AAAAI 2021:PHA121治疗遗传性血管性水肿(HAE)取得积极结果

2021-02-21 Allan MedSci原创

在用PHA121治疗的所有受试者中,有25%的受试者报告了不良事件(AEs),与安慰剂的25%发生率相同。

遗传性血管性水肿(HAE)是一种以血管性水肿反复发作为特征的疾病,不伴有荨麻疹或瘙痒,最常累及皮肤或上呼吸道和胃肠道的黏膜组织。

生物制药公司Pharvaris近日宣布,在2021年美国过敏性哮喘和免疫学学会(AAAAI)虚拟年度会议上发表了PHA121(PHA-022121)治疗遗传性血管性水肿(HAE)的药代动力学(PK)和药效学(PD)数据。

在两项双盲、安慰剂对照单次剂量研究中,通过非线性混合效应PK / PD模型(分别使用12 mg和22 mg剂量)评估PD效果,并与历史数据进行比较。PK / PD分析显示,平均复合EC50为2.4 ng / mL,EC85为13.8 ng / mL。

在用PHA121治疗的所有受试者中,有25%的受试者报告了不良事件(AEs),与安慰剂的25%发生率相同。所有不良事件均为轻度或中度,并迅速完全消失。

Pharvaris首席医学官Peng Lu博士说:“口服PHA121在有或没有食物的情况下,在15分钟内迅速吸收并超过了预期的有效治疗阈值。使用缓激肽激发的替代指标,药效学结果提示PHA121单一口服剂量可能比icatibant具有更长的药理作用”。

 

原始出处:

https://www.firstwordpharma.com/node/1802502?tsid=4

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    2021-11-15 changfy
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    2021-04-01 ay2000fy
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  5. 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    2021-03-15 123b8705m26暂无昵称

    0

  6. 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    2021-02-23 小华子
  7. 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GetPortalCommentsPageByObjectIdResponse(id=926187, encodeId=bf6792618e7b, content=好文章!, beContent=null, objectType=article, channel=null, level=null, likeNumber=100, replyNumber=0, topicName=null, topicId=null, topicList=[], attachment=null, authenticateStatus=null, createdAvatar=http://cacheapi.medsci.cn/resource/upload/20160806/IMG57A5698BDB0244113.jpg, createdBy=32a91358059, createdName=jyzxjiangqin, createdTime=Sun Feb 21 18:32:19 CST 2021, time=2021-02-21, status=1, ipAttribution=)]
  8. 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GetPortalCommentsPageByObjectIdResponse(id=926187, encodeId=bf6792618e7b, content=好文章!, beContent=null, objectType=article, channel=null, level=null, likeNumber=100, replyNumber=0, topicName=null, topicId=null, topicList=[], attachment=null, authenticateStatus=null, createdAvatar=http://cacheapi.medsci.cn/resource/upload/20160806/IMG57A5698BDB0244113.jpg, createdBy=32a91358059, createdName=jyzxjiangqin, createdTime=Sun Feb 21 18:32:19 CST 2021, time=2021-02-21, status=1, ipAttribution=)]
    2021-02-22 rabiby

    长知识了

    0

  9. 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    2021-02-21 ms2000001051330459

    学习了,涨知识了!

    0

  10. 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GetPortalCommentsPageByObjectIdResponse(id=926187, encodeId=bf6792618e7b, content=好文章!, beContent=null, objectType=article, channel=null, level=null, likeNumber=100, replyNumber=0, topicName=null, topicId=null, topicList=[], attachment=null, authenticateStatus=null, createdAvatar=http://cacheapi.medsci.cn/resource/upload/20160806/IMG57A5698BDB0244113.jpg, createdBy=32a91358059, createdName=jyzxjiangqin, createdTime=Sun Feb 21 18:32:19 CST 2021, time=2021-02-21, status=1, ipAttribution=)]
    2021-02-21 jyzxjiangqin

    好文章!

    0

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遗传性血管性水肿患者眼科手术麻醉一例

患者,女,55岁,56kg,160 cm,因车祸伤致“右侧眼球破裂伤、右眼眶骨折”入院,拟在全麻下行“右眼内容物剜出伴义眼置入术+眼窝成形术+眼睑裂伤缝合术”。10年前在北京协和医院诊断为“遗传性血管性水肿(hereditary angioedema,HAE)”。

EAACI 2020:长期临床数据证实Berotralstat可稳定持久地减少遗传性血管性水肿患者的发作

2020年欧洲过敏和临床免疫学会(EAACI)大会:每日口服一次血浆激肽释放酶抑制Berotralstat(BCX7353),可以使遗传性血管性水肿(HAE)患者在48周内发作频率持续下降。

NEJM:反义疗法治疗遗传性血管性水肿,初见有效性端倪

IONIS-PKKRx和IONIS-PKK-LRx是研究性反义药物,旨在减少前激肽释放酶的产生。

ZENITH-1试验:口服BCX7353治疗急性遗传性血管性水肿发作具有显著效果

BioCryst制药公司近日公布了II期ZENITH-1试验的最新数据,包括来自250毫克和500毫克剂量组的新数据。来自ZENITH-1试验的数据证实了先前报道的结果,显示单剂量口服750毫克 BCX7353耐受良好,且优于安慰剂(p <0.05),在治疗急性发作的遗传性血管性水肿(HAE)患者中达到了疗效终点,并证明在三个剂量水平上有明确的剂量反应。

拓展阅读

《新英格兰杂志》:遗传性血管性水肿KLKB1基因的CRISPR-Cas9体内基因编辑疗法

在探索性分析中,在所有剂量水平下均观察到每月血管性水肿发作次数减少,且未没有观察到严重的不良事件。

诊断篇|长时间不明原因水肿,专家揭开罕见病背后的神秘面纱

到底是什么样的疾病令人如此迷惑?40多年的谜团背后真相究竟为何?

遗传性血管性水肿患者的家系筛查与基因检测

HAE需要通过基因检测进行诊断吗?HAE患者有必要进行家系筛查吗?

NEJM:Donidalorsen可降低遗传性血管性水肿发作风险改善患者生活质量

这项遗传性血管性水肿患者参与的小规模II期试验中,Donidalorsen治疗可显著降低患者血管性水肿发作率,提高生活质量

Lancet:Garadacimab可有效预防C1酯酶抑制剂缺乏性遗传性血管性水肿患者的水肿发作

Garadacimab可显著降低 C1 酯酶抑制剂缺乏性遗传性血管性水肿患者的水肿发作,而且耐受性良好。