Last updated on September 2018

Study of OSE2101 Versus Standard Treatment as 2nd or 3rd Line in HLA-A2 Positive Patients With Advanced NSCLC After Failure of Immune Checkpoint Inhibitor


Brief description of study

The aim of this study is to determine if the Investigational Medicinal Product Tedopi (OSE2101) is more effective than standard treatment in treating patients with stage IIIB NSCLC unsuitable for radiotherapy or metastatic NSCLC in second- or third-line treatment after failure of immune checkpoint-inhibitor regimens.

Clinical Study Identifier: NCT02654587

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Gesinger Medical Center

Danville, PA United States
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CHU Montpellier

Montpellier, France
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Krajsk nemocnice Liberec

Liberec, Czech Republic
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Cancer Center at West Jefferson

New Orleans, LA United States
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Meridian Health

Neptune, NJ United States
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Gettysburg Cancer Center

Gettysburg, PA United States
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Millenium Oncology

Houston, TX United States
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Stephenson Cancer Center

Oklahoma City, OK United States
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Pontchartrain Cancer Center

Covington, LA United States
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Georgetown University Hospital

Washington, WA United States
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Pardubick krajsk nemocnice

Pardubice, Czech Republic
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CHU Grenoble

Grenoble, France
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Genesis Cancer Center

Hot Springs, AR United States
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Pennington Cancer Center

Baton Rouge, LA United States
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Matrai Gyogyint zet

Mátraháza, Hungary
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Recruitment Status: Open


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