Retigabine

Retigabine
Clinical data
Trade namesTrobalt, Potiga
Other namesD-23129, ezogabine (USAN US)
AHFS/Drugs.comProfessional Drug Facts
MedlinePlusa612028
License data
Routes of
administration
By mouth
ATC code
Legal status
Legal status
Pharmacokinetic data
Bioavailability60%
Protein binding60–80%
MetabolismLiver glucuronidation and acetylation. CYP not involved
Elimination half-life8 hours (mean), range: 7–11 hours
ExcretionKidney (84%)
Identifiers
  • Ethyl N-[2-amino-4-[(4-fluorophenyl)methylamino]phenyl]carbamate
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.158.123
Chemical and physical data
FormulaC16H18FN3O2
Molar mass303.337 g·mol−1
3D model (JSmol)
  • O=C(OCC)Nc1ccc(cc1N)NCc2ccc(F)cc2
  • InChI=1S/C16H18FN3O2/c1-2-22-16(21)20-15-8-7-13(9-14(15)18)19-10-11-3-5-12(17)6-4-11/h3-9,19H,2,10,18H2,1H3,(H,20,21)
  • Key:PCOBBVZJEWWZFR-UHFFFAOYSA-N

Retigabine (INN) or ezogabine (USAN) is an anticonvulsant used as an adjunctive treatment for partial epilepsies in treatment-experienced adult patients. The drug was developed by Valeant Pharmaceuticals and GlaxoSmithKline. It was approved by the European Medicines Agency under the trade name Trobalt on March 28, 2011, and by the United States Food and Drug Administration (FDA), under the trade name Potiga, on June 10, 2011. Production was discontinued in June 2017.

Retigabine works primarily as a potassium channel opener—that is, by activating a certain family of voltage-gated potassium channels in the brain. This mechanism of action is unique among antiepileptic drugs, and may hold promise for the treatment of other neurologic conditions, including tinnitus, migraine and neuropathic pain. The manufacturer withdrew retigabine from clinical use in 2017.