-
1
-
-
3042664421
-
Design and analysis of pilot studies: Recommendations for good practice
-
Lancaster GA, Dodd S, Williamson PR,. Design and analysis of pilot studies: recommendations for good practice. J Eval Clin Pract 2004; 10: 307-312.
-
(2004)
J Eval Clin Pract
, vol.10
, pp. 307-312
-
-
Lancaster, G.A.1
Dodd, S.2
Williamson, P.R.3
-
2
-
-
58849098735
-
The design and interpretation of pilot trials in clinical research in critical care
-
Arnold DM, Burns KEA, Adhikari NKJ, et al. The design and interpretation of pilot trials in clinical research in critical care. Crit Care Med 2009; 37: S69-S74.
-
(2009)
Crit Care Med
, vol.37
, pp. S69-S74
-
-
Arnold, D.M.1
Burns, K.E.A.2
Adhikari, N.K.J.3
-
3
-
-
77954554568
-
What is a pilot or feasibility study? A review of current practice and editorial policy
-
Arain M, Campbell MJ, Cooper CL, et al. What is a pilot or feasibility study? A review of current practice and editorial policy. BMC Med Res Methodol 2010; 10: 67.
-
(2010)
BMC Med Res Methodol
, vol.10
, pp. 67
-
-
Arain, M.1
Campbell, M.J.2
Cooper, C.L.3
-
4
-
-
77249142355
-
A tutorial on pilot studies: The what, why and how
-
Thabane L, Ma J, Chu R, et al. A tutorial on pilot studies: the what, why and how. BMC Med Res Methodol 2010; 10: 1.
-
(2010)
BMC Med Res Methodol
, vol.10
, pp. 1
-
-
Thabane, L.1
Ma, J.2
Chu, R.3
-
7
-
-
84970977633
-
-
EMA. Guideline on clinical trials in small populations. European Medicines Agency CHMP/EWP/83561/2005, (2006, accessed 29 October 2014)
-
EMA. Guideline on clinical trials in small populations. European Medicines Agency CHMP/EWP/83561/2005, http://www.ema.europa.eu/docs/en-GB/document-library/Scientific-guideline/2009/09/WC500003615.pdf (2006, accessed 29 October 2014).
-
-
-
-
8
-
-
84970989055
-
-
EMA. Concept paper on extrapolation of efficacy and safety in medicine development. European Medicines Agency EMA/129698/2012, (2013, accessed 29 October 2014)
-
EMA. Concept paper on extrapolation of efficacy and safety in medicine development. European Medicines Agency EMA/129698/2012, http://www.ema.europa.eu/docs/en-GB/document-library/Scientific-guideline/2013/04/WC500142358.pdf (2013, accessed 29 October 2014).
-
-
-
-
9
-
-
84971001295
-
-
Institute of Medicine. Small clinical trials: issues and challenges. National Academy Press, (2001, accessed 29 October 2014)
-
Institute of Medicine. Small clinical trials: issues and challenges. National Academy Press, http://www.nap.edu/catalog/10078.htm (2001, accessed 29 October 2014).
-
-
-
-
10
-
-
84925297669
-
Rare Cancers Europe (RCE) methodological recommendations for clinical studies in rare cancers: A European consensus position paper
-
Casali PG, Bruzzi P, Bogaerts J, et al. Rare Cancers Europe (RCE) methodological recommendations for clinical studies in rare cancers: a European consensus position paper. Ann Oncol 2015; 26 (2): 300-306.
-
(2015)
Ann Oncol
, vol.26
, Issue.2
, pp. 300-306
-
-
Casali, P.G.1
Bruzzi, P.2
Bogaerts, J.3
-
15
-
-
0141907309
-
A gridding method for Bayesian sequential decision problems
-
Brockwell AE, Kadane JB,. A gridding method for Bayesian sequential decision problems. J Computat Graphic Statist 2003; 12: 566-584.
-
(2003)
J Computat Graphic Statist
, vol.12
, pp. 566-584
-
-
Brockwell, A.E.1
Kadane, J.B.2
-
16
-
-
0141679233
-
Hybrid methods for calculating optimal few-stage sequential strategies: Data monitoring for a clinical trial
-
Kadane J, Vlachos P,. Hybrid methods for calculating optimal few-stage sequential strategies: Data monitoring for a clinical trial. Stat Comput 2002; 12: 147-152.
