Expanded Access Program for Idebenone in Patients With Leber's Hereditary Optic Neuropathy Who Completed the LEROS Study

NCT04381091 · Status: NO_LONGER_AVAILABLE · Type: EXPANDED_ACCESS

Last updated 2023-04-21

No results posted yet for this study

Summary

Expanded Access Program for Idebenone in Patients with Leber's Hereditary Optic Neuropathy who completed the LEROS Study

Conditions

  • Leber's Hereditary Optic Neuropathy

Interventions

DRUG

Idebenone 150 MG Oral Tablet

idebenone 900 mg/day

Sponsors & Collaborators

  • Santhera Pharmaceuticals

    lead INDUSTRY

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

More Related Trials

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 NCT04381091 on ClinicalTrials.gov