Drug

Fibrinolysin, human

As of the edition of 20 October 2026, Fibrinolysin, human is a drug: marketed, first approved in 1964 (US); acts on FGA, FGB and FGG; US protection ended in 1976.

Sources: FDA Orange Book and Purple Book, other approval registers, ClinicalTrials.gov, ChEMBL.

The drug

Status
Marketed; latest approval 1964
Kind
Unknown
Brand name
Elase-chloromycetin
First approved
1 April 1964 (US)
Approvals on record
2 in 1 region
Holder of the most recent approval
Pfizer; 2 holders in all
Registered trials
5, 2 stopped early
Disease areas
Heart and blood vessels; Nervous system

US protection

US protection ended in 1976.

US protection ended in 1976, computed as 12 years from the first US licence because FDA publishes no date for this product. The application that gives this date is held by Pfizer. The date is computed, not published.

This is the US only, and it is not the date generics or biosimilars can enter.

The exact date and the listings behind it

In the product

1 listing counts towards this date. The exact date and each listing are in the product.

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Targets

GeneProteinUniProt
FGAFibrinogen alpha chain [Cleaved into: Fibrinopeptide A; Fibrinogen alpha chain]P02671
FGBFibrinogen beta chain [Cleaved into: Fibrinopeptide B; Fibrinogen beta chain]P02675
FGGFibrinogen gamma chainP02679

Registered trials

PhaseTrialsCompletedActiveStopped early
Phase 11100
Phase 24202
All trials5