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Selegiline

Alternative Names: selegiline, emsam, zelapar, l-deprenyl, SELEGILINA, eldepryl
Latest Update: 2024-09-23
Latest Update Note: Clinical Trial Update

Product Description

Selegiline, a monoamine oxidase (MAO) inhibitor, is FDA-approved as an adjunct treatment in the management of patients with Parkinson disease and as a treatment for a major depressive disorder (MDD) in adults. Selegiline is also used off-label for early Parkinson disease and the treatment of attention-deficit/hyperactivity disorder (ADHD). (Sourced from: https://www.ncbi.nlm.nih.gov/books/NBK526094/)

Mechanisms of Action: MAO Inhibitor

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Transdermal,Oral

FDA Designation: None *

Approval Status: Approved

Approved Countries: Argentina | Australia | Bangladesh | Belgium | Brazil | Bulgaria | Canada | Chile | Colombia | Croatia | Cyprus | Czech | Denmark | Dominican Republic | Ecuador | Egypt | Finland | France | Germany | Greece | Hong Kong | Hungary | India | Ireland | Israel | Italy | Japan | Korea | Latvia | Luxembourg | Malta | Mexico | Netherlands | New Zealand | Norway | Pakistan | Peru | Philippines | Poland | Portugal | Romania | Russia | Singapore | Slovenia | South Africa | Spain | Sweden | Taiwan | Turkey | Ukraine | United Kingdom | United States | Uruguay | Venezuela

Approved Indications: None

Known Adverse Events: None

Company: None
Company Location:
Company CEO:
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Selegiline

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Trial

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