Study of the Efficacy and Safety PF-06741086 in Adult and Teenage Participants With Severe Hemophilia A or Moderately Severe to Severe Hemophilia B

  • STATUS
    Recruiting
  • End date
    Sep 27, 2024
  • participants needed
    145
  • sponsor
    Pfizer
Updated on 26 May 2022
treatment regimen
replacement therapy
Factor VIII
coagulation factor
hemophilia
severe haemophilia a
antihemophilic factor
acute hemorrhage
acute bleeding

Summary

Treatment with PF-06741086 is anticipated to demonstrate a clinically relevant advantage and/or a major contribution to patient care in comparison to current methods of treatment for hemophilia A or B because it works differently than factor replacement products and will work in the presence of inhibitors. The potential for once weekly (QW) subcutaneous (SC) administration provides for treatment options in the absence of reliable vascular access, increased convenience and may enable better compliance. Combined, these qualities should result in a reduction of bleeding episodes.

Details
Condition Hemophilia A, Hemophilia B
Treatment PF-06741086
Clinical Study IdentifierNCT03938792
SponsorPfizer
Last Modified on26 May 2022

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