Your browser doesn't support javascript.
loading
Characterisation of the safety profile of evobrutinib in over 1000 patients from phase II clinical trials in multiple sclerosis, rheumatoid arthritis and systemic lupus erythematosus: an integrated safety analysis.
Montalban, Xavier; Wallace, Daniel; Genovese, Mark C; Tomic, Davorka; Parsons-Rich, Dana; Le Bolay, Claire; Kao, Amy H; Guehring, Hans.
Afiliación
  • Montalban X; Department of Neurology-Neuroimmunology, Centre d'Esclerosi Múltiple de Catalunya (Cemcat), Vall d'Hebron University Hospital, Barcelona, Spain xavier.montalban@cem-cat.org.
  • Wallace D; Cedars-Sinai Medical Center, David Geffen School of Medicine, University of California, Los Angeles, California, USA.
  • Genovese MC; Division of Immunology and Rheumatology, Stanford University, Palo Alto, California, USA.
  • Tomic D; Global Clinical Development, Ares Trading SA, Eysins, Switzerland, an affiliate of Merck KGaA.
  • Parsons-Rich D; Global Clinical Development, EMD Serono Research & Development Institute, Inc, Billerica, Massachusetts, USA, an affiliate of Merck KGaA (affiliation at the time the research was conducted).
  • Le Bolay C; ECD-Early Clinical Development, Pfizer, Cambridge, Massachusetts, USA.
  • Kao AH; Biostatistics, Merck Healthcare KGaA, Darmstadt, Germany.
  • Guehring H; Translational Innovation Platform in Immunology & Neuroscience, EMD Serono Research & Development Institute, Inc, Billerica, Massachusetts, USA, an affiliate of Merck KGaA.
J Neurol Neurosurg Psychiatry ; 94(1): 1-9, 2023 01.
Article en En | MEDLINE | ID: mdl-36418156
OBJECTIVE: Analyse the integrated safety profile of evobrutinib, a Bruton's tyrosine kinase inhibitor (BTKi), using pooled data from multiple sclerosis (MS), rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE) trials. METHODS: Phase II, randomised, double-blind, placebo-controlled trial data were analysed (N=1083; MS: n=213, 48 weeks (W); RA: n=390, 12W; SLE: n=480, 52W). The analysis included all patients who received ≥1 dose of evobrutinib (25 mg or 75 mg once daily, or 50 mg or 75 mgtwice daily) or placebo. Descriptive statistics and exposure-adjusted incidence rates (EAIR) were used to report treatment-emergent adverse events (TEAEs). RESULTS: Data from 1083 patients were pooled: evobrutinib, n=861; placebo, n=271 (sum >1083 due to MS trial design: n=49 received both placebo (W0-24) and evobrutinib 25 mg (W25-48)); median follow-up time (pt-years): evobrutinib, 0.501; placebo, 0.463. Across indications, the proportion of patients with TEAEs and the EAIR were similar for evobrutinib and placebo (66.2% (247.6 events/100 pt-years) vs 62.4% (261.4 events/100 pt-years)). By indication, the EAIR (events/100 pt-years) of TEAEs for evobrutinib versus placebo were: MS: 119.7 vs 148.3; RA: 331.8 vs 306.8; SLE: 343.0 vs 302.1. Two fatal events occurred (in SLE). The serious infections EAIR was 2.7 and 2.1 events/100 pt-years for evobrutinib and placebo. For previously reported BTKi-class effects, the EAIR of transient elevated alanine aminotransferase/aspartate aminotransferase TEAEs (events/100 pt-years) with evobrutinib versus placebo was 4.8 vs 2.8/3.5 vs 0.7, respectively. IgG levels were similar in evobrutinib/placebo-treated patients. CONCLUSIONS: This is the first BTKi-integrated safety analysis that includes patients with MS. Overall, evobrutinib treatment (all doses) was generally well tolerated across indications. TRIAL REGISTRATION NUMBERS: NCT02975349, NCT03233230, NCT02975336.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Artritis Reumatoide / Lupus Eritematoso Sistémico / Esclerosis Múltiple Tipo de estudio: Clinical_trials Límite: Humans Idioma: En Revista: J Neurol Neurosurg Psychiatry Año: 2023 Tipo del documento: Article País de afiliación: España Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Artritis Reumatoide / Lupus Eritematoso Sistémico / Esclerosis Múltiple Tipo de estudio: Clinical_trials Límite: Humans Idioma: En Revista: J Neurol Neurosurg Psychiatry Año: 2023 Tipo del documento: Article País de afiliación: España Pais de publicación: Reino Unido