Abstract
AbstractDespite regulatory changes designed to stimulate investment in therapies for rare diseases, many of these conditions lack government-approved treatments. Advanced regenerative medicines, which are therapies and clinical interventions aimed at healing or replacing damaged or defective human cells, tissues, and organs, offer great promise for addressing many rare diseases. A major challenge facing advanced regenerative medicines for rare diseases is securing financial support to assist in bringing a therapy to market. This paper describes the factors cited by pharmaceutical industry players globally for sponsoring the development of advanced regenerative medicines for rare diseases. The paper examines the motivations of 53 sponsors that meet the latter criteria. The motivations behind investments were broadly similar amongst sponsors and map closely onto regulatory requirements for clinical development and marketing authorization of advanced therapeutic products, including the presence of accelerated or attenuated pathways for regulatory approval, use for indications with high unmet medical needs, and/or that have advantages over existing therapies, and robust preclinical data. Other factors include availability of investment incentives and opportunities for off-label use in the post-approval stages.
Publisher
Springer Science and Business Media LLC
Reference62 articles.
1. Health Canada. About orphan drugs and rare diseases in Canada. 2018. https://www.canada.ca/en/health-canada/services/licences-authorizations-registrations-drug-health-products/regulatory-approach-drugs-rare-diseases/about-drugs-rare-diseases.html
2. Chung CC, Chu AT, Chung BH. Rare disease emerging as a global public health priority. Front Public Health. 2022;10. https://doi.org/10.3389/fpubh.2022.1028545.
3. Planning and International Affairs Directorate. Health Products Food Branch. Initial draft discussion document for a Canadian orphan drug regulatory framework. 2012.
4. European Commission. EU research on rare diseases. https://research-and-innovation.ec.europa.eu/research-area/health/rare-diseases_en
5. United States Government. Federal Food, Drug, and Cosmetic Act. 2018.