The purpose of drug development is to evaluate a drug's efficacy and safety profile. For a personalized medicine, it is important for patients and health care providers to understand the efficacy and safety trade-off when selecting a dose for a patient. In this article, we propose three different methods for jointly modeling the clinical safety and efficacy endpoints. These three methods model the correlation relationship in three different ways: modeling the joint distribution by a copula method, modeling conditional distributions, and modeling their correlations through individual means by a hierarchical model. We compare these three methods through simulations and apply these methods to a data set from a diabetes study.
机构:
Shengjing Hospital of China Medical University,Department of PharmacyShengjing Hospital of China Medical University,Department of Pharmacy
Yuqiang Liu
Yu Wang
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机构:
Changzhi People’s Hospital,Department of PharmacyShengjing Hospital of China Medical University,Department of Pharmacy
Yu Wang
Minglu Wang
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机构:
Changzhi People’s Hospital,Department of OncologyShengjing Hospital of China Medical University,Department of Pharmacy
Minglu Wang
Suodi Zhai
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机构:
Changzhi People’s Hospital,Department of PharmacyShengjing Hospital of China Medical University,Department of Pharmacy
Suodi Zhai
Chunxia Hou
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机构:
Peking University Third Hospital,Department of PharmacyShengjing Hospital of China Medical University,Department of Pharmacy
Chunxia Hou
Feng Sun
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机构:
Changzhi People’s Hospital,Department of PharmacyShengjing Hospital of China Medical University,Department of Pharmacy
Feng Sun
Lingyan Jian
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机构:
Peking University,Department of Epidemiology and Biostatistics, School of Public HealthShengjing Hospital of China Medical University,Department of Pharmacy