Peking University People's Hospital
Beijingcun, Hebei, China
Location status: Recruiting
NCT Number: NCT06254261
The main purpose of this study is to learn more about the Tolerability of RAY1225 in participants with Obesity. The study will also explore the efficacy of RAY1225. The study will last about six months for each participant.
Interested in participating?
Request Info18 year–70 year
All sexes
Interventional
Phase 2
Beijingcun, Hebei, China
Location status: Recruiting
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Administered SC
Placebo
Time frame: Baseline,Week26
Percent Change from Baseline in Body Weight
Time frame: Baseline,Week26
Time frame: Baseline,Week26
Time frame: Baseline,Week26
Time frame: Baseline,Week26
Contact information is provided by the study sponsor or research team.
Guangdong Raynovent Biotech Co., Ltd
Industry
A Multicenter, Randomized, Double-blind, Placebo-controlled Phase 2 Study Evaluating the Safety, Tolerability, and Efficacy of RAY1225 in Participants With Obesity
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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