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Clinical Trial Summary

To assess safety and tolerability at increasing dose levels of IO-202 in successive cohorts of participants with AML with monocytic differentiation and CMML in order to estimate the maximum tolerated dose (MTD) or maximum administered dose (MAD) and select the recommended Phase 2 dose (RP2D)


Clinical Trial Description

This is a Phase 1, Multicenter, Open-Label, Dose-Escalation and Expansion, Safety, Pharmacokinetic, Pharmacodynamic, and Clinical Activity Study of Intravenously Administered IO-202 and IO-202 + Azacitidine ± Venetoclax in Acute Myeloid Leukemia (AML) Patients with Monocytic Differentiation and in Chronic Myelomonocytic Leukemia (CMML) Patients ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04372433
Study type Interventional
Source Immune-Onc Therapeutics
Contact Yasuhiro Tabata, MD, PhD
Phone 650-457-1741
Email yasuhiro.tabata@immuneonc.com
Status Recruiting
Phase Phase 1
Start date September 14, 2020
Completion date January 31, 2027

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