Last reviewed · How we verify

Ceredase (ALGLUCERASE)

Sanofi · FDA-approved approved Enzyme Quality 25/100

Ceredase (ALGLUCERASE) is a hydrolytic lysosomal glucocerebroside-specific enzyme used to treat chronic non-neuropathic Gaucher's disease. It was originally developed and is currently owned by Genzyme. This small molecule modality was FDA-approved in 1991 for its approved indications. The commercial status of Ceredase is not explicitly stated, but it is likely patented. Key safety considerations include the potential for hypersensitivity reactions and the need for careful monitoring of patients.

At a glance

Generic nameALGLUCERASE
SponsorSanofi
Drug classHydrolytic Lysosomal Glucocerebroside-specific Enzyme
ModalityEnzyme
Therapeutic areaNeuroscience
PhaseFDA-approved
First approval1991

Approved indications

Common side effects

No common side effects on file.

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape: