Study Evaluating Refacto For Pharmacovigilance

CompletedOBSERVATIONAL
Enrollment

288

Participants

Timeline

Start Date

July 31, 1999

Primary Completion Date

January 31, 2010

Study Completion Date

January 31, 2010

Conditions
Hemophilia A
Interventions
DRUG

Moroctocog alfa

Patients will be treated in accordance with the requirements of the labeling of ReFacto (Moroctocog alfa) in Germany. The dosage and duration of therapy is to be determined by the physician to meet the patients' individual needs for treatment.

Trial Locations (26)

10249

Pfizer Investigational Site, Berlin

13353

Pfizer Investigational Site, Berlin

14467

Pfizer Investigational Site, Potsdam

18055

Pfizer Investigational Site, Rostock

19049

Pfizer Investigational Site, Schwerin

20246

Pfizer Investigational Site, Hamburg

23538

Pfizer Investigational Site, Lübeck

28205

Pfizer Investigational Site, Bermen

30625

Pfizer Investigational Site, Hanover

35385

Pfizer Investigational Site, Giessen

53105

Pfizer Investigational Site, Bonn

60594

Pfizer Investigational Site, Frankfurt A. M.

60596

Pfizer Investigational Site, Frankfurt am Main

65191

Pfizer Investigational Site, Wiesbaden

66424

Pfizer Investigational Site, Homburg

69123

Pfizer Investigational Site, Heidelberg

80336

Pfizer Investigational Site, München

80337

Pfizer Investigational Site, München

89081

Pfizer Investigational Site, Ulm

91054

Pfizer Investigational Site, Erlangen

A-1090

Pfizer Investigational Site, Vienna

06120

Pfizer Investigational Site, Halle

07646

Pfizer Investigational Site, Stadtroda

01665

Pfizer Investigational Site, Klipphausen

04103

Pfizer Investigational Site, Leipzig

D-48143

Pfizer Investigational Site, Münster

All Listed Sponsors
lead

Wyeth is now a wholly owned subsidiary of Pfizer

INDUSTRY

NCT00195442 - Study Evaluating Refacto For Pharmacovigilance | Biotech Hunter | Biotech Hunter