EICHORCondition: Sleep Apnea · Obstructive · Obesity · Sponsor: Innovent Biologics (Suzhou) Co. Ltd.
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.
This description comes directly from the study's public registry record.
baiyi yan · 0512-69566088 · baiyi.yan@innoventbio.com
Always discuss trial participation with your own doctor first.
| Peking University Third Hospital | Beijing, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06931028