drugset / Trial / NCT06579092
Effects of AZD5004 in Adults Who Are Living With Obesity or Overweight With at Least 1 Weight-related Comorbidity
RandomizedParallel-groupTriple-blindTreatment
Summary
A Phase IIb, global, randomized, parallel-group, double-blind, placebo-controlled, multicenter study to assess the efficacy and safety of AZD5004 compared with placebo, given once daily as an oral tablet(s) for 36 weeks, in male and female participants at least 18 years of age who are living with obesity (body mass index \[BMI\] ≥ 30 kg/m2), or overweight (BMI ≥ 27 kg/m2) who have at least 1 weight-related comorbidity
Timeline
- Start
- 2024-10-08
- Primary completion
- 2025-11-21
- Completion
- 2025-11-21
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Elecoglipron | Unknown | 5 mg | Oral |
| Subject | Elecoglipron | Unknown | 15 mg | Oral |
| Subject | Elecoglipron | Unknown | 50 mg | Oral |
| Subject | Elecoglipron | Unknown | 75 mg | Oral |