26
Participants
Start Date
September 30, 2006
Primary Completion Date
September 30, 2008
Study Completion Date
September 30, 2008
AVE1642
For Part 1, AVE1642 was administered on Day 1 and then every three weeks intra-venously with the dose escalation step starting at 3 mg/kg/infusion with a classical dose escalation schema of 3+3. For Part 2, AVE1642 was administered at doses ranging from 0.5 mg/kg to 12 mg/kg
Velcade
For Part 2 ONLY, fixed dose of 1.3 mg/m² administered on Days 1, 4, 8, and 11.
Sanofi-Aventis Investigational Site Number 380001, Torino
Sanofi-Aventis Investigational Site Number 250001, Nantes
Sanofi-Aventis Investigational Site Number 250003, Vandœuvre-lès-Nancy
Sanofi-Aventis Investigational Site Number 250002, Lille
Lead Sponsor
Sanofi
INDUSTRY