Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Randomized Controlled Trial
. 2023 Apr 19;18(1):89.
doi: 10.1186/s13023-023-02702-9.

Randomized controlled trial data for successful new drug application for rare diseases in the United States

Yosuke Kubota  1   2 , Mamoru Narukawa  3
Affiliations
Randomized Controlled Trial

Randomized controlled trial data for successful new drug application for rare diseases in the United States

Yosuke Kubota et al. Orphanet J Rare Dis. .

Abstract

Background: Randomized controlled trial (RCT) data have important implications in drug development. However, the feasibility and cost of conducting RCTs lower the motivation for drug development, especially for rare diseases. We investigated the potential factors associated with the need for RCTs in the clinical data package for new drug applications for rare diseases in the United States (US). This study focused on 233 drugs with orphan drug designations approved in the US between April 2001 and March 2021. Univariable and multivariable logistic regression analyses were conducted to investigate the association between the presence or absence of RCTs in the clinical data package for new drug applications.

Results: Multivariable logistic regression analysis showed that the severity of the disease outcome (odds ratio [OR] 5.63, 95% confidence interval [CI] 2.64-12.00), type of drug usage (odds ratio [OR] 2.95, 95% confidence interval [CI] 1.80-18.57), and type of primary endpoint (OR 5.57, 95% CI 2.57-12.06) were associated with the presence or absence of RCTs.

Conclusions: Our results indicated that the presence or absence of RCT data in the clinical data package for successful new drug application in the US was associated with three factors: severity of disease outcome, type of drug usage, and type of primary endpoint. These results highlight the importance of selecting target diseases and potential efficacy variables to optimize orphan drug development.

Keywords: Clinical trials; Efficacy endpoint; Logistic regression analysis; Orphan drugs; Randomization; Rare diseases.

PubMed Disclaimer

Conflict of interest statement

Yosuke Kubota is an employee of Astellas Pharma Inc., Tokyo, Japan and has no conflicts of interest that are directly relevant to the content of this article.

Figures

Fig. 1
Fig. 1
Flow diagram of drug selection
See this image and copyright information in PMC

Similar articles

See all similar articles

Cited by

References

    1. Hanna H, Timothy C, Jonathan R, et al. Saving orphan drug legislations: misconceptions and clarifications. Expert Rev Pharmacoecon Outcomes Res. 2016;16(1):111–7. doi: 10.1586/14737167.2016.1141052. - DOI - PubMed
    1. Dean B, Heike W, et al. A decade of FDA-Approved drugs (2010–2019): Trends and future directions. J Med Chem. 2021 Mar;11(5):2312–38. - PubMed
    1. US Food and Drug Administration. OrphanDrug Act—Relevant Excerpts. Available from: https://www.fda.gov/industry/medical-products-rare-diseases-and-conditio...
    1. Rare Diseases at FDA. https://www.fda.gov/patients/rare-diseases-fda The current as of: 09/21/2022
    1. Haendel M, Vasilevsky N, Unni D, et al. How many rare diseases are there? Nat Rev Drug Discov. 2020;19:77–8. doi: 10.1038/d41573-019-00180-y. - DOI - PMC - PubMed

Publication types