15/10/02说明:此前论坛服务器频繁出错,现已更换服务器。今后论坛继续数据库备份,不备份上传附件。

肝胆相照论坛

 

 

肝胆相照论坛 论坛 学术讨论& HBV English HBV核心抑制剂NVR3-778的联合核苷类似物
查看: 7192|回复: 51
go

HBV核心抑制剂NVR3-778的联合核苷类似物   [复制链接]

Rank: 10Rank: 10Rank: 10

现金
20661 元 
精华
帖子
12793 
注册时间
2013-12-29 
最后登录
2024-11-2 
1
发表于 2015-5-2 18:46 |只看该作者 |倒序浏览 |打印
Effect of the combination of the HBV core inhibitor NVR 3-778 with Nucleoside Analogs or other HBV core inhibitors on the inhibition of HBV DNA Replication in HepG2.2.15 cells


http://www.natap.org/2015/EASL/EASL_74.htm
已有 1 人评分现金 收起 理由
MP4 + 3

总评分: 现金 + 3   查看全部评分

Rank: 10Rank: 10Rank: 10

现金
20661 元 
精华
帖子
12793 
注册时间
2013-12-29 
最后登录
2024-11-2 
2
发表于 2015-5-2 18:47 |只看该作者
HBVCURER能不能解释一下?

Rank: 7Rank: 7Rank: 7

现金
3543 元 
精华
帖子
2934 
注册时间
2001-10-26 
最后登录
2018-12-25 
3
发表于 2015-5-2 20:34 |只看该作者
看不明白!
建议有实力的众筹基金会,十亿元级以上,真劝慰雷军、地产商、首富、百度,强生战略入股,全球重金悬赏求拜攻克乙肝的美国古巴专家英才及技术!!齐参与、正能量,或许好药就在转角间被发现,如果没有?就用真实去验证及考证中草药民间名医,延长寿命
嘤其鸣矣,求其友声! 相彼鸟矣,犹求友声;矧伊人矣,不求友生?神之听之,

Rank: 7Rank: 7Rank: 7

现金
3543 元 
精华
帖子
2934 
注册时间
2001-10-26 
最后登录
2018-12-25 
4
发表于 2015-5-2 20:37 |只看该作者
newchinabok 发表于 2015-5-2 18:47
HBVCURER能不能解释一下?

HBVCURER大神帮助解释下
建议有实力的众筹基金会,十亿元级以上,真劝慰雷军、地产商、首富、百度,强生战略入股,全球重金悬赏求拜攻克乙肝的美国古巴专家英才及技术!!齐参与、正能量,或许好药就在转角间被发现,如果没有?就用真实去验证及考证中草药民间名医,延长寿命
嘤其鸣矣,求其友声! 相彼鸟矣,犹求友声;矧伊人矣,不求友生?神之听之,

Rank: 10Rank: 10Rank: 10

现金
6875 元 
精华
帖子
977 
注册时间
2006-10-2 
最后登录
2024-5-28 

版主勋章 才高八斗

5
发表于 2015-5-17 01:23 |只看该作者
不同靶点协同用药好,就像hiv里面的鸡尾酒疗法一样
论坛里面忽悠不少,不能简单听信别人,关系自己健康,多了解一些乙肝治疗常识是有必要的(乙肝治疗指南+骆抗先博客)

Rank: 7Rank: 7Rank: 7

现金
3216 元 
精华
帖子
1331 
注册时间
2004-7-29 
最后登录
2019-8-21 
6
发表于 2015-5-18 20:25 |只看该作者
由于HBV核心(衣壳)蛋白在病毒复制和持久性的多重作用,HBV核心蛋白抑制剂通过抑制HBV DNA复制、病毒组装、补充cccDNA和肝脏再感染循环,具有提高持久应答率的潜力。 NVR3-778是一种HBV核心蛋白抑制剂,在体外抗HBV活性类似于强效核苷(酸)。

本文是关于核心蛋白抑制剂叠加核苷类药物的结果。结论是替诺福韦叠加性最好。
已有 1 人评分现金 收起 理由
StephenW + 10

总评分: 现金 + 10   查看全部评分

Rank: 7Rank: 7Rank: 7

现金
3378 元 
精华
帖子
2638 
注册时间
2007-4-5 
最后登录
2022-11-8 
7
发表于 2015-5-19 08:50 |只看该作者
回复 baobao7676 的帖子

谢谢您的总结归纳!
病友交流,仅供参考.

