Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Santhera Pharmaceuticals
Age
8–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Documented diagnosis of DMD (severe dystrophinopathy) and clinical features consistent of typical DMD at diagnosis (i.e., documented delayed motor skills and muscle weakness by age 5 years) and who in the opinion of the Treating physician would benefit from treatment with idebenone. DMD should be confirmed by mutation analysis in the dystrophin gene or by substantially reduced levels of dystrophin protein (i.e., absent or \<5% of normal) on Western blot or immunostaining.
Minimum 8 years old at Prescreening.
PEF or FVC ≤80% and \>25% of predicted value based on most recent assessment noted in the patient's medical record and subsequently confirmed at the Enrollment Visit.
Able to understand program requirements and swallow program medication.
Signed and dated Informed Consent Form (to be obtained at the Enrollment Visit from patient or parent/legal guardian (if applicable) prior to performing any program-specific procedures and dispensing idebenone to the patient).
You may not be if
Eligible for and able to participate in an ongoing clinical trial of idebenone.
Is at high-risk of a fatal outcome from lung infection and/or advanced cardiomyopathy in the opinion of the Treating physician.
Known moderate or severe impairment of hepatic function or severe impairment of renal function.
Prior or ongoing medical condition or laboratory abnormality which in the Treating physician's opinion may put the patient at significant risk or may interfere significantly with the patient's participation in the program.
Abuse of drugs or alcohol, which in Treating physician's opinion would interfere with the compliance to treatment.
Known individual hypersensitivity to idebenone or to any of the ingredients/excipients of the program medication.
Clareo Health | Expanded Access Program for Idebenone in Participants With Duchenne Muscular Dystrophy (DMD)
