drugset / Trial / NCT06579092

Effects of AZD5004 in Adults Who Are Living With Obesity or Overweight With at Least 1 Weight-related Comorbidity

NCT06579092

Phase 2 Completed 310 enrolled AstraZeneca
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

EvaluationDrugModalityDoseRoute
Subject Elecoglipron Unknown 5 mg Oral
Subject Elecoglipron Unknown 15 mg Oral
Subject Elecoglipron Unknown 50 mg Oral
Subject Elecoglipron Unknown 75 mg Oral

Indications