4.7 Article

AAV2-GAD gene therapy for advanced Parkinson's disease: a double-blind, sham-surgery controlled, randomised trial

Journal

LANCET NEUROLOGY
Volume 10, Issue 4, Pages 309-319

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/S1474-4422(11)70039-4

Keywords

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Funding

  1. Neurologix
  2. Allergan
  3. Boehringer-Ingelheim
  4. Chelsea Therapeutics
  5. The Michael J Fox Foundation for Parkinson's Research
  6. Merz
  7. Novartis
  8. Santhera
  9. UCB
  10. Medtronic Neurological
  11. Schwartz Biosciences
  12. Molecular Biometrics
  13. IMPAX Pharmaceuticals
  14. Ohio State University
  15. Chalmers P Wiley VA Medical Center
  16. National Institute of Health
  17. Huntington's Disease Society of America
  18. Teva
  19. Acadia
  20. Ipsen
  21. Impair
  22. Chelsea Pharmaceuticals
  23. US Department of Defense, National Institutes of Health
  24. National Institutes of Health Neurological Disorders and Stroke
  25. Kyowa
  26. Boehringer Ingelheim
  27. Eli Lilly
  28. Ceregene
  29. Genzyme
  30. National Institutes of Health
  31. The Dana Foundation
  32. Thomas Hartman Foundation for Parkinson's Research

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Background Gene transfer of glutamic acid decarboxylase (GAD) and other methods that modulate production of GABA in the subthalamic nucleus improve basal ganglia function in parkinsonism in animal models. We aimed to assess the effect of bilateral delivery of AAV2-GAD in the subthalamic nucleus compared with sham surgery in patients with advanced Parkinson's disease. Methods Patients aged 30-75 years who had progressive levodopa-responsive Parkinson's disease and an overnight off-medication unified Parkinson's disease rating scale (UPDRS) motor score of 25 or more were enrolled into this double-blind, phase 2, randomised controlled trial, which took place at seven centres in the USA between Nov 17, 2008, and May 11, 2010. Infusion failure or catheter tip location beyond a predefined target zone led to exclusion of patients before unmasking for the efficacy analysis. The primary outcome measure was the 6-month change from baseline in double-blind assessment of off-medication UPDRS motor scores. This trial is registered with ClinicalTrials.gov, NCT00643890. Findings Of 66 patients assessed for eligibility, 23 were randomly assigned to sham surgery and 22 to AAV2-GAD infusions; of those, 21 and 16, respectively, were analysed. At the 6-month endpoint, UPDRS score for the AAV2-GAD group decreased by 8.1 points (SD 1.7, 23.1%; p < 0.0001) and by 4.7 points in the sham group (1.5, 12-7%; p=0.003). The AAV2-GAD group showed a significantly greater improvement from baseline in UPDRS scores compared with the sham group over the 6-month course of the study (RMANOVA, p=0.04). One serious adverse event occurred within 6 months of surgery; this case of bowel obstruction occurred in the AAV2-GAD group, was not attributed to treatment or the surgical procedure, and fully resolved. Other adverse events were mild or moderate, likely related to surgery and resolved; the most common were headache (seven patients in the AAV2-GAD group vs two in the sham group) and nausea (six vs two). Interpretation The efficacy and safety of bilateral infusion of AAV2-GAD in the subthalamic nucleus supports its further development for Parkinson's disease and shows the promise for gene therapy for neurological disorders.

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