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Results: 1 to 20 of 133

Similar articles for PubMed (Select 23307913)

1.

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

Sugimoto T, Sozu T, Hamasaki T, Evans SR.

Biostatistics. 2013 Jul;14(3):409-21. doi: 10.1093/biostatistics/kxs057. Epub 2013 Jan 10.

2.
3.

Designing exploratory cancer trials using change in tumour size as primary endpoint.

Jaki T, André V, Su TL, Whitehead J.

Stat Med. 2013 Jul 10;32(15):2544-54. doi: 10.1002/sim.5716. Epub 2012 Dec 19.

PMID:
23280944
4.

A group sequential Holm procedure with multiple primary endpoints.

Ye Y, Li A, Liu L, Yao B.

Stat Med. 2013 Mar 30;32(7):1112-24. doi: 10.1002/sim.5700. Epub 2012 Dec 14.

PMID:
23239078
5.

A hierarchical rank test for crossover trials with censored data.

Brittain E, Follmann D.

Stat Med. 2011 Dec 30;30(30):3507-19. doi: 10.1002/sim.4398. Epub 2011 Dec 5.

PMID:
22139739
6.

Sample size determination in clinical trials with multiple co-primary binary endpoints.

Sozu T, Sugimoto T, Hamasaki T.

Stat Med. 2010 Sep 20;29(21):2169-79. doi: 10.1002/sim.3972.

PMID:
20687162
7.

Sample size in cluster-randomized trials with time to event as the primary endpoint.

Jahn-Eimermacher A, Ingel K, Schneider A.

Stat Med. 2013 Feb 28;32(5):739-51. doi: 10.1002/sim.5548. Epub 2012 Aug 2.

PMID:
22865817
8.

Analysis and design of randomised clinical trials involving competing risks endpoints.

Tai BC, Wee J, Machin D.

Trials. 2011 May 19;12:127. doi: 10.1186/1745-6215-12-127.

9.

Statistics in clinical trials.

Green SJ, Pauler DK.

Curr Oncol Rep. 2004 Jan;6(1):36-41. Review.

PMID:
14664759
10.

Estimating the distribution of nonterminal event time in the presence of mortality or informative dropout.

Jiang H, Chappell R, Fine JP.

Control Clin Trials. 2003 Apr;24(2):135-46.

PMID:
12689735
11.

Sample size determination in clinical trials with multiple co-primary endpoints including mixed continuous and binary variables.

Sozu T, Sugimoto T, Hamasaki T.

Biom J. 2012 Sep;54(5):716-29. doi: 10.1002/bimj.201100221. Epub 2012 Jul 25.

PMID:
22829198
12.

Sample size determination in superiority clinical trials with multiple co-primary correlated endpoints.

Sozu T, Sugimoto T, Hamasaki T.

J Biopharm Stat. 2011 Jul;21(4):650-68. doi: 10.1080/10543406.2011.551329.

PMID:
21516562
13.

Considerations in choosing a primary endpoint that measures durability of virological suppression in an antiretroviral trial.

Gilbert PB, Ribaudo HJ, Greenberg L, Yu G, Bosch RJ, Tierney C, Kuritzkes DR.

AIDS. 2000 Sep 8;14(13):1961-72.

PMID:
10997401
14.

A review of statistical issues with progression-free survival as an interval-censored time-to-event endpoint.

Sun X, Li X, Chen C, Song Y.

J Biopharm Stat. 2013;23(5):986-1003. doi: 10.1080/10543406.2013.813524.

PMID:
23957511
15.

Simultaneous use of weighted logrank and standardized Kaplan-Meier statistics.

Yang P, Fleming TR.

J Biopharm Stat. 2006;16(2):241-52.

PMID:
16584070
16.

Viral suppression in HIV studies: combining times to suppression and rebound.

Gouskova NA, Cole SR, Eron JJ, Fine JP.

Biometrics. 2014 Jun;70(2):441-8. doi: 10.1111/biom.12140. Epub 2014 Jan 21.

17.

Power and sample size determination in clinical trials with multiple primary continuous correlated endpoints.

Lafaye de Micheaux P, Liquet B, Marque S, Riou J.

J Biopharm Stat. 2014;24(2):378-97. doi: 10.1080/10543406.2013.860156.

PMID:
24605975
18.

Statistical considerations for the next generation of clinical trials.

Wu W, Shi Q, Sargent DJ.

Semin Oncol. 2011 Aug;38(4):598-604. doi: 10.1053/j.seminoncol.2011.05.014. Review.

PMID:
21810519
19.

Sample size determination for clinical trials with co-primary outcomes: exponential event times.

Hamasaki T, Sugimoto T, Evans S, Sozu T.

Pharm Stat. 2013 Jan-Feb;12(1):28-34. doi: 10.1002/pst.1545. Epub 2012 Oct 19.

20.

Statistical considerations when using a composite endpoint for comparing treatment groups.

Gómez G, Lagakos SW.

Stat Med. 2013 Feb 28;32(5):719-38. doi: 10.1002/sim.5547. Epub 2012 Aug 1.

PMID:
22855368
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