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发表于 2018-4-3 22:55 |只看该作者 |倒序浏览 |打印
Replicor to disclose updated data demonstrating functional remission of HBV and HDV at the EASL International Liver Conference 2018



MONTREAL, April 3, 2018 – Replicor Inc., a privately held biopharmaceutical company targeting a cure for chronic hepatitis B and D patients, today announced that new additional follow-up data from its latest NAP-based combination trials in HBV infection (REP 401 study) and HBV / HDV co-infection (REP 301-LTF study) will be presented at the 2018 International Liver Conference (ILC) hosted by the European Society for the Study of the Liver (EASL) to be held April 11-15, 2018 in Paris, France.

The REP 401 study (NCT02565719) is a randomized, controlled trial assessing the safety and efficacy of Replicor’s lead HBsAg release inhibitor, REP 2139-Mg and of a REP 2139 derivative with enhanced plasma and tissue clearance (REP 2165-Mg) in combination with tenofovir disoproxil fumarate (TDF) and pegylated interferon alpha 2a (peg-IFN) in 40 patients with chronic HBeAg negative HBV infection.  Poster FRI-343 will feature further extended follow-up in patients in the experimental arm as well as new follow up data from patients in the adaptive control arm (who crossed over to experimental therapy in the absence of a HBsAg response during TDF and pegIFN).

The REP 301-LTF study (NCT02876419) provides a long term follow-up on patients with chronic HBV / HDV co-infection completing combination therapy with REP 2139-Ca and pegIFN in the REP 301 study (NCT02233075).  Poster FRI-326 (also featured during the HDV oral e-poster session on Saturday) will include follow-up data now extended to 1.5-2 years.

Updated modelling of viral kinetics during REP 2139-Ca monotherapy in HBeAg+ chronic HBV infection in the REP 102 study (NCT02646189) will also be featured in Poster FRI-324.

Replicor’s presentations from EASL ILC 2018 will be available on the company’s website following their disclosure at the meeting at www.replicor.com/science/conference-presentations.  For further information about the EASL ILC 2018 visit: http://www.easl.eu/discover/even ... iver-congress-2018.

About Replicor

Replicor is a privately held biopharmaceutical company with the most advanced animal and human clinical data in the development of the cure for HBV and HDV. The company is dedicated to accelerating the development of an effective treatment for patients with HBV and HBV/HDV co-infection. For further information about Replicor please visit our website at www.replicor.com.

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发表于 2018-4-3 22:55 |只看该作者
Replicor在2018年EASL国际肝脏会议上披露证明HBV和HDV功能缓解的更新数据



蒙特利尔,2018年4月3日 - 生物制药公司Replicor Inc.是一家针对慢性乙型肝炎和D患者治疗的私人生物制药公司,今天宣布其最新的基于NAP的HBV感染联合试验的新的后续数据(REP 401研究)和欧洲肝脏研究学会(EASL)于2018年4月11 - 15日举办的2018年国际肝脏会议(ILC)上发表了一篇关于HBV / HDV共同感染(REP 301-LTF研究) 2018年在法国巴黎。

REP 401研究(NCT02565719)是一项随机对照试验,评估Replicor的主要HBsAg释放抑制剂REP 2139-Mg和具有增强的血浆和组织清除率的REP 2139衍生物(REP 2165-Mg)的安全性和有效性,以及40名慢性HBeAg阴性HBV感染患者使用替诺福韦酯替罗非昔酯(TDF)和聚乙二醇干扰素α2a(peg-IFN)。海报FRI-343将在实验组患者中进一步延长随访时间,以及适应性对照组患者的新随访数据(在TDF和pegIFN期间没有HBsAg应答的情况下跨越实验性治疗) 。

REP 301-LTF研究(NCT02876419)为REP 301研究(NCT02233075)中的REP 2139-Ca和pegIFN慢性HBV / HDV共同感染完成联合治疗的患者提供了长期随访。海报FRI-326(也是周六在HDV口头电子海报会议期间的特色)将包括现在延长到1.5 - 2年的后续数据。

海报FRI-324中还将更新REP 102研究中REP 2139-Ca单药治疗HBeAg +慢性HBV感染病毒动力学模型(NCT02646189)。

Replicor从EASL ILC 2018发布的信息将在公司网站www.replicor.com/science/conference-presentations上公布后在公司网站上公布。有关EASL ILC 2018访问的更多信息,请访问:http://www.easl.eu/discover/even ... liver-congress-2018

关于Replicor

Replicor是一家私人控股的生物制药公司,在开发治疗HBV和HDV方面拥有最先进的动物和人类临床数据。该公司致力于加速为HBV和HBV / HDV合并感染患者开发有效的治疗方案。有关Replicor的更多信息,请访问我们的网站www.replicor.com

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发表于 2018-4-4 19:37 |只看该作者
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