Obstructive Sleep Apnea (OSA) and Obesity

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Review clinical trials related to Obstructive Sleep Apnea (OSA) and Obesity. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

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 Receiving Positive Airway Pressure (PAP) Therapy

This is a 56-week randomized, double blinded, parallel-controlled study evaluating the efficacy and safety of the HDM1005 in patients with obstructive sleep apnea (OSA) and obesity receiving positive airway pressure (PAP) therapy. Eligible participants will be screened and randomized to the HDM1005 group or the placebo group at a ratio of 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.

Participants needed: 200
Trial details
Phase: Phase 3Age: 18-75Biological sex: AllType: InterventionalSponsor: Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd.Updated: Aug 31, 2026Locations: 1
Eligibility criteria

Age between 18 and 75 years, male or female, at the time of signing the informed... [+4]

History of any type of diabetes mellitus (history of gestational diabetes is per... [+9]

Status: Not yet recruiting

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

This is a 56-week randomized, double blinded, parallel-controlled study evaluating the efficacy and safety of the HDM1005 in patients with obstructive sleep apnea (OSA) and obesity not receiving positive airway pressure (PAP) therapy. Eligible participants will be screened and randomized to the HDM1005 group or the placebo group at a ratio of 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.

Participants needed: 200
Trial details
Phase: Phase 3Age: 18-75Biological sex: AllType: InterventionalSponsor: Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd.Updated: Aug 26, 2026Locations: 1
Eligibility criteria

Age between 18 and 75 years, male or female, at the time of signing the informed... [+4]

History of any type of diabetes mellitus (history of gestational diabetes is per... [+9]