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BTK抑制剂Rilzabrutinib治疗免疫性血小板减少症:被授予FDA快速通道指定

2020-11-19 MedSci原创 MedSci原创

Rilzabrutinib很可能成为治疗免疫性血小板减少症(ITP)的首款BTK抑制剂。

美国食品和药物管理局(FDA)为赛诺菲的口服Bruton酪氨酸激酶(BTK)抑制剂rilzabrutinib授予了快速通道指定(FTD),该药物很可能成为治疗免疫性血小板减少症(ITP)的首款BTK抑制剂。在获得1/2期阳性研究结果之后,赛诺菲现已启动3期研究,评估rilzabrutinib用于治疗ITP。Rilzabrutinib治疗ITP于2018年10月获得FDA的孤儿药指定。

关于免疫性血小板减少症

ITP是由于免疫介导的血小板破坏和生成受损,进而导致下游血小板减少和易出血。在皮质类固醇激素(corticosteroids)复发或难治性ITP患者中,仍存在尚未满足的医疗需求。

Idiopathic Thrombocytopenic Purpura Clinical: • Gingival • Menorrhagia • GI

图片来源:www.grepmed.com

关于Rilzabrutinib

Rilzabrutinib是一种口服可逆的BTK抑制剂,正在研究中用于治疗免疫介导的疾病。BTK参与先天和适应性免疫应答,是免疫介导疾病中的信号分子。Rilzabrutinib的数据证明其在不耗尽B细胞的情况下,具有阻断炎症性免疫细胞、消除自身抗体破坏性信号以及防止新的自身抗体产生的能力。这些机制的临床意义目前正在研究中,其安全性和有效性尚未得到监管机构的审查。

图片来源:www.streetinsider.com

原始出处:

https://www.firstwordpharma.com/node/1775442?tsid=4

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    2021-01-21 jklm09
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    学习

    0

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    2020-11-22 gqylhd

    临床有很多难治性的血小板降低的患者

    0

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    2020-11-21 fengting7

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2019 ASH指南:免疫性血小板减少症

2019年12月,美国血液病学会(ASH)发布了免疫性血小板减少症管理指南。ASH专家组共形成了21条循证指导建议,内容涉及新诊断,持续性以及一线疗法难治的无出血性生命危险的成人和儿童免疫性血小板减少症的管理。治疗方法包括:观察,皮质类固醇类药物,IV免疫球蛋白,抗-D免疫球蛋白,英夫利昔单抗,脾切除以及血小板生成素受体激动剂。

Brit J Heamatol:免疫性血小板减少症对儿童疲劳、执行功能和心理的影响

该研究的发现为ITP儿童受到的影响提供了宝贵的见识,这可能有助于提供整体治疗策略,可能有助于做出相关医疗决定,并指导未来的研究。

Blood:ITP患儿确诊时予以IVIg预治疗可提高早期缓解率,但不影响慢性ITP发生率

中心点:对于新确诊的ITP患儿,确诊时予以IVIg治疗并不能降低慢性ITP的发生率。用IVIg进行预治疗有助于快速恢复、减少重度出血事件。摘要:对于新确诊的免疫性血小板减少症(ITP)患儿可予以密切观察或免疫调节治疗。观察性研究提示静脉输注免疫球蛋白(IVIg)治疗可降低患儿慢性ITP的发生率。Katja M.J. Heitink-Pollé等人开展一多中心的随机试验,招募3个月-16岁的新确诊的

Lancet子刊:高剂量地塞米松对于免疫性血小板减少症效果并不理想

高剂量地塞米松对于未经治疗过的免疫性血小板减少症患者的长期疗效和安全性尚不清楚。研究人员做了一项随机试验的系统回顾和荟萃分析,旨在确定与泼尼松相比,高剂量地塞米松对于血小板计数的长期效果。研究人员检索了MEDLINE,Embase,护理及相关健康文献累计索引(CINAHL),和Cochrane图书馆数据库在1970年至2016年七月发表的研究,并检索了从2004年到2015年美国血液协会年度会议发

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