High development cost, low development success, cost-disciplined health-care policies, and intense competition demand an efficient drug development process. New compounds need to bring value to patients by being safe, efficacious, and cost-effective as compared with existing treatment options. Model-based meta-analysis (MBMA) facilitates integration and utilization of summary-level efficacy and safety data, providing a quantitative framework for comparative efficacy and safety assessment. This Commentary discusses the application and limitations of MBMA in drug development.
2011 年 12 月 1 日
Author(s): Jaap Mandema, Megan Gibbs, Rebecca Boyd, Russell Wada, Marc Pfister
Year: 2011 年 12 月 1 日
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