Fibrinogen Concentrate (Human) - Efficacy and Safety Study

PHASE3WithdrawnINTERVENTIONAL
0
Timeline

Start Date

October 31, 2009

Primary Completion Date

March 31, 2014

Study Completion Date

March 31, 2014

Conditions
AfibrinogenemiaHypofibrinogenemiaFibrinogen Deficiency
Interventions
BIOLOGICAL

Fibrinogen Concentrate, Human (FCH)

"Intravenous (IV) infusion to reach the peak target levels of 100 mg/dL with an accepted lower limit of 80 mg/dL on at least 3 subsequent days for minor bleeding episodes and 150 mg/dL with an accepted lower limit of 130 mg/dL on at least 7 subsequent days for major bleeding episodes.~If a subject's fibrinogen level is not known on Day 1, at the time treatment is initiated for the acute bleed (e.g., because they did not have a screening visit), the starting dose is to be 70 mg/kg b.w. Otherwise, the dose will be calculated individually."

BIOLOGICAL

Cryoprecipitate

Patients that received on-demand treatment with Cryoprecipitate for a classified bleeding event (minor or major) with a documented hemostatic efficacy assessment.

Sponsors

Lead Sponsor

All Listed Sponsors
lead

CSL Behring

INDUSTRY