Last updated on April 2017

A Study to Evaluate Escalating Doses of AGS62P1 Given as Monotherapy in Subjects With Acute Myeloid Leukemia (AML)


Brief description of study

The purpose of this study is to evaluate the safety and tolerability of AGS62P1 given at two dosing schedules (Schedule A, every three weeks [Q3W] or Schedule B, weekly), in subjects with acute myeloid leukemia (AML) and determine the maximum tolerated dose (MTD). In addition, this study will assess the pharmacokinetics (PK), the immunogenicity and the anti-leukemic activity of AGS62P1.

Clinical Study Identifier: NCT02864290

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Agensys Clinical Research and Development

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Duarte, CA United States
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Agensys Clinical Research and Development

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Baltimore, MD United States
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Agensys Clinical Research and Development

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New York, NY United States
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Agensys Clinical Research and Development

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Houston, TX United States
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