersNo

About this study

This is a 56-week randomized, open-label, controlled study evaluating the efficacy and safety of the HDM1005 compared to tirzepatide in adults with obesity but without diabetes. Eligible participants will be screened and randomized to different dose group of HDM1005 or the tirzepatide group at a ratio of 1:1:1 :1, HDM1005 or tirzepatide 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

Ling Tao  ·  +86 021-64041990  ·  cxytaoling@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/NCT07521631