From: Pathophysiology of ion channels in amyotrophic lateral sclerosis
Drug | Structure | Target | Effect | Stage | References |
---|---|---|---|---|---|
Riluzole |
| Na+ channels | Reduces persistent Na+ current | In use | [30] |
K+ channels | Activates channels and inhibits slow inactivation of voltage-gated K+ current | ||||
Ca2+ channels | Inhibits persistent and transient Ca2+ currents | ||||
Gabapentin |
| Voltage-gated Ca2+ channels | Inhibits channel expression | Phase III | [151] |
Pimozide |
| T-type Ca2+ channels | Inhibits Ca2+ currents | Phase II | [154] |
FPL 64176 |
| L-type Ca2+ channels | Activates channels | Preliminary testing | [155] |
Bay K 8644 | L-type Ca2+ channels | Activates channels | Preliminary testing | [155] | |
Mexiletine |
| Na+ channels | Inhibits persistent Na+ current | Phase IV | [156] |
Ezogabine |
| K+ channels | Activates channels | Phase II | |
QRL-101 | Â | K+ channels | Activates channels | Phase I | [163] |
4AP |
| K+ channels | Inhibits K+ currents | Preliminary testing | [120] |