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vir三季报节选 [复制链接]

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发表于 2022-11-16 13:34 |只看该作者 |倒序浏览 |打印
Hepatitis B Virus (HBV) and Hepatitis D Virus (HDV)

VIR-2218 is an investigational HBV-targeting siRNA. VIR-3434 is an investigational HBV-neutralizing mAb that incorporates Xencor’s Xtend and other Fc technologies.


In October 2022, we announced multiple abstracts (two oral presentations, one poster and one late-breaker poster featuring real-world data from a 20-year trial evaluating treatment patterns for chronic HBV) were accepted for presentation at the American Association for the Study of Liver Diseases, or AASLD, The Liver Meeting® 2022, taking place November 4-8, 2022. Both oral presentations have been selected by AASLD for inclusion in the “Best of the Liver Meeting” summary.

Initial data from Part B of the ongoing Phase 2 Monoclonal Antibody siRNA Combination against Hepatitis B (MARCH) trial evaluating VIR-2218 in combination with VIR-3434 for 24 and 48 weeks, and in triple combination with VIR-3434 and interferon for 24 and 48 weeks, are expected in the second half of 2023. Previously reported results from the MARCH Part A trial demonstrated that the combination of VIR-3434 and VIR-2218 resulted in an approximate 3 log decline in hepatitis B surface antigen, or HBsAg, with no safety signals reported to date.

Initiation of the Phase 2 PREVAIL platform trial and its THRIVE/STRIVE sub-protocols of VIR-2218 in combination with VIR-3434 in viremic patients is expected in the fourth quarter of 2022, with initial data expected in the second half of 2023.

Initial data from the Phase 2 trial led by Brii Biosciences Offshore Limited, or Brii Bio, evaluating VIR-2218 in combination with BRII-179, an investigational T cell vaccine, for the potential treatment of chronic HBV infection are expected by the end of 2022.

In September 2022, we initiated the Phase 2 SOLSTICE trial evaluating VIR-2218 and VIR-3434 as monotherapy and in combination for the treatment of people living with chronic HDV, the most aggressive form of viral hepatitis. The trial is assessing the ability of the combination to reduce HDV viremia and block viral entry, which recent research suggests could be effective in suppressing chronic HDV infection. Initial data are expected in the second half of 2023

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发表于 2022-11-16 13:36 |只看该作者
正在进行的2期抗乙型肝炎单克隆抗体siRNA联合试验(MARCH) B部分的初步数据预计将在2023年下半年发布,该试验评估了VIR-2218与VIR-3434联合用药24和48周,以及与VIR-3434和干扰素联合用药24和48周。此前报道的MARCH A部分试验结果显示,VIR-3434和VIR-2218联合使用可导致乙肝表面抗原(HBsAg)下降约3 log,但迄今为止没有安全信号报道。

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发表于 2022-11-16 13:38 |只看该作者
vir2218+vir3434+干挠素,24周,48周

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发表于 2022-11-16 13:43 |只看该作者
本帖最后由 newchinabok 于 2022-11-16 13:43 编辑

所有的新药都加干挠素,干挠素plus版,没有干挠素大概率都反弹

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发表于 2022-11-16 13:44 |只看该作者
本帖最后由 tim889 于 2022-11-15 21:45 编辑
newchinabok 发表于 2022-11-15 21:36
正在进行的2期抗乙型肝炎单克隆抗体siRNA联合试验(MARCH) B部分的初步数据预计将在2023年下半年发布,该试 ...

不是“ 没有安全信号报道” ,而是“ 没有不安全的报道” 哈哈 翻译软件不够聪明

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发表于 2022-11-16 13:46 |只看该作者
“ Initiation of the Phase 2 PREVAIL platform trial and its THRIVE/STRIVE sub-protocols of VIR-2218 in combination with VIR-3434 in viremic patients is expected in the fourth quarter of 2022, with initial data expected in the second half of 2023. ”

这个trial适合我,但我从来没听过呢,clinicaltrial.gov 也没有找到

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发表于 2022-11-16 13:48 |只看该作者
本帖最后由 newchinabok 于 2022-11-16 13:48 编辑
tim889 发表于 2022-11-16 13:46
“ Initiation of the Phase 2 PREVAIL platform trial and its THRIVE/STRIVE sub-protocols of VIR-2218  ...

有机会可以试试,下载个药智数据APP可以查查

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发表于 2022-11-16 13:50 |只看该作者
本帖最后由 newchinabok 于 2022-11-16 13:52 编辑
tim889 发表于 2022-11-16 13:46
“ Initiation of the Phase 2 PREVAIL platform trial and its THRIVE/STRIVE sub-protocols of VIR-2218  ...

给你个vir三季报英文版https://basic.10jqka.com.cn/ajax ... ck_source=hyperlink,可能美国那边做,可以试试

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发表于 2022-11-16 13:54 |只看该作者
newchinabok 发表于 2022-11-15 21:50
给你个vir三季报英文版https://basic.10jqka.com.cn/ajax ... ck_source=hyperlink,可能美国那边做,可以 ...

查了下。原来只在新西兰做,而且只有TDF 没有TAF

https://www.isrctn.com/ISRCTN29337285

关注一下 ,看看明年初的结果。我email的vir的人,问了下美国site的情况,等回复
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