A Single-Patient Study Using AGS 006 as an Immunotherapeutic in a Subject With Newly Diagnosed Resectable Pancreatic Cancer
Single-patient, open-label clinical study:
- Events during Pre-Treatment Period:
1. Resection of pancreatic cancer,
2. RNA acquisition from tumor specimen,
3. RNA amplification,
4. Infectious disease testing,
5. Autoimmune disease testing,
6. Two blood draws for immune response monitoring,
7. Production leukapheresis, and
8. Dendritic cell electroporation with RNA and immunotherapeutic production;
- Events during Induction Period:
1. Administer investigative treatment every 2 weeks for a total of five doses,
followed by dosing every 4 weeks for a total of four doses,
2. Two Induction Period blood draws (Week 6 and Week 12) for immune response
monitoring, and
3. One leukapheresis (Week 14) for immune response monitoring;
- Events during Booster Period:
1. Dose every 3 months until progression or 2 years after first AGS treatment,
2. Potentially, one leukapheresis for immune response monitoring 12 months from the
first dose, and
3. One blood draw 2 weeks following dosing at Week 36 (1st booster dose)
(approximately Week 38); and,
- Events during study Close-Out:
1. Close-Out upon progression or 28 days following immune response monitoring 2 years
after first dose
Interventional
Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Treatment-emergent changes in vital signs (blood pressure, heart rate, respiratory rate, and body temperature) from baseline values obtained prior to each investigative treatment
Yes
Sarah J Schlesinger, MD
Principal Investigator
Rockefeller University
United States: Food and Drug Administration
AGS-006-001
NCT00664482
May 2007
October 2011
Name | Location |
---|---|
Rockefeller University | New York, New York 10021 |