<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>2(4)</volume><submitter>Aribi A</submitter><pubmed_abstract>IO-202 is a humanized immunoglobulin G1 monoclonal antibody with high affinity and specificity for leukocyte immunoglobulin-like receptor B4 (LILRB4; ILT3), which is predominantly expressed in monocytes and monocytic blasts. IO-202 induces antibody-dependent cellular cytotoxicity and antibody-dependent cellular phagocytosis in vitro and in patients with leukemia. Herein, we present the phase 1a dose escalation data of IO-202 as monotherapy and in combination with azacitidine (AZA) in patients with relapsed/refractory (R/R) acute myeloid leukemia (AML) and R/R chronic myelomonocytic leukemia (CMML), and the phase 1b dose expansion data of IO-202 combined with AZA for the treatment of hypomethylating agent (HMA)-naïve CMML. IO-202 was well tolerated as monotherapy and in combination with AZA</pubmed_abstract><journal>Blood neoplasia</journal><pagination>100126</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12409809</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A phase 1 study of IO-202, an anti-LILRB4 antibody, in chronic myelomonocytic leukemia and acute myeloid leukemia.</pubmed_title><pmcid>PMC12409809</pmcid><pubmed_authors>Liu H</pubmed_authors><pubmed_authors>Madanat YF</pubmed_authors><pubmed_authors>Xiang H</pubmed_authors><pubmed_authors>Klencke B</pubmed_authors><pubmed_authors>Mannis GN</pubmed_authors><pubmed_authors>Jonas BA</pubmed_authors><pubmed_authors>Roboz GJ</pubmed_authors><pubmed_authors>Garcia-Manero G</pubmed_authors><pubmed_authors>Liao XC</pubmed_authors><pubmed_authors>Blum W</pubmed_authors><pubmed_authors>Pollyea DA</pubmed_authors><pubmed_authors>Aribi A</pubmed_authors><pubmed_authors>Huang T</pubmed_authors><pubmed_authors>DiNardo CD</pubmed_authors><pubmed_authors>Carraway HE</pubmed_authors><pubmed_authors>Saultz JN</pubmed_authors><pubmed_authors>Schiller G</pubmed_authors><pubmed_authors>Jeyakumar D</pubmed_authors><pubmed_authors>Woodard P</pubmed_authors><pubmed_authors>Dunavin N</pubmed_authors></additional><is_claimable>false</is_claimable><name>A phase 1 study of IO-202, an anti-LILRB4 antibody, in chronic myelomonocytic leukemia and acute myeloid leukemia.</name><description>IO-202 is a humanized immunoglobulin G1 monoclonal antibody with high affinity and specificity for leukocyte immunoglobulin-like receptor B4 (LILRB4; ILT3), which is predominantly expressed in monocytes and monocytic blasts. IO-202 induces antibody-dependent cellular cytotoxicity and antibody-dependent cellular phagocytosis in vitro and in patients with leukemia. Herein, we present the phase 1a dose escalation data of IO-202 as monotherapy and in combination with azacitidine (AZA) in patients with relapsed/refractory (R/R) acute myeloid leukemia (AML) and R/R chronic myelomonocytic leukemia (CMML), and the phase 1b dose expansion data of IO-202 combined with AZA for the treatment of hypomethylating agent (HMA)-naïve CMML. IO-202 was well tolerated as monotherapy and in combination with AZA</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Nov</publication><modification>2026-06-02T05:22:03.296Z</modification><creation>2026-04-14T03:13:47.119Z</creation></dates><accession>S-EPMC12409809</accession><cross_references><pubmed>40919482</pubmed><doi>10.1016/j.bneo.2025.100126</doi></cross_references></HashMap>