drugset / Trial / NCT05051579

A Study of LY3502970 in Participants With Obesity or Overweight With Weight-related Comorbidities

NCT05051579 ↗

Phase 2 Completed 272 enrolled Eli Lilly and Company
RandomizedParallel-groupDouble-blindTreatment

Summary

The main purpose of the study was to assess the effect of LY3502970 in participants who have obesity or are overweight.

Timeline

Start
2021-09-29
Primary completion
2022-08-25
Completion
2022-11-22

Outcome

Met primary endpoint

registry analysis (superiority test); 12 mg LY3502970 vs Placebo; p <0.001; LS Mean difference (Final Values) -6.5 (95% CI -8.9 to -4.2); Mixed Models Analysis NCT05051579 ↗

paper At week 26, the mean change from baseline in body weight ranged from -8.6% to -12.6% across the orforglipron dose cohorts and was -2.0% in the placebo group. PMID 37351564 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Orforglipron Small molecule 12 mg Oral
Subject Orforglipron Small molecule 24 mg Oral
Subject Orforglipron Small molecule 36 mg Oral
Subject Orforglipron Small molecule 45 mg Oral

Indications