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Use of PRO Measures to Inform Tolerability in Oncology Trials: Implications for Clinical Review, IND Safety

Janice Kim1, Harpreet Singh2, Kassa Ayalew3

  • 1Office of Hematology and Oncology Products, Center for Drug Evaluation and Research (CDER), U.S. Food and Drug Administration, Silver Spring, Maryland. Janice.Kim@fda.hhs.gov.

Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|December 15, 2017
PubMed

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