recombinant factor VIII SQ: Clinical Trials

14 trials of recombinant factor VIII SQ, newest first

ClinicalTrials Daily  ·  Areas  ·  Conditions  ·  Drugs  ·  Sponsors  ·  

9 completed, 3 withdrawn, 2 terminated. 4 Phase 4, 3 Phase 3, 2 Not applicable, 1 Phase 1.

By phase and status

PhaseTrialsStatus
Phase 44Completed 2, Terminated 1, Withdrawn 1
Phase 33Completed 2, Terminated 1
Not applicable2Completed 1, Withdrawn 1
Phase 11Completed 1

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Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.

TrialPhaseStatusSponsorEnrollmentStartUpdated
Patient-reported Outcomes in Subjects Treated With ReFacto AF Routine Prophylaxis
Refacto AF - Hemophilia A
WithdrawnPfizer2019-09-012020-11-16
Post Marketing Surveillance To Observe Safety And Efficacy Of Xyntha® In Subjects With Hemophilia A
Xyntha : coagulation factor IIIV (recombinant) - Hemophilia A
CompletedPfizer422014-02-012015-08-17
Relative Bioavailability Of Two Formulations Of Moroctocog Alfa (AF-CC)
moroctocog alfa (AF-CC) - Hemophilia A
Phase 1CompletedPfizer162012-08-012013-02-08
Study Evaluating Safety And Efficacy Of Moroctocog Alfa (AF-CC) In Previously Treated Hemophilia A Patients
Moroctocog alfa ( AF-CC), Laboratory tests - Hemophilia A
Phase 4CompletedPfizer372009-12-012017-02-10
Study of First TIME Immunotolerance Induction in Severe Hemophilia A Patients With Inhibitor at High Risk of Failure: Comparison With FVIII Concentrates With or Without Von Willebrand Factor - RES.I.S.T. Naive
FVIII Concentrates, FVIII/VWF concentrates - Severe Hemophilia A
Not applicableWithdrawnCity of Hope Medical Center2009-09-252020-12-17
Study Evaluating Pharmacovigilance Of Refacto AF
ReFacto AF (Moroctocog alfa) - Hemophilia A
CompletedPfizer1012009-07-172018-07-17
Study Evaluating The Efficacy And Safety Of Xyntha In Children Less Than 6 Years Of Age
Moroctocog alfa - Hemophilia A
Phase 3TerminatedWyeth is now a wholly owned subsidiary of Pfizer12009-06-012022-06-15
Study Evaluating Safety Of Patients Switching To ReFacto AF In Usual Care Settings
moroctocog alfa (AF-CC) (ReFacto AF), Laboratory tests - Hemophilia A
Phase 4TerminatedPfizer2082009-05-012014-09-01
Study Evaluating Prophylaxis Treatment & Characterizing Efficacy, Safety, & PK Of B-Domain Deleted Recombinant FVIII
Moroctocog alfa (AF-CC) - Hemophilia A
Phase 3CompletedPfizer662007-12-012019-01-11
Clot Formation and Clot Stability in Patients With Severe Haemophilia A
ReFacto (Recombinant factor VIII) and Tranexamic acid - Hemophilia A
Not applicableCompletedUniversity of Aarhus82006-01-012006-11-16
Study to Establish Bioequivalence of ReFacto AF (BDDrFVIII) With Advate (FLrFVIII) in Hemophilia A
ReFacto AF, B-Domain deleted Recombinant Factor VIII, BDDrFVIII - Hemophilia A
Phase 3CompletedWyeth is now a wholly owned subsidiary of Pfizer1002005-07-012008-04-22
Study Comparing Blood Levels of ReFacto and Advante in Hemophilia A
ReFacto, Advante - Hemophilia A
Phase 4WithdrawnWyeth is now a wholly owned subsidiary of Pfizer2005-04-012018-09-25
Study Evaluating ReFacto® in Hemophilia A Undergoing Major Surgery
ReFacto - Hemophilia A
Phase 4CompletedWyeth is now a wholly owned subsidiary of Pfizer152003-02-012007-12-28
Study Evaluating Refacto For Pharmacovigilance
Moroctocog alfa - Hemophilia A
CompletedWyeth is now a wholly owned subsidiary of Pfizer2881999-07-012011-02-11

Conditions studied

Hemophilia A (14)  ·  Hemostatic Disorders (1)

Sponsors

Pfizer (7)  ·  Wyeth is now a wholly owned subsidiary of Pfizer (5)  ·  City of Hope Medical Center (1)  ·  University of Aarhus (1)

Countries

Germany (5)  ·  Austria (4)  ·  Italy (4)  ·  United States (4)  ·  Belgium (3)  ·  Finland (3)  ·  France (3)  ·  Hungary (3)  ·  Netherlands (3)  ·  New Zealand (3)  ·  Romania (3)  ·  Spain (3)  ·  Sweden (3)  ·  United Kingdom (3)  ·  Denmark (2)

Top investigators

Anne-Mette Hvas, MD, Ph.D. (1)  ·  Nadia P Ewing, MD (1)

Results publications

PMID 27140804

NIH funding

2008 (2)