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Vir Biotechnology在EASL数字国际肝病大会™上提供有关治疗乙型 [复制链接]

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发表于 2020-8-21 11:58 |只看该作者 |倒序浏览 |打印
Vir Biotechnology Presents Data on VIR-2218 from Clinical Studies for the Treatment of Hepatitis B at the EASL Digital International Liver Congress™
Vir Biotechnology, Inc.
August 20, 2020, 10:00 PM GMT+10·7 mins read

SAN FRANCISCO, Aug. 20, 2020 (GLOBE NEWSWIRE) -- Vir Biotechnology, Inc. (Nasdaq: VIR), a clinical-stage immunology company focused on treating and preventing serious infectious diseases, today announced that data from its VIR-2218 clinical program will be featured at the European Association for the Study of the Liver (EASL) Digital International Liver Congress™ from August 27-29, 2020. VIR-2218 is an investigational small interfering ribonucleic acid (siRNA) that mediates RNA interference (RNAi) for the potential treatment of chronic hepatitis B virus (HBV) infection and is the first investigational medicine from Vir’s partnership with Alnylam Pharmaceuticals, Inc. to enter clinical trials.

Among the accepted abstracts is an oral presentation of preliminary antiviral activity and safety results from an ongoing Phase 2 study of VIR-2218 in patients with chronic HBV on nucleotide/nucleoside reverse transcriptase inhibitors (NRTIs), which are standard of care. The data demonstrate that two monthly doses of VIR-2218 resulted in substantial, dose-dependent and durable reductions in hepatitis B surface antigen (HBsAg), a marker of active hepatitis B infection. The data also suggests that the Enhanced Stabilization Chemistry-Plus (ESC+) incorporated into VIR-2218 may result in an improved hepatic safety profile. Additional abstracts include safety and pharmacokinetic data from a Phase 1 study of VIR-2218, as well as preclinical data.

“Chronic HBV infection is a major public health condition impacting almost 300 million people worldwide, and innovative approaches that do not require lifelong treatment are needed to sustainably address the disease,” said Phillip Pang, M.D., Ph.D., Chief Medical Officer of Vir. “By suppressing HBV protein expression, VIR-2218 is not only a potent antiviral, but also may serve to remove antigenic inhibition of T and B cell activity directed against HBV, enabling immunologic control. The well-tolerated and substantial dose-dependent reduction in HBsAg demonstrated to date by VIR-2218 supports our belief that it has the potential to serve as the backbone of a finite treatment regimen aimed at providing a functional cure for HBV.”

VIR-2218 Scientific Research Presented at EASL

Oral Presentation:

    Preliminary safety and antiviral activity of VIR-2218, an X-targeting HBV RNAi therapeutic, in chronic hepatitis B patients
    Abstract: AS068
    Date: Friday, August 28, 2020
    Time: 11:15-11:30 a.m. CET, includes a live Q&A session
    Lead author: Gane E

The following poster presentations will be available on demand:

    Impact of ESC+ Technology on the Hepatic Safety Profile of GalNAc-Delivered, HBV-Targeted RNAi Therapeutics
    Abstract: SAT424
    Lead author: Gane E

    Pharmacokinetics of VIR-2218, an RNAi Therapeutic for the Treatment of HBV Infection, in Healthy Volunteers
    Abstract: SAT462
    Lead author: Gupta SV

    In Vitro and In Vivo Characterization of VIR-2218, an Investigational RNAi Therapeutic Targeting Hepatitis B Virus
    Abstract: SAT426
    Lead author: Anglero-Rodriguez Y

Advancing Clinical Trials for HBV Therapies

Based on preliminary Phase 2 results, Vir initiated a Phase 2 trial of VIR-2218 administered in combination with pegylated interferon alpha-2a, an approved immunomodulatory agent. Initial clinical data are expected next year.

In May 2020, Vir initiated a Phase 1 clinical trial of VIR-3434, an HBV-neutralizing monoclonal antibody with the potential to also be a therapeutic T cell vaccine. Recently, the first chronic HBV patient was treated in the program, following the study design to progress from healthy volunteers to HBV patients in a staggered, parallel fashion.

A Phase 2 clinical trial of VIR-2218 in combination with VIR-3434 is expected in 2021.

About VIR-2218
VIR-2218 is a subcutaneously administered HBV-targeting siRNA that has the potential to stimulate an effective immune response and have direct antiviral activity against HBV. It is the first siRNA in the clinic to include Enhanced Stabilization Chemistry Plus (ESC+) technology to enhance stability and minimize off-target activity, which potentially can result in an increased therapeutic index. VIR-2218 is the first asset in the company’s collaboration with Alnylam Pharmaceuticals, Inc. to enter clinical trials.

About VIR-3434
VIR-3434 is a subcutaneously administered HBV-neutralizing monoclonal antibody designed to block entry of all 10 genotypes of HBV into hepatocytes and also to reduce the level of virions and subviral particles in the blood. VIR-3434 has been engineered to have an extended half-life as well as to potentially function as a T cell vaccine against HBV in infected patients.