-
(2002)
Stat Comput
, vol.12
, pp. 147-152
-
-
Kadane, J.1
Vlachos, P.2
-
17
-
-
84970940818
-
-
Elsevier. Scopus Content Overview, (accessed 20 October 2014)
-
Elsevier. Scopus Content Overview, http://www.elsevier.com/online-tools/scopus/content-overview (accessed 20 October 2014).
-
-
-
-
18
-
-
33749364344
-
Adaptive two-stage designs in phase II clinical trials
-
Banerjee A, Tsiatis AA,. Adaptive two-stage designs in phase II clinical trials. Stat Med 2006; 25: 3382-3395.
-
(2006)
Stat Med
, vol.25
, pp. 3382-3395
-
-
Banerjee, A.1
Tsiatis, A.A.2
-
19
-
-
0028558336
-
Sample sizes for phase II clinical trials derived from Bayesian decision theory
-
Brunier HC, Whitehead J,. Sample sizes for phase II clinical trials derived from Bayesian decision theory. Stat Med 1994; 13: 2493-2502.
-
(1994)
Stat Med
, vol.13
, pp. 2493-2502
-
-
Brunier, H.C.1
Whitehead, J.2
-
20
-
-
67651027168
-
Optimal cost-effective designs of phase II proof of concept trials and associated go-no go decisions
-
Chen C, Beckman RA,. Optimal cost-effective designs of phase II proof of concept trials and associated go-no go decisions. J Biopharm Stat 2009; 19: 424-436.
-
(2009)
J Biopharm Stat
, vol.19
, pp. 424-436
-
-
Chen, C.1
Beckman, R.A.2
-
21
-
-
84874491035
-
Evaluation of early efficacy endpoints for proof-of-concept trials
-
Chen C, Sun L, Li CL,. Evaluation of early efficacy endpoints for proof-of-concept trials. J Biopharm Stat 2013; 23: 413-424.
-
(2013)
J Biopharm Stat
, vol.23
, pp. 413-424
-
-
Chen, C.1
Sun, L.2
Li, C.L.3
-
22
-
-
70449372331
-
Adaptive group sequential design for phase II clinical trials: A Bayesian decision theoretic approach
-
Chen Y, Smith BJ,. Adaptive group sequential design for phase II clinical trials: A Bayesian decision theoretic approach. Stat Med 2009; 28: 3347-3362.
-
(2009)
Stat Med
, vol.28
, pp. 3347-3362
-
-
Chen, Y.1
Smith, B.J.2
-
23
-
-
49749135478
-
Bayesian optimal design for phase II screening trials
-
Ding M, Rosner GL, Müller P,. Bayesian optimal design for phase II screening trials. Biometrics 2008; 64: 886-894.
-
(2008)
Biometrics
, vol.64
, pp. 886-894
-
-
Ding, M.1
Rosner, G.L.2
Müller, P.3
-
24
-
-
84870860958
-
Designing a series of decision-theoretic phase II trials in a small population
-
Hee SW, Stallard N,. Designing a series of decision-theoretic phase II trials in a small population. Stat Med 2012; 31: 4337-4351.
-
(2012)
Stat Med
, vol.31
, pp. 4337-4351
-
-
Hee, S.W.1
Stallard, N.2
-
25
-
-
1142275380
-
Admissible two-stage designs for phase II cancer clinical trials
-
Jung SH, Lee T, Kim KM, et al. Admissible two-stage designs for phase II cancer clinical trials. Stat Med 2004; 23: 561-569.
-
(2004)
Stat Med
, vol.23
, pp. 561-569
-
-
Jung, S.H.1
Lee, T.2
Kim, K.M.3
-
26
-
-
84876344450
-
Adaptation in clinical development plans and adaptive clinical trial designs
-
Lai TL, Liao OYW, Zhu RG,. Adaptation in clinical development plans and adaptive clinical trial designs. Statist Interf 2012; 5: 431-442.
-
(2012)
Statist Interf
, vol.5
, pp. 431-442
-
-
Lai, T.L.1
Liao, O.Y.W.2
Zhu, R.G.3
-
27
-
-
73949122617
-
The rheumatoid arthritis drug development model: A case study in Bayesian clinical trial simulation
-
Nixon RM, O'Hagan A, Oakley J, et al. The rheumatoid arthritis drug development model: A case study in Bayesian clinical trial simulation. Pharm Stat 2009; 8: 371-389.
