| Literature DB >> 23294774 |
Kimberly Spencer1, Kelly Colvin, Brad Braunecker, Marcia Brackman, Joyce Ripley, Paul Hines, Zachary Skrivanek, Brenda Gaydos, Mary Jane Geiger.
Abstract
A wide variety of operational issues were encountered with the planning and implementation of an adaptive, dose-finding, seamless phase 2/3 trial for a diabetes therapeutic. Compared with a conventional design, significant upfront planning was required, as well as earlier, more integrated cross-functional coordination. The existing infrastructure necessitated greater flexibility to meet the needs of the adaptive design. Rapid data acquisition, analysis, and reporting were essential to support the successful implementation of the adaptive algorithm. Drug supply for nine treatment arms had to be carefully managed across many sites worldwide. Details regarding these key operational challenges and others will be discussed along with resolutions taken to enable successful implementation of this adaptive, seamless trial.Entities:
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Year: 2012 PMID: 23294774 PMCID: PMC3570869 DOI: 10.1177/193229681200600608
Source DB: PubMed Journal: J Diabetes Sci Technol ISSN: 1932-2968