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Clinical Trial Summary

This is the first-in-human trial with BYON4413 to evaluate safety, PK, immunogenicity, and anti-leukemia activity of BYON4413 in patients with AML or MDS.


Clinical Trial Description

This trial includes two parts. Part 1 is a dose escalation study in which the maximum tolerated dose and recommended dose for expansion of BYON4413 will be determined. Part 2 is an expansion study to evaluate the anti-leukemia activity and safety of BYON4413. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06359002
Study type Interventional
Source Byondis B.V.
Contact Glenn van Wigcheren
Phone +31 24 679 5100
Email clinicaltrials@byondis.com
Status Not yet recruiting
Phase Phase 1
Start date May 2024
Completion date March 2027