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Only qualified physicians treating a Lafora Disease patient may request VAL-1221 Expanded Access treatment under the Parasail Lafora Expanded Access Protocol (LEAP). According to FDA guidance, this protocol can enroll up to 10 patients. However, individual patient inclusion will ultimately be dependent on protocol eligibility, site geography, treatment requirements, and available supply of the investigational therapy. Inquiring physicians can submit a request by contacting the Central Contact personnel listed below in Contacts/Locations.
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| VAL-1221 | Drug | VAL-1221 20mg/kg intravenous (IV) infusion every other week |
Inclusion Criteria:
Documented genetic diagnosis of Lafora Disease (LD) based on likely pathogenic or pathogenic variants in both alleles of either the EPM2A or the EPM2B gene
Mid-stage in evolution of LD between 12 and 28 years of age
Able and willing to comply with the protocol, including travel to Protocol Center, procedures, measurements and visits, including:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Dustin Armstrong, PhD | Contact | (617) 462-3084 | dustin.armstrong@parasailllc.com |
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| ID | Term |
|---|---|
| D020192 | Lafora Disease |
| D006008 | Glycogen Storage Disease |
| D020191 | Myoclonic Epilepsies, Progressive |
| ID | Term |
|---|---|
| D004831 | Epilepsies, Myoclonic |
| D004829 | Epilepsy, Generalized |
| D004827 | Epilepsy |
| D001927 | Brain Diseases |
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| D002493 |
| Central Nervous System Diseases |
| D009422 | Nervous System Diseases |
| D000073376 | Epileptic Syndromes |
| D020271 | Heredodegenerative Disorders, Nervous System |
| D019636 | Neurodegenerative Diseases |
| D030342 | Genetic Diseases, Inborn |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| D002239 | Carbohydrate Metabolism, Inborn Errors |
| D008661 | Metabolism, Inborn Errors |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |