An Open Label Study to Evaluate G17DT Compared to Gemcitabine

PHASE3CompletedINTERVENTIONAL
Enrollment

103

Participants

Timeline

Start Date

August 14, 2000

Primary Completion Date

September 24, 2001

Study Completion Date

September 19, 2002

Conditions
Pancreatic Cancer
Interventions
BIOLOGICAL

G17DT

250 µg/0.2 mL administered by intramuscular injection at Weeks 0, 2 and 6. 125 µg booster administered at Week 24.

DRUG

Gemcitabine

1000 µg/m\^2 intravenously administered once weekly for seven weeks starting at Week 0 followed by one week of rest. After, treatments will occur in cycles of 3 weeks of treatment followed by one week of rest.

Sponsors
All Listed Sponsors
lead

Cancer Advances Inc.

INDUSTRY

NCT03200821 - An Open Label Study to Evaluate G17DT Compared to Gemcitabine | Biotech Hunter | Biotech Hunter