TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

GALAFOLD

MIGALASTAT HYDROCHLORIDE
Approved 2018-08-10
1
Indication
--
Phase 3 Trials
1
Priority Reviews
7
Years on Market

Details

Status
Prescription
First Approved
2018-08-10
Routes
ORAL
Dosage Forms
CAPSULE

Companies

Active Ingredient: MIGALASTAT HYDROCHLORIDE

GALAFOLD Approval History

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What GALAFOLD Treats

1 indications

GALAFOLD is approved for 1 conditions since its original approval in 2018. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Fabry Disease
Source: FDA Label

GALAFOLD Competitors

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9 other drugs also target MET. Compare mechanisms, indications, and trial activity.

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Drug = Competitor name Company = Manufacturer N indic. = FDA-approved indications → Date = Patent/exclusivity expiry

Competitors share the same molecular target (MET). Earlier expiry dates signal biosimilar/generic opportunities.

Drugs Similar to GALAFOLD

FDA-approved drugs for similar conditions. Compare mechanisms and indications to understand treatment alternatives.

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Active Pipeline

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Ongoing clinical trials by development phase

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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.

GALAFOLD FDA Label Details

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Indications & Usage

FDA Label (PDF)

GALAFOLD is indicated for the treatment of adults with a confirmed diagnosis of Fabry disease and an amenable galactosidase alpha gene ( GLA ) variant based on in vitro assay data [see Dosage and Administration and Clinical Pharmacology ] . This indication is approved under accelerated approval based on reduction in kidney interstitial capillary cell globotriaosylceramide (KIC GL-3) substrate [see Clinical Studies ] . Continued approval for this indication may be contingent upon verification and description of clinical benefit in confirmatory trials. GALAFOLD is an alpha-galactosidase A (alpha...

GALAFOLD Patents & Exclusivity

Latest Patent: Jan 2042

Patents (63 active)

US11833164 Expires Jan 11, 2042
US11633388 Expires Mar 25, 2039
US11622962 Expires Mar 17, 2039
US11642334 Expires Feb 20, 2039
US11826360 Expires Feb 16, 2039
US11357784 Expires Feb 6, 2039
US11903938 Expires Aug 17, 2038
US10251873 Expires May 30, 2038
US10471053 Expires May 30, 2038
US12280042 Expires May 30, 2038
+ 53 more patents
Source: FDA Orange Book

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Data Sources

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