-
1
-
-
0036063208
-
The effects of inhaled corticosteroids in chronic obstructive pulmonary disease: A systematic review of randomized placebo-controlled trials
-
Alsaeedi, A., Sin, D. D. and McAlister, F. A. (2002). The effects of inhaled corticosteroids in chronic obstructive pulmonary disease: A systematic review of randomized placebo-controlled trials. The American Journal of Medicine 113, 59-65.
-
(2002)
The American Journal of Medicine
, vol.113
, pp. 59-65
-
-
Alsaeedi, A.1
Sin, D.D.2
McAlister, F.A.3
-
2
-
-
84919436881
-
Multiparameter hypothesis testing and acceptance sampling
-
Berger, R. L. (1982). Multiparameter hypothesis testing and acceptance sampling. Technometrics 24, 295-300.
-
(1982)
Technometrics
, vol.24
, pp. 295-300
-
-
Berger, R.L.1
-
3
-
-
33847749911
-
A combined superiority and non-inferiority approach to multiple endpoints in clinical trials
-
Bloch, D. A., Lai, T. L., Su, Z. and Tubert-Bitter, P. (2007). A combined superiority and non-inferiority approach to multiple endpoints in clinical trials. Statistics in Medicine 26, 1193-1207.
-
(2007)
Statistics in Medicine
, vol.26
, pp. 1193-1207
-
-
Bloch, D.A.1
Lai, T.L.2
Su, Z.3
Tubert-Bitter, P.4
-
4
-
-
0035186576
-
One-sided tests in clinical trials with multiple endpoints
-
Bloch, D. A., Lai, T. L. and Tubert-Bitter, P. (2001). One-sided tests in clinical trials with multiple endpoints. Biometrics 57, 1039-1047.
-
(2001)
Biometrics
, vol.57
, pp. 1039-1047
-
-
Bloch, D.A.1
Lai, T.L.2
Tubert-Bitter, P.3
-
5
-
-
15244348837
-
Superior safety in non-inferiority trials
-
Bristol, D. R. (2005). Superior safety in non-inferiority trials. Biometrical Journal 47, 75-81.
-
(2005)
Biometrical Journal
, vol.47
, pp. 75-81
-
-
Bristol, D.R.1
-
6
-
-
33847172367
-
Salmeterol and fluticasone propionate and survival in chronic obstructive pulmonary disease
-
for the TORCH investigators
-
Calverley, P. M. A., Anderson, J. A., Celli, B., Ferguson, G. T., Jenkins, C., Jones, P. W., Yates, J. C. and Vestbo, J., for the TORCH investigators. (2007). Salmeterol and fluticasone propionate and survival in chronic obstructive pulmonary disease. New England Journal of Medicine 356, 775-789.
-
(2007)
New England Journal of Medicine
, vol.356
, pp. 775-789
-
-
Calverley, P.M.A.1
Anderson, J.A.2
Celli, B.3
Ferguson, G.T.4
Jenkins, C.5
Jones, P.W.6
Yates, J.C.7
Vestbo, J.8
-
7
-
-
21244472033
-
-
Marcel Dekker, Inc., New York
-
Chow, S. C., Shao, J. and Wang, H. (2003). Sample Size Calculations in Clinical Research. Marcel Dekker, Inc., New York.
-
(2003)
Sample Size Calculations in Clinical Research
-
-
Chow, S.C.1
Shao, J.2
Wang, H.3
-
8
-
-
27544475840
-
-
Committee for Medicinal Products for Human Use (CHMP). Doc. Ref. EMEA/CPMP/EWP/2158/99. European Medicines Agency Pre-authorisation Evaluation of Medicines for Human Use
-
Committee for Medicinal Products for Human Use (CHMP). (2005). Guideline on the choice of the non-inferiority margin. Doc. Ref. EMEA/CPMP/EWP/2158/99. European Medicines Agency Pre-authorisation Evaluation of Medicines for Human Use.
