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春季银行配药报告临床数据的SB 9200的使用恩替卡韦乙肝病毒 [复制链接]

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发表于 2015-12-9 17:50 |只看该作者 |倒序浏览 |打印
Spring Bank Pharmaceuticals Reports Preclinical Data on the Use of SB 9200 with Entecavir in the Woodchuck Model of HBV
Data Supports Clinical Evaluation of SB 9200 in Combination with Anti-Viral Nucleos(t)ides in HBV

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MILFORD, Mass., Dec. 8, 2015 /PRNewswire/ -- Spring Bank Pharmaceuticals, Inc., a clinical-stage biopharmaceutical company developing novel therapeutics for the treatment of viral infections, today announced data from a preclinical study of its lead small molecule nucleic acid hybrid (SMNH) antiviral compound, SB 9200, in the woodchuck model of Hepatitis B (HBV) infection.

SB 9200 is a small orally bioavailable dinucleotide that selectively activates within infected cells the cellular viral sensors RIG-I and NOD2 to inhibit viral replication and cause the induction of intracellular interferon signaling pathways for antiviral defense.

The Company previously presented results of a 12-week study evaluating SB 9200 as a monotherapy in woodchucks at the 2015 Annual Meeting of the European Association for the Study of Liver Disease (EASL). In that study, treatment with SB 9200 resulted in significant reductions in viral load, including viral replication intermediates, and in surface antigen. The aim of this recent study was to evaluate the overall antiviral response in woodchucks when SB 9200 is used in a sequential-dosing fashion with entecavir, an antiviral nucleoside indicated for the treatment of HBV.

In this study, oral dosing with SB 9200 at 30 mg/kg for 12 weeks followed by four weeks of oral dosing with entecavir at 0.5 mg/kg/day in woodchucks resulted in statistically-significant, average declines of 6.4 log10 in viral DNA, and 3.3 log10 in viral surface antigen (sAg), along with significant reductions of hepatic viral DNA, viral RNA and cccDNA. This study presents evidence that SB 9200, when used with entecavir in an add-on regimen, can result in highly potent antiviral activity in woodchucks against the woodchuck hepatitis virus (WHV).

"We continue to assemble positive data suggesting that SB 9200 may potentially be an effective treatment against Hepatitis B," said Dr. Kris Iyer, Chief Scientific Officer of Spring Bank. "We are excited about the results from this important preclinical study and look forward to initiating our Phase 2 trial of SB 9200 in HBV during the first half of 2016."

The Company anticipates that the results of this preclinical study of SB 9200 and entecavir will be presented in an international antiviral conference in the near future.

About Spring Bank Pharmaceuticals

Spring Bank Pharmaceuticals is a clinical-stage biopharmaceutical company engaged in the discovery and development of a novel class of orally bioavailable therapeutics based on its proprietary small molecule nucleic acid hybrid, or SMNH, chemistry platform. SMNH compounds are small segments of nucleic acids that the company designs to selectively target and modulate the activity of specific proteins implicated in various disease states. The company is developing its most advanced SMNH product candidate, SB 9200, for the treatment of viral diseases. SB 9200 has been designed to selectively activate the host cellular proteins, RIG-I and NOD2, which have been implicated in the body's immune response to viral infections. Spring Bank believes that SB 9200 may play an important role in antiviral therapy by modulating host immune response to fight viral infections such as HBV and RSV.

Note Regarding NIH-Funded Research:

Certain studies mentioned in this press release were partly supported by the National Institute of Allergy and Infectious Diseases of the National Institutes of Health under Award Number R01AI094469 and NIAID contract laboratories. The content of this press release is solely the responsibility of Spring Bank Pharmaceuticals and does not necessarily represent the official views of the National Institutes of Health.

Contact:
Maeve Conneighton
Argot Partners
(212) 600-1902
[email protected]

SOURCE Spring Bank Pharmaceuticals, Inc.


