Efficacy and Safety of BC-819 and Gemcitabine in Patients With Locally Advanced Pancreatic Adenocarcinoma

PHASE2TerminatedINTERVENTIONAL
Enrollment

12

Participants

Timeline

Start Date

September 30, 2011

Primary Completion Date

January 31, 2013

Study Completion Date

May 31, 2014

Conditions
Pancreas, Adenocarcinoma
Interventions
BIOLOGICAL

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)"

Trial Locations (9)

11501

Winthrop University Hospital, Mineola

19107

Thomas Jefferson University, Philadelphia

79410

Joe Arrington Cancer Research & Treatment Center, Lubbock

Unknown

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

All Listed Sponsors
lead

Anchiano Therapeutics Israel Ltd.

INDUSTRY

NCT01413087 - Efficacy and Safety of BC-819 and Gemcitabine in Patients With Locally Advanced Pancreatic Adenocarcinoma | Biotech Hunter | Biotech Hunter