Evidence map›Paper›PMID 42405844›Full record

ArticleMovement disorders : official journal of the Movement Disorder Society2026

A Phase 1 Study of Convection-Enhanced Delivery of Intraputaminal AAV2-GDNF in Advanced Parkinson's Disease.

John D Heiss, Debra J Ehrlich, Codrin Lungu, Joseph Y Choi, Gretchen Scott, Irene Dustin, Dima A Hammoud, Peter Herscovitch, Russell R Lonser, Kareem A Zaghloul and 1 more

Abstract readClinical Trial, Phase I
In one paragraph

Article in Movement disorders : official journal of the Movement Disorder Society, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

John D HeissSurgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA.
Debra J EhrlichParkinson's Disease Clinic, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA.
Codrin LunguParkinson's Disease Clinic, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA.
Joseph Y ChoiSurgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA.ORCID https://orcid.org/0009-0009-2408-138X
Gretchen ScottSurgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA.
Irene DustinParkinson's Disease Clinic, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA.
Dima A HammoudRadiology and Imaging Sciences, Clinical Center, National Institutes of Health, Bethesda, Maryland, USA.
Peter HerscovitchPositron Emission Tomography Department, Clinical Center, National Institutes of Health, Bethesda, Maryland, USA.
Russell R LonserDepartment of Neurological Surgery, The Ohio State University College of Medicine, Columbus, Ohio, USA.
Kareem A ZaghloulSurgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA.ORCID https://orcid.org/0000-0001-8575-3578
Krystof BankiewiczDepartment of Neurological Surgery, The Ohio State University College of Medicine, Columbus, Ohio, USA.

Funding

Central Nervous System Drug Delivery TechniquesZ01NS003051 · NINDS · NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE · PI LONSER, RUSSELL · 2008 to 2008
$2.1M
Intramural NIH HHS Z01 NS003051NIH HHS X01NS065758-01NINDS NIH HHS NS-003032-17NINDS NIH HHS NS003051-18
6 · The paper itself

Abstract

backgroundParkinson's disease (PD) is a progressive neurodegenerative disorder. Neurotrophic therapeutic approaches have been limited in part by incomplete delivery to the putamen. We developed image-guided convection-enhanced delivery with real-time monitoring to improve intraputaminal distribution of neurotrophic gene therapy.

objectivesTo evaluate the 5-year safety and tolerability of bilateral putaminal delivery of adeno-associated virus serotype 2 encoding glial cell line-derived neurotrophic factor (AAV2-GDNF), and to describe exploratory long-term clinical outcomes.

methodsThis was a single-center, open-label, phase 1, dose-escalation study in adults with advanced PD. Thirteen participants received bilateral putaminal infusions across three dose cohorts (six low-dose, six medium-dose, one high-dose) and were followed for 5 years. Adverse events, including serious adverse events, were collected, and their relationship to the study agent was determined. Longitudinal clinical outcomes were analyzed with a mixed-effects model.

resultsAcross follow-up, 562 adverse events were recorded; 45 were considered possibly or probably related to the study drug. The 13 serious adverse events that occurred were not attributed to the study drug. One participant died 45 months after infusion from aspiration pneumonia following cervical spine surgery at an outside institution. The study drug had a mean putaminal coverage of 26% ± 10%. Exploratory clinical measures did not change significantly between baseline and final follow-up.

conclusionsBilateral putaminal neurotrophic gene therapy delivered with real-time image guidance was well tolerated over 5 years, without protocol-defined stopping events. © 2026 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society. This article has been contributed to by U.S. Government employees and their work is in the public domain in the USA.

Indexed as

Genetic TherapyGlial Cell Line-Derived Neurotrophic FactorParkinson DiseasePutamenAgedConvectionDependovirusFemaleGene Therapy AgentsHumansMaleMiddle AgedTreatment OutcomeGlial Cell Line-Derived Neurotrophic FactorConvectionDrug delivery systemsGenetic therapyGenetic vectorGlial cell line‐derived neurotrophic factorParkinson disease

Identifiers

PMID42405844
PMCPMC13602296

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.