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Items: 1 to 20 of 156

1.
2.

A two one-sided tests procedure for assessment of individual bioequivalence.

Liu J, Chow SC.

J Biopharm Stat. 1997 Mar;7(1):49-61.

PMID:
9056588
3.

A distribution-free procedure for the statistical analysis of bioequivalence studies.

Hauschke D, Steinijans VW, Diletti E.

Int J Clin Pharmacol Ther Toxicol. 1990 Feb;28(2):72-8.

PMID:
2307548
4.

A distribution-free procedure for the statistical analysis of bioequivalence studies.

Hauschke D, Steinijans VW, Diletti E.

Int J Clin Pharmacol Ther Toxicol. 1992;30 Suppl 1:S37-43.

PMID:
1601530
5.

Types of bioequivalence and related statistical considerations.

Hauck WW, Anderson S.

Int J Clin Pharmacol Ther Toxicol. 1992 May;30(5):181-7. Review.

PMID:
1592546
6.

[Review and use of decision rules for bioequivalence trials].

Nicolas P, Tod M, Petitjean O.

Therapie. 1993 Jan-Feb;48(1):15-22. Review. French.

PMID:
8356540
7.

On TIER method for assessment of individual bioequivalence.

Ju HL.

J Biopharm Stat. 1997 Mar;7(1):63-85.

PMID:
9056589
8.

Sample size determination for bioequivalence assessment by means of confidence intervals.

Diletti E, Hauschke D, Steinijans VW.

Int J Clin Pharmacol Ther Toxicol. 1991 Jan;29(1):1-8.

PMID:
2004861
9.

Sample size determination for bioequivalence assessment by means of confidence intervals.

Diletti E, Hauschke D, Steinijans VW.

Int J Clin Pharmacol Ther Toxicol. 1992;30 Suppl 1:S51-8.

PMID:
1601532
10.

A note on statistical methods for assessing therapeutic equivalence.

Chow SC, Shao J.

Control Clin Trials. 2002 Oct;23(5):515-20.

PMID:
12392865
11.

Bias of two one-sided tests procedures in assessment of bioequivalence.

Liu JP, Weng CS.

Stat Med. 1995 Apr 30;14(8):853-61.

PMID:
7644864
12.

Subgroup analyses in randomised controlled trials: quantifying the risks of false-positives and false-negatives.

Brookes ST, Whitley E, Peters TJ, Mulheran PA, Egger M, Davey Smith G.

Health Technol Assess. 2001;5(33):1-56. Review.

13.

Trimmed weighted Simes' test for two one-sided hypotheses with arbitrarily correlated test statistics.

Brannath W, Bretz F, Maurer W, Sarkar S.

Biom J. 2009 Dec;51(6):885-98. doi: 10.1002/bimj.200900132.

PMID:
20014203
14.

Non-inferiority trials: the 'at least as good as' criterion.

Laster LL, Johnson MF.

Stat Med. 2003 Jan 30;22(2):187-200.

PMID:
12520556
15.

Sample size determination: extended tables for the multiplicative model and bioequivalence ranges of 0.9 to 1.11 and 0.7 to 1.43.

Diletti E, Hauschke D, Steinijans VW.

Int J Clin Pharmacol Ther Toxicol. 1992;30 Suppl 1:S59-62.

PMID:
1601533
16.

On population and individual bioequivalence.

Schall R, Luus HG.

Stat Med. 1993 Jun 30;12(12):1109-24.

PMID:
8210816
17.
18.

Sample size determination: extended tables for the multiplicative model and bioequivalence ranges of 0.9 to 1.11 and 0.7 to 1.43.

Diletti E, Hauschke D, Steinijans VW.

Int J Clin Pharmacol Ther Toxicol. 1992 Aug;30(8):287-90.

PMID:
1526691
19.

Robust and bootstrap testing procedures for bioequivalence.

Shen CF, Iglewicz B.

J Biopharm Stat. 1994 Mar;4(1):65-90.

PMID:
8019585
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