drugset / Trial / NCT06370715

A Study of LY900014 in Adult Participants With Type 2 Diabetes Mellitus in India

NCT06370715

Phase 4 Completed 150 enrolled Eli Lilly and Company Cipla Ltd. · collab
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the safety of insulin lispro-aabc in adult participants with Type 2 diabetes mellitus in India. The study will last about 33 weeks for each participant, including screening (1 week), Lead-in period (4 weeks), treatment period (26 weeks) and follow up period (2 weeks).

Timeline

Start
2024-04-18
Primary completion
2025-09-02
Completion
2025-09-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Insulin Lispro-aabc Unknown Subcutaneous
Background insulin glargine Protein / enzyme biologic Subcutaneous