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Published on: March 2, 2018
Systematic Review of Patient Focused Drug Development Meeting Reports for Conditions Affecting Neurodevelopment
Cristan Farmer1, Victoria Kim2, Tanvi Das2
1Neurodevelopmental and Behavioral Phenotyping Service, National Institute of Mental Health, National Institutes of Health, Bethesda, MD, USA. Cristan.Farmer@NIH.gov.
Background:
Researchers 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.
Methods:
Sixteen 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.
Results:
Full 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.
Conclusions:
This 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.
Insights
Patients with rare neurodevelopmental diseases prioritize communication and cognitive/developmental concepts. This finding supports unifying clinical outcome assessment development for rare conditions, accelerating clinical trial readiness.
Area of Science:
- Neuroscience
- Rare Diseases
- Clinical Outcome Assessment Development
Background:
- Researchers face challenges in identifying concepts and outcomes for rare neurodevelopmental diseases.
- The collective commonness of rare diseases is underutilized for creating large-scale clinical outcome assessments.
- Identifying shared concepts across conditions can accelerate outcome assessment development.
Purpose of the Study:
- To systematically review patient-focused drug development (PFDD) meeting reports.
- To identify concepts prioritized by patients and caregivers across rare neurodevelopmental conditions.
Main Methods:
- Systematic review of 16 PFDD meeting reports for rare neurodevelopmental conditions.
- Coded responses on troublesome symptoms and ideal treatment targets into general concepts.
- Aggregated endorsement rates of concepts across conditions.
Main Results:
- No single symptom or treatment target achieved full consensus across all conditions.
- For 11 of 16 conditions, over 30% of respondents prioritized Communication or Cognitive/Developmental concepts.
- These prioritized concepts were relevant as both troublesome symptoms and ideal treatment targets.
Conclusions:
- Empirical evidence supports shared prioritization of developmental concepts across diverse rare diseases.
- This shared prioritization is crucial for unifying clinical outcome assessment development.
- Unification efforts can enhance clinical trial readiness for rare disease populations.
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