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Terminated Phase 3 Interventional

Phase III Study With Idebenone in Patients With Duchenne Muscular Dystrophy (SIDEROS-E)

ClinicalTrials.gov ID: NCT03603288

Public ClinicalTrials.gov record NCT03603288. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 24, 2026, 7:34 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase III Open-Label Extension Study to Assess the Long-Term Safety and Efficacy of Idebenone in Patients With Duchenne Muscular Dystrophy (DMD) Who Completed the SIDEROS Study

Study identification

NCT ID
NCT03603288
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Santhera Pharmaceuticals
Industry
Enrollment
161 participants

Conditions and interventions

Interventions

  • idebenone 150 mg film-coated tablets Drug

Drug

Eligibility (public fields only)

Age range
11 Years and older
Sex
Male
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 3, 2018
Primary completion
Nov 24, 2020
Completion
Nov 24, 2020
Last update posted
Dec 2, 2021

2018 – 2020

United States locations

U.S. sites
13
U.S. states
11
U.S. cities
13
Facility City State ZIP Site status
University of Alabama - Birmingham, Child Health Research Birmingham Alabama 35233
Banner University of Arizona Medical Center Tucson Arizona 85724
Children's Hospital of Los Angeles Los Angeles California 90027
UC Davis Department of Physical Medicine and Rehabilitation Sacramento California 95817
Center for Integrative Rare Disease Research, Rare Disease Research, LLC Atlanta Georgia 30318
University of Iowa, Department of Pediatrics Iowa City Iowa 52242
Johns Hopkins University Baltimore Maryland 21287
Children's Hospital Boston, Harvard Medical School, Department of Neurology Boston Massachusetts 02115
Gillette Children's Specialty Healthcare Saint Paul Minnesota 55101
Neurosciences Institute, Neurology - Charlotte Carolinas Healthcare System Charlotte North Carolina 28207
Cincinnati Children's Hospital Cincinnati Ohio 45229
MetroHealth Medical Center Cleveland Ohio 44109-1988
Children's Hospital of Philadelphia, Division of Pulmonology Philadelphia Pennsylvania 19104-1771

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 26 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03603288, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 2, 2021 · Synced Jul 24, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03603288 live on ClinicalTrials.gov.

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