Congenital Fibrinogen Deficiency

What is a congenital fibrinogen deficiency?

Congenital fibrinogen deficiency (CFD) is a rare inherited bleeding disorder that occurs when your body is unable to produce ample fibrinogen (also called Factor I) to help the body form blood clots to stop bleeding. 

CFD is an umbrella term for several related disorders: Afibrinogenemia (a complete lack of fibrinogen), hypofibrinogenemia (low levels of fibrinogen), dysfibrinogenemia (fibrinogen does not work properly), and hypodysfibrinogenemia (a combined defect that involves both low levels of fibrinogen and impaired function). CSL Behring offers fibrinogen replacement therapies to help the body clot properly.

Resources for you

Signs of Bleeding The 5 signs of a bleeding disorder View Website
World Federation of Hemophilia A global organization aiming to improve and sustain care for people with inherited bleeding disorders.
View Website
National Hemophilia Foundation A U.S. organization dedicated to finding better treatments and cures for inheritable bleeding disorders.
View Website
Hemophilia Federation of America A U.S. a national nonprofit organization that assists and advocates for the bleeding disorders community.
View Website

Treatments Available

Availability of treatments may vary from country to country. Please be sure to visit your local site for further information.

RiaSTAP®  Fibrinogen Concentrate (Human) Visit RiaSTAP® Website  
Haemocomplettan P® Fibrinogen Concentrate (Human) Visit Haemocomplettan P® Website

Current Clinical Trials

Please see below for any current clinical trials for this condition.

Condition Description
Congenital Fibrinogen Deficiency An Observational Cohort Study of the Safety and Efficacy of Fibrinogen Concentrate, Human (FCH) in Subjects With Congenital Fibrinogen Deficiency Learn More
Looking down into microscope and taking notes

Participate in Clinical Trials

Discover what is involved in participating in one of our clinical trials and how you can enroll.

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