Ozmosi | Fampridine Drug Profile
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Fampridine

Alternative Names: fampridine, 4-aminopyridine, dalfampridine, ampyra, fampridine-sr, fampyra, fampridine-pr, dalfampridine-er, 4-ap
Clinical Status: Inactive
Latest Update: 2025-12-12
Latest Update Note: Clinical Trial Update

Product Description

Fampridine is a drug that has been shown to improve walking speed for some adults with multiple sclerosis. (Sourced from: https://mstrust.org.uk/a-z/fampridine-fampyra)

Mechanisms of Action: Potassium Channel Blocker

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: *

Approval Status: Approved

Approved Countries: Argentina | Australia | Austria | Belgium | Brazil | Canada | Chile | Colombia | Croatia | Cyprus | Czech | Denmark | Dominican Republic | Ecuador | Egypt | Estonia | European Medicines Agency | Finland | France | Germany | Greece | Hungary | Iceland | India | Ireland | Israel | Italy | Jordan | Korea | Latvia | Lebanon | Lithuania | Luxembourg | Malta | Netherlands | New Zealand | Norway | Peru | Poland | Portugal | Romania | Russia | Saudi Arabia | Slovakia | Slovenia | South Africa | Spain | Sweden | Switzerland | Turkey | United Arab Emirates | United Kingdom | United States | Uruguay | Venezuela

Approved Indications: None

Known Adverse Events: None

Company: Acorda
Company Location:
Company CEO: Ron Cohen
Additional Commercial Interests: None

Clinical Description

Countries in Clinic:

Active Clinical Trial Count: 1

Recent & Upcoming Milestones

Highest Development Phases

Phase 2: Chronic Inflammatory Demyelinating Polyradiculoneuropathy

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

2020-002438-34

2020-002438-34

P2

Completed

Chronic Inflammatory Demyelinating Polyradiculoneuropathy

2024-09-30

2025-06-05

Primary Completion Date|Study Completion Date|Treatments