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Activity Details

113 * ! Mon, 7/31/2017, 8:30 AM - 10:20 AM CC-317
Clinical Outcome Assessments: Measurement, Evaluation, and Interpretation — Topic Contributed Papers
Biopharmaceutical Section
Organizer(s): Xu Shu, Novartis
Chair(s): Dong Xi, Novartis Pharmaceuticals Corporation
8:35 AM Generalizability Theory for Clinician-Rated Outcomes Joseph Cappelleri, Pfizer Inc
8:55 AM Exploring the Cognitive Endpoints in Alzheimer's Disease Cohort Data Using Item Response Theory Models Xu Shu, Novartis
9:15 AM Estimating Real Cigarette Counts from Heaped Time-Line Follow-Back Data Chelsea McCarty Allen, Southern Methodist University ; Daniel F. Heitjan, Southern Methodist University
9:35 AM Patient-Reported Outcomes: Observations of Regulatory Approvals by the Center for Biologics Evaluation and Research Hussein Ezzeldin, FDA/CBER ; Megan Moncur, FDA/CBER ; Yuqun Abigail Luo, FDA/CBER ; Telba Irony, Office of Biostatistics and Epidemiology, CBER, FDA
9:55 AM Mixed Methods for Analyzing Factors Important to Patients in Choosing a Dialysis Modality Jarcy Zee, Arbor Research Collaborative for Health ; Lalita Subramanian, Arbor Research Collaborative for Health ; Junhui Zhao, Arbor Research Collaborative for Health ; Francesca Tentori, Arbor Research Collaborative for Health; Vanderbilt University
10:15 AM Floor Discussion
 
 
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