69
Participants
Start Date
December 31, 2007
Primary Completion Date
December 31, 2010
Study Completion Date
February 28, 2011
Aprepitant
Subjects will be randomized to receive aprepitant 125mg PO day 3 then 80mg on days 4-7 on either cycle 1 or cycle 2.
Placebo
Subjects will be randomized to receive placebo on days 3-7 on either cycle 1 or cycle 2.
University of Pennsylvania, Philadelphia
Indiana University Simon Cancer Center, Indianapolis
Medical Consultants, P.C., Muncie
Froedtert/Medical College of Wisconsin, Milwaukee
Siteman Cancer Center, St Louis
Providence Portland Medical Center, Portland
Lead Sponsor
Merck Sharp & Dohme LLC
INDUSTRY
Hoosier Cancer Research Network
OTHER