Trends in orphan drug use and spending among children and adolescents during 2010–2020 in Korea

Background: Since 2014 in Korea, the Ministry of Food and Drug Safety has designated orphan drugs (ODs) for the treatment of rare diseases. This study investigated the market share and 20 most frequently prescribed therapeutic subgroups of ODs among children and adolescents in Korea. Methods: This study referenced the Korean national health insurance database from January 2010 through December 2020. The outcome measures were the number of prescriptions and expenditures on ODs. Results: Among children aged 0–12 years, the number of patients using ODs increased from 11,264 in 2010 to 14,017 in 2020. Expenditures on ODs and their proportion of total pharmaceutical expenditures also tripled from 13.3 million USD (1.2%) in 2010 to 46.4 million USD (6.2%) in 2020. Among the overall population and adolescents aged 13–17 years, the percentage of total pharmaceutical expenditures for ODs increased from 0.4% in 2010 to 3.2% in 2020 and from 2.1% in 2010 to 11.2% in 2020, respectively. The highest numbers and drug costs of child patients were for H01 (pituitary and hypothalamic hormones and analogues, 44,839) and A16 (other alimentary tract and metabolism products, 160 million USD). The individual ODs with the highest drug costs were A16AB09 (idursulfase, 82.4 million USD) and M09AX07 (nusinersen, 36.2 million USD). Conclusion: Although the market size of ODs remained small in Korea, both the number of approved ODs and the proportion of total pharmaceutical expenditures for ODs have increased. Additional policies related to designation and reimbursement should be put in place to ensure timely access to ODs.

[1]  Y. le Cam,et al.  Orphan Medicine Incentives: How to Address the Unmet Needs of Rare Disease Patients by Optimizing the European Orphan Medicinal Product Landscape Guiding Principles and Policy Proposals by the European Expert Group for Orphan Drug Incentives (OD Expert Group) , 2021, Frontiers in Pharmacology.

[2]  Dong-Sook Kim,et al.  Determinants of Growth in Prescription Drug Spending Using 2010–2019 Health Insurance Claims Data , 2021, Frontiers in Pharmacology.

[3]  Jong Hyuk Lee Pricing and Reimbursement Pathways of New Orphan Drugs in South Korea: A Longitudinal Comparison , 2021, Healthcare.

[4]  R. Conti,et al.  Trends In Orphan Drug Spending And Out-Of-Pocket Spending Among US Children, 2013-18. , 2020, Health affairs.

[5]  Jong Hyuk Lee,et al.  Patient Accessibility and Budget Impact of Orphan Drugs in South Korea: Long-Term and Real-World Data Analysis (2007–2019) , 2020, International journal of environmental research and public health.

[6]  Joshua T. Cohen,et al.  Orphan Drugs Offer Larger Health Gains but Less Favorable Cost-effectiveness than Non-orphan Drugs , 2020, Journal of General Internal Medicine.

[7]  O. Blin,et al.  Orphan drug designation in Europe: A booster for the research and development of drugs in rare diseases. , 2020, Therapie.

[8]  S. Vogler,et al.  Public spending on orphan medicines: a review of the literature , 2019, Journal of Pharmaceutical Policy and Practice.

[9]  Tudor I. Oprea,et al.  Therapies for rare diseases: therapeutic modalities, progress and challenges ahead , 2019, Nature Reviews Drug Discovery.

[10]  A. Hutchings,et al.  An analysis of orphan medicine expenditure in Europe: is it sustainable? , 2019, Orphanet Journal of Rare Diseases.

[11]  R. Ahonen,et al.  Policies and availability of orphan medicines in outpatient care in 24 European countries , 2018, European Journal of Clinical Pharmacology.

[12]  R. Wade,et al.  Orphan Drug Expenditures In The United States: A Historical And Prospective Analysis, 2007-18. , 2016, Health affairs.

[13]  R. Wade,et al.  Pharmaceutical expenditure on drugs for rare diseases in Canada: a historical (2007–13) and prospective (2014–18) MIDAS sales data analysis , 2016, Orphanet Journal of Rare Diseases.

[14]  Christine Y. Lu,et al.  Access to Orphan Drugs: A Comprehensive Review of Legislations, Regulations and Policies in 35 Countries , 2015, PloS one.

[15]  Jatinder Singh,et al.  The portal for rare diseases and orphan drugs , 2013, Journal of pharmacology & pharmacotherapeutics.

[16]  Steven Simoens,et al.  Paying for the Orphan Drug System: break or bend? Is it time for a new evaluation system for payers in Europe to take account of new rare disease treatments? , 2012, Orphanet Journal of Rare Diseases.

[17]  A. Hutchings,et al.  Estimating the budget impact of orphan medicines in Europe: 2010 - 2020 , 2011, Orphanet journal of rare diseases.

[18]  I. Oyagüez,et al.  Global spending on orphan drugs in France, Germany, the UK, Italy and Spain during 2007 , 2010, Applied health economics and health policy.

[19]  T. Umeda,et al.  35 years of Japanese policy on rare diseases , 2008, The Lancet.

[20]  J G Thornton,et al.  Clinical trials and rare diseases: a way out of a conundrum , 1995, BMJ.