Your browser doesn't support javascript.
loading
Effects of vadadustat on hemoglobin concentrations in patients receiving hemodialysis previously treated with erythropoiesis-stimulating agents.
Haase, Volker H; Chertow, Glenn M; Block, Geoffrey A; Pergola, Pablo E; deGoma, Emil M; Khawaja, Zeeshan; Sharma, Amit; Maroni, Bradley J; McCullough, Peter A.
Afiliación
  • Haase VH; Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
  • Chertow GM; Stanford University School of Medicine, Palo Alto, CA, USA.
  • Block GA; Denver Nephrology, Denver, CO, USA.
  • Pergola PE; Renal Associates PA, San Antonio, TX, USA.
  • deGoma EM; Akebia Therapeutics Inc., Cambridge, MA, USA.
  • Khawaja Z; Akebia Therapeutics Inc., Cambridge, MA, USA.
  • Sharma A; Akebia Therapeutics Inc., Cambridge, MA, USA.
  • Maroni BJ; Akebia Therapeutics Inc., Cambridge, MA, USA.
  • McCullough PA; Baylor University Medical Center, Baylor Heart and Vascular Institute, Baylor Jack and Jane Hamilton Heart and Vascular Hospital, Dallas, TX, USA.
Nephrol Dial Transplant ; 34(1): 90-99, 2019 01 01.
Article en En | MEDLINE | ID: mdl-29672740
Background: Vadadustat, an inhibitor of hypoxia-inducible factor prolyl-4-hydroxylase domain dioxygenases, is an oral investigational agent in development for the treatment of anemia secondary to chronic kidney disease. Methods: In this open-label Phase 2 trial, vadadustat was evaluated in 94 subjects receiving hemodialysis, previously maintained on epoetin alfa. Subjects were sequentially assigned to one of three vadadustat dose cohorts by starting dose: 300 mg once daily (QD), 450 mg QD or 450 mg thrice weekly (TIW). The primary endpoint was mean hemoglobin (Hb) change from pre-baseline average to midtrial (Weeks 7-8) and end-of-trial (Weeks 15-16) and was analyzed using available data (no imputation). Results: Overall, 80, 73 and 68% of subjects in the 300 mg QD, 450 mg QD, and 450 mg TIW dose cohorts respectively, completed the study. For all dose cohorts no statistically significant mean change in Hb from pre-baseline average was observed, and mean Hb concentrations-analyzed using available data-remained stable at mid- and end-of-trial. There was one subject with an Hb excursion >13 g/dL. Overall, 83% of subjects experienced an adverse event (AE); the proportion of subjects who experienced at least one AE was similar among the three dose cohorts. The most frequently reported AEs were nausea (11.7%), diarrhea (10.6%) and vomiting (9.6%). No deaths occurred during the study. No serious AEs were attributed to vadadustat. Conclusions: Vadadustat maintained mean Hb concentrations in subjects on hemodialysis previously receiving epoetin. These data support further investigation of vadadustat to assess its long-term safety and efficacy in subjects on hemodialysis.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Ácidos Picolínicos / Hemoglobinas / Diálisis Renal / Insuficiencia Renal Crónica / Glicina / Hematínicos / Anemia Tipo de estudio: Clinical_trials / Etiology_studies / Prognostic_studies Límite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Nephrol Dial Transplant Asunto de la revista: NEFROLOGIA / TRANSPLANTE Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Ácidos Picolínicos / Hemoglobinas / Diálisis Renal / Insuficiencia Renal Crónica / Glicina / Hematínicos / Anemia Tipo de estudio: Clinical_trials / Etiology_studies / Prognostic_studies Límite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Nephrol Dial Transplant Asunto de la revista: NEFROLOGIA / TRANSPLANTE Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido