Study of Personalized Immunotherapy in Adults With Metastatic Colorectal Cancer
Status: | Active, not recruiting |
---|---|
Conditions: | Colorectal Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 9/28/2018 |
Start Date: | May 2, 2017 |
End Date: | December 2020 |
A Phase 1 Safety and Tolerability Study of Personalized Live, Attenuated, Double-Deleted Listeria Monocytogenes (pLADD) Immunotherapy in Adults With Metastatic Colorectal Cancer
This study will evaluate the safety and tolerability of a personalized live, attenuated,
double-deleted Listeria monocytogenes (pLADD) treatment in adults with metastatic colorectal
cancer.
double-deleted Listeria monocytogenes (pLADD) treatment in adults with metastatic colorectal
cancer.
This single arm study is designed to evaluate the safety and tolerability of a personalized
treatment in adults with metastatic colorectal cancer by first analyzing the expression of
tumor-associated antigens and then treating the patients with a personalized live,
attenuated, double-deleted Listeria monocytogenes (pLADD)-based immunotherapy. pLADD is based
on the attenuated form of Listeria monocytogenes that has been genetically modified to reduce
its ability to cause disease, while maintaining its ability to stimulate a potent immune
response. pLADD is manufactured using patient-specific antigens and is therefore
individualized to each patient.
treatment in adults with metastatic colorectal cancer by first analyzing the expression of
tumor-associated antigens and then treating the patients with a personalized live,
attenuated, double-deleted Listeria monocytogenes (pLADD)-based immunotherapy. pLADD is based
on the attenuated form of Listeria monocytogenes that has been genetically modified to reduce
its ability to cause disease, while maintaining its ability to stimulate a potent immune
response. pLADD is manufactured using patient-specific antigens and is therefore
individualized to each patient.
Inclusion Criteria:
- metastatic colorectal cancer (mCRC) that is microsatellite stable (MSS)
- able to provide adequate tumor tissue from at least 1 accessible tumor site
- completed or have developed intolerance to a course of oxaliplatin- or
irinotecan-based frontline therapy at Screening
- on maintenance standard-of-care chemotherapies or on treatment holiday
- Eastern Cooperative Oncology Group (ECOG) 0 or 1
- adequate organ function
- progression of disease at the time of Enrollment
Exclusion Criteria:
- BRAF V600E mutation
- known allergy to both penicillin and sulfa drugs
- implanted devices that cannot be easily removed
- immunodeficiency, immune compromised state or receiving immunosuppressive therapy
We found this trial at
5
sites
Stanford, California 94304
Principal Investigator: George Fisher, MD, PhD
Phone: 650-724-2056
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Los Angeles, California 90095
310-825-4321
Principal Investigator: Zev A Wainberg, MD
Phone: 310-582-4069
University of California at Los Angeles The University of California, Los Angeles (UCLA) is an...
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7777 Forest Lane
Dallas, Texas 75230
Dallas, Texas 75230
Principal Investigator: James F Strauss, MD
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1500 East Duarte Road
Duarte, California 91010
Duarte, California 91010
626-256-HOPE (4673)
Principal Investigator: Marwan G Fakih, MD
Phone: 626-218-7073
City of Hope National Medical Center City of Hope is dedicated to making a difference...
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Sacramento, California 95817
Principal Investigator: May T. Cho, MD
Phone: 916-734-3089
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