Study of AVE1642 Anti-IGF1R Monoclonal Antibody in Patients With Advanced Multiple Myeloma

PHASE1CompletedINTERVENTIONAL
Enrollment

26

Participants

Timeline

Start Date

September 30, 2006

Primary Completion Date

September 30, 2008

Study Completion Date

September 30, 2008

Conditions
Multiple Myeloma
Interventions
DRUG

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

DRUG

Velcade

For Part 2 ONLY, fixed dose of 1.3 mg/m² administered on Days 1, 4, 8, and 11.

Trial Locations (4)

10126

Sanofi-Aventis Investigational Site Number 380001, Torino

44093

Sanofi-Aventis Investigational Site Number 250001, Nantes

54511

Sanofi-Aventis Investigational Site Number 250003, Vandœuvre-lès-Nancy

59037

Sanofi-Aventis Investigational Site Number 250002, Lille

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Sanofi

INDUSTRY