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标题: 杨梅将出席TKM-HBV数据在2015年AASLD肝病会议 [打印本页]

作者: StephenW    时间: 2015-10-2 09:32     标题: 杨梅将出席TKM-HBV数据在2015年AASLD肝病会议

Press Release
Arbutus to Present TKM-HBV Data at the 2015 AASLD Liver Meeting

Published: Oct 1, 2015 10:00 a.m. ET

   
        

VANCOUVER, British Columbia and DOYLESTOWN, Pa., Oct 01, 2015 (GLOBE NEWSWIRE via COMTEX) --

Arbutus Biopharma Corporation ABUS, +2.13% an industry-leading therapeutic solutions company focused on developing a cure for chronic hepatitis B virus infection (HBV), today announced presentation of data at the 2015 American Association for the Study of Liver Diseases (AASLD) Liver Meeting being held on November 13 – 17, 2015, at the Moscone West Convention Center, San Francisco.

"We are encouraged by the supportive data generated for TKM- HBV, our lead HBV clinical candidate, and are focused on advancing the development of this product as well as our other HBV candidates," said Dr. Mark J. Murray, Arbutus' President and CEO. "Our preclinical data support reduction of hepatitis B surface antigen (HBsAg) by TKM-HBV, as well as complementary effects when combined with currently approved nucleos(t)ide analogs."
Presentation Information and Abstract Summaries:
      
Session:      Hepatitis B: Treatment
Date:      November 17, 2015
Time:      8.00am – 12.00pm (PT) /11.00am –3.00pm (ET)

    Abstract #1: "TKM-HBV, a Novel RNA Interference Treatment for Chronic Hepatitis B, Rapidly Reduces Surface Antigen and other Viral Proteins in Both Intrahepatic and Peripheral Compartments"

Summary: TKM-HBV effectively removed viral antigens from both the intrahepatic and peripheral compartments within days after treatment initiation in hydrodynamic injection (HDI) mice. These viral elements include immunomodulatory surface and core proteins which are implicated in mediating the immune-repressed condition of chronic HBV infection.

    Abstract #2: "TKM-HBV, a Novel RNA Interference Treatment for Chronic Hepatitis B, has a Complementary Mode of Action to Current Standard of Care Nucleos(t)ide Analogs"

Summary: Results show that TKM-HBV and nucleos(t)ide analog modes of action are complementary, and combination therapy allows effective disease targeting at multiple critical nodes of the viral life cycle.

    Abstract #3: "Development of a Direct RNA Interference Therapy for Hepatitis Delta Virus Infection"

Summary: A direct hepatitis delta virus (HDV)-targeted siRNA-LNP approach can effectively suppress positive and negative strand HDV RNAs and hepatitis D antigen (HDAg) protein in vitro, and provides a promising novel strategy to treat HDV infection. The efficacy of direct HDV targeting relative to indirect effects from HBV gene silencing are currently under investigation.

About TKM-HBV

The goal of TKM-HBV is to facilitate HBsAg loss in patients with chronic hepatitis B. The continued presence of HBsAg in chronic HBV is believed to be responsible for disease pathogenesis and impairing the body's ability to clear the virus. Blocking HBsAg may lead to a functional cure by promoting immune-mediated clearance and control of HBV, potentially through HBsAg seroconversion. TKM-HBV is a novel lipid nanoparticle (LNP) formulated RNAi therapy that uniquely targets three highly conserved regions of the HBV viral genome. Targeting multiple sites on the HBV genome allows for potent reduction of multiple viral antigens, knockdown across a broad range of HBV genotypes, and a decrease in the probability of developing antiviral resistance. Preclinical studies with TKM-HBV have shown reductions of HBsAg and other important viral markers across the most prevalent HBV genotypes, demonstrating that TKM-HBV has the potential to treat patients with chronic HBV.

About Arbutus

Arbutus Biopharma Corporation is a biopharmaceutical company dedicated to discovering, developing and commercializing a cure for patients suffering from chronic hepatitis B infection (HBV). Our strategy is to target the three pillars necessary to develop a curative regimen for HBV: suppressing HBV replication within liver cells, stimulating and reactivating the body's immune system so that it can mount an effective defense against the virus and, eliminating the reservoir of viral genomic material known as covalently closed circular DNA, or cccDNA that is the source of HBV persistence. Our portfolio of assets includes a broad pipeline of drug candidates for use in combination to develop a cure for HBV. To support continuous discovery of potential novel drug candidates and technologies, Arbutus has a research collaboration agreement with the Baruch S. Blumberg Institute that provides exclusive rights to in-license any intellectual property generated through the relationship. The Baruch S. Blumberg Institute was established in 2003 by the Hepatitis B Foundation.

Arbutus is headquartered in Vancouver, BC, Canada with offices in Doylestown, PA, USA. For more information, visit www.arbutusbio.com.

CONTACT: Investors Adam Cutler Senior Vice President, Corporate Affairs Phone: 604.419.3200 Email: [email protected] Helia Baradarani Manager, Investor Relations Phone: 604.419.3200 Email: [email protected] Media Please direct all media inquiries to: [email protected]

Copyright (C) 2015 GlobeNewswire, Inc. All rights reserved.