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Vir Biotechnology在EASL数字国际肝病大会™上提供有关治疗乙型肝炎的临床研究的VIR-2218数据
维尔生物技术有限公司
2020年8月20日,格林尼治标准时间+ 10·7分钟,晚上10:00

旧金山,2020年8月20日(全球新闻)-专注于治疗和预防严重传染病的临床阶段免疫学公司Vir Biotechnology,Inc.(纳斯达克股票代码:VIR)今天宣布,其VIR-2218临床数据该计划将在2020年8月27日至29日举行的欧洲肝脏研究协会(EASL)数字国际肝脏大会™上进行专题报道。VIR-2218是一种研究中的小干扰核糖核酸(siRNA),可介导RNA干扰(RNAi)。是Vir与Alnylam Pharmaceuticals,Inc.的合作伙伴关系中首款进入临床试验的研究药物,可用于治疗慢性乙型肝炎病毒(HBV)的潜在治疗。

在接受的摘要中,有一项口服正在进行的初步抗病毒活性和安全性研究结果的口服报告,该研究正在进行中,VIR-2218在慢性HBV患者中使用核苷酸/核苷逆转录酶抑制剂(NRTIs)进行了VIR-2218治疗,这是常规治疗方法。数据表明,每月两次服用VIR-2218可导致活性肝炎感染的标志物乙型肝炎表面抗原(HBsAg)显着,剂量依赖性和持久性降低。数据还表明,纳入VIR-2218的增强稳定化学加号(ESC +)可能会改善肝脏的安全性。其他摘要包括来自VIR-2218的1期研究的安全性和药代动力学数据,以及临床前数据。

“慢性HBV感染是一种主要的公共卫生状况,影响着全球近3亿人,因此需要不需要终生治疗的创新方法来可持续地应对这种疾病,”美国国家卫生研究院首席医学官Phillip Pang博士说。 Vir。通过抑制HBV蛋白表达,VIR-2218不仅是有效的抗病毒药,而且还可以消除针对HBV的T细胞和B细胞活性的抗原性抑制,从而实现免疫控制。迄今为止,VIR-2218所证实的HBsAg耐受性良好且基本呈剂量依赖性,这支持了我们的信念,即它有可能成为旨在为HBV提供功能性治疗的有限治疗方案的骨干。”

VIR-2218科学研究在EASL上发表

口头表达:

    靶向X线的HBV RNAi治疗剂VIR-2218在慢性乙型肝炎患者中的初步安全性和抗病毒活性
    摘要:AS068
    日期:2020年8月28日,星期五
    时间:欧洲中部时间上午11:15-11:30,包括现场问答环节
    主要作者:甘恩E

以下海报演示将按需提供:

    ESC +技术对GalNAc传递,HBV靶向的RNAi治疗药物的肝安全性的影响
    摘要:SAT424
    主要作者:甘恩E

    VIR-2218(一种用于治疗HBV感染的RNAi治疗药物)在健康志愿者中的药代动力学
    摘要:SAT462
    主要作者:Gupta SV

    VIR-2218的体外和体内表征,这是一种针对RNAi治疗性乙型肝炎病毒的研究性药物
    摘要:SAT426
    主要作者:安格洛·罗德里格斯Y

推进HBV治疗的临床试验

根据第2阶段的初步结果,Vir启动了VIR-2218与聚乙二醇化干扰素α-2a(一种批准的免疫调节剂)联合给药的第2阶段试验。预计明年将获得初步临床数据。

2020年5月,Vir启动了VIR-3434的1期临床试验,VIR-3434是一种中和HBV的单克隆抗体,也有可能成为治疗性T细胞疫苗。最近,按照研究设计,以交错,平行的方式从健康志愿者发展为HBV患者,该方案治疗了第一位慢性HBV患者。

预计2021年将VIR-2218与VIR-3434结合进行2期临床试验。

关于VIR-2218
VIR-2218是皮下注射的靶向HBV的siRNA,具有刺激有效免疫应答和对HBV具有直接抗病毒活性的潜力。它是临床上首个包含增强稳定化学增强(ESC +)技术的siRNA,以增强稳定性并最大程度地降低脱靶活性,这有可能导致治疗指数的提高。 VIR-2218是公司与Alnylam Pharmaceuticals,Inc.合作进行临床试验的第一项资产。

关于VIR-3434
VIR-3434是皮下注射的中和HBV的单克隆抗体,旨在阻止HBV的所有10个基因型进入肝细胞,并降低血液中病毒体和亚病毒颗粒的水平。 VIR-3434已被设计为具有延长的半衰期,并可能在感染的患者中充当针对HBV的T细胞疫苗。

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发表于 2020-8-21 15:09 |只看该作者
和免疫药组合试验是正解
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