Phase 2b, Trial of Intravesical DTA-H19/PEI in Patients With Intermediate-Risk Superficial Bladder Cancer

PHASE2CompletedINTERVENTIONAL
Enrollment

47

Participants

Timeline

Start Date

January 31, 2008

Primary Completion Date

January 31, 2013

Study Completion Date

January 31, 2013

Conditions
Superficial Bladder Cancer
Interventions
BIOLOGICAL

BC-819/PEI

Papillary tumors will be resected with the exception of one marker tumor that will remain to examine the effects of the treatment on the remaining tumor. Study treatments will consist of an induction course of six weekly instillations of 20 mg of DTA-H19/PEI into the urinary bladder. Intravesical therapy will be delivered through a Foley catheter. Patients will be instructed to hold the dose in the bladder for two hours after administration. If the patient has a complete response, then she/he will be eligible to receive three additional courses of 3 weekly intravesical administrations of the same dose of investigational product every 12 weeks.

Trial Locations (6)

85032

BCG Oncology, Phoenix

Unknown

Bnai Zion Medical Center, Haifa

Edith Wolfson Medical Center, Holon

Hadassah and Hebrew University Medical Center, Jerusalem

Meir Medical Center, Kfar Saba

Assaf Harofeh, Zrifin

All Listed Sponsors
lead

Anchiano Therapeutics Israel Ltd.

INDUSTRY

NCT00595088 - Phase 2b, Trial of Intravesical DTA-H19/PEI in Patients With Intermediate-Risk Superficial Bladder Cancer | Biotech Hunter | Biotech Hunter