drugset / Trial / NCT03495102

A Study of the Efficacy and Safety of Dulaglutide (LY2189265) in Participants With Type 2 Diabetes

NCT03495102 ↗

Phase 3 Completed 1842 enrolled Eli Lilly and Company
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of investigational doses of once weekly dulaglutide when added to metformin in participants with type 2 diabetes with inadequate blood sugar control.

Timeline

Start
2018-04-05
Primary completion
2019-05-28
Completion
2019-10-10

Outcome

Met primary endpoint

paper At 36 weeks, dulaglutide 4.5 mg provided superior HbA1c reductions compared with 1.5 mg PMID 33397768 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Dulaglutide Peptide 1.5 mg Subcutaneous
Subject Dulaglutide Peptide 3 mg Subcutaneous
Subject Dulaglutide Peptide 4.5 mg Subcutaneous