A logrank test-based method for sizing clinical trials with two co-primary time-to-event endpoints-Reference-Cited by-同舟云学术

A logrank test-based method for sizing clinical trials with two co-primary time-to-event endpoints

Author:

Sugimoto Tomoyuki¹,Sozu Takashi²,Hamasaki Toshimitsu³,Evans Scott R.⁴

Affiliation:

1. Department of Mathematical Sciences, Hirosaki University Graduate School of Science and Technology, 3 Bunkyocho, Hirosaki, Aomori 036-8561, Japan

2. Department of Biostatistics, Kyoto University School of Public Heath, Kyoto 606-8501, Japan

3. Department of Biomedical Statistics, Osaka University Graduate School of Medicine, Suita 565-0871, Japan

4. Department of Biostatistics, Harvard University School of Public Heath, Boston, MA 02115-6018, USA

Funder

JSPS KAKENHI

Pfizer Health Research Foundation, Japan

Data Management Center of the Adult AIDS Clinical Trials Group

Publisher

Oxford University Press (OUP)

Subject

Statistics, Probability and Uncertainty,General Medicine,Statistics and Probability

Link

Reference14 articles.

2. Sample size determination for clinical trials with co-primary endpoints: exponential event times;Hamasaki;Pharmaceutical Statistics,2012

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