B cell depletion and BAFF receptor blockade with ianalumab (VAY736) for the treatment of moderate-to-severe systemic lupus erythematosus: a phase 2 randomised, double-blind, placebo-controlled trial with subsequent open-label treatment

dc.contributor.authorAgmon-Levin N.
dc.contributor.authorIgnatenko S.
dc.contributor.authorGordienko A.
dc.contributor.authorCortés-Hernández J.
dc.contributor.authorNarongroeknawin P.
dc.contributor.authorRomanowska-Próchnicka K.
dc.contributor.authorShen N.
dc.contributor.authorCiferská H.
dc.contributor.authorKodera M.
dc.contributor.authorCheng-Chung W.J.
dc.contributor.authorLeszczynski P.
dc.contributor.authorLan J.L.
dc.contributor.authorMysler E.
dc.contributor.authorWojciechowski R.
dc.contributor.authorTarr T.
dc.contributor.authorVishneva E.
dc.contributor.authorChen Y.H.
dc.contributor.authorKaneko Y.
dc.contributor.authorFinzel S.
dc.contributor.authorHoi A.
dc.contributor.authorOkada M.
dc.contributor.authorKoolvisoot A.
dc.contributor.authorLee S.S.
dc.contributor.authorLie D.
dc.contributor.authorKaneko H.
dc.contributor.authorRojkovich B.
dc.contributor.authorSun L.
dc.contributor.authorZotkin E.
dc.contributor.authorViallard J.F.
dc.contributor.authorLópez B.P.M.
dc.contributor.authorGhanshani S.A.
dc.contributor.authorLau C.
dc.contributor.authorAvrameas A.
dc.contributor.authorSips C.
dc.contributor.authorOliver S.J.
dc.contributor.correspondenceAgmon-Levin N.
dc.contributor.otherMahidol University
dc.date.accessioned2025-12-27T18:19:39Z
dc.date.available2025-12-27T18:19:39Z
dc.date.issued2025-01-01
dc.description.abstractObjectives: B cell depletion or B cell activating factor (BAFF) blockade has shown benefits in systemic lupus erythematosus (SLE). We compared ianalumab, a monoclonal antibody targeting BAFF receptor (BAFF-R)-expressing B cells to lyse B cells and block BAFF-R, with placebo for SLE treatment combined with standard therapies. Methods: Patients with active SLE were randomised (1:1) to monthly subcutaneous ianalumab 300 mg or placebo. The primary outcome was a composite of SLE Responder Index (SRI)-4 at week 28 in patients successfully achieving corticosteroid (CS) tapering criteria. Patients subsequently received open-label (OL) ianalumab until week 48, followed by exploratory assessments at week 52 and off-treatment to week 68. Safety monitoring continued until B cell recovery. This report describes interim analyses conducted on the week 68 dataset. Results: Sixty-seven patients were randomised and received blinded treatments until week 28. The primary composite endpoint was more frequently achieved with ianalumab vs placebo: 15/34 (44.1%) vs 3/33 (9.1%), with responses sustained to week 52 and replicated by placebo transitioned to OL ianalumab: 15/33 (45.5%) and 13/32 (40.6%). Positive treatment effects were consistently observed across other lupus disease activity outcomes (SRI-6, Definition of Remission in SLE, Lupus Low Disease Activity State, flare reduction, and CS use) at week 28, with clinical benefits until weeks 52 and 68. Ianalumab was not associated with increased serious adverse events or serious infections. Nonserious local injection site reactions occurred more frequently with ianalumab. Conclusions: At week 28, reduced disease activity was observed in patients with SLE receiving ianalumab plus standard therapies compared with those receiving standard therapies alone, with sustained benefits with further treatment until 1 year, which was well tolerated.
dc.identifier.citationAnnals of the Rheumatic Diseases (2025)
dc.identifier.doi10.1016/j.ard.2025.11.015
dc.identifier.eissn14682060
dc.identifier.issn00034967
dc.identifier.pmid41353079
dc.identifier.scopus2-s2.0-105025241510
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/113678
dc.rights.holderSCOPUS
dc.subjectBiochemistry, Genetics and Molecular Biology
dc.subjectMedicine
dc.subjectImmunology and Microbiology
dc.titleB cell depletion and BAFF receptor blockade with ianalumab (VAY736) for the treatment of moderate-to-severe systemic lupus erythematosus: a phase 2 randomised, double-blind, placebo-controlled trial with subsequent open-label treatment
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105025241510&origin=inward
oaire.citation.titleAnnals of the Rheumatic Diseases
oairecerif.author.affiliationMonash University
oairecerif.author.affiliationSun Yat-Sen University
oairecerif.author.affiliationTel Aviv University
oairecerif.author.affiliationCharles University
oairecerif.author.affiliationCharité – Universitätsmedizin Berlin
oairecerif.author.affiliationUniversitätsklinikum Freiburg
oairecerif.author.affiliationChina Medical University
oairecerif.author.affiliationMedical University of Warsaw
oairecerif.author.affiliationSemmelweis Egyetem
oairecerif.author.affiliationHospital Universitari Vall d'Hebron
oairecerif.author.affiliationNovartis International AG
oairecerif.author.affiliationChina Medical University Hospital
oairecerif.author.affiliationPoznan University of Medical Sciences
oairecerif.author.affiliationKeio University School of Medicine
oairecerif.author.affiliationMedical School of Nanjing University
oairecerif.author.affiliationHospital de La Santa Creu I Sant Pau
oairecerif.author.affiliationRenji Hospital
oairecerif.author.affiliationSiriraj Hospital
oairecerif.author.affiliationChung Shan Medical University Hospital
oairecerif.author.affiliationÁltalános Orvostudományi Kar
oairecerif.author.affiliationVeterans General Hospital-Taichung Taiwan
oairecerif.author.affiliationChonnam National University Medical School
oairecerif.author.affiliationHopital Haut-Lévêque C.H.U de Bordeaux
oairecerif.author.affiliationMilitary Medical Academy, Saint Petersburg
oairecerif.author.affiliationSt. Luke's International Hospital Tokyo
oairecerif.author.affiliationV.A. Nasonova Research Institute of Rheumatology
oairecerif.author.affiliationPhramongkutklao College of Medicine
oairecerif.author.affiliationJapan Community Healthcare Organization Chukyo Hospital
oairecerif.author.affiliationNovartis India Limited
oairecerif.author.affiliationOrganizacion Medica de Investigacion
oairecerif.author.affiliationUniversity Hospital No. 2
oairecerif.author.affiliationNational Centre for Global Health and Medicine
oairecerif.author.affiliationLLC Family Clinic

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