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发表于 2017-3-24 09:12 |只看该作者 |倒序浏览 |打印
Hepatera completed patient recruitment for clinical trials of an innovative drug against Hepatitis B with Delta Agent Ronan Leonard
March 22, 2017
BiotechCutting EdgeFuture TrendsHealthMedTechWorld News

                                                                                                                       
Hepatera LLC, a biotechnology company of Maxwell Biotech Group and a resident of the Skolkovo Foundation Biomed Cluster, has completed the patient recruitment for phase 2b clinical trials of Myrcludex B innovative medical drug.
Hepatera is implementing a clinical program for patients suffering from chronic viral hepatitis B with delta agent, which includes two clinical trials and extensive laboratory research intended for comprehensive study of the pharmacological activity of Myrcludex B innovative drug.
A clinical trial according to MYR 202 protocol involves the assessment of a viral load, activity of liver ferments and a histologic pattern for three dosages. The patients take Myrcludex B in a combination with a nucleotide analogue tenofovir to suppress the replication of hepatitis B virus. The trial includes 120 patients in 15 clinical centres of Russia and Germany. The active therapy stage duration will be 24 weeks.
The second clinical trial according to MYR 203 protocol assesses safety and anti-viral activity of various Myrcludex B dosages in combination with pegylated interferon ?-2a. The trial includes 60 Russian patients who will undergo an active therapy stage during 48 weeks.
Aleksandr Aleksandrov, Medical Director, Hepatera: “We do everything possible to speed up the market launch of Myrcludex B, awaited by the patients who suffer from the most severe form of viral hepatitis and have no treatment alternatives. Hepatera is implementing the world’s largest clinical program for the patients with this rare but very serious disease, and has recently completed the recruitment of 180 patients for two parallel trials.”
The program of clinical trials has been supported by the Skolkovo Foundation. A grant received in the end of 2015 allowed the company to focus its strategy of Myrcludex B studies on an orphan hepatitis B disease with delta agent, while the commercialization strategy switched to the accelerated market launch of the drug.
Kirill Kaem, VP, Executive Director of ?iomed Cluster, Skolkovo Foundation: “Hepatera, which is one of a few Russian startups to independently launch clinical trials both in Russia and Germany, has overcome all regulatory obstacles and quickly completed the patient recruitment, thus emphasizing a high market demand for the drug being developed. The Foundation and the patients’ community are eagerly waiting for the results of the clinical trials that will determine the further strategy for the commercialization of Myrcludex B innovative medical drug.”

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发表于 2017-3-24 09:12 |只看该作者
Hepatera完成了针对乙型肝炎与Delta Agent的创新药物临床试验的临床试验
罗安·伦纳德,2017年3月22日
BiotechCutting EdgeFuture TrendsHealthMedTechWorld新闻

作为麦克斯韦生物科技集团的生物技术公司和Skolkovo基金会生物群集群的居民Hepatera LLC完成了Myrcludex B创新药物的2b期临床试验的病人招聘。

Hepatera正在为患有慢性病毒性乙型肝炎患者的delta药物实施临床计划,其中包括两项临床试验和广泛的实验室研究,旨在全面研究Myrcludex B创新药物的药理活性。

根据MYR 202方案的临床试验涉及评估病毒载量,肝发酵活性和三种剂量的组织学模式。患者服用Myrcludex B与核苷酸类似物替诺福韦组合以抑制乙型肝炎病毒的复制。该试验包括俄罗斯和德国15个临床中心的120例患者。主动治疗期持续时间为24周。

根据MYR 203方案的第二次临床试验评估了各种Myrcludex B剂量与聚乙二醇化干扰素α-2a组合的安全性和抗病毒活性。该试验包括60名在48周内进行积极治疗阶段的俄罗斯患者。

Hepatera医学主任Aleksandr Aleksandrov:“我们尽全力加快Myrcludex B的市场推出,等待患有最严重形式的病毒性肝炎的患者,并没有治疗方法。 Hepatera正在为这种罕见但非常严重的疾病的患者实施世界上最大的临床计划,并且最近完成了180名患者的两次并行试验。

临床试验方案得到Skolkovo基金会的支持。 2015年底收到的赠款使公司能够将梅多库特B研究的战略集中在带有德尔塔药剂的孤儿乙型肝炎病毒,而商业化战略转向药物加速市场推出。

斯柯尔科沃基金会执行总监Kirill Kaem:“俄罗斯和德国独立开展临床试验的几家俄罗斯创业公司之一的Hepatera已经克服了所有监管障碍,并迅速完成了患者招聘强调对正在开发的药物的市场需求很高。基金会和患者社区正在急切地等待临床试验的结果,这将决定Myrcludex B创新药物商业化的进一步战略。“
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