Vatiquinone Expanded Access Protocol

NCT07159139 · Status: NO_LONGER_AVAILABLE · Type: EXPANDED_ACCESS

Last updated 2026-04-09

No results posted yet for this study

Summary

The purpose of this study is to provide participants who successfully completed the study titled "An Open-label, Safety Study for Previously Treated Vatiquinone (PTC743) Subjects With Inherited Mitochondrial Disease" with liquid Vatiquinone through an intermediate patient population expanded access protocol.

Conditions

Interventions

DRUG

Vatiquinone

Vatiquinone will be administered per dose and schedule specified in the arm description.

Sponsors & Collaborators

  • PTC Therapeutics

    collaborator INDUSTRY
  • Medical University of South Carolina

    lead OTHER

Principal Investigators

  • Thomas Koch, MD · Medical University of South Carolina

Eligibility

Min Age
1 Year
Sex
ALL
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 NCT07159139 on ClinicalTrials.gov