Canadian Hemophilia Prophylaxis Study

PHASE4CompletedINTERVENTIONAL
Enrollment

56

Participants

Timeline

Start Date

June 26, 1997

Primary Completion Date

December 31, 2012

Study Completion Date

December 31, 2014

Conditions
Severe Hemophilia A
Interventions
BIOLOGICAL

Recombinant Factor VIII (Advate/Helixate FS/KoegenateFS)

escalating dose prophylaxis

BIOLOGICAL

Recombinant Factor VIII (Advate/Helixate FS/KoegenateFS)

escalating dose

Trial Locations (1)

M5G 1X8

The Hospital for Sick Children, Toronto

All Listed Sponsors
lead

The Hospital for Sick Children

OTHER

NCT01085344 - Canadian Hemophilia Prophylaxis Study | Biotech Hunter | Biotech Hunter