Considerations for therapeutic targets for clinical trials in biomarker-characterized prodromal Parkinson's disease populations
- 1Department of Neurology, , Rochester, NY, USA
- 2, New York, NY, USA
- 3Department of Neurology, , Chicago, IL, USA
Abstract
Parkinson's disease (PD) is a growing public health problem and biologically targeted therapeutics (BTTs) that slow disease progression are urgently needed. However, the development of effective BTTs is challenging as PD is a clinically defined syndrome with pathobiological heterogeneity and the pathobiological process begins many years before the onset of clinically detectable motor symptoms. Testing BTTs in a biomarker-defined population at an earlier stage in the disease course, before a clinical PD diagnosis, may be the key to achieving this objective. The recent emergence of biological definitions of neuronal α-synuclein disease (NSD) and research frameworks for staging disease represent the first step towards testing BTTs in biomarker-defined prodromal populations. While biomarker-defined populations are essential for implementing precision therapeutic approaches, selecting and prioritizing BTTs for testing in early-stage populations is also critical, and requires consideration of biological relevance, safety, and operational feasibility. Here, in preparation for such studies, we review the landscape of publicly available PD BTTs organized by mechanistic pathways and targets, and summarize scientific, safety, and operational considerations relevant to early-stage, biomarker-defined trials targeting NSD participants prior to PD clinical diagnosis. Recognizing that there are shared biological mechanisms across neurodegenerative disorders, we complement this review of the PD therapeutic target landscape with a review of publicly available Alzheimer's dementia and amyotrophic lateral sclerosis BTTs and provide a comprehensive list of agents for reference.
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BibTeX
@article{schneider2026considerations,
title = {{Considerations for therapeutic targets for clinical trials in biomarker-characterized prodromal Parkinson's disease populations}},
author = {RB Schneider and G Skibinski and B Fiske and CM Kopil and K Merchant and T Simuni},
journal = {Journal of Parkinson’s Disease},
year = {2026},
month = nov,
doi = {10.1177/1877718x261493297},
url = {https://doi.org/10.1177/1877718x261493297},
note = {CC BY},
}
RIS
TY - JOUR
TI - Considerations for therapeutic targets for clinical trials in biomarker-characterized prodromal Parkinson's disease populations
AU - RB Schneider
AU - G Skibinski
AU - B Fiske
AU - CM Kopil
AU - K Merchant
AU - T Simuni
PY - 2026
DA - 2026/11/04
JO - Journal of Parkinson’s Disease
DO - 10.1177/1877718x261493297
UR - https://doi.org/10.1177/1877718x261493297
AB - Parkinson's disease (PD) is a growing public health problem and biologically targeted therapeutics (BTTs) that slow disease progression are urgently needed. However, the development of effective BTTs is challenging as PD is a clinically defined syndrome with pathobiological heterogeneity and the pathobiological process begins many years before the onset of clinically detectable motor symptoms. Testing BTTs in a biomarker-defined population at an earlier stage in the disease course, before a clinical PD diagnosis, may be the key to achieving this objective. The recent emergence of biological definitions of neuronal α-synuclein disease (NSD) and research frameworks for staging disease represent the first step towards testing BTTs in biomarker-defined prodromal populations. While biomarker-defined populations are essential for implementing precision therapeutic approaches, selecting and prioritizing BTTs for testing in early-stage populations is also critical, and requires consideration of biological relevance, safety, and operational feasibility. Here, in preparation for such studies, we review the landscape of publicly available PD BTTs organized by mechanistic pathways and targets, and summarize scientific, safety, and operational considerations relevant to early-stage, biomarker-defined trials targeting NSD participants prior to PD clinical diagnosis. Recognizing that there are shared biological mechanisms across neurodegenerative disorders, we complement this review of the PD therapeutic target landscape with a review of publicly available Alzheimer's dementia and amyotrophic lateral sclerosis BTTs and provide a comprehensive list of agents for reference.
SN - 1877-7171
SN - 1877-718X
ER -