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| ID | Type | Description | Link |
|---|---|---|---|
| SPIES-007 | Other Identifier | StealthBiotherapeutics |
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Choosing to participate in an expanded access program is an important personal decision. Talk with your doctor to learn more about this program. The treating physician must contact StealthBiotherapeutics using the Expanded Access Program Contacts provided. Elamipretide will only be made available after careful review of an individual request submitted by the treating physician. The initiation and conduct of the treatment with elamipretide for an individual patient, and compliance with this treatment guideline, will be under the full and sole responsibility of the treating physician.
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| elamipretide | Drug | Elamipretide is an aromatic-cationic tetrapeptide that readily penetrates cell membranes and transiently localizes to the inner mitochondrial membrane. |
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Key Inclusion Criteria:
≥1 year and ≤ 80 years of age or ≥12 years for Barth Syndrome in SPIES-007
Patients with genetically confirmed rare primary mitochondrial diseases including Barth Syndrome
Patients without genetic confirmation of a rare disease with known mitochondrial dysfunction but do exhibit serious or life-threatening clinical manifestations of mitochondrial dysfunction.
Is self-able or has caregiver willing and able to administer SC injection.
Would potentially benefit from treatment with elamipretide and cannot be treated satisfactorily with any approved medicinal product in the opinion of the treating physician.
Key Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Donna Cowan | Contact | 617.600.6888 | donna.cowan@stealthbt.com | |
| Stealth EAP | Contact | EAP@stealthbt.com |
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| ID | Term |
|---|---|
| D028361 | Mitochondrial Diseases |
| D056889 | Barth Syndrome |
| ID | Term |
|---|---|
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
| D006330 | Heart Defects, Congenital |
| D018376 | Cardiovascular Abnormalities |
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| ID | Term |
|---|---|
| C506540 | arginyl-2,'6'-dimethyltyrosyl-lysyl-phenylalaninamide |
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| D002318 | Cardiovascular Diseases |
| D006331 | Heart Diseases |
| D000015 | Abnormalities, Multiple |
| D000013 | Congenital Abnormalities |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| D040181 | Genetic Diseases, X-Linked |
| D030342 | Genetic Diseases, Inborn |
| D008052 | Lipid Metabolism, Inborn Errors |
| D008661 | Metabolism, Inborn Errors |
| D052439 | Lipid Metabolism Disorders |