BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

82 related articles for article (PubMed ID: 30345693)

  • 1. Blinded continuous monitoring in clinical trials with recurrent event endpoints.
    Friede T; Häring DA; Schmidli H
    Pharm Stat; 2019 Jan; 18(1):54-64. PubMed ID: 30345693
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The inclusion of real world evidence in clinical development planning.
    Martina R; Jenkins D; Bujkiewicz S; Dequen P; Abrams K;
    Trials; 2018 Aug; 19(1):468. PubMed ID: 30157904
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Analysis and design of randomised clinical trials involving competing risks endpoints.
    Tai BC; Wee J; Machin D
    Trials; 2011 May; 12():127. PubMed ID: 21595883
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Sample size reestimation and Bayesian predictive probability for single-arm clinical trials with a time-to-event endpoint using Weibull distribution with unknown shape parameter.
    Waleed M; He J; Phadnis MA
    J Biopharm Stat; 2024 Jul; 34(4):469-487. PubMed ID: 37545144
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Adaptive clinical trial designs with blinded selection of binary composite endpoints and sample size reassessment.
    Roig MB; Melis GG; Posch M; Koenig F
    Biostatistics; 2023 Dec; 25(1):237-252. PubMed ID: 36150142
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Statistical Considerations and Software for Designing Sequential, Multiple Assignment, Randomized Trials (SMART) with a Survival Final Endpoint.
    Kravets S; Ruppert AS; Jacobson SB; Le-Rademacher JG; Mandrekar SJ
    J Biopharm Stat; 2024 Jul; 34(4):539-552. PubMed ID: 37434437
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Bayesian analysis of multi-type recurrent events and dependent termination with nonparametric covariate functions.
    Lin LA; Luo S; Chen BE; Davis BR
    Stat Methods Med Res; 2017 Dec; 26(6):2869-2884. PubMed ID: 26546256
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Distributional imputation for the analysis of censored recurrent events.
    Fairfax SR; Yang S
    Stat Med; 2024 Jun; 43(13):2622-2640. PubMed ID: 38684331
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Sample size considerations for split-mouth design.
    Zhu H; Zhang S; Ahn C
    Stat Methods Med Res; 2017 Dec; 26(6):2543-2551. PubMed ID: 26303156
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Optimal allocation strategies in platform trials with continuous endpoints.
    Bofill Roig M; Glimm E; Mielke T; Posch M
    Stat Methods Med Res; 2024 May; 33(5):858-874. PubMed ID: 38505941
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Sample size calculation in clinical trials with two co-primary endpoints including overdispersed count and continuous outcomes.
    Homma G; Yoshida T
    Pharm Stat; 2024; 23(1):46-59. PubMed ID: 38267827
    [TBL] [Abstract][Full Text] [Related]  

  • 12. An audit strategy for time-to-event outcomes measured with error: application to five randomized controlled trials in oncology.
    Dodd LE; Korn EL; Freidlin B; Gu W; Abrams JS; Bushnell WD; Canetta R; Doroshow JH; Gray RJ; Sridhara R
    Clin Trials; 2013 Oct; 10(5):754-60. PubMed ID: 23935162
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Design and monitoring of clinical trials with an interim analysis and a negative binomial endpoint.
    Quan H; Xu Y; Liu Y; Chen X
    Contemp Clin Trials; 2024 Mar; 138():107467. PubMed ID: 38331382
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of causal effects on binary outcomes using structural mean models.
    Clarke PS; Windmeijer F
    Biostatistics; 2010 Oct; 11(4):756-70. PubMed ID: 20522728
    [TBL] [Abstract][Full Text] [Related]  

  • 15. An audit strategy for progression-free survival.
    Dodd LE; Korn EL; Freidlin B; Gray R; Bhattacharya S
    Biometrics; 2011 Sep; 67(3):1092-9. PubMed ID: 21210772
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Sample size determination.
    Dell RB; Holleran S; Ramakrishnan R
    ILAR J; 2002; 43(4):207-13. PubMed ID: 12391396
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical Trial Adaptation by Matching Evidence in Complementary Patient Sub-groups of Auxiliary Blinding Questionnaire Responses.
    Arandjelović O
    PLoS One; 2015; 10(7):e0131524. PubMed ID: 26161797
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Sample Size Considerations in Clinical Trials when Comparing Two Interventions using Multiple Co-Primary Binary Relative Risk Contrasts.
    Ando Y; Hamasaki T; Evans SR; Asakura K; Sugimoto T; Sozu T; Ohno Y
    Stat Biopharm Res; 2015 Jun; 7(2):81-94. PubMed ID: 26167243
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Simulation-based sample size calculations of marginal proportional means models for recurrent events with competing risks.
    Furberg JF; Andersen PK; Scheike T; Ravn H
    Pharm Stat; 2024 Mar; ():. PubMed ID: 38509020
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Longitudinal design considerations to optimize power to detect variances and covariances among rates of change: simulation results based on actual longitudinal studies.
    Rast P; Hofer SM
    Psychol Methods; 2014 Mar; 19(1):133-54. PubMed ID: 24219544
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.