首页>Clinical Pharmacology and Therapeutics>Shift from surrogate end point to outcome trials: Implications for cardiovascular safety assessment in development programs for antidiabetic drugs
Shift from surrogate end point to outcome trials: Implications for cardiovascular safety assessment in development programs for antidiabetic drugs
作者单位:Takeda Global Research and Development Center Inc., Deerfield, IL, United States, Abbott[1]Takeda Global Research and Development Center Inc., Deerfield, IL, United States[2]