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Not yet taking people in BelgiumPhase 3

Migalastat in Young Children with Fabry Disease

Tests migalastat in children aged 2 to under 12 with Fabry disease.

Key facts

Who runs it
Amicus Therapeutics Inc.
Where
Leuven, BelgiumSee the siteAlso in 2 other countries, 2 sites
Registry title
An Open-label Study of the Safety, Pharmacokinetics, Pharmacodynamics, and Efficacy of 12-month Treatment with Migalastat in Pediatric Subjects (aged 2 to < 12 years) with Fabry Disease and Amenable GLA Variants
Status
Not yet recruiting
Phase
Phase 3
People taking part
3 people, planned
Started
1 Nov 2025
Expected to end
31 Dec 2027
Type of study
Interventional
Record updated
24 April 2026

Who can take part

AI summary

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for children aged 2 to under 12 years with Fabry disease and a GLA gene variant that migalastat can work on. It tests safety and how the body handles the drug.

Age
2 to under 12 years at randomization (11-year-olds must have a birthday more than 30 days after randomization).
Sex
Boys and girls can both join.
Disease stage
Fabry disease with at least 1 documented complication, for example corneal whorls, nerve pain, stomach or bowel symptoms, reduced sweating, heart, kidney, hearing problems or stroke signs.
Earlier treatment
No enzyme replacement therapy (ERT, e.g. Replagal or Fabrazyme) for at least 14 days before the baseline visit.
Biomarker or test result
A GLA variant documented as amenable to migalastat. If the variant is not known, a lab result showing an amenable variant is needed before Visit 2.

Main reasons for not taking part

  • Moderate or severe kidney impairment (eGFR below 60 mL/min/1.73 m2) or kidney disease needing dialysis or transplant
  • Allergy or sensitivity to migalastat or other iminosugars (e.g. miglustat, miglitol)
  • Any gene therapy at any time, or planned during the study
  • Treatment with miglitol (Glyset) or miglustat (Zavesca) within 6 months before screening or during the study
  • Pregnant or breastfeeding, or planning pregnancy during the study

The registry criteria, word for word

Show all 15 criteriaShow less

Who can take part

  • Male or female subjects, diagnosed with Fabry disease who are between ages 2 and < 12 years at randomization (subjects aged 11 years must have birthdays > 30 days after randomization)
  • Subject’s parent or legally authorized representative is willing and able to provide written informed consent and authorization for use and disclosure of personal health information or research-related health information, and subject provides assent, if applicable
  • Subject has a GLA variant documented in his/her medical record that is amenable to migalastat prior to Visit 2. • For subjects without a known GLA variant, an amenable GLA genotyping result from the local laboratory must be received prior to Visit 2
  • Subject has not received ERT (eg, Replagal® [agalsidase alfa] or Fabrazyme® [agalsidase beta]) for at least 14 days prior to Baseline visit
  • Subject has at least 1 documented complication (ie, historical or current laboratory abnormality or sign/symptom) of Fabry disease, including but not limited to: a. corneal whorls b. neuropathic pain and/or acroparesthesia and/or acute crises persisting or recurring at least twice over the previous 3 months or longer, or requiring management with analgesia c. Fabry disease-related gastrointestinal signs and symptoms (eg, diarrhea, abdominal pain) persisting or recurring at least twice over the previous 3 months or longer d. hypohidrosis (present for at least 3 months) e. left ventricular mass index (LVMi) above the normal range for age and sex f. rhythm and/or conduction disturbances, for example: − episode of tachycardia or bradycardia, − arrhythmia, or; − abnormal PR, QRS, or QT interval g. reduced estimated glomerular filtration rate (eGFR) (using the Schwartz formula) for age and sex, or hyperfiltration (> 135 mL/min/1.73 m2) h. proteinuria or albuminuria in a spot urine (early morning preferable) or as determined by the investigator i. elevated plasma globotriaosylsphingosine (lyso-Gb3) j. hearing impairment and/or tinnitus k. transient ischemic attack/stroke
  • If of reproductive potential, both male and female subjects agree to use a medically accepted method of contraception throughout the duration of the study and for up to 30 days after their last dose of migalastat

Who cannot take part

  • Subject received any investigational/experimental drug, biologic, or device within 30 days or 5 half-lives of the investigational product (whichever is longer) before Visit 1 (screening)
  • Subject has received any gene therapy at any time or anticipates starting gene therapy during the study period
  • Subject requires treatment with Glyset® (miglitol) or Zavesca® (miglustat), within 6 months before Visit 1 (screening) or throughout the study
  • Subject has advanced kidney disease requiring dialysis or kidney transplantation
  • Subject has a history of allergy or sensitivity to migalastat (including excipients) or other iminosugars (eg, miglustat, miglitol)
  • Subject has any intercurrent illness or condition at Visit 1 (screening) or Visit 2 (baseline) that may preclude the subject from fulfilling the protocol requirements or suggests to the investigator that the potential subject may have an unacceptable risk by participating in this study
  • Subject has moderate or severe renal impairment (eGFR < 60 mL/min/1.73 m2 at Visit 1 [screening])
  • Female subject is pregnant or breastfeeding or is planning to become pregnant during the study period
  • In the opinion of the investigator, the subject and/or parent or legally-authorized representative is unlikely or unable to comply with the study requirements

Where in Belgium

Also in 2 other countries, 2 sites

  • UZ LeuvenLeuven, BelgiumNot yet recruiting

About the trial

What the trial wants to find out

to characterize the pharmacokinetics (PK) and to confirm pediatric dose regimens predicted to provide plasma migalastat exposure levels similar to adolescents and adults in pediatric subjects aged 6 to < 12 years old and 2 to < 6 years old with Fabry disease and who have the gene encoding α-galactosidase A (α-Gal A) (GLA) variants amenable to treatment with migalastat to evaluate the safety of migalastat treatment in pediatric subjects diagnosed with Fabry disease and who have GLA variants amenable to treatment with migalastat

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record

Print a page for my doctor

Data and sources

Registry record
Listed on the EU's official list of trials (CTIS).
Official title
An Open-label Study of the Safety, Pharmacokinetics, Pharmacodynamics, and Efficacy of 12-month Treatment with Migalastat in Pediatric Subjects (aged 2 to < 12 years) with Fabry Disease and Amenable GLA Variants
Plain-language title
Migalastat in Young Children with Fabry DiseaseGenerated from the registry record. The registry title is the official one.
AI summary
From the trial's eligibility criteria. Read by machine on 9 November 2026.
Record updated
24 April 2026