-
(2009)
Pharm Stat
, vol.8
, pp. 371-389
-
-
Nixon, R.M.1
O'Hagan, A.2
Oakley, J.3
-
28
-
-
0035560898
-
A decision analytic approach to a futility analysis of a phase II pharmaceutical study
-
Pallay A,. A decision analytic approach to a futility analysis of a phase II pharmaceutical study. J Biopharm Stat 2001; 11: 209-225.
-
(2001)
J Biopharm Stat
, vol.11
, pp. 209-225
-
-
Pallay, A.1
-
29
-
-
0025816336
-
A comparative phase II clinical trials procedure for choosing the best of three treatments
-
Palmer CR,. A comparative phase II clinical trials procedure for choosing the best of three treatments. Stat Med 1991; 10: 1327-1340.
-
(1991)
Stat Med
, vol.10
, pp. 1327-1340
-
-
Palmer, C.R.1
-
31
-
-
0031697980
-
Approximately optimal designs for phase II clinical studies
-
Stallard N,. Approximately optimal designs for phase II clinical studies. J Biopharm Stat 1998; 8: 469-487.
-
(1998)
J Biopharm Stat
, vol.8
, pp. 469-487
-
-
Stallard, N.1
-
32
-
-
0031898459
-
Sample size determination for phase II clinical trials based on Bayesian decision theory
-
Stallard N,. Sample size determination for phase II clinical trials based on Bayesian decision theory. Biometrics 1998; 54: 279-294.
-
(1998)
Biometrics
, vol.54
, pp. 279-294
-
-
Stallard, N.1
-
33
-
-
0038545822
-
Decision-theoretic designs for phase II clinical trials allowing for competing studies
-
Stallard N,. Decision-theoretic designs for phase II clinical trials allowing for competing studies. Biometrics 2003; 59: 402-409.
-
(2003)
Biometrics
, vol.59
, pp. 402-409
-
-
Stallard, N.1
-
34
-
-
84861183854
-
Optimal sample sizes for phase II clinical trials and pilot studies
-
Stallard N,. Optimal sample sizes for phase II clinical trials and pilot studies. Stat Med 2012; 31: 1031-1042.
-
(2012)
Stat Med
, vol.31
, pp. 1031-1042
-
-
Stallard, N.1
-
35
-
-
67549145644
-
Optimal choice of the number of treatments to be included in a clinical trial
-
Stallard N, Posch M, Friede T, et al. Optimal choice of the number of treatments to be included in a clinical trial. Stat Med 2009; 28: 1321-1338.
-
(2009)
Stat Med
, vol.28
, pp. 1321-1338
-
-
Stallard, N.1
Posch, M.2
Friede, T.3
-
36
-
-
0035186577
-
Decision-theoretic designs for pre-phase II screening trials in oncology
-
Stallard N, Thall PF,. Decision-theoretic designs for pre-phase II screening trials in oncology. Biometrics 2001; 57: 1089-1095.
-
(2001)
Biometrics
, vol.57
, pp. 1089-1095
-
-
Stallard, N.1
Thall, P.F.2
-
37
-
-
0032885857
-
Decision theoretic designs for phase II clinical trials with multiple outcomes
-
Stallard N, Thall PF, Whitehead J,. Decision theoretic designs for phase II clinical trials with multiple outcomes. Biometrics 1999; 55: 971-977.
-
(1999)
Biometrics
, vol.55
, pp. 971-977
-
-
Stallard, N.1
Thall, P.F.2
Whitehead, J.3
-
38
-
-
0017392125
-
A decision theory approach to phase II clinical trials
-
Staquet M, Sylvester R,. A decision theory approach to phase II clinical trials. Biomedicine 1977; 26: 262-266.
-
(1977)
Biomedicine
, vol.26
, pp. 262-266
-
-
Staquet, M.1
Sylvester, R.2
-
39
-
-
0023777558
-
A Bayesian approach to the design of phase II clinical trials
-
Sylvester RJ,. A Bayesian approach to the design of phase II clinical trials. Biometrics 1988; 44: 823-836.
-
(1988)
Biometrics
, vol.44
, pp. 823-836
-
-
Sylvester, R.J.1
-
40
-
-
0018982068
-
Design of phase II clinical trials in cancer using decision theory
-
Sylvester RJ, Staquet MJ,. Design of phase II clinical trials in cancer using decision theory. Cancer Treat Rep 1980; 64: 519-524.
