BAX 326 Pediatric Study

PHASE2/PHASE3CompletedINTERVENTIONAL
Enrollment

23

Participants

Timeline

Start Date

December 20, 2011

Primary Completion Date

May 14, 2013

Study Completion Date

May 14, 2013

Conditions
Hemophilia B
Interventions
BIOLOGICAL

BAX326

All participants underwent a pharmacokinetic evaluation with BAX326 (recombinant Factor IX) followed by twice weekly prophylactic treatment for 6 months or for at least 50 exposure days, whichever occurred last.

Trial Locations (11)

11156

S.C. Sanador SRL, Bucharest

79044

"State Institution Institute of Blood Pathology and Transfusion Medicine of the Academy of Medical Sciences of Ukraine", Lviv

110002

LNJP Maulana Azad Medical College & Associated Hospitals, New Delhi

195213

Republican Center for Hemophilia Treatment, Saint Petersburg

300011

Louis Turcanu Emergency Children's Hospital, Timișoara

350007

Pediatric Regional Clinical Hospital, Hematology Department, Krasnodar

620149

Regional Clinical Hospital, Yekaterinburg

30-663

University Pediatric Hospital, Krakow

10-561

Stanislaw Popowski Provincial Specialist Pediatric Hospital, Olsztyn

71-252

Professor Tadeusz Sokolowski Independent Public Teaching Hospital of the Pomeranian Medical University in Szczecin, Szczecin

M13 9WL

Manchester Children´s Hospital, Manchester

All Listed Sponsors
lead

Baxalta now part of Shire

INDUSTRY

NCT01488994 - BAX 326 Pediatric Study | Biotech Hunter | Biotech Hunter