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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