Wednesday, July 8, 2026

Drug profile · INN

elosulfase alfa

elosulfase alfa (VIMIZIM) is a chondroitin-6-sulfate hydrolytic enzyme. Associated with BioMarin Pharmaceutical Australia Pty Ltd. Route of administration: injection. Current US regulatory status: approved.

FDA: approved EMA: approved Alimentary tract and metabolism (A16) A16AB12
US status approved
Patents linked 20
Pipeline programs 0
News articles 0
Drug details — elosulfase alfa
US status
approved
Class
Alimentary tract and metabolism (A16)
Route
INJECTION
Patents
20
Programs
0
Data quality
0.89

Quick answer

elosulfase alfa (VIMIZIM) is a chondroitin-6-sulfate hydrolytic enzyme. Associated with BioMarin Pharmaceutical Australia Pty Ltd. Route of administration: injection. Current US regulatory status: approved.

Key facts

INN elosulfase alfa
Brand VIMIZIM
Mechanism Chondroitin-6-sulfate hydrolytic enzyme
Target Chondroitin-6-sulfate
Therapeutic class Alimentary tract and metabolism (A16)
Route INJECTION
Formulation INJECTABLE
ATC code A16AB12

Mechanism of action

Chondroitin-6-sulfate hydrolytic enzyme

Primary target: Chondroitin-6-sulfate

Approval history

Authority Status Date
FDA approved
EMA approved

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Frequently asked questions

What is elosulfase alfa?

elosulfase alfa (VIMIZIM) is a chondroitin-6-sulfate hydrolytic enzyme. Associated with BioMarin Pharmaceutical Australia Pty Ltd. Route of administration: injection. Current US regulatory status: approved.

What is the brand name for elosulfase alfa?

VIMIZIM is a marketed brand name for elosulfase alfa. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of elosulfase alfa?

elosulfase alfa has approved status in the United States according to our Drugs@FDA-derived records. Verify on the official FDA label before clinical or commercial decisions.