Spinal Muscular Atrophy is a hereditary neuromuscular disease affecting motor neurons in the spinal cord, characterized by weakness and progressive muscle wasting. It is caused by a mutation in the survival motor neuron gene 1 (SMN1).
Spinal Muscular Atrophy is a hereditary neuromuscular disease affecting motor neurons in the spinal cord, characterized by weakness and progressive muscle wasting. It is caused by a mutation in the survival motor neuron gene 1 (SMN1).
| Name | Drug Class | Updated |
|---|---|---|
| Risdiplam | Miscellaneous uncategorized agents | 12-Aug-2023 |
| Onasemnogene abeparvovec (zolgensma) | Miscellaneous uncategorized agents | 11-Aug-2023 |
| Nusinersen (injection) | Miscellaneous uncategorized agents | 11-Aug-2023 |
| Zolgensma | Miscellaneous uncategorized agents | 14-Jul-2023 |
| Evrysdi | Miscellaneous uncategorized agents | 13-Jul-2023 |
| Spinraza | Miscellaneous uncategorized agents | 12-Jul-2023 |