BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

82 related articles for article (PubMed ID: 7613559)

  • 1. Dose response studies. II. Analysis and interpretation.
    Ruberg SJ
    J Biopharm Stat; 1995 Mar; 5(1):15-42. PubMed ID: 7613559
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Dose response studies. I. Some design considerations.
    Ruberg SJ
    J Biopharm Stat; 1995 Mar; 5(1):1-14. PubMed ID: 7613556
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Factorial dose-response studies using frequency and magnitude of dose.
    Hafner KB; Ruberg SJ
    J Biopharm Stat; 1996 Jul; 6(3):253-62. PubMed ID: 8854230
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A multiple comparison procedure to control the strong stagewise family error rate in comparing test treatments and a control.
    Chen M; Kianifard F
    J Biopharm Stat; 1997 Jul; 7(3):355-67. PubMed ID: 9252830
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identifying the maximum safe dose: a multiple testing approach.
    Hothorn LA; Hauschke D
    J Biopharm Stat; 2000 Feb; 10(1):15-30. PubMed ID: 10709798
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Application of response surface methodology and factorial designs to clinical trials for drug combination development.
    Stewart WH
    J Biopharm Stat; 1996 Jul; 6(3):219-30. PubMed ID: 8854227
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Measuring social functioning with the personal and social performance scale in patients with acute symptoms of schizophrenia: interpretation of results of a pooled analysis of three Phase III trials of paliperidone extended-release tablets.
    Patrick DL; Burns T; Morosini P; Gagnon DD; Rothman M; Adriaenssen I
    Clin Ther; 2010 Feb; 32(2):275-92. PubMed ID: 20206786
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Using the partitioning principle to adaptively design dose-response studies.
    Ling X; Hsu J
    J Biopharm Stat; 2006; 16(5):733-43. PubMed ID: 17037268
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Non-parametric estimators of a monotonic dose-response curve and bootstrap confidence intervals.
    Dilleen M; Heimann G; Hirsch I
    Stat Med; 2003 Mar; 22(6):869-82. PubMed ID: 12627406
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Efficacy and tolerability of nebivolol monotherapy by baseline systolic blood pressure: a retrospective analysis of pooled data from two multicenter, 12-week, randomized, double-blind, placebo-controlled, parallel-group, dose-ranging studies in patients with mild to moderate essential hypertension.
    Germino FW
    Clin Ther; 2009 Sep; 31(9):1946-56. PubMed ID: 19843484
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identifying effective and/or safe doses by stepwise confidence intervals for ratios.
    Bretz F; Hothorn LA; Hsu JC
    Stat Med; 2003 Mar; 22(6):847-58. PubMed ID: 12627404
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Statistical methods for a three-period crossover design in which high dose cannot be used first.
    Peace KE; Koch GG
    J Biopharm Stat; 1993 Mar; 3(1):103-16. PubMed ID: 8485531
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Desvenlafaxine 50 and 100 mg/d in the treatment of major depressive disorder: an 8-week, phase III, multicenter, randomized, double-blind, placebo-controlled, parallel-group trial and a post hoc pooled analysis of three studies.
    Tourian KA; Padmanabhan SK; Groark J; Brisard C; Farrington D
    Clin Ther; 2009 Jun; 31 Pt 1():1405-23. PubMed ID: 19698901
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Imputation strategies for missing continuous outcomes in cluster randomized trials.
    Taljaard M; Donner A; Klar N
    Biom J; 2008 Jun; 50(3):329-45. PubMed ID: 18537126
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A practical limit to trials needed in one-person randomized controlled experiments.
    Alemi R; Alemi F
    Qual Manag Health Care; 2007; 16(2):130-4. PubMed ID: 17426611
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The analysis of a multiple-dose, combination-drug clinical trial using response surface methodology.
    Phillips JA; Cairns V; Koch GG
    J Biopharm Stat; 1992; 2(1):49-67. PubMed ID: 1300205
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Dose finding - a challenge in statistics.
    Bretz F; Hsu J; Pinheiro J; Liu Y
    Biom J; 2008 Aug; 50(4):480-504. PubMed ID: 18663758
    [TBL] [Abstract][Full Text] [Related]  

  • 18. How to deal with multiple treatment or dose groups in randomized clinical trials?
    Hothorn LA
    Fundam Clin Pharmacol; 2007 Apr; 21(2):137-54. PubMed ID: 17391286
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A logistic dose-ranging method for phase I clinical investigations trials.
    Murphy JR; Hall DL
    J Biopharm Stat; 1997 Nov; 7(4):635-47. PubMed ID: 9358335
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Efficacy of botulinum toxin type A for the prophylaxis of episodic migraine headaches: a meta-analysis of randomized, double-blind, placebo-controlled trials.
    Shuhendler AJ; Lee S; Siu M; Ondovcik S; Lam K; Alabdullatif A; Zhang X; Machado M; Einarson TR
    Pharmacotherapy; 2009 Jul; 29(7):784-91. PubMed ID: 19558252
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.