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Toviaz (Fesoterodine)

Weill Medical College of Cornell University · FDA-approved active Small molecule

Fesoterodine is a muscarinic M3 receptor antagonist that relaxes bladder smooth muscle to reduce urinary incontinence and overactive bladder symptoms.

Fesoterodine is a muscarinic M3 receptor antagonist that relaxes bladder smooth muscle to reduce urinary incontinence and overactive bladder symptoms. Used for Overactive bladder with symptoms of urge incontinence, urgency, and frequency.

At a glance

Generic nameToviaz (Fesoterodine)
Also known asToviaz
SponsorWeill Medical College of Cornell University
Drug classMuscarinic M3 receptor antagonist
TargetM3 muscarinic acetylcholine receptor
ModalitySmall molecule
Therapeutic areaUrology
PhaseFDA-approved

Mechanism of action

Fesoterodine blocks M3 muscarinic acetylcholine receptors on the detrusor muscle of the bladder, preventing involuntary contractions. This anticholinergic action increases bladder capacity and reduces the urge to urinate, thereby decreasing episodes of urgency incontinence and frequency. The drug is a prodrug that is rapidly hydrolyzed to its active metabolite.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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