Expediting treatments in the 21st century: orphan drugs and accelerated approvals
Although the typical timings for AA to be confirmed or withdrawn has not changed significantly over the decades, the disease areas utilizing orphan drug designation and AA have changed significantly over time. Both programs have had increases in their use for therapies targeting oncological diseases. The re-use of surrogate markers for oncological diseases has been an advantage in a way that may not be scientifically feasible in many other disease areas that have greater differentiation across disease etiology. For non-oncological diseases, applicability of AA is, in part, dependent upon greater focus on characterization and acceptance of novel surrogate markers.
Authors
- Annie Kennedy (ORCID: https://orcid.org/0000-0002-0987-675X)
- Reuben Domike (ORCID: https://orcid.org/0000-0002-5653-0890)
- G. K. Raju
- Jamie Sullivan
Institutions
- nLIGHT (United States) (US)
- University of Prince Edward Island (CA)
- Acceleron Pharma (United States) (US)
- Massachusetts Institute of Technology (US)
Publication Details
- Journal
- Orphanet Journal of Rare Diseases
- Published
- 2024-11-08
- DOI
- https://doi.org/10.1186/s13023-024-03398-1
- Citations
- 2
- Primary Topic
- Neurogenetic and Muscular Disorders Research
- Type
- article
- Field-Weighted Citation Impact
- 0.88
Funders
- Massachusetts Institute of Technology