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Long-term safety profile of tolvaptan in autosomal dominant polycystic kidney disease patients: TEMPO Extension Japan Trial [Corrigendum]

Authors Muto S, Okada T, Yasuda M, Tsubouchi H, Nakajima K, Horie S

Received 29 May 2018

Accepted for publication 29 May 2018

Published 16 July 2018 Volume 2018:10 Pages 67—68

DOI https://doi.org/10.2147/DHPS.S175655


Muto S, Okada T, Yasuda M, et al. Drug Healthc Patient Saf. 2017;9:93–104.

On page 97, ‘Discussion’ section, lines 10–13, left column, the sentence: ‘Similarly, placebo patients who crossed over onto active treatment discontinued at a similar rate (24.0%), while those who continued on tolvaptan treatment discontinued at a much lower rate (11.8%)’ should read: ‘Similarly, placebo patients who crossed over onto active treatment discontinued at a similar rate (26.0%), while those who continued on tolvaptan treatment discontinued at a much lower rate (10.6%)’. On page 101, Figure 6, the number of patients of ‘Completed trial’ in the TEMPO Extension Japan trial should be revised from ‘n=75’ to ‘n=76’, and ‘Withdrawal rate’ should also be revised from ‘11.8%’ to ‘10.6%’ in the allocated to tolvaptan in TEMPO 3:4 trial. The number of patients of ‘Completed trial’ in TEMPO Extension Japan trial should be revised from ‘n=38’ to ‘n=37’, and ‘Withdrawal rate’ should also be revised from ‘24.0%’ to ‘26.0%’ in the allocated to placebo in TEMPO 3:4 trial.

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