drugset / Trial / NCT05963022

A Study of Tirzepatide (LY3298176) in Chinese Participants With Type 2 Diabetes (SURPASS-CN-MONO)

NCT05963022 ↗

Phase 3 Completed 206 enrolled Eli Lilly and Company
RandomizedParallel-groupDouble-blindTreatment

Summary

The main purpose of this study is to investigate the efficacy and safety of Tirzepatide monotherapy in Chinese participants with Type 2 Diabetes.

Timeline

Start
2023-08-21
Primary completion
2024-10-09
Completion
2024-10-09

Outcome

Met primary endpoint

registry analysis (superiority test); 5 mg Tirzepatide vs Placebo; p <0.001; LS Mean Difference -1.42 (95% CI -1.76 to -1.07); ANCOVA NCT05963022 ↗

registry analysis (superiority test); 10 mg Tirzepatide vs Placebo; p <0.001; LS Mean Difference -0.98 (95% CI -1.34 to -0.63); ANCOVA NCT05963022 ↗

registry analysis (superiority test); 15 mg Tirzepatide vs Placebo; p <0.001; LS Mean Difference -1.26 (95% CI -1.61 to -0.92); ANCOVA NCT05963022 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Tirzepatide Peptide 5 mg Subcutaneous
Subject Tirzepatide Peptide 10 mg Subcutaneous
Subject Tirzepatide Peptide 15 mg Subcutaneous