drugset / Trial / NCT02367976

Efficacy and Safety on Prouk for STEMI Patients in China

NCT02367976

Phase 3 Unknown 450 enrolled Suzhou RxD Biopharmaceutical Co., Ltd
RandomizedParallel-groupSingle-blindTreatment

Summary

The purpose of the study is to evaluate the efficacy and safety of rh-prouk as pharmacoinvasive therapy on those ST Elevated Myocardial Infarctions patients, it is designed as a multicenter, active controlled, single blinded study. The primary endpoint is to assess the coronary recanalization 90 minutes after thrombolysis. The secondary endpoint is to evaluate the mortality rate at day 30.

Timeline

Start
2015-01
Primary completion
2016-12
Completion
2017-12

Drugs

EvaluationDrugModalityDoseRoute
Subject rhPro-UK Protein / enzyme biologic