4.1 Review

IPX066: a novel carbidopa-levodopa extended-release formulation

Journal

EXPERT REVIEW OF NEUROTHERAPEUTICS
Volume 12, Issue 2, Pages 133-140

Publisher

EXPERT REVIEWS
DOI: 10.1586/ERN.11.195

Keywords

carbidopa; dyskinesia; extended release; fluctuations; Impax; IPX066; levodopa; medication; Parkinson's disease; treatment

Funding

  1. Impax Pharmaceuticals
  2. Bial
  3. Lundbeck
  4. Biogen Idec
  5. Boehringer Ingelheim
  6. Chelsea Therapeutics
  7. GE Healthcare
  8. Impax
  9. Santhera Pharmaceuticals
  10. Merck Serono/EMD Serono
  11. Solvay Pharmaceuticals
  12. Synosia Therapeutics
  13. Schering-Plough
  14. Shire Pharmaceuticals, Inc.
  15. XenoPort, Inc.
  16. Medivation, Inc.
  17. Addex
  18. Adamas Pharmaceuticals
  19. Noven Pharmaceuticals
  20. PICO-Tesla
  21. Schwartz Pharma
  22. Genzyme
  23. Acadia
  24. TEVA Neuroscience
  25. (Merck) Serono
  26. Novartis Pharmaceuticals
  27. IPSEN Pharmaceuticals
  28. XenoPort Pharmaceuticals
  29. Allergan Neuroscience
  30. Molecular Biometrics
  31. Michael J Fox Foundation for Parkinson's Research
  32. National Parkinson Foundation
  33. University of South Florida

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Levodopa (LD) remains the most effective medication to treat Parkinson's disease (PD). However, most patients develop motor fluctuations and dyskinesias with long-term LD use. It is thought that these response complications are due, at least in part, to LD's short half-life. Thus, there is great interest in long-acting LD preparations that might be able to provide robust antiparkinsonian benefit through the day and potentially avoid the development of motor fluctuations and dyskinesias. IPX066 is an investigational extended-release carbidopa-levodopa (CD-LD) formulation. It is designed to achieve rapid absorption and onset of clinical benefit, similar to CD-LD immediate release, and to provide more sustained therapeutic LD levels and longer duration of clinical benefit. In Phase III clinical trials, IPX066 was demonstrated to be efficacious in early PD compared with placebo, and in moderate-to-advanced PD, it provided more sustained clinical benefit with fewer dose administrations than CD-LD immediate release, as reported in published abstracts.

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