Fampridine sustained-release

Drug Profile

Fampridine sustained-release

Alternative Names: 4-Aminopyridine modified release - Acorda Therapeutics; 4-AP - Acorda Therapeutics; Ampyra; BIIB 041; Dalfampridine ER; Dalfampridine extended-release; Dalfampridine QD; Dalfampridine-SR; EL 970; Fampridine ER; Fampridine extended-release; Fampridine-PR; Fampridine-SR; Fampyra; Neurelan; PR-FAM

Latest Information Update: 25 Mar 2017

Price : $50

At a glance

  • Originator Elan Drug Technologies
  • Developer Acorda Therapeutics; Biogen; Kessler Foundation; University of California at Los Angeles; University of Florida; University of Miami
  • Class Aminopyridines; Small molecules
  • Mechanism of Action Potassium channel antagonists
  • Orphan Drug Status

    Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.

    Yes - Spinal cord injuries; Multiple sclerosis
  • On Fast track

    Fast track status is assigned by the US FDA so therapies with the potential to address unmet needs can move faster through development.

  • New Molecular Entity Yes

Highest Development Phases

  • Marketed Multiple sclerosis
  • Phase III Ataxia
  • Phase II Spinal cord injuries; Spinocerebellar degeneration
  • Phase I/II Parkinson's disease
  • No development reported Cerebral palsy
  • Discontinued Neurological disorders

Most Recent Events

  • 09 Mar 2017 The USPTO’s Patent Trials and Appeal Board (PTAB) uphelds four patents related to use of dalfampridine extended release tablets
  • 21 Nov 2016 Discontinued - Phase-III for Neurological disorders in USA (PO)
  • 21 Nov 2016 Efficacy and adverse events data from the phase III trial in Neurological disorders (Post-stroke) released by Acorda
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