Clinical data | |
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Other names | LP352; LP-352; AN352; AN-352 |
Routes of administration | Oral[1] |
Drug class | Serotonin 5-HT2C receptor agonist[1][2] |
Pharmacokinetic data | |
Elimination half-life | 5–7 hours[2] |
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Chemical and physical data | |
Formula | C15H19F2N3O |
Molar mass | 295.334 g·mol−1 |
3D model (JSmol) | |
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Bexicaserin (INN ; developmental code names LP352 and AN352) is a selective serotonin 5-HT2C receptor agonist which is under development for the treatment of seizures in developmental disabilities such as Dravet syndrome and Lennox-Gastaut syndrome.[1][3][2] It is taken by mouth.[2][1]
The drug is highly selective for the serotonin 5-HT2C receptor, with negligible affinity for the serotonin 5-HT2A and 5-HT2B receptors.[2] Because it does not activate the serotonin 5-HT2B receptor, bexicaserin is not expected to pose a risk of cardiac valvulopathy, unlike the existing agent fenfluramine.[2]
As of October 2024, bexicaserin is in phase 3 clinical trials for treatment of developmental disabilities.[1][3] It is being developed by Longboard Pharmaceuticals.[1][3]