JSM 2012 Online Program
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Online Program HomeActivity Details
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522 | Wed, 8/1/2012, 10:30 AM - 12:20 PM | CC-Sails Pavilion | |
Contributed Oral Poster Presentations: Biopharmaceutical Section — Contributed Poster Presentations | |||
Biopharmaceutical Section | |||
Chair(s): Jianwei Chen, San Diego State University | |||
01: | Did Adult Liver Transplant Recipients Who Had Hepatitis C Prior to Transplant Receive Antiviral Therapy, January 1997 to June 2009 — Feifei Wei, University of Arkansas for Medical Science ; Robin R. Whitebird, HealthPartners Research Foundation | ||
02: | Multivariate Statistical Methods Used for Lymphoblastoid Cell Lines Drug Response Shows Promise in Pharmacogenomics Gene Discovery — Chad C Brown, North Carolina State University ; Tammy Havener, The University of North Carolina at Chapel Hill ; Ronald Krauss, Children's Hospital Oakland Research Institute ; Marisa Wong-Medina, Children's Hospital Oakland Research Institute ; Kevin Long, The University of North Carolina at Chapel Hill ; Howard McLeod, The University of North Carolina at Chapel Hill ; Alison Anne Motsinger-Reif, North Carolina State University | ||
04: | Development of Software for Simulation and Implementation of Optimal Response-Adaptive Randomization Designs in Time-to-Event Trials — Oleksandr Sverdlov, Bristol-Myers Squibb ; Yevgen Ryeznik, Kharkov National University of Economics ; Weng-Kee Wong, University of California at Los Angeles Fielding School of Public Health | ||
05: | Precision Study for a Qualitative Assay — Paul Hshieh, FDA/CBER ; Tie-Hua Ng, FDA/CBER | ||
06: | Comparability of CTCAE Grading and Clinical Significance in Abnormal Clinical Laboratory Results — Brian Hetzell, Rho, Inc. ; Ashley Marie Pinckney, Rho, Inc. ; Katharine Marie Poole, Rho, Inc. | ||
07: | Methods for Responder Analysis of Patient-Reported Outcomes — Alexandra I. Barsdorf, Pfizer Inc. ; Kelly Zou, Pfizer Inc. ; Martin M Carlsson, Pfizer Inc. ; Joseph Cappelleri, Pfizer Inc. | ||
08: | Study at a Glance: Old Wine in a New Bottle — William Coar | ||
09: | Estimators of a Dose-Reduction Factor: A Comparison Study — Reid Landes, University of Arkansas for Medical Sciences ; Shelly Y. Lensing, University of Arkansas for Medical Sciences ; Ralph L Kodell, University of Arkansas for Medical Sciences ; Martin Hauer-Jensen, University of Arkansas for Medical Sciences | ||
10: | A General Approach for Estimating Stopping Probabilities of Large Group Sequential Trials in Life-Threatening Conditions Monitoring Binary Efficacy and Safety Outcomes — Yanqiu Weng, Medical University of South Carolina ; Wenle Zhao, Medical University of South Carolina ; Yuko Palesch, Medical University of South Carolina | ||
11: | Escalation with Overdose Control Using Ordinal Toxicity Grades for Cancer Phase I Clinical Trials — Galen Cook-Wiens, Cedars Sinai Medical Center ; Mourad Tighiouart, Cedars Sinai Medical Center ; Andre Rogatko, Cedars Sinai Medical Center | ||
12: | Matching-Adjusted Indirect Comparison Using Bootstrapping for Comparative Effectiveness: Individual Patient Data vs. Published Aggregated Data — Daniel Parks, GlaxoSmithKline ; Xiwu Lin, GlaxoSmithKline ; Alan J Menius, GlaxoSmithKline ; Kwan R. Lee, GlaxoSmithKline | ||
13: | Analyzing Hypoglycemia Events eith Negative Binomial Regression Model — Junxiang Luo, Eli Lilly and Company ; Yongming Qu, Eli Lilly and Company | ||
14: | A Comparison of Multivariate Methods for Measuring Change from Pre-Test to Post-Test — Justin Rogers, Abbott Laboratories ; Daniel Mundfrom, Eastern Kentucky University | ||
