A Long-term Safety Study of Orforglipron (LY3502970) in Participants With Type 2 Diabetes

3期 已完成 NCT06010004

摘要

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.

Number of Participants With Treatment Emergent Adverse Events (TEAEs)

Baseline to Week 54 · Participants

在 BENITIONS 中查看 查看 ClinicalTrials.gov 原文

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