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. 2019 Oct 1;93(14):647. doi: 10.1212/WNL.0000000000008186

Clinical trials of disease-modifying agents in pediatric MS

Opportunities, challenges, and recommendations from the IPMSSG

PMCID: PMC7987956  PMID: 31570644

In the article “Clinical trials of disease-modifying agents in pediatric MS: Opportunities, challenges, and recommendations from the IPMSSG" by Waubant et al.,1 first published online May 1, 2019, the Coinvestigator appendix—the list of those who reviewed and approved the consensus statement—should have included Investigators Angelo Ghezzi (Centro Studi Sclerosi Multipla, Ospedale di Gallarate, Gallarate, Italy), Amit Bar-Or (Center for Neuroinflammation and Experimental Therapeutics and the Department of Neurology, University of Pennsylvania, Philadelphia, PA), and Andrew Kornberg (University of Melbourne, Parkville, Australia), who each reviewed the manuscript. The authors regret the errors.

Reference

  • 1.Waubant E, Banwell B, Wassmer E, et al. Clinical trials of disease-modifying agents in pediatric MS: opportunities, challenges, and recommendations from the IPMSSG. Neurology 2019;92:e2538–2549. [DOI] [PMC free article] [PubMed] [Google Scholar]

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