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Tracing the path of non-industry-driven medicine development for rare diseases through regulatory interactions at the European Medicines Agency

  • Noa Rosenberg
  • , Carla E M Hollak
  • , V A Haverhoek
  • , Violeta Stoyanova-Beninska
  • , A M G Pasmooij*
  • , Saco J de Visser
  • *Corresponding author for this work
  • Utrecht University
  • MetabERN
  • European Medicines Agency
  • Platform at Amsterdam UMC - University of Amsterdam

Research output: Contribution to journalReview articlepeer-review

Abstract

Non-industry organizations, including academia, charities, and public institutes, increasingly contribute to rare disease medicine development. In this study, we reviewed orphan designations (ODs) granted between 2000 and 2022, comparing non-industry and industry outcomes. Of 2734 ODs, 183 (6.7%) originated from non-industry organizations. Protocol assistance was obtained for 33% of non-industry and 35% of industry ODs, with distinct peaks for non-industry ODs in 2015 and 2017 linked to European grant calls promoting regulatory engagement. Only six non-industry ODs led to marketing authorization, all post transfer to industry. Our findings indicate lower transition rates yet partial long-term convergence, highlighting the value of targeted grants and regulatory support.

Original languageEnglish
Article number104631
JournalDrug Discovery Today
Volume31
Issue number2
Early online date19 Feb 2026
DOIs
Publication statusPublished - Mar 2026

Bibliographical note

Publisher Copyright:
© 2026 The Author(s).

Keywords

  • medicines development
  • orphan designation
  • orphan medicine
  • protocol assistance
  • rare disease
  • regulatory interaction

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