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Spots Global Cancer Trial Database for Personalizing Immune Checkpoint Inhibitor Therapy

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

Trial Identification

Brief Title: Personalizing Immune Checkpoint Inhibitor Therapy

Official Title: Personalizing Immune Checkpoint Inhibitor Therapy for Solid Tumors

Study ID: NCT03409341

Study Description

Brief Summary: This prospective, observational study will evaluate whether vitro testing of tumor tissue and white blood cells from patients with lung cancer who are being treated with immune checkpoint inhibitors and other standard of care approaches, predicts clinical response to these agents.

Detailed Description: Overall Goal: The long-term goal of this study is to predict whether checkpoint inhibitors will be effective in individual patients with solid tumors. Objectives: In this pilot study to be conducted in ten subjects with lung cancer who are to receive checkpoint inhibitors, we will use cellular and molecular techniques to characterize * tumor immunogenicity * anti-tumor T-cell response * effect of checkpoint inhibitors on antigen presentation and T-cell response, and * the tumor microenvironment Planned enrollment: • Ten subjects with lung cancer Methods for Informed Consent: Investigators will approach subjects for informed consent

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Holy Cross Hospital, Silver Spring, Maryland, United States

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

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