Clinical trial
A Study of SGB-7342 in Subjects With Obesity or Overweight
Opening soon · Phase 1 · 0 countries · Registry ID NCT07324850
Opening soonPhase 1Interventional
What this study is about
The purpose of this study is to evaluate the safety and tolerability of subcutaneously administered SGB-7342 in adult subjects with obesity and overweight.
A promising-looking record is not the same as confirmed eligibility. The study team must review the full criteria and current recruitment status.
Basic eligibility
Age18 Years to 55 Years
SexAll
Healthy volunteersNot accepted
ConditionObesity & Overweight
Full registry criteria
Inclusion Criteria: * Body Mass Index (BMI) within the range of 26.0 to 35.0 kg/m² * Have a stable body weight within 3 months * Participants must agree to use adequate contraception from signing the informed consent until 6 months after completion of the follow-up visit. * Willing to comply with the protocol required visit schedule and visit requirements and provide written informed consent. Exclusion Criteria: * A history of or a current surgical or medical condition that, in the opinion of the Investigator, may put the subject at significant risk (according to Investigator's judgment) or interfere with the subject's participation in the clinical study. * Use of GLP-1R agonists for any indication within 6 months prior to administering the investigational drug. * Use of non-GLP1R medications for weight loss within 3 months prior to administering the investigational drug. * Alanine aminotransferase (ALT), total bilirubin (TBIL), aspartate aminotransferase (AST)\> 1.5 × ULN, and deemed clinically significant by the Investigators
Treatments and study arms
SGB-7342
Drug
SC injection, single dose
SGB-7342-Matching placebo
Drug
Normal saline (0.9% NaCl) in a matching volume, SC injection, single dose
Primary outcomes
Number of Participants with Adverse Events (AEs)up to approximately 6 months
Study locations
0 locations were listed when this page was built. The first 40 are shown.
No public site location was included in this record. Check the original registry for updates.