|
Tweet | ||
657 ! | Thu, 8/13/2015, 8:30 AM - 10:20 AM | CC-603 | |
Clinical Trial Design V — Contributed Papers | |||
Biopharmaceutical Section | |||
Chair(s): Diqiong Xie, FDA | |||
8:35 AM | Nonparametric Method for Analyzing Recurrence of Adverse Events in Randomized Clinical Trials — Masanori Ito, Astellas Pharma Global Development ; Misun Lee, Astellas Pharma Global Development | ||
8:50 AM | Conservativeness of T-Test Following Stratified Randomization — Yanqing Hu, West Virginia University | ||
9:05 AM | Phase I Dose Finding in Clinical Trials---An Interface for Designs — Yunfei Wang, Children's National | ||
9:20 AM | A Flexible Cure Rate Model in Population-Based Cancer Survival Analysis — Myron Chang, University of Florida ; Yang Li, University of Florida | ||
9:35 AM | Exchangeability and Nonexchangeability in Subgroup Analysis — Margaret Gamalo-Siebers, FDA/CDER ; Ram Tiwari, FDA/CDER/OT/OB | ||
9:50 AM | Sample Size Calculations for Equivalence Trials with Poisson Data — Lori Davis, ProNAi Therapeutics | ||
10:05 AM | Floor Discussion |
For program information, contact the JSM Registration Department or phone (888) 231-3473.
For Professional Development information, contact the Education Department.
The views expressed here are those of the individual authors and not necessarily those of the JSM sponsors, their officers, or their staff.
2015 JSM Online Program Home
ASA Meetings Department
732 North Washington Street, Alexandria, VA 22314
(703) 684-1221 • meetings@amstat.org
Copyright © American Statistical Association.