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Spots Global Cancer Trial Database for A Study of Combination Therapies With Viagenpumatucel-L (HS-110) in Patients With Non-Small Cell Lung Cancer

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We do not endorse or review these studies in any way.

Trial Identification

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

Study Description

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.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

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

Contact Details

Name: Daniel Morgensztern, MD

Affiliation: Washington University School of Medicine in St. Louis

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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