44
Participants
Start Date
April 30, 2003
Primary Completion Date
December 31, 2006
Study Completion Date
December 31, 2006
ABR-217620
Starting dose: 0.5 mcg/kg; subsequent doses: individual, based on pre-treatment level of anti-SEA/E-120, body weight, and toxicities observed in prior patients on study; IV; one bolus injection each day for 5 consecutive days; up to 3 cycles
Fox Chase Cancer Center, Philadelphia
Det Norske Radiumhospitalet, Oslo
Paterson Institute for Cancer Research, Christie Hospital NHS Trust and Research Institute, Manchester
Lead Sponsor
Active Biotech AB
INDUSTRY