Clinical trial

Efficacy and Safety Study of a Recombinant and Protein-Free Factor VIII…

NCT00189982 · Baxalta now part of Shire, Industry · Completed

Key facts

NCT number NCT00189982
Title Efficacy and Safety Study of a Recombinant and Protein-Free Factor VIII (rAHF-PFM) in Pediatric Patients in Canada With Hemophilia A - A Continuation of Baxter Study 060101
Official title Recombinant Antihemophilic Factor Manufactured and Formulated Without Added Human or Animal Proteins (ADVATE rAHF-PFM): Safety Monitoring in Pediatric Patients Diagnosed With Severe to Moderately Severe Hemophilia A - A Continuation of Baxter Clinical Study 060101
Lead sponsor Baxalta now part of Shire, Industry
Status Completed
Phase Phase 2/Phase 3
Study type Interventional
Conditions Hemophilia A
Intervention type Drug
Interventions Antihemophilic Factor Manufactured and Formulated without Added Human or Animal Proteins (rAHF-PFM)
Enrollment 4
Start date Dec 17, 2004
Primary completion Nov 10, 2006
Completion Nov 10, 2006
First posted Sep 19, 2005
Last update posted May 5, 2021
Countries Canada

At a glance

  • 1–9 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About ClinicalTrials.gov studies

ClinicalTrials.gov is the U.S. National Library of Medicine's registry of clinical studies conducted around the world. Contact and investigator details are not shown here.

Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

Browse all ClinicalTrials.gov studies