Survodutide once weekly for the treatment of adults with obesity (Registro nro. 22855)

000 -Cabecera
Campo de control interno 03306nam a2200289 4500
001 - Número de control
control field ESSALUD
005 - Fecha y hora de la última transacción
Campo de control 20260821125939.0
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 Le Roux, Carel W.
Rol del Autor Autor
9 (RLIN) 54269
245 ## - Titulo
Titulo Survodutide once weekly for the treatment of adults with obesity
300 ## - Páginas
Paginación páginas: 776-787
520 ## - Resumen
Resumen Background: Although medications with glucagon-like peptide-1 (GLP-1) receptor agonist activity have transformed the management of obesity and shown substantial cardiometabolic benefits, unmet needs remain. Survodutide, an investigational glucagon receptor–GLP-1 receptor dual agonist, led to substantial weight reduction in a phase 2 trial involving adults with obesity without diabetes. Methods: In this phase 3, double-blind trial, we randomly assigned adults with a body-mass index (BMI; the weight in kilograms divided by the square of the height in meters) of 30 or higher, or 27 or higher with at least one obesity-related complication (excluding diabetes), in a 1:1:1 ratio to receive once-weekly survodutide administered subcutaneously at a dose adjusted up to 3.6 mg or 6.0 mg or placebo, in addition to counseling for lifestyle modification. The two primary end points were the percent change in body weight and a reduction in body weight of at least 5% from baseline to week 76. The primary efficacy analysis was conducted according to the treatment-regimen estimand, which incorporates the effects of any early discontinuation of survodutide or placebo, the use of protocol-prohibited obesity medications, and a prolonged dose-escalation period. Results: Among 725 participants (241 in the 3.6-mg survodutide group, 242 in the 6.0-mg survodutide group, and 242 in the placebo group), the mean age was 47.1 years; 294 participants (40.6%) were men. At baseline, the mean BMI was 37.9, and the mean body weight was 108.8 kg. At week 76, the mean change in body weight from baseline according to the treatment-regimen estimand was –12.2% (95% confidence interval [CI], −13.6 to −10.8) in the 3.6-mg group, –13.0% (95% CI, −14.4 to −11.6) in the 6.0-mg group, and –5.4% (95% CI, −6.9 to −4.0) in the placebo group; 72.6%, 71.9% and 46.3% of the participants, respectively, had weight reduction of at least 5% (P<0.001 for all comparisons with placebo). The most common adverse events were gastrointestinal symptoms (typically mild to moderate), which occurred in 80.9% of the participants in the 3.6-mg group, in 89.7% of those in the 6.0-mg group, and in 47.9% of those in the placebo group. No deaths were reported. Conclusions: Survodutide led to significantly greater reductions in body weight than placebo in adults with obesity without diabetes.
650 ## - Temas - Descriptores
Temas - Descriptores CARDIOLOGÍA GENERAL
9 (RLIN) 53638
650 ## - Temas - Descriptores
Temas - Descriptores MEDICINA CLÍNICA GENERAL
9 (RLIN) 53666
650 ## - Temas - Descriptores
Temas - Descriptores ENDOCRINOLOGÍA GENERAL
9 (RLIN) 54270
650 ## - Temas - Descriptores
Temas - Descriptores HIPERTENSIÓN
650 ## - Temas - Descriptores
Temas - Descriptores OBESIDAD
9 (RLIN) 1238
700 ## - Autor Personal
Autor Personal Wharton, Sean
9 (RLIN) 54271
700 ## - Autor Personal
Autor Personal Startseva, Elena
9 (RLIN) 54272
700 ## - Autor Personal
Autor Personal Kloer, Isabel M.
9 (RLIN) 54273
700 ## - Autor Personal
Autor Personal Ajaz Hussain, Samina
9 (RLIN) 54274
773 0# - Revista (Relacion con el numero)
Host Biblionumber 22717
Host Itemnumber 22650
Ciudad, Editorial Massachusetts NEJM Group
Codigo barras item/ejemplar NEJM12
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 2026-08-21
Catalogador sqb

No hay ítems disponibles.