13
Participants
Start Date
September 25, 2020
Primary Completion Date
March 10, 2022
Study Completion Date
March 10, 2022
Tenecteplase
First 20 patients randomized to treatment arm will receive 0.25 mg/kg of tenecteplase. Next 20 patients randomized to treatment arm will receive 0.50 mg/kg of tenecteplase. Both will receive concomitant heparin to maintain activated partial thromboplastin time between 2.0 and 2.5 upper limit of normal.
Placebo
Patients will receive placebo with concomitant heparin to maintain activated partial thromboplastin time between 2.0 and 2.5 upper limit of normal.
Mount Sinai Hospital, New York
Collaborators (1)
Genentech, Inc.
INDUSTRY
Hooman Poor
OTHER