12
Participants
Start Date
September 30, 2011
Primary Completion Date
January 31, 2013
Study Completion Date
May 31, 2014
Biological/Vaccine: BC-819
"Post screening and prior to randomization, all patients will receive gemcitabine by IV infusion at a dose of 1000mg/m2 once weekly for four weeks. They may also enter the study if they received up to 4 doses of gemcitabine before entering the study. In this case, they will be randomized immediately provided there is no evidence of disease progression.~After randomization patients will receive 6 weekly IV infusions of gemcitabine at a dose of 1000mg/m2 + 7 intratumoral injections of BC-819 (8 mg or 12 mg according to allocations by randomization)"
Winthrop University Hospital, Mineola
Thomas Jefferson University, Philadelphia
Joe Arrington Cancer Research & Treatment Center, Lubbock
Carmel Medical Center, Haifa
Rambam Medical Center, Haifa
Hadassah Medical Organization, Jerusalem
Meir Medical Center, Kfar Saba
Galil Maaravi, Nahariya
Tel Aviv Medical Center, Tel Aviv
Lead Sponsor
Anchiano Therapeutics Israel Ltd.
INDUSTRY