Neurology · 2021 · 80 citations · 23 references
MedicineNeurologyNeuroscienceClinical NeuroscienceClinical PharmacologyGene TherapyNeurodegenerative DiseasesNeurodegenerative DisordersNeurological Gene TherapyParkinson DiseaseParkinsonian DisordersSafety Of Gene TherapyAromatic L-amino Acid DecarboxylaseGene-targeted TherapyLarge Bowel ObstructionParkinson Disease Gene Therapy
<h3>Background and Objectives</h3> To report final, 36-month safety and clinical outcomes from the PD-1101 trial of NBIb-1817 (VY-AADC01) in participants with moderately advanced Parkinson disease (PD) and motor fluctuations. <h3>Methods</h3> PD-1101 was a phase 1b, open-label, dose escalation trial of VY-AADC01, an experimental AAV2 gene therapy encoding the human aromatic l-amino acid decarboxylase (AADC) enzyme. VY-AADC01 was delivered via bilateral, intraoperative MRI-guided putaminal infusions to 3 cohorts (n = 5 participants per cohort): cohort 1, ≤7.5 × 10<sup>11</sup> vector genomes (vg); cohort 2, ≤1.5 × 10<sup>12</sup> vg; cohort 3, ≤4.7 × 10<sup>12</sup> vg. <h3>Results</h3> No serious adverse events (SAEs) attributed to VY-AADC01 were reported. All 4 non-vector–related SAEs (atrial fibrillation and pulmonary embolism in 1 participant and 2 events of small bowel obstruction in another participant) resolved. Requirements for PD medications were reduced by 21%–30% in the 2 highest dose cohorts at 36 months. Standard measures of motor function (PD diary, Unified Parkinson9s Disease Rating Scale III “off”-medication and “on”-medication scores), global impressions of improvement (Clinical Global Impression of Improvement, Patient Global Impression of Improvement), and quality of life (39-item Parkinson9s Disease Questionnaire) were stable or improved compared with baseline at 12, 24, and 36 months following VY-AADC01 administration across cohorts. <h3>Discussions</h3> VY-AADC01 and the surgical administration procedure were well-tolerated and resulted in stable or improved motor function and quality of life across cohorts, as well as reduced PD medication requirements in cohorts 2 and 3 over 3 years. <h3>Trial Registration Information</h3> NCT01973543. <h3>Classification of Evidence</h3> This study provides Class IV evidence that, in patients with moderately advanced PD and motor fluctuations, putaminal infusion of VY-AADC01 is well tolerated and may improve motor function.
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