MEDI2228 in Subjects With Relapsed/Refractory Multiple Myeloma

Study Overview

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.

Study Description

A Phase 1, Open-label Study to Evaluate the Safety, Pharmacokinetics, Immunogenicity, and Preliminary Efficacy of MEDI2228 in Subjects with Relapsed/Refractory Multiple Myeloma

  • ClinicalTrials.gov Identifier: NCT03489525
  • Protocol Number: 18-165
  • Principal Investigator: Jacalyn Rosenblatt

Recruitment Status

Open

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