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Comment
. 2020 Feb;59(2):283-285.
doi: 10.1007/s40262-019-00852-3.

Authors' Reply to Yu et al.: "Levothyrox® New and Old Formulations: Are They Switchable for Millions of Patients?"

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Comment

Authors' Reply to Yu et al.: "Levothyrox® New and Old Formulations: Are They Switchable for Millions of Patients?"

Didier Concordet et al. Clin Pharmacokinet. 2020 Feb.
No abstract available

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Conflict of interest statement

Didier Concordet, Peggy Gandia, Jean-Louis Montastruc, Alain Bousquet-Mélou, Peter Lees, Aude A. Ferran, and Pierre-Louis Toutain have no conflicts of interest that are directly relevant to the content of this reply.

Comment on

References

    1. Yu Y, Maliepaard M. Comment on: “Levothyrox® new and old formulations: are they switchable for millions of patients?”. Clin Pharmacokinet. 2019 doi: 10.1007/s40262-019-00850-5. - DOI - PubMed
    1. U.S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER). Guidance for industry: statistical approaches to establishing bioequivalence. January 2001. https://www.fda.gov/media/70958/download. [Accessed 26 Nov 2019].
    1. Concordet D, Gandia P, Montastruc J-L, Bousquet-Mélou A, Lees P, Ferran AA, et al. Authors’ reply to Coste et al.: Levothyrox® new and old formulations: are they switchable for millions of patients? Clin Pharmacokinet. 2019;58(7):967–968. doi: 10.1007/s40262-019-00747-3. - DOI - PMC - PubMed
    1. Concordet D, Gandia P, Montastruc J-L, Bousquet-Mélou A, Lees P, Ferran AA, et al. Why were more than 200 subjects required to demonstrate the bioequivalence of a new formulation of levothyroxine with an old one? Clin Pharmacokinet. 2019 doi: 10.1007/s40262-019-00812-x. - DOI - PMC - PubMed
    1. Anonymous. Draft guidance on levothyroxine sodium. Food and Drug Administration; 2018: :p. 2. https://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformat.... Accessed 4 Oct 2019.

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