Abstract
Background: The multifaceted challenges of rare disease research remain, leaving a large proportion of rare disease patients without treatment options. This study aims to identify the challenges of rare disease drug development. Research design & methods: Ten semi-structured interviews were carried out with a range of stakeholders. Thematic analysis was conducted to identify common and important themes. Results: Four overarching themes of stakeholder engagement, regulatory structure, data, and patient support were identified, encompassing fifteen subthemes. Conclusion: The presence of an active patient group is a significant factor in reducing barriers to rare diseases treatment development. Effective collaboration between the various stakeholders of rare disease research is crucial.
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Joshi, S., Chen, J., Sultan, M., Singh, S., Abedi, S., & Zheng, S. (2021). European stakeholder perspectives on challenges to rare disease drug development–a qualitative study. Expert Opinion on Orphan Drugs, 9(6), 181–188. https://doi.org/10.1080/21678707.2021.1953469
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