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Clinical Trial Summary

The purpose of this study is to determine the long-term safety of the study intervention orforglipron as a monotherapy or in combination with oral antihyperglycemic medication. This study includes 3 periods as follows: - screening and lead-in period: up to 4 weeks - treatment period: 52 weeks, including 20 weeks of dose escalation, and - safety follow-up period: 2 weeks.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06010004
Study type Interventional
Source Eli Lilly and Company
Contact
Status Active, not recruiting
Phase Phase 3
Start date September 28, 2023
Completion date June 21, 2025

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