-
(1980)
Cancer Treat Rep
, vol.64
, pp. 519-524
-
-
Sylvester, R.J.1
Staquet, M.J.2
-
41
-
-
84901048582
-
Using joint utilities of the times to response and toxicity to adaptively optimize schedule-dose regimes
-
Thall PF, Nguyen HQ, Braun TM, et al. Using joint utilities of the times to response and toxicity to adaptively optimize schedule-dose regimes. Biometrics 2013; 69: 673-682.
-
(2013)
Biometrics
, vol.69
, pp. 673-682
-
-
Thall, P.F.1
Nguyen, H.Q.2
Braun, T.M.3
-
42
-
-
84858864984
-
Bayesian enrichment strategies for randomized discontinuation trials
-
Trippa L, Rosner GL, Müller P,. Bayesian enrichment strategies for randomized discontinuation trials. Biometrics 2012; 68: 203-211.
-
(2012)
Biometrics
, vol.68
, pp. 203-211
-
-
Trippa, L.1
Rosner, G.L.2
Müller, P.3
-
43
-
-
84863994177
-
Bayesian decision theoretic two-stage design in phase II clinical trials with survival endpoint
-
Zhao L, Taylor JM, Schuetze SM,. Bayesian decision theoretic two-stage design in phase II clinical trials with survival endpoint. Stat Med 2012; 31: 1804-1820.
-
(2012)
Stat Med
, vol.31
, pp. 1804-1820
-
-
Zhao, L.1
Taylor, J.M.2
Schuetze, S.M.3
-
44
-
-
67549151410
-
Bayesian decision sequential analysis with survival endpoint in phase II clinical trials
-
Zhao L, Woodworth G,. Bayesian decision sequential analysis with survival endpoint in phase II clinical trials. Stat Med 2009; 28: 1339-1352.
-
(2009)
Stat Med
, vol.28
, pp. 1339-1352
-
-
Zhao, L.1
Woodworth, G.2
-
45
-
-
0023914909
-
One-sided sequential stopping boundaries for clinical trials: A decision-theoretic approach
-
Berry DA, Ho CH,. One-sided sequential stopping boundaries for clinical trials: A decision-theoretic approach. Biometrics 1988; 44: 219-227.
-
(1988)
Biometrics
, vol.44
, pp. 219-227
-
-
Berry, D.A.1
Ho, C.H.2
-
46
-
-
84872851208
-
Determining optimal sample sizes for multistage adaptive randomized clinical trials from an industry perspective using value of information methods
-
Chen MH, Willan AR,. Determining optimal sample sizes for multistage adaptive randomized clinical trials from an industry perspective using value of information methods. Clin Trials 2013; 10: 54-62.
-
(2013)
Clin Trials
, vol.10
, pp. 54-62
-
-
Chen, M.H.1
Willan, A.R.2
-
47
-
-
34548537745
-
Optimal adaptive randomized designs for clinical trials
-
Cheng Y, Berry DA,. Optimal adaptive randomized designs for clinical trials. Biometrika 2007; 94: 673-687.
-
(2007)
Biometrika
, vol.94
, pp. 673-687
-
-
Cheng, Y.1
Berry, D.A.2
-
48
-
-
24144464254
-
Bayesian adaptive designs for clinical trials
-
Cheng Y, Shen Y,. Bayesian adaptive designs for clinical trials. Biometrika 2005; 92: 633-646.
-
(2005)
Biometrika
, vol.92
, pp. 633-646
-
-
Cheng, Y.1
Shen, Y.2
-
49
-
-
84867702983
-
An efficient sequential design of clinical trials
-
Cheng Y, Shen Y,. An efficient sequential design of clinical trials. J Stat Plan Inference 2013; 143: 283-295.
-
(2013)
J Stat Plan Inference
, vol.143
, pp. 283-295
-
-
Cheng, Y.1
Shen, Y.2
-
50
-
-
3843053372
-
Choosing sample size for a clinical trial using decision analysis
-
Cheng Y, Su F, Berry DA,. Choosing sample size for a clinical trial using decision analysis. Biometrika 2003; 90: 923-936.
-
(2003)
Biometrika
, vol.90
, pp. 923-936
-
-
Cheng, Y.1
Su, F.2
Berry, D.A.3
-
51
-
-
0347217096
-
Sequential medical trials involving paired data
-
Chernoff H, Petkau AJ,. Sequential medical trials involving paired data. Biometrika 1981; 68: 119-132.
-
(1981)
Biometrika
, vol.68
, pp. 119-132
-
-
Chernoff, H.1
Petkau, A.J.2
-
52
-
-
0030281042
-
An economic approach to clinical trial design and research priority-setting
-
Claxton K, Posnett J,. An economic approach to clinical trial design and research priority-setting. Health Econ 1996; 5: 513-524.
