About this trial
This trial is conducted in China. The purpose of the 24-week trial is to investigate the efficacy of henagliflozin to induce body weight loss and the purpose of the extension is to evaluate the hypoglycemic effect of henagliflozin in obese subjects without diabetes.
Trial has the following two periods: 1) A 12-week randomized, double-blind, placebo-controlled, multi-center trial for evaluating the efficacy of henagliflozin to induce body weight loss; 2) A 12-week multicenter randomized controlled open-label trial for evaluating the hypoglycemic effect of henagliflozin followed by a 24-week extension period.
Eligibility criteria
Qualifiers
18 years old≤age≤65 years old, regardless of gender and race
Nondiabetic population: without hypoglycemic treatment, FPG<7.0 mmol/l, PPG<11.1 mmol/l, and HbA1c<6.5%
obesity: BMI≥28 kg/m2
Stable weight: weight change less than 5kg in the past 3 months
Disqualifiers
Allergies to Henagliflozin or its formulations;
Participants have been definitely diagnosed with diabetes;
HbA1c≥6.5 % or FPG≥7.0 mmol/l, or PPG≥11.1 mmol/l;
Participants have used glucagon-like peptide-1 (GLP-1) receptor agonists, sodium glucose linked transporter-2 (SGLT-2) inhibitors, or other weight loss related drugs within the past 3 months;
Trial design
Treatments tested in this trial
- Henagliflozin
- Placebo
Treatment groups
Locations
Sponsors and collaborators
The First People's Hospital of Changzhou
Lead sponsor
The Second Hospital of Nanjing Medical University
Collaborator
The First Affiliated Hospital of Soochow University
Collaborator
Second Affiliated Hospital of Soochow University
Collaborator
Wuxi People's Hospital
Collaborator
Northern Jiangsu People's Hospital
Collaborator
The Affiliated Hospital of Xuzhou Medical University
Collaborator
The First People's Hospital of Lianyungang
Collaborator
Affiliated Hospital of Jiangsu University
Collaborator
The fourth affiliated hospital of nantong university
Collaborator