| Literature DB >> 32380083 |
Kaijun Su1, Zhihong Li1, Yancheng Yu1, Xiaojin Zhang2.
Abstract
Prolyl hydroxylase (PHD) inhibitors, such as roxadustat, can stabilize hypoxia-inducible factor (HIF)-2α and induce erythropoietin (EPO) production under normal conditions. Roxadustat was recently approved as a first-in-class orally active drug for the treatment of renal anemia. In addition, it has garnered growing therapeutic interest for use against various diseases, such as carcinoma, neurological diseases, ocular diseases, and tissue and organ injuries. In this review, we systemically review target validation, hit identification, and further key clinical trials of roxadustat. The prospective clinical applications of PHD inhibitors are then discussed based on this marketed drug.Entities:
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Year: 2020 PMID: 32380083 DOI: 10.1016/j.drudis.2020.04.017
Source DB: PubMed Journal: Drug Discov Today ISSN: 1359-6446 Impact factor: 7.851