-
(1996)
Health Econ
, vol.5
, pp. 513-524
-
-
Claxton, K.1
Posnett, J.2
-
53
-
-
0034898832
-
A dynamic programming approach to the efficient design of clinical trials
-
Claxton K, Thompson KM,. A dynamic programming approach to the efficient design of clinical trials. J Health Econ 2001; 20: 797-822.
-
(2001)
J Health Econ
, vol.20
, pp. 797-822
-
-
Claxton, K.1
Thompson, K.M.2
-
54
-
-
33846820176
-
Expected value of information and decision making in HTA
-
Eckermann S, Willan AR,. Expected value of information and decision making in HTA. Health Econ 2007; 16: 195-209.
-
(2007)
Health Econ
, vol.16
, pp. 195-209
-
-
Eckermann, S.1
Willan, A.R.2
-
56
-
-
0034039532
-
A behavioral Bayes method for determining the size of a clinical trial
-
Gittins J, Pezeshk H,. A behavioral Bayes method for determining the size of a clinical trial. Drug Inf J 2000; 34: 355-363.
-
(2000)
Drug Inf J
, vol.34
, pp. 355-363
-
-
Gittins, J.1
Pezeshk, H.2
-
57
-
-
0036448951
-
A decision theoretic approach to sample size determination in clinical trials
-
Gittins JC, Pezeshk H,. A decision theoretic approach to sample size determination in clinical trials. J Biopharm Stat 2002; 12: 535-551.
-
(2002)
J Biopharm Stat
, vol.12
, pp. 535-551
-
-
Gittins, J.C.1
Pezeshk, H.2
-
58
-
-
0035970746
-
The sample size for a clinical trial: A Bayesian-decision theoretic approach
-
Halpern J, Brown Jr BW, Hornberger J,. The sample size for a clinical trial: A Bayesian-decision theoretic approach. Stat Med 2001; 20: 841-858.
-
(2001)
Stat Med
, vol.20
, pp. 841-858
-
-
Halpern, J.1
Brown, B.W.2
Hornberger, J.3
-
59
-
-
0026596626
-
A decision-theoretic evaluation of early stopping rules
-
Heitjan DF, Houts PS, Harvey HA,. A decision-theoretic evaluation of early stopping rules. Stat Med 1992; 11: 673-683.
-
(1992)
Stat Med
, vol.11
, pp. 673-683
-
-
Heitjan, D.F.1
Houts, P.S.2
Harvey, H.A.3
-
60
-
-
0032054154
-
The cost-benefit of a randomized trial to a health care organization
-
Hornberger J, Eghtesady P,. The cost-benefit of a randomized trial to a health care organization. Control Clin Trials 1998; 19: 198-211.
-
(1998)
Control Clin Trials
, vol.19
, pp. 198-211
-
-
Hornberger, J.1
Eghtesady, P.2
-
61
-
-
84904513484
-
Interim monitoring of clinical trials: Decision theory, dynamic programming and optimal stopping
-
Jennison C, Turnbull BW,. Interim monitoring of clinical trials: Decision theory, dynamic programming and optimal stopping. Kuwait J Sci 2013; 40: 43-59.
-
(2013)
Kuwait J Sci
, vol.40
, pp. 43-59
-
-
Jennison, C.1
Turnbull, B.W.2
-
62
-
-
84877621591
-
A Bayesian decision-theoretic sequential response-adaptive randomization design
-
Jiang F, Lee JJ, Müller P,. A Bayesian decision-theoretic sequential response-adaptive randomization design. Stat Med 2013; 32: 1975-1994.
-
(2013)
Stat Med
, vol.32
, pp. 1975-1994
-
-
Jiang, F.1
Lee, J.J.2
Müller, P.3
-
63
-
-
69949095120
-
A behavioral Bayes method to determine the sample size of a clinical trial considering efficacy and safety
-
Kikuchi T, Gittins J,. A behavioral Bayes method to determine the sample size of a clinical trial considering efficacy and safety. Stat Med 2009; 28: 2293-2306.
-
(2009)
Stat Med
, vol.28
, pp. 2293-2306
-
-
Kikuchi, T.1
Gittins, J.2
-
64
-
-
80051867134
-
A behavioural Bayes approach to the determination of sample size for clinical trials considering efficacy nd safety: Imbalanced sample size in treatment groups
-
Kikuchi T, Gittins J,. A behavioural Bayes approach to the determination of sample size for clinical trials considering efficacy nd safety: Imbalanced sample size in treatment groups. Stat Methods Med Res 2011; 20: 389-400.