作者: StephenW    时间: 2015-10-2 09:32

新闻稿
杨梅将出席TKM-HBV数据在2015年AASLD肝病会议

发布时间:2015年10月1日上午10:00 ET



        
        

温哥华,不列颠哥伦比亚省和DOYLESTOWN,宾夕法尼亚州,2015年10月1日(GLOBE通过COMTEX商业电讯) -

杨梅生物制药公司安博,+ 2.13%的业界领先的治疗解决方案的公司,致力于开发治​​疗慢性乙型肝炎病毒感染治愈(HBV)今天宣布,在肝病的研究2015年美国协会(AASLD)肝演示数据会议正在举行11月13日至17日,2015年,在Moscone West会议中心会议中心,旧金山。

“我们正在为TKM- HBV,我们的领先优势乙肝临床候选人中产生的数据支持鼓励,并重点推进该产品的发展,以及我们的其他乙肝病毒的考生,”马克博士J.默里,杨梅“总统说和首席执行官。 “我们的临床前数据支撑乙肝表面抗原的减少(乙肝表面抗原)由TKM-HBV,以及何时与目前批准的核苷(酸)类似物联合。互补效应”
提示信息与摘要摘要:
  
会议:乙型肝炎:治疗
日期:2015年11月17日
时间:上午8点00分 - 下午12点00分(PT)/11.00am -3.00pm(ET)

    摘要#1:“TKM-HBV,新型RNA干扰治疗慢性乙型肝炎,迅速降低表面抗原和在肝内及外围车厢其它病毒蛋白”

摘要:TKM-HBV治疗开始在高压注射(HDI)小鼠后有效去除病毒抗原来自在几天内肝内和外围车厢。这些病毒的因素包括那些参与介导的慢性HBV感染者的免疫抑制状态的免疫调节表面和核心蛋白​​。

    摘要#2:“TKM-HBV,新型RNA干扰治疗慢性乙型肝炎,有行动的互补模式,以护理核苷的现行标准(T)类似物”

摘要:研究结果表明,TKM-HBV和核苷(酸)IDE模拟操作模式是相辅相成的,联合治疗可以有效的疾病的病毒生命周期的多个关键节点目标。

    摘要#3:“直接的RNA干扰治疗丁型肝炎病毒感染的发展”

摘要:一种直接型肝炎病毒(HDV)-targeted的siRNA-LNP方法可以有效地抑制在体外正和负链的HDV RNA和丁型肝炎抗原(HDAg的)蛋白,并提供了一​​个有希望的新的策略来治疗HDV感染。直接针对HDV相对于从HBV基因沉默间接影响疗效目前正在调查中。

关于TKM-HBV

TKM - HBV的目标是促进HBsAg消失在慢性乙型肝炎的HBsAg在慢性HBV的继续存在被认为是负责疾病的发病机制和损害人体的清除病毒能力。阻断的HBsAg可能导致功能治愈促进免疫介导的清除和HBV的控制,有可能通过HBsAg血清。 TKM-HBV是一种新型脂质纳米粒(LNP)制定的RNAi疗法是唯一针对乙肝病毒基因组三个高度保守的区域。靶向多个站点上的HBV基因组允许有力的减少的多个病毒抗原,在广泛的范围内HBV基因型的拦截,而在显影抗病毒药阻力的可能性降低。与TKM - HBV的临床前研究已经显示HBsAg及其它重要的病毒标记物的减少在整个最普遍的HBV基因型,表明TKM - HBV具有治疗慢性HBV的潜力。

关于杨梅

杨梅生物制药公司是一家生物制药公司,致力于发现,开发和商业化的治疗方法患慢性乙肝病毒感染(HBV)的痛苦。我们的策略是瞄准必要制定一个治疗方案治疗乙肝的三大支柱:抑制HBV复制的肝细胞中,刺激和重新激活人体的免疫系统,使其可以安装反病毒有效的防御和,消除了病毒基因组的水库材料被称为共价闭合环状DNA,或cccDNA的是乙肝病毒的持久性的来源。我们的资产组合包括候选药物的广泛的管道用于联合开发一种治疗乙肝。为了支持潜在的新候选药物和技术的不断发现,杨梅与巴鲁克S. Blumberg的研究所提供独家经营权的许可通过关系产生的任何知识产权方面的研究合作协议。巴鲁克S. Blumberg的研究所成立于2003年由乙型肝炎基金会。

杨梅总部设在温哥华,加拿大的Doylestown,宾夕法尼亚州,美国均设有办事处。欲了解更多信息,请访问www.arbutusbio.com

联系方式:投资者亚当·卡特勒高级副总裁,公司事务部电话:604.419.3200电子邮件:[email protected]贺莉亚Baradarani投资者关系经理电话:604.419.3200电子邮件:[email protected]媒体请直接将媒体询问:媒体@ arbutusbio.com

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作者: 重韧    时间: 2015-10-3 23:17

拜托速度快点就行。全面推进新药的临床才是正道 。
作者: 默然10    时间: 2015-10-4 15:17

TKM-HBV  这个会议上会发布一期试验数据吗?
作者: StephenW    时间: 2015-10-4 15:50

默然10 发表于 2015-10-4 15:17
TKM-HBV  这个会议上会发布一期试验数据吗?

http://hbvhbv.info/forum/thread-1392407-1-1.html
作者: zgct    时间: 2015-10-4 20:49

有讲到可以很好干掉整合到肝细胞内HBV的基因吗?integrated DNA?
作者: zgct    时间: 2015-10-4 21:03

怕它是否是一种快速吹起来的不同输送方式新药核苷药!圈钱药
作者: StephenW    时间: 2015-10-4 22:23

zgct 发表于 2015-10-4 21:03
怕它是否是一种快速吹起来的不同输送方式新药核苷药!圈钱药

不同输送方式和不同"货物" 的RNAi, 不是核苷药.
作者: newchinabok    时间: 2015-10-30 10:50

http://files.shareholder.com/dow ... f_Amy_Lee_Final.pdf




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