Fesoterodine

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Fesoterodine
Systematic (IUPAC) name
[2-[(1R)-3-(Di(propan-2-yl)amino)-1-phenylpropyl]-4-(hydroxymethyl)phenyl] 2-methylpropanoate
Clinical data
Trade names Toviaz
AHFS/Drugs.com monograph
MedlinePlus a609021
Licence data EMA:LinkUS FDA:link
Pregnancy cat. C(US)
Legal status Prescription only
Routes Oral
Pharmacokinetic data
Bioavailability 52% (active metabolite)
Protein binding 50% (active metabolite)
Metabolism Hepatic (CYP2D6- and 3A4-mediated)
Half-life 7–8 hours (active metabolite)
Excretion Renal (70%) and fecal (7%)
Identifiers
CAS number 286930-03-8 N
ATC code G04BD11
PubChem CID 6918558
DrugBank DB06702
ChemSpider 5293755 YesY
UNII 621G617227 YesY
KEGG D07226 YesY
ChEMBL CHEMBL1201764 N
Chemical data
Formula C26H37NO3 
Mol. mass 411.278 g/mol
SMILES eMolecules & PubChem
 N(what is this?)  (verify)

Fesoterodine (INN, used as the fumarate under the brand name Toviaz) is an antimuscarinic drug developed by Schwarz Pharma AG to treat overactive bladder syndrome (OAB).[1] It was approved by the European Medicines Agency in April 2007[2] and was approved by the US Food and Drug Administration on October 31, 2008.[3]

Fesoterodine is a prodrug. It is broken down into its active metabolite, 5-hydroxymethyl tolterodine, by plasma esterases.

[edit] Efficacy

In two large, 12-week, randomized, double-blind multicentre Phase III trials, oral fesoterodine 4 or 8mg once daily improved the symptoms of OAB significantly more than placebo.[4]

[edit] References


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