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.

Abstract

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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