Post Trial Access to Lucerastat for Patients With Fabry Disease Who Participated in Study ID-069A302

NCT07762638 · Status: AVAILABLE · Type: EXPANDED_ACCESS

Last updated 2026-08-13

No results posted yet for this study

Summary

This is a Post Trial Access program for patients with Fabry Disease who previously participated in the ID-069A302 (MODIFY OLE) trial and who were still enrolled in the study at the time the Sponsor decided to discontinue ID-069A302. The program is designed to provide continued access to lucerastat.

Conditions

Interventions

DRUG

Lucerastat

Sponsors & Collaborators

  • Idorsia Pharmaceuticals Ltd.

    lead INDUSTRY

Eligibility

Sex
Healthy Volunteers
No

Timeline & Regulatory

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07762638 on ClinicalTrials.gov