19
Participants
Start Date
April 30, 2013
Primary Completion Date
May 31, 2016
Study Completion Date
September 30, 2017
BPX-201 vaccine plus AP1903
The trial design consists of 3 cohorts of 6 patients each, receiving escalating doses of BPX-201 of 10 million (M), 20M and 40M cells, respectively. Dose escalation will occur according to a 3+3 design. Patients will receive administration of BPX-201 every other week for 6 cycles (1 cycle equals 2 weeks). Approximately 1.6 mL of BPX-201 will be administered as 8 intradermal injections (200μL each) at each treatment visit. On the day following each vaccination, a single 40 mg dose of the activating agent, AP1903, will be administered via intravenous (IV) infusion over 2 hours.
UAB Comprehensive Cancer Center, Birmingham
Baylor Charles Sammons Cancer Center, Dallas
Lead Sponsor
Bellicum Pharmaceuticals
INDUSTRY