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Clinical Trial Summary

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 Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03489525
Study type Interventional
Source MedImmune LLC
Contact
Status Completed
Phase Phase 1
Start date May 8, 2018
Completion date March 21, 2022

See also
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