-
(2011)
Stat Methods Med Res
, vol.20
, pp. 389-400
-
-
Kikuchi, T.1
Gittins, J.2
-
65
-
-
38849173686
-
A Bayesian cost-benefit approach to the determination of sample size in clinical trials
-
Kikuchi T, Pezeshk H, Gittins J,. A Bayesian cost-benefit approach to the determination of sample size in clinical trials. Stat Med 2008; 27: 68-82.
-
(2008)
Stat Med
, vol.27
, pp. 68-82
-
-
Kikuchi, T.1
Pezeshk, H.2
Gittins, J.3
-
66
-
-
13044274375
-
Group sequential clinical trials: A classical evaluation of Bayesian decision-theoretic designs
-
Lewis RJ, Berry DA,. Group sequential clinical trials: A classical evaluation of Bayesian decision-theoretic designs. J Am Stat Assoc 1994; 89: 1528-1534.
-
(1994)
J Am Stat Assoc
, vol.89
, pp. 1528-1534
-
-
Lewis, R.J.1
Berry, D.A.2
-
67
-
-
34250366338
-
Bayesian decision-theoretic group sequential clinical trial design based on a quadratic loss function: A frequentist evaluation
-
Lewis RJ, Lipsky AM, Berry DA,. Bayesian decision-theoretic group sequential clinical trial design based on a quadratic loss function: A frequentist evaluation. Clin Trial 2007; 4: 5-14.
-
(2007)
Clin Trial
, vol.4
, pp. 5-14
-
-
Lewis, R.J.1
Lipsky, A.M.2
Berry, D.A.3
-
68
-
-
84901301869
-
An optimization approach to calculating sample sizes with binary responses
-
Maroufy V, Marriott P, Pezeshk H,. An optimization approach to calculating sample sizes with binary responses. J Biopharm Stat 2014; 24: 715-731.
-
(2014)
J Biopharm Stat
, vol.24
, pp. 715-731
-
-
Maroufy, V.1
Marriott, P.2
Pezeshk, H.3
-
69
-
-
33748576736
-
Adaptive, group sequential and decision theoretic approaches to sample size determination
-
Mehta CR, Patel NR,. Adaptive, group sequential and decision theoretic approaches to sample size determination. Stat Med 2006; 25: 3250-3269.
-
(2006)
Stat Med
, vol.25
, pp. 3250-3269
-
-
Mehta, C.R.1
Patel, N.R.2
-
70
-
-
58149503911
-
Bayesian sequential analysis for multiple-arm clinical trials
-
Orawo LA, Christen JA,. Bayesian sequential analysis for multiple-arm clinical trials. Stat Comput 2009; 19: 99-109.
-
(2009)
Stat Comput
, vol.19
, pp. 99-109
-
-
Orawo, L.A.1
Christen, J.A.2
-
71
-
-
35949003229
-
A Bayesian approach for incorporating economic factors in sample size design for clinical trials of individual drugs and portfolios of drugs
-
Patel NR, Ankolekar S,. A Bayesian approach for incorporating economic factors in sample size design for clinical trials of individual drugs and portfolios of drugs. Stat Med 2007; 26: 4976-4988.
-
(2007)
Stat Med
, vol.26
, pp. 4976-4988
-
-
Patel, N.R.1
Ankolekar, S.2
-
72
-
-
84876441697
-
A mathematical model for maximizing the value of phase 3 drug development portfolios incorporating budget constraints and risk
-
Patel NR, Ankolekar S, Antonijevic Z, et al. A mathematical model for maximizing the value of phase 3 drug development portfolios incorporating budget constraints and risk. Stat Med 2013; 32: 1763-1777.
-
(2013)
Stat Med
, vol.32
, pp. 1763-1777
-
-
Patel, N.R.1
Ankolekar, S.2
Antonijevic, Z.3
-
73
-
-
0036186473
-
A fully Bayesian approach to calculating sample sizes for clinical trials with binary responses
-
Pezeshk H, Gittins J,. A fully Bayesian approach to calculating sample sizes for clinical trials with binary responses. Drug Inf J 2002; 36: 143-150.
