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Orphanet Journal of Rare Diseases logoLink to Orphanet Journal of Rare Diseases
. 2024 Mar 21;19:131. doi: 10.1186/s13023-024-03136-7

Correction to: Analysis of the first ten years of FDA’s rare pediatric disease priority review voucher program: designations, diseases, and drug development

Catherine Mease 1,, Kathleen L Miller 1, Lewis J Fermaglich 1, Jeanine Best 2, Gumei Liu 3, Erika Torjusen 1
PMCID: PMC10958872  PMID: 38515155

Correction to: Orphanet Journal of Rare Diseases (2024) 19:86

10.1186/s13023-024-03097-x

Following publication of the original article [1], we have been notified that there should be a disclaimer published in the Acknowledgement note.

Acknowledgement note now is:

Acknowledgements

The authors would like to thank Sandra Retzky and Dionna Green for their input on this research project.

Acknowledgement note should be:

Acknowledgements

The authors would like to thank Sandra Retzky and Dionna Green for their input on this research project.

This manuscript reflects the views of the authors and should not be construed to represent FDA’s and the Department of Health and Human Services (HHS)’s views or policies.

Footnotes

The online version of the original article can be found at 10.1186/s13023-024-03097-x.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

  • 1.Mease et al. Analysis of the first ten years of FDA’s rare pediatric disease priority review voucher program: designations, diseases, and drug development. Orphanet J Rare Dis. 2024;19:86. 10.1186/s13023-024-03097-x. [DOI] [PMC free article] [PubMed]

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