{ "abstract": "Background: Warm autoimmune hemolytic anemia (wAIHA) is a rare, potentially life-threatening disease characterized by autoantibody (typically IgG)-mediated premature destruction of red blood cells (RBCs). Nipocalimab is a fully human monoclonal antibody that binds FcRn with high specificity and affinity to block the IgG-recycling pathway, thus lowering total IgG (including pathogenic anti-RBC IgG autoantibodies) without impacting other key humoral and cellular immune functions. Aim: This analysis characterized the pharmacodynamic (PD) effect of nipocalimab on total IgG and anti-RBC IgG and the correlation with the change in hemoglobin (Hgb) and hemolytic markers during the 24-week double blind (DB) period of the phase 2/3 ENERGY trial (ClinicalTrials.gov Identifier: NCT04119050). Methods: Adults with wAIHA (Hgb <10 g/dL, laboratory evidence of hemolysis, and positive direct antiglobulin test) who received ≥1 prior therapy and consented to participate were randomized 1:1:1 to intravenous nipocalimab 30 mg/kg q4w, 15 mg/kg q2w, or placebo. Serum total IgG and anti-RBC IgG levels were measured in the DB period, and percent change from baseline was determined at all timepoints with available samples. Total IgG was measured with an immunonephelometric assay at a central lab. A semiquantitative multiplex flow cytometry based-assay was used to measure binding of anti-RBC IgG at 37oC to 12 reference RBC populations (representing warm autoantibodies pathogenic in wAIHA). The median percent change values for all positive reference RBC types were used to represent the overall percent change in anti-RBC IgG. Spearman correlations of change in total and anti-RBC IgG levels with changes in Hgb and hemolytic markers (ie, reticulocyte counts, indirect bilirubin) were determined. Results: Of the 118 patients in the ENERGY trial, 114 were included in the total IgG analysis (38, 37, and 39 in nipocalimab 30 mg/kg q4w, 15 mg/kg q2w, and placebo groups, respectively) and 89 were included in the anti-RBC IgG analysis (30, 31, and 28 in nipocalimab 30 mg/kg q4w, 15 mg/kg q2w, and placebo groups, respectively) based on patient consent and sample availability. Baseline clinical characteristics for individuals in the PD analysis set were similar between treatment groups and to those of the overall study population. Rapid and persistent reduction in total IgG was observed from Week 1 (W1) through W24 in the nipocalimab groups. Similarly, rapid and persistent reduction in anti-RBC IgG was observed in nipocalimab treatment groups, with consistent trends across the 12 reference RBC types. The median overall reduction in anti-RBC IgG was 41% and 35% at W1 and 23% and 16% at W24 for the 30 mg/kg q4w and 15 mg/kg q2w groups, respectively. Correlations were observed between total IgG reduction and Hgb improvement (R=-0.22; p<0.0001) as well as anti-RBC IgG reduction and Hgb improvement (R=-0.33, p<0.0001). In addition, anti-RBC IgG reduction was correlated with improvement in hemolytic markers. Conclusion: Nipocalimab reduced both total IgG as well as pathogenic anti-RBC IgG autoantibodies in wAIHA, supporting its mechanism of action as an FcRn blocker. A correlation was observed between anti-RBC IgG reduction and improvement in disease biomarkers, most notably increase in Hgb, consistent with nipocalimab targeting autoantibody-mediated disease mechanisms in wAIHA.", "abstract_shown": true, "affiliations": [ "Hematology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico; Department of Oncology and Hemato-Oncology, University of Milan, Milan, Italy", "Albert Einstein College of Medicine/Montefiore Medical Center, Bronx, NY, United States", "4The University of Osaka, Suita, Osaka, Japan", "Department of Hematology and Amsterdam Institute for Infection and Immunity, Amsterdam UMC, University of Amsterdam; Department of Immunohematology Diagnostics, Sanquin Diagnostics Services, Amsterdam, Netherlands", "Johnson & Johnson, Cambridge, MA, United States", "Johnson & Johnson, Spring House, PA, United States", "Sanquin Research and Landsteiner Laboratory, Amsterdam UMC, University of Amsterdam, Amsterdam, Netherlands", "Hospital das Clínicas da Universidade Federal de Goias (HC UFG), Goiania, GO, Brazil" ], "article_type": null, "arxiv": null, "author_total": 16, "authors": [ { "affs": [ 0 ], "name": "Bruno FATTIZZO" }, { "affs": [ 1 ], "name": "Irina MURAKHOVSKAYA" }, { "affs": [ 2 ], "name": "Yasutaka UEDA" }, { "affs": [ 3 ], "name": "Josephine M I VOS" }, { "affs": [ 4 ], "name": "Eugene MYSHKIN" }, { "affs": [ 5 ], "name": "Vani LAKSHMINARAYANAN" }, { "affs": [ 5 ], "name": "Kristen BROWN" }, { "affs": [ 4 ], "name": "Leona E LING" }, { "affs": [ 6 ], "name": "Emile VAN DEN AKKER" }, { "affs": [ 6 ], "name": "Kerly FU" }, { "affs": [ 5 ], "name": "Cathye SHU" }, { "affs": [ 5 ], "name": "Kristen SWEET" }, { "affs": [ 4 ], "name": "Carolyn A CUFF" }, { "affs": [ 5 ], "name": "Sheng GAO" }, { "affs": [ 5 ], "name": "Marcia T SANTOS" }, { "affs": [ 7 ], "name": "Renato S TAVARES" } ], "bibtex": "https://research.draconitic.com/paper/3xvkrgg4r1bdz.bib", "cited_by": 0, "doi": "10.1016/j.htct.2026.106690", "fulltext_url": "http://www.sciencedirect.com/science/article/pii/S2531137926004372", "id": "3xvkrgg4r1bdz", "issns": [ "2531-1379", "2531-1387" ], "landing_url": "https://doi.org/10.1016/j.htct.2026.106690", "language": "en", "licence": "CC-BY", "licence_label": "CC BY", "licence_source": "journal", "licence_url": "https://creativecommons.org/licenses/by/4.0/", "metadata_licence": null, "native_subjects": [ [ "lcc", "RC633-647.5" ], [ "openalex", "2720|Blood groups and transfusion" ] ], "openalex": "W7223128897", "pdf_url": null, "pmcid": null, "pmid": null, "published": "2026-10-23", "publisher": "Elsevier", "ris": "https://research.draconitic.com/paper/3xvkrgg4r1bdz.ris", "sources": [ { "first_seen": "2026-10-30T12:17:23Z", "native_id": "0efa44892f1c4ff390288704b370ed47", "source": "doaj", "url": "https://doi.org/10.1016/j.htct.2026.106690" } ], "subjects": [ { "field": "medicine", "origin": "lcc:RC633-647.5", "subfield": "endocrinology-metabolism" } ], "title": "PHARMACODYNAMIC EFFECT OF NIPOCALIMAB IN WARM AUTOIMMUNE HEMOLYTIC ANEMIA (WAIHA) AND CORRELATION WITH CLINICAL IMPROVEMENT", "title_text": "PHARMACODYNAMIC EFFECT OF NIPOCALIMAB IN WARM AUTOIMMUNE HEMOLYTIC ANEMIA (WAIHA) AND CORRELATION WITH CLINICAL IMPROVEMENT", "type": "peer-reviewed", "updated_at": "2026-10-30T13:43:18Z", "url": "https://research.draconitic.com/paper/3xvkrgg4r1bdz", "venue": "Hematology, Transfusion and Cell Therapy", "versions": [] }