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Keyword Search Criteria: adverse event returned 10 record(s)
Sunday, 07/30/2017
Sources of Safety Data and Statistical Strategies for Design and Analysis in Clinical Trials
Richard C. Zink, JMP Life Sciences, SAS Institute, Inc.
2:05 PM

Statistical Monitoring of Safety via a Bayesian Predictive Approach
LiAn Lin; Greg Ball, Merck; William W Wang, Merck & Co Inc
2:20 PM

Monday, 07/31/2017
Modeling Excess Zeroes in an Integrated Analysis of Vaccine Safety
Roger Maansson, Pfizer Inc.; David Radley, Pfizer Inc.; Qin Jiang, Pfizer Inc.; Scott Patterson, Pfizer Inc.; Judith Absalon, Pfizer Inc.; John Perez, Pfizer Inc.


Analysis of Adverse Event Relationships in Clinical Trials Using JMP
Anastasia Dmitrienko; Kelci Miclaus, JMP Life Sciences, SAS Institute Inc.; Richard C. Zink, JMP Life Sciences, SAS Institute, Inc.


Inverse Probability of Treatment Weighted Estimator for Exposure Adjusted Incidence Rate Ratio for Rare Adverse Event in Pooled Studies Controlling for Confounding by Study
Hui Wang, Astrazeneca; Sudipta Bhattacharya, AstraZeneca
9:20 AM

Tuesday, 08/01/2017
Discriminant Analysis (DA) Based Methods in Safety Evaluation
Angang Zhang, Merck; Richard Baumgartner, Merck; William W Wang, Merck & Co Inc


Discriminant Analysis (DA) Based Methods in Safety Evaluation
Angang Zhang, Merck; Richard Baumgartner, Merck; William W Wang, Merck & Co Inc
9:15 AM

Optimal Individualized Early Warning for Inpatient Adverse Events
Hossein Soleimani, Johns Hopkins University; Suchi Saria, Johns Hopkins University
10:35 AM

Statistical Methods to Analyze PRO-CTCAE Data in Oncology Clinical Trials
Amylou Dueck, Mayo Clinic
3:05 PM

Wednesday, 08/02/2017
Analysis of Clinical Trial Adverse Event Data
Michael Fries, CSL Behring; Judy X. Li, Regeneron Pharmaceuticals; Matilde Sanchez-Kam
10:55 AM

 
 
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