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1.
Allergy Asthma Proc ; 45(4): 232-239, 2024 Jul 01.
Artículo en Inglés | MEDLINE | ID: mdl-38760164

RESUMEN

Background: The clinical development program of the SQ grass, ragweed, tree, and house dust mite (HDM) sublingual immunotherapy (SLIT)-tablets for allergic rhinitis/conjunctivitis (AR/C) included clinical trials conducted in North America, Europe, and Japan. Objective: Data from these trials were analyzed to assess efficacy, immunologic mechanisms, and safety outcomes across allergens and geographic regions. Methods: Thirteen phase III, double-blind, placebo controlled trials in the subjects with AR/C were conducted in North America, Europe (including Russia), and Japan (N = 7763 analyzed). Trials were generally similar with respect to medical practice, target population, eligibility criteria, and efficacy and safety monitoring. Data were analyzed for the approved doses in North America and Europe. Four statistical models were used to enhance comparison of the efficacy end points among the trials. Results: The SLIT-tablets demonstrated consistent efficacy across allergens and regions, regardless of the statistical analysis used. Relative improvement in the primary efficacy end point compared with placebo by using the predefined protocol analysis ranged from 17.9% to 32.8%, 17.5% to 19.3%, 20.6% to 38.3%, and 39.6% with the grass, HDM, ragweed, and tree SLIT-tablets, respectively. The kinetics of specific immunoglobulin E (IgE) and IgG4 responses were similar among the allergens and regions. Local application-site reactions were the most common adverse events for all allergens and in all regions. Most treatment-related adverse events for all allergens and in all regions were mild in severity. The rate of systemic allergic reactions was similar across regions (0%-0.54%). Conclusion: Confirmatory phase III trials for SLIT-tablets in the treatment of AR/C showed consistent efficacy, immunologic, and safety outcomes across allergens and geographic regions.


Asunto(s)
Alérgenos , Inmunoterapia Sublingual , Humanos , Inmunoterapia Sublingual/métodos , Inmunoterapia Sublingual/efectos adversos , Alérgenos/inmunología , Alérgenos/administración & dosificación , Resultado del Tratamiento , Rinitis Alérgica/terapia , Rinitis Alérgica/inmunología , Conjuntivitis Alérgica/terapia , Conjuntivitis Alérgica/inmunología , Comprimidos , Europa (Continente) , Método Doble Ciego , Animales , América del Norte , Adulto , Masculino , Femenino , Japón , Ensayos Clínicos Fase III como Asunto , Niño , Adolescente
2.
Ugeskr Laeger ; 185(1)2023 01 02.
Artículo en Danés | MEDLINE | ID: mdl-36629290

RESUMEN

Anorexia nervosa (AN) is a mental disorder with the greatest incidence amongst women of the childbearing age. The prevalence of AN in pregnancy is marginal, yet the risk of exacerbation or reactivation is significant. Adverse perinatal complications of mental and physical nature pertain to both mother and child and through early diagnosis and monitoring during the perinatal period manageable. This preview describes the importance of enabling optimal perinatal care through a multidisciplinary management team.


Asunto(s)
Anorexia Nerviosa , Complicaciones del Embarazo , Trastornos Psicóticos , Femenino , Humanos , Embarazo , Madres , Periodo Posparto , Complicaciones del Embarazo/etiología , Prevalencia , Trastornos Psicóticos/complicaciones
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