-
(2002)
Drug Inf J
, vol.36
, pp. 143-150
-
-
Pezeshk, H.1
Gittins, J.2
-
74
-
-
68349092668
-
The choice of sample size: A mixed Bayesian/frequentist approach
-
Pezeshk H, Nematollahi N, Maroufy V, et al. The choice of sample size: A mixed Bayesian/frequentist approach. Stat Meth Med Res 2009; 18: 183-194.
-
(2009)
Stat Meth Med Res
, vol.18
, pp. 183-194
-
-
Pezeshk, H.1
Nematollahi, N.2
Maroufy, V.3
-
75
-
-
84888585255
-
Bayesian sample size calculation for estimation of the difference between two binomial proportions
-
Pezeshk H, Nematollahi N, Maroufy V, et al. Bayesian sample size calculation for estimation of the difference between two binomial proportions. Stat Meth Med Res 2013; 22: 598-611.
-
(2013)
Stat Meth Med Res
, vol.22
, pp. 598-611
-
-
Pezeshk, H.1
Nematollahi, N.2
Maroufy, V.3
-
76
-
-
0345945008
-
Gittins indices and constrained allocation in clinical trials
-
Wang YG,. Gittins indices and constrained allocation in clinical trials. Biometrika 1991; 78: 101-111.
-
(1991)
Biometrika
, vol.78
, pp. 101-111
-
-
Wang, Y.G.1
-
77
-
-
33745322898
-
Implementation of backward induction for sequentially adaptive clinical trials
-
Wathen JK, Christen JA,. Implementation of backward induction for sequentially adaptive clinical trials. J Computat Graphic Stat 2006; 15: 398-413.
-
(2006)
J Computat Graphic Stat
, vol.15
, pp. 398-413
-
-
Wathen, J.K.1
Christen, J.A.2
-
78
-
-
58749104400
-
Bayesian adaptive model selection for optimizing group sequential clinical trials
-
Wathen JK, Thall PF,. Bayesian adaptive model selection for optimizing group sequential clinical trials. Stat Med 2008; 27: 5586-5604.
-
(2008)
Stat Med
, vol.27
, pp. 5586-5604
-
-
Wathen, J.K.1
Thall, P.F.2
-
79
-
-
61449282534
-
Optimal sample size determinations from an industry perspective based on the expected value of information
-
Willan AR,. Optimal sample size determinations from an industry perspective based on the expected value of information. Clin Trial 2008; 5: 587-594.
-
(2008)
Clin Trial
, vol.5
, pp. 587-594
-
-
Willan, A.R.1
-
80
-
-
77951722695
-
Optimal clinical trial design using value of information methods with imperfect implementation
-
Willan AR, Eckermann S,. Optimal clinical trial design using value of information methods with imperfect implementation. Health Econ 2010; 19: 549-561.
-
(2010)
Health Econ
, vol.19
, pp. 549-561
-
-
Willan, A.R.1
Eckermann, S.2
-
81
-
-
84861050774
-
Value of information and pricing new healthcare interventions
-
Willan AR, Eckermann S,. Value of information and pricing new healthcare interventions. Pharmacoeconomics 2012; 30: 447-459.
-
(2012)
Pharmacoeconomics
, vol.30
, pp. 447-459
-
-
Willan, A.R.1
Eckermann, S.2
-
82
-
-
58149130292
-
Determining optimal sample sizes for multi-stage randomized clinical trials using value of information methods
-
Willan AR, Kowgier M,. Determining optimal sample sizes for multi-stage randomized clinical trials using value of information methods. Clin Trial 2008; 5: 289-300.
-
(2008)
Clin Trial
, vol.5
, pp. 289-300
-
-
Willan, A.R.1
Kowgier, M.2
-
83
-
-
21044450556
-
The value of information and optimal clinical trial design
-
Willan AR, Pinto EM,. The value of information and optimal clinical trial design. Stat Med 2005; 24: 1791-1806.
-
(2005)
Stat Med
, vol.24
, pp. 1791-1806
-
-
Willan, A.R.1
Pinto, E.M.2
-
84
-
-
0024536437
-
Optimal two-stage designs for phase II clinical trials
-
Simon R,. Optimal two-stage designs for phase II clinical trials. Control Clin Trials 1989; 10: 1-10.
-
(1989)
Control Clin Trials
, vol.10
, pp. 1-10
-
-
Simon, R.1
-
85
-
-
0035019379
-
Bayesian assessment of sample size for clinical trials of cost-effectiveness
-
O'Hagan A, Stevens JW,. Bayesian assessment of sample size for clinical trials of cost-effectiveness. Med Decis Making 2001; 21: 219-230.
