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339
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Tue, 7/30/2019,
10:30 AM -
12:20 PM
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CC-105
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SPEED: Biopharmaceutical and General Health Studies: Statistical Methods and Applications, Part 1 — Contributed Speed
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Biopharmaceutical Section, Section on Statistics in Epidemiology, Section on Bayesian Statistical Science, Health Policy Statistics Section, ENAR
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Chair(s): Sedigheh Mirzaei Salehabadi, St. Jude Children's Research Hospital
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Poster Presentations
for this session.
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10:35 AM
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Mediation Analysis for Longitudinal Data with Applications to Clinical Trial Data
Yun Zhang
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10:40 AM
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Adjusting Response Adaptive Allocation for Subject Dropout
Katharine Stromberg, Virginia Commonwealth University; Adam Sima, Virginia Commonwealth University
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10:45 AM
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The Use of a New Classifier to Maximize the Classification Performance
Hua Ma, Merck; Joe Heyse, Merck
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10:50 AM
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Reproducibility of Living Data - Validation of Published Research Using the Parkinson’s Progression Marker Initiative Living Database
Elliot Burghardt, University of Iowa; Christopher Coffey, University of Iowa; Chelsea Caspell-Garcia, University of Iowa; Eric Foster, Ferring Pharmaceuticals
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10:55 AM
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Blinding in Open Label Study with Adaptive Design
Bo Xu, Boston Biomedical Inc; Bo Jin, Boston Biomedical Inc; Alex Dmitrienko, Mediana Inc
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11:00 AM
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Estimating the Relative Risk for Response-Biased Samples: Calibration and Conditional Likelihood
Claudia Rivera-Rodriguez, University of Auckland
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11:05 AM
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Another Estimation Method Besides MMRM for Treatment Effects in Diabetes Clinical Trials
Yu Du, Eli Lilly and Company
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11:10 AM
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Criteria for Choosing a Futility Method for Clinical Studies
Richard McNally, Covance-Chiltern
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11:15 AM
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Random Forests for Exploring Factors Driving Opioid Prescribing in National Outpatient Health Care Data Using Complex Survey Design
Yong Ma, FDA; JaeJoon Song, FDA
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11:20 AM
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An Adaptive Phase II Dose Finding Study Using Sample Size Re-Estimation Design
Qingyang Liu, University of Connecticut; Guanyu Hu, University of Connecticut; Yaoshi Wu, Boehringer-Ingelheim ; Binqi Ye, Boehringer-Ingelheim; Susan Wang, Boehringer-Ingelheim
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11:30 AM
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Sieve Maximum Likelihood Method for Interval-Censored Data with Missing Covariates Under Proportional Hazards Model
Ruiwen Zhou, University of Missouri-Columbia; Huiqiong Li, Yunnan University; (Tony) Jianguo Sun, University of Missouri
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11:35 AM
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Quantifying the Number of Events Borrowed from External Data in Hybrid Control Arms
Brian Segal, Flatiron Health; Carrie Bennette, Flatiron Health; Somnath Sarkar, Flatiron Health
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11:40 AM
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Characterizing Irreproducibility in Drug Sensitivity Data from a Large Pharmacogenomic Study
Zoe Rehnberg, University of Michigan; Johann A Gagnon-Bartsch, University of Michigan
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11:45 AM
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Closest Similar Subset Imputation
Macaulay Okwuokenye, Brio Dexteri Pharmaceutical Consultant & UNE; Karl E Peace, Georgia Southern University
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11:50 AM
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Planning and Analyzing Clinical Trials with Competing Risks: Recommendations for Choosing Appropriate Statistical Methodology
Misun Yu Lee, Astellas Pharma; Joseph Poythress, University of Georgia; James Young, Astellas Pharma
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11:55 AM
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Estimating and Using the Attained Power Distribution to Ensure We Get the Trial Power We Expect
Yongdong Ouyang, University of British Columbia; Hubert Wong, University of British Columbia; Ehsan Karim, University of British Columbia; Paul Gustafson, University of British Columbia
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12:00 PM
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Bayesian Semiparametric Joint Modeling of Longitudinal Predictors and a Binary Outcome
Woobeen Lim, The Ohio State University; Michael Pennell, Ohio State University
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12:05 PM
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Clustering of Multivariate Data with Varying Dimensions
Xiaoqi Lu, Columbia University; Bin Cheng, Columbia University; Ying Kuen Ken Cheung, Columbia University
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12:10 PM
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Floor Discussion
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