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Fibrinogen · Tachosil

Plasma-derived product · Protein replacement · developed by Corza Medical Gmbh

Approved FDA, Apr 2010
1 Registered trials

What is Fibrinogen?

FIB Grifols is a human plasma-derived fibrinogen preparation given by slow intravenous infusion, with dosing based on target plasma fibrinogen level and measured pre-infusion level. It is studied in congenital afibrinogenemia and hypofibrinogenemia. The fibrinogen in the product converts to fibrin during blood clot formation.

Summary written with AI from the sources listed at the end of this page.

At a glance

Also known as
Tachosil, FIB Grifols
Drug type
Plasma-derived product
Mechanism
Protein replacement
Pathways
fibrin clot formation, coagulation cascade
Therapy area
Hematology
Developer
Corza Medical Gmbh
In trials of
GRFS
FDA status
Approved as Tachosil (April 5, 2010), BLA125351 · FDA label

✅ FDA-approved uses

From the indications section of the FDA label (version of Oct 8, 2025). Read the full label for the exact wording, limitations and safety information.

🧪 Clinical trials

TrialPhaseConditionStatusSponsor
NCT04636268 Phase 3 Congenital Afibrinogenemia Withdrawn GRFS

Trials of the companies BioRadar tracks, from ClinicalTrials.gov, most advanced phase first.

Conditions studied

Congenital AfibrinogenemiaHypofibrinogenemia

Sources

Updated Oct 11, 2026.

Data: FDA (Drugs@FDA, Purple Book, DailyMed), NIH (NCI Thesaurus, GSRS, RxNorm), ClinicalTrials.gov • Informational purposes only, not medical or investment advice. • All drugs A–Z

This data is for informational purposes only, not investment advice. BioRadar does not provide buy/sell recommendations. Past performance does not guarantee future results. Always do your own due diligence.