Last updated on June 2020

MEDI2228 in Subjects With Relapsed/Refractory Multiple Myeloma

Brief description of study

The purpose of this study is to assess the safety, pharmacokinetics and tolerability, describe the dose-limiting toxicities (DLTs), and determine the maximum tolerated dose (MTD) or maximum administered dose (MAD [in the absence of establishing the MTD]) for single agent MEDI2228 in adult subjects with multiple myeloma who are either transplant ineligible or post autologous stem cell transplant and are relapsed/refractory.

Clinical Study Identifier: NCT03489525

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Research Site

Melbourne, Australia
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Recruitment Status: Open

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