50
Participants
Start Date
May 31, 2005
Primary Completion Date
July 31, 2007
Study Completion Date
October 31, 2007
MLN1202
Patients received 5 intravenous (IV) infusions of the study drug. The first 3 infusions were administered at 15-day intervals, followed by 2 infusions at 30-day intervals. Patients were randomized to receive 1 of 2 doses of MLN1202 (4mg/kg or 8mg/kg).
Lead Sponsor
Millennium Pharmaceuticals, Inc.
INDUSTRY