NOT YET RECRUITING
NCT07767942
Phase III Trial of UBT251 in Moderate-to-Severe OSA With Obesity: A Randomized, Double-Blind, Placebo-Controlled, Multicenter Study.
The objective of this clinical trial is to evaluate the efficacy of investigational drug UBT251 in the treatment of moderate-to-severe obstructive sleep apnea (OSA) with obesity, as well as to assess its safety. The key research question is:
Does UBT251 reduce the Apnea-Hypopnea Index (AHI) in participants?
UBT251 will be compared with placebo (an inactive substance identical in appearance) to determine its efficacy in treating moderate-to-severe OSA.
Participants will:
Receive weekly subcutaneous injections of either UBT251 or placebo for a duration of 52 weeks
Undergo examinations and testing at protocol-specified visit windows
Have their AHI assessed following the 52-week treatment period
Gender: All
Ages: 18 Years - 75 Years
Obstructive Sleep Apnea, Obesity