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NCT03683966: MALTA-FABRY

MigALastat Therapy Adherence Among FABRY Patients: A Prospective Multicentral Observational Study

Status unknown Last updated 11 July 2022
What this trial tests

trial in Rare Diseases in 30 participants. Status unknown.

Timeline
27 October 2017
Primary endpoint
31 December 2023
31 December 2023

Quick facts

Lead sponsorWuerzburg University Hospital
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment30
Start date27 October 2017
Primary completion31 December 2023
Estimated completion31 December 2023
Sites1 location across Germany

Conditions studied

Sponsor

Wuerzburg University Hospital

Who can join

18 and older, any sex, with Rare Diseases or Fabry Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study evaluates adherence to the oral chaperone therapy migalastat in patients with Fabry disease.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Contemporary therapeutics and new drug developments for treatment of Fabry disease: a narrative review.
    Oder D, Müntze J, Nordbeck P. · · 2021 · cited 4× · PMID 33968645 · DOI 10.21037/cdt-20-743

Verify or expand the search:

Other recruiting trials for Rare Diseases

Currently open trials in the same condition.

Other Wuerzburg University Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03683966.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing