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NCT06328608 · ClinicalTrials.gov registry record · Phase 2

A Study to Learn About the Safety and Effects of the Study Drug PRX-102 in Children and Adolescents With Fabry Disease

A Phase 2 study of Fabry Disease, sponsored by Chiesi Farmaceutici S.p.A..

Recruiting
Registry status
Phase 2
Development phase
22
Enrollment target
12
Study locations

NCT06328608 is a Phase 2 study of Fabry Disease that is actively recruiting participants, run by Chiesi Farmaceutici S.p.A.. The registered enrollment target is 22 participants, below the 542-participant average among 32 other Fabry Disease trials with a reported enrollment target (96% lower). The trial reports 12 study locations across 7 states.

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The verdict

NCT06328608, a Phase 2 study of Fabry Disease, is actively recruiting participants, sponsored by Chiesi Farmaceutici S.p.A..

RECRUITING
Registry status
Phase 2
Development phase
22 participants
Enrollment target
12
Study locations

Study Summary

A Study to Learn About the Safety and Effects of the Study Drug PRX-102 in Children and Adolescents with Fabry Disease.

Conditions Studied

Interventions

  • DRUG PRX-102 1 mg/kg every two weeks

Study Locations (12)

Other

  • UK für Kinder- und Jugendheilkunde der PMU Salzburg - Salzburg
  • Centre Hospitalier Universitaire (CHU) de Bordeaux - Groupe Hospitalier Pellegrin - Bordeaux
  • Hopital Arnaud de Villeneuve - Montpellier
  • Haukeland Universitetssjukehus - Bergen
  • Hospital Clinico Universitario De Santiago De Compostela - Santiago de Compostela
  • Great Ormond Street Hospital for Children NHS Foundation Trust - London

Arizona

  • Phoenix Children's - Phoenix

Georgia

  • Emory Genetics Clinical Trials Center - Atlanta

Iowa

  • University of Iowa - Iowa City

Ohio

  • Cincinnati Children's Hospital Medical Center - Cincinnati

Utah

  • University of Utah - Salt Lake City

Virginia

  • Lysosomal and Rare Disorders Research and Treatment Center Inc - Fairfax

Trial Details

FieldValue
Enrollment Target 22 participants
Start Date 2025-07-29
Est. Completion 2031-04
Phase Phase 2

Sponsor

Chiesi Farmaceutici S.p.A.

30 total trials

What the Registry Record Tells You About NCT06328608

The ClinicalTrials.gov registry entry for NCT06328608 describes a study currently listed as recruiting, categorized as Phase 2. The registered enrollment target is 22 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 542-participant average among 32 other Fabry Disease trials with a reported enrollment target (96% lower). The listed sponsor is Chiesi Farmaceutici S.p.A., which has 30 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Fabry Disease appearing as the primary indexed condition, and to 1 intervention - of which PRX-102 1 mg/kg every two weeks is the first listed.

NCT06328608 reports 12 study locations spanning 7 distinct geographic areas - top geographies include Other, Arizona, Georgia.

Frequently Asked Questions

What is clinical trial NCT06328608 about?

NCT06328608 is a clinical study titled "A Study to Learn About the Safety and Effects of the Study Drug PRX-102 in Children and Adolescents With Fabry Disease". A Study to Learn About the Safety and Effects of the Study Drug PRX-102 in Children and Adolescents with Fabry Disease.

What is the current status of trial NCT06328608?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 22 participants. The study started on 2025-07-29. Estimated completion is 2031-04.

What conditions does trial NCT06328608 study?

This clinical trial studies the following conditions: Fabry Disease.

What interventions are being tested in trial NCT06328608?

The interventions under investigation include: PRX-102 1 mg/kg every two weeks (DRUG).

Who is sponsoring clinical trial NCT06328608?

This trial is sponsored by Chiesi Farmaceutici S.p.A., which has 30 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06328608 being conducted?

This trial has 12 study locations across Arizona, Georgia, Iowa, Ohio, Utah. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.