Study to Investigate the Long-term Efficacy and Safety of Human-cl rhFVIII in Previously Treated Patients (PTPs)

PHASE3CompletedINTERVENTIONAL
Enrollment

3

Participants

Timeline

Start Date

June 30, 2011

Primary Completion Date

August 31, 2012

Study Completion Date

August 31, 2012

Conditions
Severe Hemophilia A
Interventions
BIOLOGICAL

Human-cl rhFVIII

Human-cl rhFVIII is administered intravenously on demand for bleeding episodes and prophylactically in case of surgery. The dosage depends on the severity of the bleeding episodes and the surgery.

Trial Locations (2)

20057

Georgetown University, Washington D.C.

Unknown

"Haematological Hospital SHAT Joan Pavel", Sofia

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Octapharma

INDUSTRY