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NCT06931028·Phase 3·INTERVENTIONAL

A Study of IBI362 in Chinese Subjects With Obstructive Sleep Apnea and BMI≥28 kg/m2

Status

Recruiting

Phase

Phase 3

Enrollment

260

Locations

1

Results

Not posted

Publications

0

Study summary

What the protocol is testing.

This is a multicenter, randomized, double-blind, placebo-controlled Phase III clinical study to evaluate the efficacy and safety of IBI362 in subjects with moderate-to-severe obstructive sleep apnea (OSA) and a body mass index (BMI) ≥28 kg/m2. Subjects will be randomly assigned to IBI362 9 mg and placebo groups. All study treatment will be administered once-weekly and subcutaneously. The entire trial cycle includes a 4-week screening period, a 48-week double-blind treatment period, and a 12-week drug withdrawal follow-up period after the end of treatment.

Interventions

Treatment arms and agents.

OTHER

placebo

placebo administered subcutaneously (SC) once a week.

DRUG

IBI362

Once-weekly injections of gradually increased doses of IBI362

Timeline

From registration to results.

  1. First posted

    Apr 16, 2025

  2. Study start

    Jun 12, 2025

  3. Primary completion

    May 7, 2027

  4. Study completion

    Jun 11, 2027

  5. Results posted

    Not reported

  6. Registry updated

    Jun 29, 2025

Outcomes

What the study measures.

Primary outcomes

Change from Baseline in Apnea-Hypopnea Index (AHI)

Time frame · Week 48

AHI is defined as the average number of apnea and hypopnea events per hour of sleep, which is determined by polysomnography. The lower the value, the better, and the normal range is \<5 events/hour.

Secondary outcomes

Percent Change from Baseline in Body Weight

Time frame · Week 48

Change from Baseline in Systolic Blood Pressure (SBP)

Time frame · Week 48

Percent Change from Baseline in Apnea-Hypopnea Index (AHI)

Time frame · Week 48

AHI is defined as the average number of apnea and hypopnea events per hour of sleep, which is determined by polysomnography. The lower the value, the better, and the normal range is \<5 events/hour.

Percentage of Participants with ≥50% AHI Reduction from Baseline

Time frame · Week 48

Percentage of Participants with AHI <5 or with AHI 5-14 with Epworth Sleepiness Scale (ESS) ≤10

Time frame · Week 48

Change from Baseline in Sleep Apnea-Specific Hypoxic Burden (SASHB)

Time frame · Week 48

SASHB is an indicator that quantifies the cumulative effect of hypoxia caused by apnea or hypopnea events during sleep. It is also calculated based on the results of polysomnography. It combines the severity, duration and frequency of hypoxia, and can more comprehensively reflect the systemic damage of hypoxia to the body. It is an important predictive factor for increased CVD risk. The lower the value, the better.

Eligibility

Who can take part.

Minimum age
18 Years
Maximum age
Not reported
Sex
ALL
Healthy volunteers
No

Inclusion Criteria: * For PAP s: Subjects who have received positive airway pressure (PAP) therapy for at least 3 consecutive months prior to screening and plan to continue PAP therapy during the study. * For non-PAP s:Subjects who are unable or unwilling to undergo PAP therapy. PAP must not have been used for at least 4 weeks prior to screening. * For all subjects: 1. Age ≥18 years at the time of signing informed consent. 2. Polysomnography (PSG) during screening shows an apnea-hypopnea index (AHI) ≥15 events/hour. 3. Body mass index (BMI) ≥28.0 kg/m² at screening. Exclusion Criteria: For PAPs: * Have personal or job-related responsibilities, or in the opinion of the investigator have any situation, that would make it unsafe to stop PAP therapy for 7 days prior to PSG testing during the course of the study * Are unwilling to stop PAP therapy for 7 days prior to polysomnography (PSG) testing during the course of the study For all subjects: * Have type 1 diabetes mellitus (T1DM) or type 2 diabetes mellitus (T2DM). * Any previous or planned surgery for sleep apnea or major ear, nose or throat surgery, including tonsillectomy and adenoidectomy that still may affect breathing at time of baseline * Have significant craniofacial abnormalities that may affect breathing at baseline * Diagnosis of Obesity Hypoventilation Syndrome or daytime hypercapnia. * Active device treatment of OSA other than PAP therapy (for example, dental appliance), or other treatment, that in the opinion of the investigator, may interfere with study outcomes, unless willing to stop treatment at baseline and throughout the study. * Respiratory and neuromuscular diseases that could interfere with the results of the trial in the opinion of the investigator. * Have achieved a \>5% change in body weight through diet and exercise alone for at least 12 weeks prior to screening.

Study locations

1 registered sites.

China. Showing up to 24 locations stored in the fast local snapshot.

Peking University Third Hospital

Beijing, China

Publications

Results and literature.

No PMID-linked publications were present in this registry snapshot.

Primary links

Continue at the source.

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