Getting Started Brochure

GETTING STARTED ON EXONDYS 51

An informational guide for your English-speaking patients that explains DMD, how EXONDYS 51 works, and starting and staying on EXONDYS 51 therapy.

 

 

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EXONDYS 51 PATIENT WEBSITE.

Our patient site covers topics such as genetic mutations, exon skipping, how EXONDYS 51 works, and SareptAssist support services, with patient-friendly language and informative videos. Share it with patients seeking additional information

UNDERSTANDING EXON-SKIPPING TECHNOLOGY.
UNDERSTANDING EXON-SKIPPING TECHNOLOGY.

Our animated video explains how exon skipping works in a patient-friendly way.

View Patient Video

INFORMATION FOR PATIENTS STARTING THERAPY.
INFORMATION FOR PATIENTS STARTING THERAPY.

This overview will help patients know what to expect when starting EXONDYS 51 therapy.

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INDICATION

EXONDYS 51 (eteplirsen) is indicated for the treatment of Duchenne muscular dystrophy (DMD) in patients who have a confirmed mutation of the DMD gene that is amenable to exon 51 skipping. This indication is approved under accelerated approval based on an increase in dystrophin in skeletal muscle observed in some patients treated with EXONDYS 51. Continued approval for this indication may be contingent upon verification of a clinical benefit in confirmatory trials.

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IMPORTANT SAFETY INFORMATION

Hypersensitivity reactions, including bronchospasm, chest pain, cough, tachycardia and urticaria, have occurred in patients who were treated with EXONDYS 51. If a hypersensitivity reaction occurs, institute appropriate medical treatment and consider slowing the infusion or interrupting the EXONDYS 51 therapy.

Adverse reactions in DMD patients (N=8) treated with EXONDYS 51 30 or 50 mg/kg/week by intravenous (IV) infusion with an incidence of at least 25% more than placebo (N=4) (Study 1, 24 weeks) were (EXONDYS 51, placebo): balance disorder (38%, 0%), vomiting (38%, 0%) and contact dermatitis (25%, 0%). The most common adverse reactions were balance disorder and vomiting. Because of the small numbers of patients, these represent crude frequencies that may not reflect the frequencies observed in practice. The 50 mg/kg once weekly dosing regimen of EXONDYS 51 is not recommended.

The most common adverse reactions from observational clinical studies (N=163) seen in greater than 10% of patients were headache, cough, rash, and vomiting.

Please see the full Prescribing Information for EXONDYS 51 (eteplirsen).