-
(2001)
Med Decis Making
, vol.21
, pp. 219-230
-
-
O'Hagan, A.1
Stevens, J.W.2
-
86
-
-
84920889664
-
Adaptive designs for subpopulation analysis optimizing utility functions
-
Graf AC, Posch M, Koenig F,. Adaptive designs for subpopulation analysis optimizing utility functions. Biometric J 2015; 57: 76-89.
-
(2015)
Biometric J
, vol.57
, pp. 76-89
-
-
Graf, A.C.1
Posch, M.2
Koenig, F.3
-
87
-
-
84888318018
-
Adaptive enrichment designs for clinical trials
-
Simon N, Simon R,. Adaptive enrichment designs for clinical trials. Biostatistics 2013; 14: 613-625.
-
(2013)
Biostatistics
, vol.14
, pp. 613-625
-
-
Simon, N.1
Simon, R.2
-
88
-
-
66349125688
-
Adaptive patient enrichment designs in therapeutic trials
-
Wang S-J, Hung HMJ, O'Neill RT,. Adaptive patient enrichment designs in therapeutic trials. Biometric J 2009; 51: 358-374.
-
(2009)
Biometric J
, vol.51
, pp. 358-374
-
-
Wang, S.-J.1
Hung, H.M.J.2
O'Neill, R.T.3
-
90
-
-
0022782492
-
Application of statistical decision theory to treatment choices: Implications for the design and analysis of clinical trials
-
Simes RJ,. Application of statistical decision theory to treatment choices: implications for the design and analysis of clinical trials. Stat Med 1986; 5: 411-420.
-
(1986)
Stat Med
, vol.5
, pp. 411-420
-
-
Simes, R.J.1
-
91
-
-
24944501851
-
ASTIN: A Bayesian adaptive dose-response trial in acute stroke
-
Grieve AP, Krams M,. ASTIN: A Bayesian adaptive dose-response trial in acute stroke. Clin Trial 2005; 2: 340-351.
-
(2005)
Clin Trial
, vol.2
, pp. 340-351
-
-
Grieve, A.P.1
Krams, M.2
-
94
-
-
84891584370
-
-
Hoboken, NJ: John Wiley & Sons
-
Gittins JC, Weber R, Glazebrook KD,. Multi-armed bandit allocation indices, Hoboken, NJ: John Wiley & Sons, 2011.
-
(2011)
Multi-armed Bandit Allocation Indices
-
-
Gittins, J.C.1
Weber, R.2
Glazebrook, K.D.3
-
97
-
-
0346856880
-
Eliciting expert beliefs in substantial practical applications
-
O'Hagan A,. Eliciting expert beliefs in substantial practical applications. J Royal Stat Soc: Ser D (The Statistician) 1998; 47: 21-35.
-
(1998)
J Royal Stat Soc: Ser D (The Statistician)
, vol.47
, pp. 21-35
-
-
O'Hagan, A.1
-
98
-
-
0005959185
-
Being an expert
-
In: (ed). New York: Wiley
-
Blanck TJJ, Conahan TJ, Merin RG, et al.Being an expert. In: Kadane JB, (ed). Bayesian methods and ethics in a clinical trial design, New York: Wiley, 1996, pp. 159-162.
-
(1996)
Bayesian Methods and Ethics in A Clinical Trial Design
, pp. 159-162
-
-
Blanck, T.J.J.1
Conahan, T.J.2
Merin, R.G.3
Kadane, J.B.4
-
99
-
-
84874977112
-
Structured approach to the elicitation of expert beliefs for a Bayesian-designed clinical trial: A case study
-
Kinnersley N, Day S,. Structured approach to the elicitation of expert beliefs for a Bayesian-designed clinical trial: a case study. Pharm Stat 2013; 12: 104-113.
-
(2013)
Pharm Stat
, vol.12
, pp. 104-113
-
-
Kinnersley, N.1
Day, S.2
-
102
-
-
84882928974
-
Whether to participate in a clinical trial: The patient's view
-
In: (eds). New York: Wiley
-
Emrich LJ, Sedransk N, Whether to participate in a clinical trial: The patient's view. In: Kadane JB, (eds). Bayesian methods and ethics in a clinical trial design, New York: Wiley, 1996, pp. 267-305.
-
(1996)
Bayesian Methods and Ethics in A Clinical Trial Design
, pp. 267-305
-
-
Emrich, L.J.1
Sedransk, N.2
Kadane, J.B.3
|