CompletedNot applicableNCT04187768

Immunological Profile Changes In Patients With Advanced Non-Small Cell Lung Cancer

This is a blood collection study being conducted to better understand and describe the immunological blood profile changes in patients with advanced non small cell lung cancer undergoing treatment with checkpoint inhibitor therapy. Blood will be collected from healthy volunteers and patients with non small cell lung cancer

Checked against the public recordLast updated Jul 20, 2022 · Source: ClinicalTrials.gov

StatusCompleted
PhaseNot applicable
U.S. locations1
SponsorIndiana University
01
Study overview

What this study is about

Purpose
Not specified
Study type
Observational
Phase
Not applicable
Sponsor
Indiana University
Interventions being studied
Not specified
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

03
Public criteria

Who may be able to participate

Inclusion Criteria: 1. ≥ 18 years old at the time of informed consent 2. Written informed consent and HIPAA authorization for release of personal health information. 3. Subjects with histologically and radiographically confirmed NSCLC. 4. Subjects must have stage IV disease or recurrent disease. 5. Subjects should be treatment naïve (systemic therapies) or have received prior chemotherapy in the first line setting. Prior radiation or surgery is permissible. 6. Subjects who are eligible to receive single agent immunotherapy must have documentation of a PD-L1 Tumor Proportion Score (TPS) of at least 1%. 7. Subjects with Eastern Cooperative Oncology Group (ECOG) performance status of 0-2. Exclusion Criteria: 1. Subjects with curable or potentially curable NSCLC. 2. Subjects should not have contraindications to treatment with immune checkpoint inhibitors per standard criteria. 3. Patients with targetable mutations eligible for treatment with molecularly targeted small molecule inhibitor therapy. 4. Subjects eligible for combination treatment with chemoimmunotherapy.

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • Indiana University Melvin & Bren Simon Cancer CenterIndianapolis, Indiana

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Jul 20, 2022. Always confirm current availability with the study team.

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