Active Ingredient History
Amifampridine (Firdapse), currently approved in the European Union, is the first and only approved drug for the symptomatic treatment of Lambert-Eaton Myasthenic Syndrome (LEMS) in adults, a rare autoimmune disease with the primary symptoms of muscle weakness. In LEMS, the body’s own immune system attacks connections between nerves and muscles and disrupts the ability of nerve cells to send signals to muscle cells. Amifampridine blocks voltage-dependent potassium channels, thereby prolonging pre-synaptic cell membrane depolarization. Prolonging the action potential enhances the transport of calcium into the nerve ending. The resulting increase in intracellular calcium concentrations facilitates exocytosis of acetylcholine containing vesicles, which in turn enhances neuromuscular transmission. Amifampridine phosphate has been granted Orphan Drug Designation and Breakthrough Therapy designation by the FDA for the treatment of Lambert-Eaton Myasthenic Syndrome (LEMS). NCATS
Drug Pricing (per unit)
Note: This drug pricing data is preliminary, incomplete, and may contain errors.
| Organization | Org Type | FDA approvals | Clinical Trials involvement | Org ID | Force Sort |
|---|
| Organization | Org Type | FDA approvals | Clinical Trials involvement | Org ID | Force Sort |
|---|
Lambert-Eaton Myasthenic Syndrome (approved 2009)
Botulism (Phase 2/Phase 3)
Brugada Syndrome (Phase 3)
Fatigue (Phase 2)
Lambert-Eaton Myasthenic Syndrome (Phase 3)
Multiple Sclerosis (Phase 3)
Muscular Atrophy (Phase 2)
Muscular Atrophy, Spinal (Phase 2)
Myasthenia Gravis (Phase 3)
Myasthenic Syndromes, Congenital (Phase 3)
Vocal Cord Dysfunction (Phase 2)
| Trial | Phase | Start Date | Organizations | Indications |
|---|
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