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Although the typical timings for AA to be confirmed or withdrawn has not changed significantly over the decades, the disease areas utilizing orphan drug designation and AA have changed significantly over time.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.

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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

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article

Expediting treatments in the 21st century: orphan drugs and accelerated approvals

Annie Kennedy, Reuben Domike, G. K. Raju, Jamie Sullivan
2 citations
Orphanet Journal of Rare Diseases
Neurogenetic and Muscular Disorders Research
0.88
article

Expediting treatments in the 21st century: orphan drugs and accelerated approvals

Annie Kennedy, Reuben Domike, G. K. Raju, Jamie Sullivan
article en
2 citations

Abstract

Although the typical timings for AA to be confirmed or withdrawn has not changed significantly over the decades, the disease areas utilizing orphan drug designation and AA have changed significantly over time.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.

Orphanet Journal of Rare DiseasesVol. 19(1)
nLIGHT (United States) (US), University of Prince Edward Island (CA), Acceleron Pharma (United States) (US), Massachusetts Institute of Technology (US)
Massachusetts Institute of Technology
Good health and well-being
Openalex Percentile: Top 23%
Neurogenetic and Muscular Disorders Research
0.88
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Expediting treatments in the 21st century: orphan drugs and accelerated approvals — Annie Kennedy, Reuben Domike, et al. · Orphanet Journal of Rare Diseases (2024) | TGRS Research Map | TGRS