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FDA ovarian cancer clinical trial endpoints workshop: A Society of Gynecologic Oncology White Paper.

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a University of Cincinnati Cancer Institute, Dept. of Ob/Gyn, University of Cincinnati, United States b Office of Hematology Oncology Products, OND, CDER, FDA, United States c Division of Gynecologic Oncology,… Click to show full abstract

a University of Cincinnati Cancer Institute, Dept. of Ob/Gyn, University of Cincinnati, United States b Office of Hematology Oncology Products, OND, CDER, FDA, United States c Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, Vanderbilt University Medical Center, Nashville, TN, United States d Johns Hopkins Sidney Kimmel Comprehensive Cancer Center, United States e Division of Biometrics V, OB, OTS, CDER, FDA, United States f Ovarian Cancer Alliance of San Diego, United States g Department of Gynecologic Oncology & Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, United States h U.S. Oncology, Phoenix, AZ, United States i Oncology Center of Excellence, OMPT, FDA, United States j Ovarian Cancer Survivor, White Plains, New York

Keywords: ovarian cancer; united states; gynecologic oncology; oncology; fda

Journal Title: Gynecologic oncology
Year Published: 2017

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