-
(2005)
Guideline on the choice of the non-inferiority margin
-
-
-
9
-
-
0029022868
-
Multivariate tests for multiple endpoints in clinical trials
-
Follmann, D. (1995). Multivariate tests for multiple endpoints in clinical trials. Statistics in Medicine 14, 1163-1175.
-
(1995)
Statistics in Medicine
, vol.14
, pp. 1163-1175
-
-
Follmann, D.1
-
10
-
-
85163224722
-
-
International Conference on Harmonization (ICH) of Technical Requirements for Regulations of Pharmaceuticals for Human use. Statistical Principles for Clinical trials, 5 February 1998
-
International Conference on Harmonization (ICH) of Technical Requirements for Regulations of Pharmaceuticals for Human use. (1998). ICH Tripartite Guideline E-9 Document, Statistical Principles for Clinical trials, 5 February 1998.
-
(1998)
ICH Tripartite Guideline E-9 Document
-
-
-
11
-
-
0027425644
-
Group sequential tests for bivariate response: Interim analyses of clinical trials with both efficacy and safety endpoints
-
Jennison, C. and Turnbull, B. W. (1993). Group sequential tests for bivariate response: Interim analyses of clinical trials with both efficacy and safety endpoints. Biometrics 49, 741-752.
-
(1993)
Biometrics
, vol.49
, pp. 741-752
-
-
Jennison, C.1
Turnbull, B.W.2
-
12
-
-
0029843085
-
Exact t and F test for analyzing studies with multiple endpoints
-
Erratum: Biometrics 56, 324-325
-
Läuter, J. (1996). Exact t and F test for analyzing studies with multiple endpoints. Biometrics, 52, 964-970. Erratum: Biometrics 56, 324-325.
-
(1996)
Biometrics
, vol.52
, pp. 964-970
-
-
Läuter, J.1
-
13
-
-
0032971979
-
Carvedilol and the Food and Drug Administration (FDA) approval process: the FDA paradigm and reflection upon hypothesis testing
-
Lloyd, D. F. (1999). Carvedilol and the Food and Drug Administration (FDA) approval process: the FDA paradigm and reflection upon hypothesis testing. Controlled Clinical Trials 20, 16-39.
-
(1999)
Controlled Clinical Trials
, vol.20
, pp. 16-39
-
-
Lloyd, D.F.1
-
14
-
-
0021666221
-
Procedures for comparing samples with multiple endpoints
-
O'Brien, P. C. (1984). Procedures for comparing samples with multiple endpoints. Biometrics 40, 1079-1087.
-
(1984)
Biometrics
, vol.40
, pp. 1079-1087
-
-
O'Brien, P.C.1
-
15
-
-
1642341945
-
A note on one-sided tests with multiple endpoints
-
Perlman, M. D. and Wu, L. (2004). A note on one-sided tests with multiple endpoints. Biometrics 60, 276-280.
-
(2004)
Biometrics
, vol.60
, pp. 276-280
-
-
Perlman, M.D.1
Wu, L.2
-
16
-
-
0023598472
-
The analysis of multiple endpoints in clinical trials
-
Pocock, S. J., Geller, N. L. and Tsiatis, A. A. (1987). The analysis of multiple endpoints in clinical trials. Biometrics 43, 487-498.
-
(1987)
Biometrics
, vol.43
, pp. 487-498
-
-
Pocock, S.J.1
Geller, N.L.2
Tsiatis, A.A.3
-
17
-
-
33846235440
-
On testing simultaneously non-inferiority in two multiple primary endpoints and superiority in at least one of them
-
Röhmel, J., Gerlinger, C., Benda, N. and Läuter, J. (2006). On testing simultaneously non-inferiority in two multiple primary endpoints and superiority in at least one of them. Biometrical Journal 48, 916-933.
