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Clinical Trial Summary

In order to reevaluate safety and efficacy of human urinary kallikrein in treating acute cerebral infarction ,a multi-center, open label , single group study was designed. Expect to enroll 60 sites and 2186 subjects. Subjects will receive kallikrein treatment according to real clinical practice (suggest above 14days treatment) and 90 days follow up


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02562183
Study type Interventional
Source Techpool Bio-Pharma Co., Ltd.
Contact
Status Enrolling by invitation
Phase Phase 4
Start date August 2015
Completion date November 30, 2018

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