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A Non-interventional Study of Clinical Experience in Patients Prescribed Raxone® for the Treatment of Leber’s Hereditary Optic Neuropathy (LHON).
Status of the trial: Completed
Orphan Drug Recognition: NA
Inclusion: Patient prescribed Raxone® for the treatment of LHON; Patient has completed an Informed Consent Form (ICF) indicating that he/ she (or a legally acceptable representative) has been informed of all pertinent aspects of the study and has agreed to participa
Exclusion: No explicit exclusion criteria exist to avoid selection bias and to allow for documentation of routine clinical practice.
Funder Type: industry
Principal location of the trial
HCP: Principal investigators
HCP: Other investigators