Rank: 10Rank: 10Rank: 10

现金
20661 元 
精华
帖子
12793 
注册时间
2013-12-29 
最后登录
2024-11-2 
8
发表于 2015-5-19 09:10 |只看该作者

Rank: 10Rank: 10Rank: 10

现金
20661 元 
精华
帖子
12793 
注册时间
2013-12-29 
最后登录
2024-11-2 
9
发表于 2015-5-19 09:10 |只看该作者
Novira Therapeutics Announces Presentation of Preclinical Antiviral Data for NVR 3-778 at EASL
Oral presentation: "High antiviral activity of the HBV core inhibitor NVR 3-778 in the humanized UPA/SCID mouse model"

Poster presentation: "Effect of the combination of the HBV core inhibitor NVR 3-778 with nucleoside analogs or other HBV core inhibitors on the inhibition of HBV DNA replication in HepG2.2.15 cells"


Google+  Share with LinkedIn   
DOYLESTOWN, Pa., April 27, 2015 /PRNewswire/ -- Novira Therapeutics, Inc., a privately held, clinical-stage biopharmaceutical company developing novel therapies for curative treatment of chronic hepatitis B virus (HBV) infection, today announced the presentation of preclinical antiviral data for its lead HBV core inhibitor candidate, NVR 3-778, at the 2015 annual meeting of the European Association for the Study of the Liver (EASL) in Vienna, Austria.

The antiviral activity of NVR 3-778 from studies performed in a humanized UPA/SCID mouse model was described in an oral presentation. As monotherapy given for a six week duration, NVR 3-778 showed HBV DNA suppression efficacy superior to pegylated interferon (PEG-IFN) and similar to that of the widely prescribed nucleoside analog entecavir. All mice responded to treatment and there was no evidence for drug resistance. The highest efficacy was observed in mice that received NVR 3-778 in combination with PEG-IFN, where all treated mice (n=11) reduced serum HBV DNA below the limit of quantitation.

In a poster session, Novira presented results from the combination of NVR 3-778 with nucleoside analogs lamivudine, tenofovir or entecavir in a cell-based model. These data showed additive and synergistic antiviral activity without cytotoxicity. NVR 3-778 also showed additive antiviral activity in combination with an HBV core inhibitor from another chemical class.

"The apparent synergy of NVR 3-778 in combination with PEG-IFN is very encouraging. This is the first time that we have seen a treatment with higher DNA suppression efficacy than entecavir in a humanized mouse model," said Klaus Klumpp, Ph.D., Novira's VP of Discovery and Biology. "Having access to a new class of Direct Acting Antivirals, or DAAs, enables the clinical testing of combination treatments that may significantly intensify the suppression of HBV production in the liver. Highly potent DAA combination treatment may be able to reduce the rate of new hepatocyte infection below that of infected hepatocyte clearance in HBV infected patients and may thereby lead to a clinically-relevant improvement in functional cure rates."

About NVR 3-778

NVR 3-778 is a small molecule, direct acting antiviral, for oral administration in patients with Chronic Hepatitis B (CHB) that inhibits the HBV core or capsid protein. HBV core is a novel and promising drug target with multiple activities required for viral replication and persistence. Inhibition of the HBV core protein function by NVR 3-778 offers the potential for more efficient suppression of virus production and replication, leading to improved durable viral suppression and functional cure rates. NVR 3-778 completed a Phase 1a clinical trial in 2014 and is currently enrolling a Phase 1b clinical trial.

