Carisbamate Trade names Comfyde (proposed) ATC code
(S )-2-O -Carbamoyl-1-o -chlorophenyl-ethanol
CAS Number PubChem CID ChemSpider UNII ChEMBL CompTox Dashboard (EPA ) Formula C 9 H 10 Cl N O 3 Molar mass 215.63 g·mol−1 3D model (JSmol )
Clc1ccccc1[C@@H](O)COC(=O)N
InChI=1S/C9H10ClNO3/c10-7-4-2-1-3-6(7)8(12)5-14-9(11)13/h1-4,8,12H,5H2,(H2,11,13)/t8-/m0/s1
Y Key:OLBWFRRUHYQABZ-QMMMGPOBSA-N
Y
N Y (what is this?)
Carisbamate (YKP 509 , proposed trade name Comfyde ) is an experimental anticonvulsant drug that was under development by Johnson & Johnson Pharmaceutical Research and Development but never marketed.
Clinical study [ ]
A phase II clinical trial in the treatment of partial seizures demonstrated that the compound has efficacy in the treatment of partial seizures and a good safety profile. Since late 2006, the compound has been undergoing a large multicenter phase III clinical trial for the treatment of partial seizures. Its mechanism of action is unknown.[1] [2]
A double-blind, placebo-controlled trial of carisbamate in 323 patients with migraine determined that carisbamate was well tolerated at doses up to 600 mg/day, but it failed to demonstrate that the drug was sufficiently more effective than placebo in migraine prophylaxis.[3]
History [ ]
In 1998, the compound was in-licensed from SK Corp. (currently Life Science Business Division of SK Holdings ), a South Korean company. On October 24, 2008, Johnson & Johnson announced that it had submitted a New Drug Application to the U.S. Food and Drug Administration (FDA) for carisbamate.[4] Johnson & Johnson received provisional approval by the FDA to market carisbamate under the brand name of Comfyde. However, on August 21, 2009, Johnson & Johnson reported that the FDA had failed to give marketing approval.
References [ ]
^ Rogawski MA (2006). "Diverse mechanisms of antiepileptic drugs in the development pipeline" . Epilepsy Res . 69 (3): 273–294. doi :10.1016/j.eplepsyres.2006.02.004 . PMC 1562526 . PMID 16621450 .
^ Novak GP, Kelley M, Zannikos P, Klein B (2007). "Carisbamate (RWJ-333369)" . Neurotherapeutics . 4 (1): 106–109. doi :10.1016/j.nurt.2006.11.016 . PMC 7479705 . PMID 17199023 .
^ Cady RK, Mathew N, Diener HC, Hu P, Haas M, Novak GP, Study Group (2009). "Evaluation of carisbamate for the treatment of migraine in a randomized, double-blind trial". Headache . 49 (2): 216–226. doi :10.1111/j.1526-4610.2008.01326.x . PMID 19222595 . S2CID 709835 .
^ "Johnson & Johnson Pharmaceutical Research & Development, L.L.C. Submits New Drug Application to FDA for Carisbamate" (Press release). Johnson & Johnson. 2008-10-24. Retrieved 2008-11-02 .
Anticonvulsants (N03 )
GABAergics
GABAA R PAMs
Barbiturates : Barbexaclone
Metharbital
Methylphenobarbital
Pentobarbital
Phenobarbital #
Primidone ; Carbamates : Cenobamate
Felbamate ; Benzodiazepines : Clobazam
Clonazepam
Clorazepate
Diazepam #
Lorazepam #
Midazolam
Nimetazepam
Nitrazepam
Temazepam ; Others: Bromide (potassium bromide , sodium bromide )
Imepitoin
Paraldehyde
Stiripentol
GABA-T inhibitors Others
Channel modulators
Sodium blockers Calcium blockers
Oxazolidinediones : Ethadione
Paramethadione
Trimethadione ; Succinimides : Ethosuximide #
Mesuximide
Phensuximide ; Gabapentinoids : Gabapentin
Pregabalin ; Others: Imepitoin
Lamotrigine #
Topiramate
Zonisamide
Potassium openers
Others
CA inhibitors
Sulfonamides : Acetazolamide
Ethoxzolamide
Sultiame
Topiramate
Zonisamide
Others
Albutoin
Beclamide
Cannabidiol
Etiracetam
Levetiracetam
Perampanel
# WHO-EM
‡ Withdrawn from market
Clinical trials :
† Phase III
§ Never to phase III
GABA A receptor positive modulatorsAlcohols
Butanol
Chloralodol
Chlorobutanol (cloretone)
Ethanol (alcohol) (alcoholic drink )
Ethchlorvynol
Isobutanol
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tert -Butanol (2M2P)
tert -Pentanol (2M2B)
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Trifluoroethanol
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Org 25,435
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(e.g., sulfonmethane (sulfonal) , tetronal , trional )
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Unsorted benzodiazepine site positive modulators: α-Pinene
See also: Receptor/signaling modulators • GABA receptor modulators • GABA metabolism/transport modulators