Amy E McKee

Summary

Affiliation: Food and Drug Administration
Country: USA

Publications

  1. doi request reprint The role of the U.S. Food and Drug Administration review process: clinical trial endpoints in oncology
    Amy E McKee
    U S Food and Drug Administration, Silver Spring, Maryland 20993, USA
    Oncologist 15:13-8. 2010

Collaborators

Detail Information

Publications1

  1. doi request reprint The role of the U.S. Food and Drug Administration review process: clinical trial endpoints in oncology
    Amy E McKee
    U S Food and Drug Administration, Silver Spring, Maryland 20993, USA
    Oncologist 15:13-8. 2010
    ..Surrogate endpoints may be acceptable for "accelerated" approval, with a sponsor commitment to provide evidence of clinical benefit in a subsequent trial...