Phase 3 results of bepirovirsen treatment for chronic hepatitis B virus infection (Registro nro. 22757)

000 -Cabecera
Campo de control interno 02883nam a2200289 4500
001 - Número de control
control field ESSALUD
005 - Fecha y hora de la última transacción
Campo de control 20260804185551.0
007 - Tipo material - Descripcion fisica - info general
Tipo material - Descripcion fisica - info general ta
008 - Elementos de Longitud Fija - Información General
Elementos de Longitud Fija - Información t pe ||||| |||| 00| 0 spa d
040 ## - Origen de la Catalogación
Origen de la Catalogación BMG
041 ## - Idioma
Idioma eng
100 ## - Autor
Autor Hou, Jinlin
Rol del Autor Autor
9 (RLIN) 53847
245 ## - Titulo
Titulo Phase 3 results of bepirovirsen treatment for chronic hepatitis B virus infection
300 ## - Páginas
Paginación páginas: 2395-2406
520 ## - Resumen
Resumen Background: Treatment with bepirovirsen, an antisense oligonucleotide targeting hepatitis B virus (HBV) transcripts, has the potential to result in a functional cure, defined by at least 24 weeks of a sustained HBV DNA level below the lower limit of quantification (LLOQ) and hepatitis B surface antigen (HBsAg) loss after fixed-duration therapy.<br/>Methods: In two replicate, double-blind trials (B-Well 1 and B-Well 2), we randomly assigned adults with noncirrhotic chronic HBV infection in a 2:1 ratio to receive subcutaneous bepirovirsen (at a weekly dose of 300 mg) or placebo for 24 weeks. All the patients were receiving stable nucleoside or nucleotide analogue (NA) therapy and had an HBsAg level of more than 100 to 3000 IU per milliliter. Eligible patients discontinued NA therapy at 48 weeks. The primary outcome was a functional cure at week 72.<br/>Results: The percentage of patients with a functional cure at week 72 was significantly higher with bepirovirsen than with placebo both in the B-Well 1 trial (in 127 of 650 patients [20%] vs. none of 328 patients) and in the B-Well 2 trial (in 106 of 570 patients [19%] vs. none of 286 patients). In a pooled analysis at 72 weeks, adverse events were reported in 91% of the patients in the bepirovirsen groups and in 73% of those in the placebo groups; serious adverse events were reported in 7% and 4% of the patients, respectively. During the treatment period, adverse events of grade 3 or higher were reported in 16% of the patients who received bepirovirsen and in 3% of those who received placebo; increases in the alanine aminotransferase level were the most common grade 3 adverse events with bepirovirsen (in 6% of the patients).<br/>Conclusions: In two phase 3 trials involving patients with chronic HBV infection, a functional cure after the discontinuation of NA therapy was reported in significantly more patients treated with bepirovirsen than in those who received placebo.
650 ## - Temas - Descriptores
Temas - Descriptores GASTROENTEROLOGÍA
9 (RLIN) 12562
650 ## - Temas - Descriptores
Temas - Descriptores ENFERMEDADES INFECCIOSAS
9 (RLIN) 6776
650 ## - Temas - Descriptores
Temas - Descriptores ENFERMEDAD HEPÁTICA
9 (RLIN) 53848
650 ## - Temas - Descriptores
Temas - Descriptores INFECCIONES VIRALES
9 (RLIN) 53766
700 ## - Autor Personal
Autor Personal Lim, Seng-Gee
9 (RLIN) 53849
700 ## - Autor Personal
Autor Personal Buti, Maria
9 (RLIN) 53850
700 ## - Autor Personal
Autor Personal Man-Fung ,Yuen
9 (RLIN) 53851
700 ## - Autor Personal
Autor Personal Gane, Edward
9 (RLIN) 53852
700 ## - Autor Personal
Autor Personal Lampertico, Pietro
9 (RLIN) 53853
773 0# - Revista (Relacion con el numero)
Host Biblionumber 22717
Host Itemnumber 22639
Ciudad, Editorial Massachusetts NEJM Group
Codigo barras item/ejemplar NEJM006
Titulo de la Revista The New England Journal of Medicine
Número de control de registro ESSALUD
ISSN 0028-4793
942 ## - Elementos de Koha
Tipo de Documento Artículos
Fecha procesamiento 2026-07-31
Catalogador SQB

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