drugset / Trial / NCT06650007

the Efficacy and Safety of HRS9531 Injection in Subjects With Type 2 Diabetes, Inadequately Controlled With Diet and Exercise Alone

NCT06650007 ↗

Phase 3 Completed 218 enrolled Fujian Shengdi Pharmaceutical Co., Ltd.
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary objective of this study is to evaluate the effectiveness of HRS9531 compared to placebo in controlling blood glucose levels after 36 weeks of treatment

Timeline

Start
2024-11-08
Primary completion
2026-01-21
Completion
2026-06-12

Outcome

Met primary endpoint

release “HRS9531-302)取得积极顶线结果,主要终点及所有关键次要终点均达到优效” hengrui.com ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject HRS9531 Unknown — —