Evidence map›Paper›PMID 41787226›Full record

SynthesisTherapeutic innovation & regulatory science2026

Systematic Review of Patient Focused Drug Development Meeting Reports for Conditions Affecting Neurodevelopment.

Cristan Farmer, Victoria Kim, Tanvi Das, Seth Cutler, Heidi Wallis, Audrey Thurm

Abstract readSystematic Review
In one paragraph

Synthesis in Therapeutic innovation & regulatory science, 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

6 authors.

Cristan FarmerNeurodevelopmental and Behavioral Phenotyping Service, National Institute of Mental Health, National Institutes of Health, Bethesda, MD, USA. Cristan.Farmer@NIH.gov.
Victoria KimNeurodevelopmental and Behavioral Phenotyping Service, National Institute of Mental Health, National Institutes of Health, Bethesda, MD, USA.
Tanvi DasNeurodevelopmental and Behavioral Phenotyping Service, National Institute of Mental Health, National Institutes of Health, Bethesda, MD, USA.
Seth CutlerNeurodevelopmental and Behavioral Phenotyping Service, National Institute of Mental Health, National Institutes of Health, Bethesda, MD, USA.
Heidi WallisAssociation for Creatine Deficiencies, Carlsbad, CA, USA.
Audrey ThurmNeurodevelopmental and Behavioral Phenotyping Service, National Institute of Mental Health, National Institutes of Health, Bethesda, MD, USA.

Funding

Neurodevelopmental and Behavioral Phenotyping ZICMH002961 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI THURM, AUDREY · 2017 to 2025
$12.6M
Intramural NIH HHS ZIC MH002961NIMH NIH HHS ZICMH002961
6 · The paper itself

Abstract

backgroundResearchers of rare diseases affecting neurodevelopment struggle with concept and outcome assessment identification issues that are uniquely associated with developmental concepts but common across conditions. However, the potential to capitalize on the collective commonness of rare disease in order to achieve the large samples often required to create and validate clinical outcome assessments is insufficiently tapped. Identifying synergies in concepts of interest across conditions affecting neurodevelopment may accelerate clinical outcome assessment development for prioritized concepts. We conducted the first systematic review of patient focused drug development (PFDD) meeting reports, to identify concepts prioritized by patients and caregivers across conditions.

methodsSixteen reports on rare conditions affecting neurodevelopment were identified. The responses to two survey items, "top three most troublesome symptoms" and "top three ideal treatment targets," were coded into general concepts and the endorsement rates were aggregated across the conditions.

resultsFull consensus about any individual troublesome symptom or treatment target was rare for any condition. Three conditions had no concept that exceeded 30% endorsement. However, for 11 of the 16 conditions, at least 30% of the respondents endorsed the developmental concepts of Communication or Cognitive/Developmental as a most troublesome symptom and as an ideal treatment target.

conclusionsThis empirical support for the shared prioritization of developmental concepts across heterogeneous conditions is an important first step in unifying clinical outcome assessment development efforts to promote clinical trial readiness in rare disease.

Indexed as

Drug DevelopmentNeurodevelopmental DisordersRare DiseasesHumansNeurodevelopmentClinical meaningfulnessLived experiencePatient focused drug developmentPublic participationRare disease

Identifiers

PMID41787226
PMCPMC13002096

What OpenQuestion holds

Textmetadata
LicenceTDM
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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.