Clinical safety, tolerability, pharmacokinetics and effects on urinary electrolyte excretion of AZD9977, a novel, selective mineralocorticoid receptor modulator

التفاصيل البيبلوغرافية
العنوان: Clinical safety, tolerability, pharmacokinetics and effects on urinary electrolyte excretion of AZD9977, a novel, selective mineralocorticoid receptor modulator
المؤلفون: M Kjaer, Krister Bamberg, Hans Ericsson, Linda Wernevik, Judith Hartleib-Geschwindner, Karin Nelander, Fredrik Erlandsson, Rasmus Jansson-Löfmark, Muna Albayaty, Carl Amilon, Ligia Chialda
المصدر: British Journal of Clinical Pharmacology. 84:1486-1493
بيانات النشر: Wiley, 2018.
سنة النشر: 2018
مصطلحات موضوعية: 0301 basic medicine, Pharmacology, Agonist, Aldosterone, medicine.drug_class, business.industry, Fludrocortisone, 030204 cardiovascular system & hematology, Natriuresis, Eplerenone, 03 medical and health sciences, chemistry.chemical_compound, 030104 developmental biology, 0302 clinical medicine, Mineralocorticoid receptor, chemistry, Pharmacokinetics, Tolerability, medicine, Pharmacology (medical), business, medicine.drug
الوصف: Aims AZD9977 is the first mineralocorticoid receptor modulator in clinical development exerting similar organ protection as eplerenone with minimal urinary electrolyte effects in preclinical studies. The aim was to perform the initial clinical assessment of AZD9977. Methods A first-in-human trial explored doses from 5 to 1200 mg. To study effects on urinary electrolyte excretion an additional randomized placebo controlled cross-over four-period clinical trial was performed. Twenty-three healthy volunteers were administered fludrocortisone alone or in combination with AZD9977, eplerenone or both. AZD9977/eplerenone combination was given to assess if AZD9977 can attenuate eplerenone induced natriuresis. Results AZD9977 at doses from 5 to 1200 mg was safe and well tolerated and pharmacokinetics were compatible with further development. AZD9977 exhibited similar effects on urinary ln [Na+ ]/[K+ ] as eplerenone when using fludrocortisone as mineralocorticoid receptor agonist, and the combination had an additive effect on ln [Na+ K+ ]. Conclusions The results in man contradict the results in rodent models driven by aldosterone, in which AZD9977 has minimal electrolyte effects. Future clinical studies with AZD9977 should be performed in presence of endogenous or exogenous aldosterone to assess potential benefit of AZD9977 in patients.
تدمد: 0306-5251
DOI: 10.1111/bcp.13562
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::22998e7eab0e9f69d707fef6451e06f7
https://doi.org/10.1111/bcp.13562
Rights: OPEN
رقم الانضمام: edsair.doi...........22998e7eab0e9f69d707fef6451e06f7
قاعدة البيانات: OpenAIRE
الوصف
تدمد:03065251
DOI:10.1111/bcp.13562