Last updated on April 2018

Safety and Efficacy of MEDI0457 and Durvalumab in Patients With HPV Associated Recurrent/Metastatic Head and Neck Cancer


Brief description of study

This is a Phase 1b/2a, open-label, multi-center study to evaluate the safety and tolerability, anti-tumor activity, and immunogenicity of MEDI0457 (also known as INO 3112) a HPV DNA vaccine in combination with durvalumab (also known as MEDI4736) which is a human monoclonal antibody directed against PD-L1, which blocks the interaction of PD-L1 with PD-1 and CD80.

An initial three to 12 patients (Safety Analysis Run-in patients) will be enrolled and assessed for safety before additional patients are enrolled.

The initial safety analysis run-in patients along with an approximate total of 50 patients with human papilloma virus associated recurrent or metastatic head and neck squamous cell cancer will be enrolled in this study and evaluated also for anti-tumor efficacy to MEDI0457 in combination with durvalumab.

Clinical Study Identifier: NCT03162224

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AstraZeneca Clinical Study Information Center

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Atlanta, GA United States
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Philadelphia, PA United States
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Detroit, MI United States
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Bronx, NY United States
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Winston-Salem, NC United States
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Chicago, IL United States
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Indianapolis, IN United States
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Baltimore, MD United States
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Creve Coeur, MO United States
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AstraZeneca Clinical Study Information Center

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Saint Louis, MO United States
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AstraZeneca Clinical Study Information Center

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Saint Peters, MO United States
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AstraZeneca Clinical Study Information Center

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Morristown, NJ United States
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AstraZeneca Clinical Study Information Center

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Summit, NJ United States
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