International PMS Study - KOGENATE Bayer

CompletedOBSERVATIONAL
Enrollment

200

Participants

Timeline

Start Date

December 31, 2002

Study Completion Date

December 31, 2005

Conditions
Hemophilia A
Interventions
DRUG

Kogenate (BAY14-2222)

Patients with severe haemophilia A (\<2% FVIII:C baseline level) treated with Kogenate Bayer as their only source of recombinant FVIII

Trial Locations (10)

Unknown

Many Locations

Many Locations

Many Locations

Many Locations

Many Locations

Many Locations

Many Locations

Many Locations

Many Locations

Many Locations

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Bayer

INDUSTRY

NCT00864552 - International PMS Study - KOGENATE Bayer | Biotech Hunter | Biotech Hunter