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Clinical Trial Summary

This is an open-label, multi-center, Phase 1/2 study to determine the MTD and assess the safety, tolerability, PK, immunogenicity, and anti-leukemia activity of IMGN632 when administered as monotherapy to patients with CD123+ disease.


Clinical Trial Description

IMGN632 is administered by IV on Day 1 of each cycle, with cycles repeating every 21 days. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03386513
Study type Interventional
Source ImmunoGen, Inc.
Contact
Status Active, not recruiting
Phase Phase 1/Phase 2
Start date January 2, 2018
Completion date December 2025

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