Evidence map›Paper›PMID 37823970›Full record

ArticleNeurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics2023

Transforming Drug Development for Neurological Disorders: Proceedings from a Multidisease Area Workshop.

Diane Stephenson, Ramona Belfiore-Oshan, Yashmin Karten, Jessi Keavney, D Kevin Kwok, Terina Martinez, Joe Montminy, Martijn L T M Müller, Klaus Romero, Sudhir Sivakumaran

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
3.7field-weighted citation impact, top 6% of its field
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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
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  5. Review
  6. Article
  7. Review
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  9. Article
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  11. 3DFrontiers in pharmacology · 2025
    Review
  12. Review
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  14. Review
  15. Article
  16. Parkinson's disease: Still waiting for a cure.Clinical and translational science · 2024
    Article
  17. Article
  18. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Diane StephensonCritical Path Institute, Tucson, AZ, USA. dstephenson@c-path.org.ORCID 0000-0002-4262-436X
Ramona Belfiore-OshanCritical Path Institute, Tucson, AZ, USA.
Yashmin KartenCritical Path Institute, Tucson, AZ, USA.
Jessi KeavneyCritical Path Institute, Tucson, AZ, USA.
D Kevin KwokCritical Path Institute, Tucson, AZ, USA.
Terina MartinezCritical Path Institute, Tucson, AZ, USA.
Joe MontminyCritical Path Institute, Tucson, AZ, USA.
Martijn L T M MüllerCritical Path Institute, Tucson, AZ, USA.
Klaus RomeroCritical Path Institute, Tucson, AZ, USA.
Sudhir SivakumaranCritical Path Institute, Tucson, AZ, USA.
Critical Path Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neurological disorders represent some of the most challenging therapeutic areas for successful drug approvals. The escalating global burden of death and disability for such diseases represents a significant worldwide public health challenge, and the rate of failure of new therapies for chronic progressive disorders of the nervous system is higher relative to other non-neurological conditions. However, progress is emerging rapidly in advancing the drug development landscape in both rare and common neurodegenerative diseases. In October 2022, the Critical Path Institute (C-Path) and the US Food and Drug Administration (FDA) organized a Neuroscience Annual Workshop convening representatives from the drug development industry, academia, the patient community, government agencies, and regulatory agencies regarding the future development of tools and therapies for neurological disorders. This workshop focused on five chronic progressive diseases: Alzheimer's disease, Parkinson's disease, Huntington's disease, Duchenne muscular dystrophy, and inherited ataxias. This special conference report reviews the key points discussed during the three-day dynamic workshop, including shared learnings, and recommendations that promise to catalyze future advancement of novel therapies and drug development tools.

Indexed as

Huntington DiseaseMuscular Dystrophy, DuchenneNervous System DiseasesParkinson DiseaseDrug DevelopmentHumansAlzheimer’s diseaseAtaxiaData sharingDuchenne muscular dystrophyHuntington’s diseaseParkinson’s disease

Identifiers

PMID37823970
PMCPMC10684834
OpenAlexW4387563701

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.