Clinical trial

Dose-Response Study of Recombinant Factor VIII Manufactured Protein-Free…

NCT00289536 · Baxalta now part of Shire, Industry · Completed

Key facts

NCT number NCT00289536
Title Dose-Response Study of Recombinant Factor VIII Manufactured Protein-Free (rAHF-PFM) in Patients With Hemophilia A
Official title Advate Antihemophilic Factor (Recombinant), Plasma/Albumin-Free Method (ADVATE rAHF-PFM): A Phase 4 Study to Determine the Pharmacokinetic Response of Patients Diagnosed With Severe Hemophilia A to Different Doses of ADVATE rAHF-PFM
Lead sponsor Baxalta now part of Shire, Industry
Status Completed
Phase Phase 4
Study type Interventional
Conditions Hemophilia A
Intervention type Biological
Interventions Antihemophilic factor, recombinant, manufactured protein-free
Enrollment 38
Start date Feb 2, 2006
Primary completion Apr 1, 2007
Completion Apr 1, 2007
First posted Feb 10, 2006
Last update posted Jun 10, 2021
Countries United States

At a glance

  • Yes Results posted
  • None Linked FDA submissions

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

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

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