Works matching IS 15391604 AND DT 2025 AND VI 24 AND IP 1
Results: 33
Sample Size Estimation for Correlated Count Data With Changes in Dispersion.
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- Pharmaceutical Statistics, 2025, v. 24, n. 1, p. 1, doi. 10.1002/pst.2469
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Estimation of the Restricted Mean Duration of Response (RMDoR) in Oncology.
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- Pharmaceutical Statistics, 2025, v. 24, n. 1, p. 1, doi. 10.1002/pst.2468
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Taylor Series Approximation for Accurate Generalized Confidence Intervals of Ratios of Log‐Normal Standard Deviations for Meta‐Analysis Using Means and Standard Deviations in Time Scale.
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- Pharmaceutical Statistics, 2025, v. 24, n. 1, p. 1, doi. 10.1002/pst.2467
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Bayesian Sample Size Calculation in Small n, Sequential Multiple Assignment Randomized Trials (snSMART).
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- Pharmaceutical Statistics, 2025, v. 24, n. 1, p. 1, doi. 10.1002/pst.2465
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A Commensurate Prior Model With Random Effects for Survival and Competing Risk Outcomes to Accommodate Historical Controls.
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- Pharmaceutical Statistics, 2025, v. 24, n. 1, p. 1, doi. 10.1002/pst.2464
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- Article
New Methods for Two‐Stage Treatment Switching Estimation.
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- Pharmaceutical Statistics, 2025, v. 24, n. 1, p. 1, doi. 10.1002/pst.2462
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- Article
Estimating the Strength of Binding Affinity via Delta–Delta‐G for Hit Screening After a Deming Regression Calibration.
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- Pharmaceutical Statistics, 2025, v. 24, n. 1, p. 1, doi. 10.1002/pst.2460
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- Article
Balance Index to Determine the Follow‐Up Duration of Oncology Trials.
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- Pharmaceutical Statistics, 2025, v. 24, n. 1, p. 1, doi. 10.1002/pst.2442
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- Article
On Some Modeling Issues in Estimating Vaccine Efficacy.
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- Pharmaceutical Statistics, 2025, v. 24, n. 1, p. 1, doi. 10.1002/pst.2440
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- Article
An Adaptive Three‐Arm Comparative Clinical Endpoint Bioequivalence Study Design With Unblinded Sample Size Re‐Estimation and Optimized Allocation Ratio.
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- Pharmaceutical Statistics, 2025, v. 24, n. 1, p. 1, doi. 10.1002/pst.2439
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- Article
Number of Repetitions in Re‐Randomization Tests.
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- Pharmaceutical Statistics, 2025, v. 24, n. 1, p. 1, doi. 10.1002/pst.2438
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- Article
Assessing the Operational Characteristics of the Individual Causal Association as a Metric of Surrogacy in the Binary Continuous Setting.
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- Pharmaceutical Statistics, 2025, v. 24, n. 1, p. 1, doi. 10.1002/pst.2437
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- Article
Propensity Score Analysis With Baseline and Follow‐Up Measurements of the Outcome Variable.
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- Pharmaceutical Statistics, 2025, v. 24, n. 1, p. 1, doi. 10.1002/pst.2436
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- Article
Generalizing Treatment Effect to a Target Population Without Individual Patient Data in a Real‐World Setting.
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- Pharmaceutical Statistics, 2025, v. 24, n. 1, p. 1, doi. 10.1002/pst.2435
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- Article
Comparative Analyses of Bioequivalence Assessment Methods for In Vitro Permeation Test Data.
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- Pharmaceutical Statistics, 2025, v. 24, n. 1, p. 1, doi. 10.1002/pst.2434
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- Article
Principles for Defining Estimands in Clinical Trials—A Proposal.
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- Pharmaceutical Statistics, 2025, v. 24, n. 1, p. 1, doi. 10.1002/pst.2432
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- Article
Bayesian Predictive Probability Based on a Bivariate Index Vector for Single‐Arm Phase II Study With Binary Efficacy and Safety Endpoints.
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- Pharmaceutical Statistics, 2025, v. 24, n. 1, p. 1, doi. 10.1002/pst.2431
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- Article
Quality by Design for Preclinical In Vitro Assay Development.
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- Pharmaceutical Statistics, 2025, v. 24, n. 1, p. 1, doi. 10.1002/pst.2430
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- Article
Sample Size Reestimation in Stochastic Curtailment Tests With Time‐to‐Events Outcome in the Case of Nonproportional Hazards Utilizing Two Weibull Distributions With Unknown Shape Parameters.
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- Pharmaceutical Statistics, 2025, v. 24, n. 1, p. 1, doi. 10.1002/pst.2429
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- Article
Simultaneous Inference Using Multiple Marginal Models.
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- Pharmaceutical Statistics, 2025, v. 24, n. 1, p. 1, doi. 10.1002/pst.2428
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- Article
Mixture Experimentation in Pharmaceutical Formulations: A Tutorial.
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- Pharmaceutical Statistics, 2025, v. 24, n. 1, p. 1, doi. 10.1002/pst.2426
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- Article
Experimental design considerations and statistical analyses in preclinical tumor growth inhibition studies.
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- Pharmaceutical Statistics, 2025, v. 24, n. 1, p. 1, doi. 10.1002/pst.2399
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- Article
Strategy for Designing In Vivo Dose–Response Comparison Studies.
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- Pharmaceutical Statistics, 2025, v. 24, n. 1, p. 1, doi. 10.1002/pst.2421
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- Article
The Role of CMC Statisticians: Co‐Practitioners of the Scientific Method.
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- Pharmaceutical Statistics, 2025, v. 24, n. 1, p. 1, doi. 10.1002/pst.2420
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- Article
Potency Assay Variability Estimation in Practice.
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- Pharmaceutical Statistics, 2025, v. 24, n. 1, p. 1, doi. 10.1002/pst.2408
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- Article
Issue Information.
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- Pharmaceutical Statistics, 2025, v. 24, n. 1, p. 1, doi. 10.1002/pst.2400
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- Article
Tutorial on Firth's Logistic Regression Models for Biomarkers in Preclinical Space.
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- Pharmaceutical Statistics, 2025, v. 24, n. 1, p. 1, doi. 10.1002/pst.2422
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- Article
The partnership between statisticians and the Institutional Animal Care and Use Committee (IACUC).
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- Pharmaceutical Statistics, 2025, v. 24, n. 1, p. 1, doi. 10.1002/pst.2390
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- Article
Synergy detection: A practical guide to statistical assessment of potential drug combinations.
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- Pharmaceutical Statistics, 2025, v. 24, n. 1, p. 1, doi. 10.1002/pst.2383
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- Article
Predictive Ppk calculations for biologics and vaccines using a Bayesian approach – a tutorial.
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- Pharmaceutical Statistics, 2025, v. 24, n. 1, p. 1, doi. 10.1002/pst.2380
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- Article
Statistical approaches to evaluate in vitro dissolution data against proposed dissolution specifications.
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- Pharmaceutical Statistics, 2025, v. 24, n. 1, p. 1, doi. 10.1002/pst.2379
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- Article
Introduction to qualification and validation of an immunoassay.
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- Pharmaceutical Statistics, 2025, v. 24, n. 1, p. 1, doi. 10.1002/pst.2370
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What they forgot to tell you about machine learning with an application to pharmaceutical manufacturing.
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- Pharmaceutical Statistics, 2025, v. 24, n. 1, p. 1, doi. 10.1002/pst.2366
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- Article