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A phase 1 study of the safety, tolerability, pharmacodynamics, and pharmacokinetics of tenapanor in healthy Japanese volunteers

BACKGROUND: Tenapanor (RDX5791, AZD1722), a small molecule with minimal systemic availability, is an inhibitor of the sodium/hydrogen exchanger isoform 3 (NHE3). Tenapanor acts locally in the gut to reduce absorption of sodium and phosphate. It is being developed for the treatment of patients with h...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Clin Exp Nephrol
Päätekijät: Johansson, Susanne, Rosenbaum, David P., Knutsson, Mikael, Leonsson-Zachrisson, Maria
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Springer Japan 2016
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5486465/
https://ncbi.nlm.nih.gov/pubmed/27368672
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10157-016-1302-8
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