15: | Zero-Inflated Poisson and Negative Binomial Models Applied to the Analysis of Colorectal Polyp Prevention Trial Data — Christopher Davidson, University of Arizona ; Chiu-Hsieh Hsu, University of Arizona | ||
16: | Sample Size Considerations When Using the Synthesis Method for Non-inferiority Trials — Huei Wang, Amgen, Inc. ; Guanghui Wei, Amgen, Inc. | ||
17: | Simulation Study on Bioequivalence Tests Under Several Variability Conditions — Denka Markova, Axio Research Inc. ; Dean Young, Baylor University | ||
18: | An Application of Adaptive Randomization to Guide Dose-Finding in a Large Multicenter Phase I Clinical Trial — Alison Marie Graham, Abbott ; Wijith Prasantha Munasinghe, Abbott Laboratories ; James Bolognese, Cytel Inc. ; Yi-Lin Chiu, Abbott Laboratories | ||
19: | 1 Plus 1 Equals 3: Searching for In Vivo Synergy — Mandy Bergquist, GlaxoSmithKline ; Jonathan Hommel, University of Texas Medical Branch ; Andrea Acker, GlaxoSmithKline ; Mark Paulik, GlaxoSmithKline | ||
20: | Aligned Rank Tests: An Application to Clinical Trials — John Kloke, University of Wisconsin-Madison ; Tom Cook, University of Wisconsin-Madison | ||
21: | Evaluating Oncology Phase II Study Designs — Zhuying Huang, PPD ; Hui Liu, PPD ; Lindsey Lian, PPD | ||
22: | On the Problem of Identifiabilityof the EMAX Model — Ha Nguyen, Pfizer Inc. ; Birol Emir, Pfizer Inc. ; Javier Cabrera, Rutgers University ; Feihan Lu, New York University | ||
23: | Power and Sample Size Investigation for Correlated Binary Data — Dar Shong Hwang, BRSI ; James Lee, Daiichi Sankyo Pharma Development ; Chyi-Hung Hsu, Janssen Pharmaceuticals, Inc. | ||
24: | An Extension of the Bland-Altman Plot — Tie-Hua Ng, FDA/CBER | ||
25: | Power and Sample Size Estimation in Clinical Trials with Multiple Co-Primary Endpoints — Zuoshun Zhang, Celgene Corporation | ||
26: | Estimating Pharmacokinetics Parameters Using Meta-Analysis and Nonlinear Mixed Effects Model — Wijith Prasantha Munasinghe, Abbott Laboratories ; Balakrishna Hosmane, Abbott Laboratories ; Rajendra Pradhan, Abbott Laboratories ; Yi-Lin Chiu, Abbott Laboratories | ||
27: | Case-Cohort Data Analyses with an Application in Vaccine Trial — Shu-Chih Su, Merck Research Laboratories ; Guanghan Liu, Merck Research Laboratories ; Ivan Chan, Merck | ||
28: | Methods for Pairwise Comparison of Treatment Levels in a Functional Data Setting — Olga Vsevolozhskaya, Montana State University ; Mark Greenwood, Montana State University ; Dmitri Holodov, Voronezh State University | ||
29: | Predicting a Binary Outcome with Dose-Response Data — Yang Zhang, University of Pittsburgh | ||
31: | Generalized Estimation of the Treatment Effects in Mixed-Effects Model: A Comparison with ML and REML — Ching-Ray Yu, Pfizer Inc. ; Kelly Zou, Pfizer Inc. ; Martin M Carlsson, Pfizer Inc. ; Samaradasa Weerahandi, Pfizer Inc. | ||
32: | A New Tool for Flagging Adverse Events of Potential Clinical Interest — Li Zhou, Axio Research Inc. ; David Kerr, Axio Research Inc. | ||
33: | The Optimal Thresholds of Biomarkers by Maximizing Various Metrics — Kelly Zou, Pfizer Inc. ; Martin M Carlsson, Pfizer Inc. ; Kezhen Liu, State University of New Jersey ; Ching-Ray Yu, Pfizer Inc. | ||
34: | Incorporating Continuity Corrections When Illustrating Noninferiority with Binomial Proportions — Brianna Bright, University of Nebraska ; Julia Soulakova, University of Nebraska | ||
35: | Considering Efficacy in Tumor Genotypes in a Two-Stage Adaptive Design for Oncology Trials — Jinwei Yuan, ICON Clinical Research | ||
36: | Creating a Better, Shorter DMC Report: A Stack of Needles, Not a Needle in a Haystack — David Kerr, Axio Research Inc. ; William Coar ; Shannon Grant, Axio Research Inc. |
2012 JSM Online Program Home
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