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Oxybutynin

Alternative Names: oxybutynin, ditropan, oxytrol, oxybutinin, ditropan xl, oxytrol for women, oxibutinina, gelnique, gelnique 3%
Latest Update: 2024-12-17
Latest Update Note: Clinical Trial Update

Product Description

Oxybutynin is an anticholinergic medication that is indicated in patients with overactive bladder or symptoms of detrusor overactivity, including urinary frequency and urgency. Oxybutynin is an anticholinergic medication that has antispasmodic activity against smooth muscle, including bladder smooth muscle. The active metabolite is N-desethyloxybutynin. It blocks the muscarinic effect of acetylcholine by competitively inhibiting the postganglionic muscarinic 1, 2, and 3 receptors. (Sourced from: https://www.ncbi.nlm.nih.gov/books/NBK499985/)

Mechanisms of Action: MR Inhibitor,mAChR Antagonist

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Oral,Transdermal

FDA Designation: None *

Approval Status: Approved

Approved Countries: Algeria | Argentina | Australia | Austria | Bangladesh | Belgium | Brazil | Bulgaria | Canada | Chile | Colombia | Croatia | Cyprus | Czech | Denmark | Dominican Republic | Ecuador | Egypt | Estonia | European Medicines Agency | Finland | France | Germany | Greece | Hong Kong | Hungary | Iceland | India | Ireland | Israel | Italy | Japan | Jordan | Korea | Latvia | Lithuania | Luxembourg | Malaysia | Malta | Mexico | Morocco | Netherlands | New Zealand | Norway | Pakistan | Peru | Philippines | Poland | Portugal | Romania | Russia | Singapore | Slovakia | Slovenia | South Africa | Spain | Sri Lanka | Sweden | Switzerland | Taiwan | Thailand | Tunisia | Turkey | Ukraine | United Arab Emirates | United Kingdom | United States | Uruguay | Venezuela | Vietnam

Approved Indications: None

Known Adverse Events: None

Company: VIATRIS & KG
Company Location:
Company CEO:
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Oxybutynin

Countries in Clinic: Japan, Korea

Active Clinical Trial Count: 4

Highest Development Phases

Phase 3: Hyperhidrosis

Phase 2: Overactive Bladder|Sleep Apnea, Obstructive|Urinary Incontinence, Urge

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

2023-000062-34

P2

Active, not recruiting

Sleep Apnea, Obstructive

2025-04-11

H-2310-153-1481

P2

Not yet recruiting

Overactive Bladder

2025-04-01

MedRing-04

P2

Active, not recruiting

Urinary Incontinence, Urge

2023-03-28

jRCT2031200143

P3

Completed

Hyperhidrosis

2022-02-04

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