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Study of rhPro-UK in Patients With Acute Ischaemic Stroke in 4.5 Hours After Stroke Onset(PROST)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT03541668
Recruitment Status : Completed
First Posted : May 30, 2018
Last Update Posted : June 22, 2020
Sponsor:
Information provided by (Responsible Party):
Tasly Biopharmaceuticals Co., Ltd.

No Study Results Posted on ClinicalTrials.gov for this Study
Recruitment Status : Completed
Actual Primary Completion Date : April 14, 2020
Actual Study Completion Date : May 24, 2020