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评估培非替尼治疗类风湿关节炎的疗效和安全性。

Efficacy and safety of peficitinib in rheumatoid arthritis.

机构信息

Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan.

出版信息

Mod Rheumatol. 2020 Sep;30(5):773-778. doi: 10.1080/14397595.2020.1794103. Epub 2020 Aug 3.

Abstract

Peficitinib is a Janus kinase (JAK) inhibitor, newly developed and approved in Japan. In contrast to other JAK inhibitors, it is a unique pan-JAK inhibitor, demonstrating inhibition of all JAKs. In patients with rheumatoid arthritis with an inadequate response to previous disease-modifying anti-rheumatic drugs, the efficacy of peficitinib (100 mg and 150 mg) has been confirmed with a comparison to placebo in Phase 2b and 3 trials conducted in Asia. Reportedly, peficitinib was well tolerated for 52 weeks during the trial duration, as well as for the next few years in a subsequent, ongoing long-term extension study. Safety signals, especially, the increased risk of herpes zoster was comparable with other JAK inhibitors.

摘要

培非替尼是一种新型的 Janus 激酶(JAK)抑制剂,在日本获得批准。与其他 JAK 抑制剂不同,它是一种独特的泛 JAK 抑制剂,对所有 JAK 均有抑制作用。在对先前的疾病修饰抗风湿药物反应不足的类风湿关节炎患者中,培非替尼(100mg 和 150mg)的疗效已在亚洲进行的 2b 期和 3 期临床试验中与安慰剂进行了比较得到证实。据报道,在试验期间以及随后的长期扩展研究的几年内,培非替尼在 52 周内耐受性良好。安全性信号,特别是带状疱疹风险增加,与其他 JAK 抑制剂相当。

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