About HBV

Hepatitis B infection presents a significant unmet medical need with an estimated 350 million people worldwide living with chronic HBV infection. A significant number of patients with chronic infection incur a higher risk of developing cirrhosis and cancer. It is estimated that 60% of hepatocellular carcinoma (liver cancer) is a direct consequence of HBV infection. Current drugs approved for the management of CHB include PEG-Interferon and nucleot(s)ides which can effectively suppress virus replication, but rarely lead to a cure.

About Novira Therapeutics

Novira Therapeutics, Inc., is a privately held biopharmaceutical company focused on discovery and development of first-in-class antiviral drugs for the treatment of chronic HBV infection (CHB), a global disease with a high level of unmet medical need. The company is employing innovative chemistry and biology technologies to discover small molecule inhibitors of the HBV core or capsid protein as well as other drugs with novel mode of action. The company's novel antivirals will offer the potential to address the limitations of current CHB therapies when used either as mono-therapy or in combination with existing standards of care.

Rank: 10Rank: 10Rank: 10

现金
20661 元 
精华
帖子
12793 
注册时间
2013-12-29 
最后登录
2024-11-2 
10
发表于 2015-5-19 09:11 |只看该作者
Novira Therapeutics宣布临床前介绍抗病毒数据的NVR 3-778在EASL
口头陈述:“HBV核心抑制剂NVR 3-778的人性化UPA / SCID小鼠模型的高抗病毒活性”

海报介绍:“HBV核心抑制剂NVR 3-778与HBV DNA复制的HepG2.2.15细胞抑制核苷类似物或其它HBV核心抑制剂的组合的效应”
 

Google+分享与LinkedIn
DOYLESTOWN,霸,2015年4月27日/新华美通/ - 。Novira Therapeutics公司是一家私人持有,临床阶段的生物技术企业,开发创新疗法治疗治疗慢性乙型肝炎病毒(HBV)感染,今天宣布的表现抗病毒的临床前数据的铅HBV核心抑制剂候选人,NVR 3-778,在欧洲协会为肝脏(EASL)在维也纳,奥地利研究2015年年度会议。

NVR 3-778从一个人性化的UPA / SCID小鼠模型进行研究的抗病毒活性在口头陈述中描述。作为单一疗法给予为六个为期一周,NVR 3-778表现出乙型肝炎病毒DNA的抑制效力优于聚乙二醇干扰素(PEG-IFN)和类似于广泛处方核苷类似物恩替卡韦。所有的小鼠对治疗有反应,并没有任何证据为耐药性。最高效力,观察在接受NVR 3-778结合PEG-IFN,小鼠,所有处理过的小鼠(n = 11)低于定量极限降低血清HBV DNA。

在海报会议,Novira提出的结果从NVR 3-778的组合的核苷类似物拉米夫定,替诺福韦或恩替卡韦在基于细胞的模型。这些数据显示,无毒性的添加剂和协同的抗病毒活性。 NVR 3-778还显示出与从另一种化学类的HBV核心抑制剂组合添加剂的抗病毒活性。

“NVR 3-778的与PEG-IFN组合的表观协同作用是非常令人鼓舞的。这是第一次,我们已经看到比恩替卡韦在人源化小鼠模型中越高的DNA抑制功效的治疗,”克劳斯Klumpp的中,Ph表示。 D.,发现和生物学Novira的副总裁。 “能够使用一类新的直接作用抗病毒药,或的DAA的,使得能够联合治疗的临床试验,可能显著加紧在肝脏HBV产生的抑制。高度有效的DAA组合治疗可以是能够减少的新肝细胞的比率下面是感染的肝细胞清除乙肝病毒感染者的感染,并可能由此导致的功能治愈率一个临床相关的改善。“
‹ 上一主题|下一主题
你需要登录后才可以回帖 登录 | 注册

肝胆相照论坛

GMT+8, 2024-11-2 22:41 , Processed in 0.013922 second(s), 12 queries , Gzip On.

Powered by Discuz! X1.5

© 2001-2010 Comsenz Inc.