Fetal Gaucher disease

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At a Glance

Live from database

Regulatory Watchboard

2 events
Aug 2014

Cerdelga: FDA approved

Long-term treatment of adult patients with Gaucher disease type 1 who are CYP2D6 extensive metabolizers (EMs), intermediate metabolizers (IMs), or poor metabolizers (PMs) as detected by an FDA-cleared test.

FDAcompleted
Apr 1991

Ceredase: FDA approved

Long-term enzyme replacement therapy for children, adolescents and adult patients with a confirmed diagnosis of Type I Gaucher disease who exhibit signs and symptoms that are severe enough to result in one or more of the following conditions: a) moderate-to-severe anemia; b) thrombocytopenia with bleeding tendency; c) bone disease; d) significant hepatomegaly or splenomegaly.

FDAcompleted

Data from FDA regulatory filings and ClinicalTrials.gov. Updated periodically.

Financial Assistance

1 program

FINANCIAL LANDSCAPE SUMMARY

1

Total programs

1

Open now

1

Copay cards

Copay Assistance1

Ceredase

Genzyme Corporation

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Approved Treatments

3 FDA-approved

Cerdelga

(ELIGLUSTAT)Orphan drug

Genzyme Corporation

Approved Aug 2014FDA label ↗

Ceredase

(Alglucerase injection)Orphan drug

Genzyme Corporation

Approved Apr 1991

Azithromycin

(AZITHROMYCIN)Orphan drugstandard

Preferred Pharmaceuticals Inc.

FDA label ↗

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Clinical Trial Landscape

No active clinical trials currently recruiting for Fetal Gaucher disease.
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Recent News & Research

No recent news articles indexed yet for Fetal Gaucher disease.
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Specialist Network

Top 1 by expertise

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