Completed Enrollment
A Study of Insulin Efsitora Alfa (LY3209590) Compared to Degludec in Adults With Type 2 Diabetes Who Are Starting Basal Insulin for the First Time (QWINT-2)
I8H-MC-BDCX - ClinicalTrials.gov - NCT05362058
The purpose of this study is to determine the effect and safety of insulin efsitora alfa (LY3209590) compared to degludec in adult participants with type 2 diabetes who are starting basal insulin for the first time. Additional participants will continue to be enrolled in a maximum extended enrollment cohort.
Trial Summary
Age Range
≥18 yearsConditions the trial is for
Type 2 DiabetesWhat the trial is testing?
LY3209590, Insulin Degludec, Insulin Efsitora AlfaCould I receive a Placebo?
NoEnrollment Goal
928Trial Dates
Jun 3, 2022 - Apr 15, 2024How long will I be in the trial?
Your participation could last about 57 weeks and may include up to 33 visits to the study center.Trial Phase
IIIKey Requirements
Clinical trials have inclusion and exclusion requirements to determine which individuals qualify for participation. Listed below are key requirements for this clinical trial, but there may be additional requirements to qualify.Participants Must:
- Participants must have type 2 diabetes mellitus (T2DM)
- Participants must be taking diabetes medication 3 months before entering the study
Participants Must Not:
- Participants must not have type 1 diabetes mellitus (T1DM)
- Participants must not have had an episode of very low blood glucose level within the last 6 months of starting the study
- Participants must not have had heart failure or other heart conditions
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Clinical Trial Resources
You will complete the questionnaire on another website.YesNo