110
Participants
Start Date
November 30, 2007
Primary Completion Date
August 31, 2010
Study Completion Date
August 31, 2010
RG4733
Administered orally daily at ascending doses to successive cohorts of patients
RG4733
Administered orally at ascending doses to successive cohorts of patients, on a 3 days on/ 4 days off schedule
RG4733
Administered orally at ascending doses to successive cohorts of patients, on days 1-7 of each 21 day cycle
Houston
Aurora
San Antonio
Boston
Boston
Boston
New Brunswick
Hoffmann-La Roche
INDUSTRY