EFFEKT - Efficacy and Safety of Long-term Treatment With KOGENATE Bayer/FS

CompletedOBSERVATIONAL
Enrollment

405

Participants

Timeline

Start Date

June 30, 2008

Primary Completion Date

November 30, 2012

Study Completion Date

April 30, 2013

Conditions
Hemophilia A
Interventions
BIOLOGICAL

Recombinant Factor VIII (Kogenate FS, BAY14-2222)

Haemophilia A patients

Trial Locations (17)

Unknown

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Sponsors

Lead Sponsor

All Listed Sponsors
lead

Bayer

INDUSTRY

NCT00874926 - EFFEKT - Efficacy and Safety of Long-term Treatment With KOGENATE Bayer/FS | Biotech Hunter | Biotech Hunter