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Clinical Trial Summary

This study evaluated the single-dose pharmacokinetics of human fibrinogen concentrate and clot strength (maximum clot firmness [MCF]) in subjects with congenital fibrinogen deficiency. MCF was measured to demonstrate the functional activity of replacement fibrinogen when a fixed dose of human fibrinogen concentrate was administered.


Clinical Trial Description

n/a


Study Design

Endpoint Classification: Pharmacokinetics Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00496262
Study type Interventional
Source CSL Behring
Contact
Status Completed
Phase Phase 2
Start date July 2007
Completion date May 2008

See also
  Status Clinical Trial Phase
Withdrawn NCT00916656 - Fibrinogen Concentrate (Human) - Efficacy and Safety Study Phase 3