Survey of Japanese Orphan Drug Program: Factors Related to Successful Marketing Approval
- PMID: 31364772
- PMCID: PMC6972571
- DOI: 10.1002/jcph.1501
Survey of Japanese Orphan Drug Program: Factors Related to Successful Marketing Approval
Abstract
The basic components of regulatory and supporting policies for orphan drug development appear similar between the United States and Japan, but drugs designated as orphan drugs have been different between the 2 countries. The probabilities of development success (ie, marketing approval) in designated orphan drugs have also been significantly different. In this study, we analyzed recent outcomes of development for orphan drugs designated from 1993 to 2017 in Japan, considering their development and approval status in the United States. Our analysis showed that success for orphan drug development in Japan was apparently associated with prior approval status in the United States. Company size, orphan development experience, and patient enrichment were also positively associated with successful marketing approval. Although similar designations and priority review systems for orphan drugs have been enacted, economic incentives and regulatory conditions provided by the systems seem to be different between the 2 countries, which may lead to varied performance in orphan designation and approval. We need to pay close attention to the impact of industrial global development strategies when comparing the outcomes and performance of different orphan drug promotion systems.
Keywords: global development; orphan drug; patient enrichment; probability of success.
© 2019 The Authors. The Journal of Clinical Pharmacology published by Wiley Periodicals, Inc. on behalf of American College of Clinical Pharmacology.
Figures
References
-
- Melnikova I. Rare diseases and orphan drugs. Nat Rev Drug Discov. 2012;11(4):267‐268. - PubMed
-
- Schieppati A, Henter JI, Daina E, Aperia A. Why rare diseases are an important medical and social issue. Lancet. 2008;371(9629):2039‐2041. - PubMed
-
- Electronic Code of Federal Regulations PART 316—Orphan Drugs. https://www.ecfr.gov/cgi-bin/text-idx?SID=7f77960f61d80d3fdca8f02993f23e.... Accessed April 21, 2019.
-
- European Medicines Agency. Orphan designation https://www.ema.europa.eu/en/human-regulatory/overview/orphan-designation. Accessed April 21, 2019.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