-
(2006)
Biometrical Journal
, vol.48
, pp. 916-933
-
-
Röhmel, J.1
Gerlinger, C.2
Benda, N.3
Läuter, J.4
-
18
-
-
0024451027
-
The consultant forum. Combining outcome measure: statistical power is irrelevant
-
Senn, S. (1989). The consultant forum. Combining outcome measure: statistical power is irrelevant. Biometrics 45, 1027-1028.
-
(1989)
Biometrics
, vol.45
, pp. 1027-1028
-
-
Senn, S.1
-
19
-
-
0242575196
-
Inhaled corticosteroids reduce the progression of airflow limitation in chronic obstructive pulmonary disease: a meta-analysis
-
Sutherland, E. R., Allmers, H., Ayas, N. T., Venn, A. J. and Martin, R. J. (2003). Inhaled corticosteroids reduce the progression of airflow limitation in chronic obstructive pulmonary disease: a meta-analysis. Thorax 58, 937-941.
-
(2003)
Thorax
, vol.58
, pp. 937-941
-
-
Sutherland, E.R.1
Allmers, H.2
Ayas, N.T.3
Venn, A.J.4
Martin, R.J.5
-
20
-
-
76149098065
-
Power and sample size calculations in clinical trials with multiple primary variables
-
Sozu, T., Kanou, T., Hamada, C. and Yoshimura, I. (2006). Power and sample size calculations in clinical trials with multiple primary variables. Japanese Journal of Biometrics 27, 83-96.
-
(2006)
Japanese Journal of Biometrics
, vol.27
, pp. 83-96
-
-
Sozu, T.1
Kanou, T.2
Hamada, C.3
Yoshimura, I.4
-
21
-
-
24944562831
-
A superiority-equivalence approach to one-sided tests on multiple endpoints in clinical trials
-
Tamhane, A. C. and Logan, B. R. (2004). A superiority-equivalence approach to one-sided tests on multiple endpoints in clinical trials. Biometrika 91, 715-727.
-
(2004)
Biometrika
, vol.91
, pp. 715-727
-
-
Tamhane, A.C.1
Logan, B.R.2
-
22
-
-
84950421583
-
Design of group sequential clinical trials with multiple endpoints
-
Tang, D. I., Gnecco, C. and Geller, N. L. (1989a). Design of group sequential clinical trials with multiple endpoints. Journal of the American Statistical Association 84, 776-779.
-
(1989)
Journal of the American Statistical Association
, vol.84
, pp. 776-779
-
-
Tang, D.I.1
Gnecco, C.2
Geller, N.L.3
-
23
-
-
0141833065
-
An approximate likelihood ratio test for a normal mean vector with nonnegative components with applications to clinical trials
-
Tang, D. I., Gnecco, C. and Geller, N. L. (1989b). An approximate likelihood ratio test for a normal mean vector with nonnegative components with applications to clinical trials. Biometrika 76, 577-583.
-
(1989)
Biometrika
, vol.76
, pp. 577-583
-
-
Tang, D.I.1
Gnecco, C.2
Geller, N.L.3
-
24
-
-
0029029276
-
Comparing the bivariate effects of toxicity and efficacy of treatments
-
Tubert-Bitter, P., Bloch, D. A. and Raynauld, J. P. (1995). Comparing the bivariate effects of toxicity and efficacy of treatments. Statistics in Medicine 14, 1129-1141.
-
(1995)
Statistics in Medicine
, vol.14
, pp. 1129-1141
-
-
Tubert-Bitter, P.1
Bloch, D.A.2
Raynauld, J.P.3
-
25
-
-
27744464827
-
Power and sample size for clinical trials when efficacy is required in multiple endpoints: application to an Alzheimer's treatment trial
-
Xiong, C., Yu, K., Gao, F., Yan, Y. and Zhang, Z. (2005). Power and sample size for clinical trials when efficacy is required in multiple endpoints: application to an Alzheimer's treatment trial. Clinical Trials 2, 387-393.
-
(2005)
Clinical Trials
, vol.2
, pp. 387-393
-
-
Xiong, C.1
Yu, K.2
Gao, F.3
Yan, Y.4
Zhang, Z.5
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