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发表于 2015-12-9 17:50 |只看该作者
春季银行配药报告临床数据的SB 9200的使用恩替卡韦乙肝病毒的土拨鼠模型
数据支持SB 9200的联合临床评价与乙肝抗病毒核苷(酸)集成开发环境

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米尔福德,马萨诸塞,2015年12月8日/新华美通/ - 春季银行制药公司是一家临床阶段的生物技术企业,开发创新疗法对病毒性感染的治疗,今天公布的数据,从它的主角小分子的临床前研究核酸杂交体(SMNH)抗病毒化合物,SB 9200,在B型肝炎(HBV)感染的土拨鼠模型。

SB 9200是一个小的口服生物可利用的二核苷酸,其选择性地激活感染细胞内的细胞的病毒传感器RIG-I和NOD2抑制病毒复制和细胞内引起干扰素信号传导途径的抗病毒防御的诱导。

该公司此前提出了一个为期12周的研究,评估SB 9200作为旱獭单一疗法在欧洲协会的2015年年度会议为肝脏疾病的研究(EASL)的结果。在这项研究中,用SB 9200治疗导致显著减少病毒载量,包括病毒复制中间体,并在表面抗原。这个最近的一项研究的目的是评估在土拨鼠的整体的抗病毒反应时的SB 9200是用在一个序贯给药方式恩替卡韦,乙肝病毒的治疗表示的抗病毒核苷。

在这项研究中,口服剂量用SB 9200在30毫克/公斤12周,然后通过四个星期口服给药恩替卡韦以0.5mg / kg /天在土拨鼠导致6.4日志10中的病毒DNA统计学-显著,平均下降,和3.3日志10在病毒表面抗原(SAG),伴随着肝病毒DNA,病毒RNA和cccDNA的显著减少。这项研究提出的证据表明,SB 9200,恩替卡韦在一个附加的方案中使用时,可能会导致非常有效的抗病毒活性,对土拨鼠肝炎病毒(WHV)旱獭。

“我们将继续组装积极数据表明,SB 9200可能潜在地对乙肝的有效治疗方法,”克里斯艾耶博士,春季银行的首席科学官说。 “我们很高兴看到这一重要的临床前研究的结果,并期待着在开始的第一个2016年上半年SB 9200在HBV我们的二期试验”

公司预计,SB 9200和恩替卡韦的临床前这一研究结果将在不久的将来,一个国际抗病毒会议上提出的。

关于春季银行制药

春季银行药业是一家临床阶段的生物制药公司从事基于其专有的小分子核酸杂交,或SMNH,化学平台一类新型的口服生物疗法的发现和开发。 SMNH化合物是,该公司设计选择性地靶向和调节涉及各种疾病状态的特定蛋白质的活性的核酸小片段。该公司正在开发其最先进的SMNH候选产品,SB 9200,用于病毒性疾病的治疗。 SB 9200被设计成选择性地激活宿主细胞蛋白质,RIG-I和NOD2,已经牵连在体内的病毒感染的免疫应答。春季银行认为,SB 9200可以通过调节宿主免疫反应,以对抗病毒感染,如乙肝病毒和呼吸道合胞病毒发挥抗病毒治疗中起重要作用。

注:关于美国国立卫生研究院资助的研究:

本新闻稿中提及的某些研究由国家过敏研究所和美国国立卫生研究院在奖号R01AI094469和NIAID的合同实验室传染病被部分支持。本新闻稿中的内容完全是春季银行药品的责任,并不一定代表美国国立卫生研究院的官方意见。

联系:
梅芙Conneighton
隐语合作伙伴
(212)600-1902
[email protected]

源春银制药公司


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3
发表于 2015-12-9 18:34 |只看该作者
本帖最后由 newchinabok 于 2015-12-9 18:40 编辑

看好sb,有图表更好,sb不傻,好像比gs9620还好,可惜是老鼠模型

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发表于 2015-12-9 19:04 |只看该作者
谢谢
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,

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发表于 2015-12-9 19:09 |只看该作者
人体实验都没开始,都是要过7.8年后了

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发表于 2015-12-9 20:31 |只看该作者

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发表于 2015-12-9 20:49 |只看该作者
箭头或古巴药物成功,此药便作古!说实话研究乙肝的企业越多,给他们的时间越少,你可以拖拉不前。但是对手却不会停下脚步。

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发表于 2015-12-9 20:54 |只看该作者
回复 jiankangren19 的帖子

2016年二期,不慢,比较快的研发速度
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