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Brief Title: A Study of Combination Therapies With Viagenpumatucel-L (HS-110) in Patients With Non-Small Cell Lung Cancer
Official Title: A Phase 1b/2 Study of Viagenpumatucel-L (HS-110) in Combination With Multiple Treatment Regimens in Patients With Non-Small Cell Lung Cancer (The "DURGA" Trial)
Study ID: NCT02439450
Brief Summary: This study will test whether vaccination with viagenpumatucel-L combined with strategies to modulate the immune response is safe for patients with non-small cell lung adenocarcinoma or squamous cell carcinoma for incurable or metastatic disease.
Detailed Description: This study will test whether vaccination with viagenpumatucel-L combined with strategies to modulate the immune response is safe for patients with non-small cell lung adenocarcinoma or squamous cell carcinoma for incurable or metastatic disease. These methods collectively use the body's immune system to target the patient's own tumor. Immunosuppression hinders that response, and may develop in NSCLC patients in a variety of ways, such as activation of checkpoint pathways in the tumor microenvironment. Drugs that disrupt checkpoint molecule signaling like anti-PD-1 monoclonal antibodies nivolumab, may release this brake on the immune system. Tumor expression of PD-L1 plays an important role in patient response to checkpoint inhibitors; in general, clinical response to checkpoint inhibitors requires tumor expression of PD-L1 and presence of Tumor Infiltrating Lymphocytes (TIL). Combining viagenpumatucel-L with anti-PD-1 agents may enhance the vaccine's anti-tumor activity while prolonging or increasing the efficacy of the checkpoint inhibitor.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
University of Arizona Cancer Center, Tucson, Arizona, United States
UC San Diego, La Jolla, California, United States
BRRH Lynn Cancer Institute, Boca Raton, Florida, United States
Memorial Cancer Institute, Pembroke Pines, Florida, United States
Horizon Oncology Research, Lafayette, Indiana, United States
Ashland-Bellefonte Cancer Center, Ashland, Kentucky, United States
Baptist Health Louisville, Louisville, Kentucky, United States
Washington University School of Medicine, Saint Louis, Missouri, United States
New York Oncology Hematology, Albany, New York, United States
Winthrop Hospital, Mineola, New York, United States
Oncology Hematology Care, Inc., Cincinnati, Ohio, United States
Cleveland Clinic, Cleveland, Ohio, United States
Providence Portland Medical Center, Portland, Oregon, United States
University of Pennsylvania, Philadelphia, Pennsylvania, United States
Rhode Island Hospital, Providence, Rhode Island, United States
Virginia Cancer Specialists, Fairfax, Virginia, United States
Name: Daniel Morgensztern, MD
Affiliation: Washington University School of Medicine in St. Louis
Role: PRINCIPAL_INVESTIGATOR