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Antihemophilic Factor (Recombinant) - Plasma/Albumin Free Method
BIOLOGICAL
3 trials
Sponsors
Baxalta now part of Shire
Conditions
Hemophilia A
Phase 1
BAX 855 Dose-Escalation Safety Study
Completed
NCT01599819
Baxalta now part of Shire
Hemophilia A
Start: 2011-09-30
End: 2012-07-27
Updated: 2021-05-05
Phase 2
Study Investigating a PEGylated Recombinant Factor VIII (BAX 855) for Hemophilia A (PROLONG-ATE Study)
Completed
NCT01736475
Baxalta now part of Shire
Hemophilia A
Start: 2013-01-31
End: 2014-07-17
Updated: 2021-05-20
Phase 3
BAX 855 Pediatric Study
Completed
NCT02210091
Baxalta now part of Shire
Hemophilia A
Start: 2014-10-31
End: 2015-10-23
Updated: 2021-05-24
Related Papers
Clinical studies of extended-half-life recombinant FVIII products for prophylaxis in adults and children: A critical review from the physician's perspective.
2022-04-04
13 citations
Subgroup analysis of a phase 2/3 study of rurioctocog alfa pegol in patients with severe hemophilia A: efficacy and safety in previously treated Korean patients.
2019-09-25
4 citations
Immunogenicity of BAX 855 in Previously Treated Patients with Congenital Severe Hemophilia Α
Blood
2016-12-02
2 citations
Pegylated, full-length, recombinant factor VIII for prophylactic and on-demand treatment of severe hemophilia A
Blood
2015-07-08
250 citations