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Safety, tolerability, pharmacokinetics and effect on serum uric acid of the myeloperoxidase inhibitor AZD4831 in a randomized, placebo-controlled, phase I study in healthy volunteers.
Gan, Li-Ming; Lagerström-Fermér, Maria; Ericsson, Hans; Nelander, Karin; Lindstedt, Eva-Lotte; Michaëlsson, Erik; Kjaer, Magnus; Heijer, Maria; Whatling, Carl; Fuhr, Rainard.
Afiliación
  • Gan LM; Early Clinical Development, IMED Biotech Unit, AstraZeneca, Gothenburg, Sweden.
  • Lagerström-Fermér M; Department of Molecular and Clinical Medicine, Institute of Medicine, Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden.
  • Ericsson H; Department of Cardiology, Sahlgrenska University Hospital, Gothenburg, Sweden.
  • Nelander K; Early Clinical Development, IMED Biotech Unit, AstraZeneca, Gothenburg, Sweden.
  • Lindstedt EL; Early Clinical Development, IMED Biotech Unit, AstraZeneca, Gothenburg, Sweden.
  • Michaëlsson E; Early Clinical Development, IMED Biotech Unit, AstraZeneca, Gothenburg, Sweden.
  • Kjaer M; Cardiovascular, Renal and Metabolism, IMED Biotech Unit, AstraZeneca, Gothenburg, Sweden.
  • Heijer M; Cardiovascular, Renal and Metabolism, IMED Biotech Unit, AstraZeneca, Gothenburg, Sweden.
  • Whatling C; Early Clinical Development, IMED Biotech Unit, AstraZeneca, Gothenburg, Sweden.
  • Fuhr R; Early Clinical Development, IMED Biotech Unit, AstraZeneca, Gothenburg, Sweden.
Br J Clin Pharmacol ; 85(4): 762-770, 2019 04.
Article en En | MEDLINE | ID: mdl-30618054
AIMS: Myeloperoxidase activity can contribute to impaired vascular endothelial function and fibrosis in chronic inflammation-related cardiovascular disease. Here, we investigated the safety, tolerability and pharmacokinetics of the myeloperoxidase inhibitor, AZD4831. METHODS: In this randomized, single-blind, placebo-controlled, phase I, first-in-human study, healthy men in five sequential cohorts were randomized 3:1 to receive a single oral dose of AZD4831 (5, 15, 45, 135 or 405 mg) or placebo, after overnight fasting. After at least 7 days' washout, one cohort additionally received AZD4831 45 mg after a high-calorie meal. RESULTS: Forty men participated in the study (eight per cohort: AZD4831, n = 6; placebo, n = 2). AZD4831 distributed rapidly into plasma, with a half-life of 38.2-50.0 hours. The area under the plasma concentration-time curve (AUC) increased proportionally with dose (AUC0-∝ slope estimate 1.060; 95% confidence interval [CI] 0.9943, 1.127). Increases in maximum plasma concentration were slightly more than dose proportional (slope estimate 1.201; 95% CI 1.071, 1.332). Food intake reduced AZD4831 absorption rate but did not substantially affect overall exposure or plasma half-life (n = 4). Serum uric acid concentrations decreased by 71.77 (95% CI 29.15, 114.39) and 84.42 (58.90, 109.94) µmol L-1 with AZD4831 135 mg and 405 mg, respectively. Maculopapular rash (moderate intensity) occurred in 4/30 participants receiving AZD4831 (13.3%). No other safety concerns were identified. CONCLUSIONS: AZD4831 was generally well tolerated, rapidly absorbed, had a long plasma half-life and lowered uric acid concentrations after single oral doses in healthy men. These findings support the further clinical development of AZD4831.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Pirimidinas / Pirroles / Ácido Úrico / Peroxidasa / Inhibidores Enzimáticos Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Adult / Humans / Male / Middle aged Idioma: En Revista: Br J Clin Pharmacol Año: 2019 Tipo del documento: Article País de afiliación: Suecia Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Pirimidinas / Pirroles / Ácido Úrico / Peroxidasa / Inhibidores Enzimáticos Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Adult / Humans / Male / Middle aged Idioma: En Revista: Br J Clin Pharmacol Año: 2019 Tipo del documento: Article País de afiliación: Suecia Pais de publicación: Reino Unido