Tenecteplase in Patients With COVID-19

PHASE2CompletedINTERVENTIONAL
Enrollment

13

Participants

Timeline

Start Date

September 25, 2020

Primary Completion Date

March 10, 2022

Study Completion Date

March 10, 2022

Conditions
COVID-19Respiratory FailureARDS
Interventions
DRUG

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.

DRUG

Placebo

Patients will receive placebo with concomitant heparin to maintain activated partial thromboplastin time between 2.0 and 2.5 upper limit of normal.

Trial Locations (1)

10029

Mount Sinai Hospital, New York

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Genentech, Inc.

INDUSTRY

lead

Hooman Poor

OTHER

NCT04505592 - Tenecteplase in Patients With COVID-19 | Biotech Hunter | Biotech Hunter