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Safety of AADC Gene Therapy for Moderately Advanced Parkinson Disease: Three-Year Outcomes From the PD-1101 Trial

BACKGROUND AND OBJECTIVES: 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. METHODS: PD-1101 was a phase 1b, open-label, dose escalation trial of VY-AADC01, a...

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Autores principales: Christine, Chadwick W., Richardson, R. Mark, Van Laar, Amber D., Thompson, Marin E., Fine, Elisabeth M., Khwaja, Omar S., Li, Chunming, Liang, Grace S., Meier, Andreas, Roberts, Eiry W., Pfau, Madeline L., Rodman, Josh R., Bankiewicz, Krystof S., Larson, Paul S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8726573/
https://www.ncbi.nlm.nih.gov/pubmed/34649873
http://dx.doi.org/10.1212/WNL.0000000000012952
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author Christine, Chadwick W.
Richardson, R. Mark
Van Laar, Amber D.
Thompson, Marin E.
Fine, Elisabeth M.
Khwaja, Omar S.
Li, Chunming
Liang, Grace S.
Meier, Andreas
Roberts, Eiry W.
Pfau, Madeline L.
Rodman, Josh R.
Bankiewicz, Krystof S.
Larson, Paul S.
author_facet Christine, Chadwick W.
Richardson, R. Mark
Van Laar, Amber D.
Thompson, Marin E.
Fine, Elisabeth M.
Khwaja, Omar S.
Li, Chunming
Liang, Grace S.
Meier, Andreas
Roberts, Eiry W.
Pfau, Madeline L.
Rodman, Josh R.
Bankiewicz, Krystof S.
Larson, Paul S.
author_sort Christine, Chadwick W.
collection PubMed
description BACKGROUND AND OBJECTIVES: 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. METHODS: 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(11) vector genomes (vg); cohort 2, ≤1.5 × 10(12) vg; cohort 3, ≤4.7 × 10(12) vg. RESULTS: 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 Parkinson's 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 Parkinson's Disease Questionnaire) were stable or improved compared with baseline at 12, 24, and 36 months following VY-AADC01 administration across cohorts. DISCUSSIONS: 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. TRIAL REGISTRATION INFORMATION: NCT01973543. CLASSIFICATION OF EVIDENCE: 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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spelling pubmed-87265732022-01-05 Safety of AADC Gene Therapy for Moderately Advanced Parkinson Disease: Three-Year Outcomes From the PD-1101 Trial Christine, Chadwick W. Richardson, R. Mark Van Laar, Amber D. Thompson, Marin E. Fine, Elisabeth M. Khwaja, Omar S. Li, Chunming Liang, Grace S. Meier, Andreas Roberts, Eiry W. Pfau, Madeline L. Rodman, Josh R. Bankiewicz, Krystof S. Larson, Paul S. Neurology Research Article BACKGROUND AND OBJECTIVES: 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. METHODS: 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(11) vector genomes (vg); cohort 2, ≤1.5 × 10(12) vg; cohort 3, ≤4.7 × 10(12) vg. RESULTS: 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 Parkinson's 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 Parkinson's Disease Questionnaire) were stable or improved compared with baseline at 12, 24, and 36 months following VY-AADC01 administration across cohorts. DISCUSSIONS: 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. TRIAL REGISTRATION INFORMATION: NCT01973543. CLASSIFICATION OF EVIDENCE: 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. Lippincott Williams & Wilkins 2022-01-04 /pmc/articles/PMC8726573/ /pubmed/34649873 http://dx.doi.org/10.1212/WNL.0000000000012952 Text en Copyright © 2021 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Research Article
Christine, Chadwick W.
Richardson, R. Mark
Van Laar, Amber D.
Thompson, Marin E.
Fine, Elisabeth M.
Khwaja, Omar S.
Li, Chunming
Liang, Grace S.
Meier, Andreas
Roberts, Eiry W.
Pfau, Madeline L.
Rodman, Josh R.
Bankiewicz, Krystof S.
Larson, Paul S.
Safety of AADC Gene Therapy for Moderately Advanced Parkinson Disease: Three-Year Outcomes From the PD-1101 Trial
title Safety of AADC Gene Therapy for Moderately Advanced Parkinson Disease: Three-Year Outcomes From the PD-1101 Trial
title_full Safety of AADC Gene Therapy for Moderately Advanced Parkinson Disease: Three-Year Outcomes From the PD-1101 Trial
title_fullStr Safety of AADC Gene Therapy for Moderately Advanced Parkinson Disease: Three-Year Outcomes From the PD-1101 Trial
title_full_unstemmed Safety of AADC Gene Therapy for Moderately Advanced Parkinson Disease: Three-Year Outcomes From the PD-1101 Trial
title_short Safety of AADC Gene Therapy for Moderately Advanced Parkinson Disease: Three-Year Outcomes From the PD-1101 Trial
title_sort safety of aadc gene therapy for moderately advanced parkinson disease: three-year outcomes from the pd-1101 trial
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8726573/
https://www.ncbi.nlm.nih.gov/pubmed/34649873
http://dx.doi.org/10.1212/WNL.0000000000012952
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