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Data updated: Mar 10, 2026

BRINEURA

CERLIPONASE ALFA
Approved 2017-04-27

Brineura (cerliponase alfa) is a hydrolytic lysosomal N-terminal tripeptidyl peptidase indicated for use in pediatric patients. It is specifically approved to slow the loss of ambulation in patients with neuronal ceroid lipofuscinosis type 2 (CLN2 disease), also known as tripeptidyl peptidase 1 (TPP1) deficiency. This neurodegenerative condition is characterized by a progressive decline in motor function caused by the deficiency of a specific lysosomal enzyme.

Source: FDA Label โ€ข BIOMARIN PHARM

How BRINEURA Works

Cerliponase alfa is a proenzyme that is taken up by target cells in the central nervous system and translocated to the lysosomes via the Cation Independent Mannose-6-Phosphate Receptor. Once inside the lysosome, the drug is activated into a proteolytic form that cleaves tripeptides from the N-terminus of proteins. This enzymatic activity addresses the deficiency of endogenous tripeptidyl peptidase-1 (TPP1), which normally catabolizes polypeptides. By replacing the missing enzyme, the treatment helps prevent the accumulation of lysosomal storage materials that lead to progressive motor decline.

Source: FDA Label
2
Indications
--
Phase 3 Trials
1
Priority Reviews
8
Years on Market

Details

Status
Prescription
First Approved
2017-04-27
Routes
INJECTION
Dosage Forms
INJECTABLE

Companies

Active Ingredient: CERLIPONASE ALFA

BRINEURA Approval History

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What BRINEURA Treats

1 indications

BRINEURA is approved for 1 conditions since its original approval in 2017. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Neuronal Ceroid Lipofuscinosis
Source: FDA Label

BRINEURA Boxed Warning

HYPERSENSITIVITY REACTIONS INCLUDING ANAPHYLAXIS Patients treated with enzyme replacement therapies have experienced life-threatening hypersensitivity reactions, including anaphylaxis. Anaphylaxis has occurred during the early course of enzyme replacement therapy and after extended duration of therapy. Initiate BRINEURA in a healthcare setting with appropriate medical monitoring and support measures, including access to cardiopulmonary resuscitation equipment. If a severe hypersensitivity reacti...

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Key Completed Trials

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Completed studies with published results, ranked by significance

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Trial Timeline

Full development history with FDA approval milestones

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Understanding FDA Approval Types
Count Type What it means
- ORIG Original approval - drug first enters market
- SUPPL - Efficacy New indication (new disease/condition approved)
- SUPPL - Labeling Label text changes (warnings, dosing updates)
- SUPPL - Manufacturing Production changes (new facility)
- SUPPL - Chemistry Formulation changes (new dosage strength)

Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.

BRINEURA FDA Label Details

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Indications & Usage

FDA Label (PDF)

BRINEURA is indicated to slow the loss of ambulation in pediatric patients with neuronal ceroid lipofuscinosis type 2 (CLN2 disease), also known as tripeptidyl peptidase 1 (TPP1) deficiency. BRINEURA is a hydrolytic lysosomal N-terminal tripeptidyl peptidase indicated to slow the loss of ambulation in pediatric patients with neuronal ceroid lipofuscinosis type 2 (CLN2 disease), also known as tripeptidyl peptidase 1 (TPP1) deficiency.

โš ๏ธ BOXED WARNING

WARNING: HYPERSENSITIVITY REACTIONS INCLUDING ANAPHYLAXIS Patients treated with enzyme replacement therapies have experienced life-threatening hypersensitivity reactions, including anaphylaxis. Anaphylaxis has occurred during the early course of enzyme replacement therapy and after extended duration...

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Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.