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两大重挫:Juno又停止JCAR015 CAR-T临床实验,礼来阿尔兹海默病药物临床III期失败

2016-11-25 奇点原创文章(公众号:geekheal_com) 奇点原创文章(公众号:geekheal_

11月23日,祸不单行。2016年最受关注的两个领域的临床研究接连受挫。先是礼来(Lilly)宣布,其轻度阿尔兹海默病III期临床药物Solanezumab没有达到主要临床终点,宣告失败;紧接着朱诺(Juno)宣布,其处于II期临床阶段的CAR-T免疫治疗方法JCAR015再次导致患者死亡,主动暂停JCAR015的临床研究。截止发稿前,礼来的股价下跌16%,朱诺的股价重挫30%。Solanez

11月23日,祸不单行。

2016年最受关注的两个领域的临床研究接连受挫。先是礼来(Lilly)宣布,其轻度阿尔兹海默病III期临床药物Solanezumab没有达到主要临床终点,宣告失败;紧接着朱诺(Juno)宣布,其处于II期临床阶段的CAR-T免疫治疗方法JCAR015再次导致患者死亡,主动暂停JCAR015的临床研究。截止发稿前,礼来的股价下跌16%,朱诺的股价重挫30%。

Solanezumab

Solanezumab是靶向β淀粉样蛋白的单克隆抗体药物,礼来在上面的投入达数亿美元。一直以来,礼来的Solanezumab被业界寄予厚望,然而2013年两个III期临床研究的失败,在业界引起了极大的震动。一度甚至动摇了「阿尔兹海默病是由β淀粉样蛋白导致的」这一主流理论。


礼来官方申明

2015年7月,礼来在华盛顿举行的阿尔茨海默氏病协会国际会议(AAIC)上,公布了Solanezumab的最新试验数据分析结果。这一回礼来重新分析研究了前面两个III期临床试验结果研究,根据阿尔茨海默病认知评估量表(Alzheimer’s Disease Assessment Scale-cognitive subscale ,ADAS-cog),重新分析了部分轻度患者的试验结果,数据显示Solanezumab能够将认知能力下降速度减缓34%,相比安慰剂组具有统计学显著性(1)。这些数据提振了礼来继续研发这个药物的热情。这一结果也是礼来启动第三个III期临床研究的根本动力。

然而,本周三上午,礼来官方宣布,Solanezumab的第三个临床试验EXPEDITION3没有达到预期结果。根据阿尔茨海默病认知评估量表分析,Solanezumab给轻度阿尔茨海默病患者带来的认知衰退减慢,与安慰剂带来的结果没有显著差异。

礼来将在12月8日,美国东部时间下午9点15在阿尔茨海默病临床试验(CTAD)会议上提供进一步的研究结果。发布会将会通过网络直播(http://www.ctad-alzheimer.com)。

受礼来Solanezumab临床结果的影响,Biogen的股票也下跌6%。

JCAR015

对于朱诺的JCAR015来讲,这已经是这半年来第二次了。

在四个月前,由于临床试验导致多人死亡,FDA叫停朱诺的CAR-T免疫疗法JCAR015在复发性或难治性B细胞急性淋巴细胞白血病患者身上展开的临床II期试验;虽然几天之后FDA又允许朱诺继续开展CAR-T免疫疗法JCAR015临床II期试验,但JCAR015的这一表现还是激起了人们对CAR-T免疫治疗的疑虑。


朱诺官方申明

在9月7日,朱诺终于再次证明了自己的实力,在《科学转化医学》期刊发表了一篇重要文章(2),CAR-T候选药物JCAR014与特定化疗药物一起使用,让一些晚期非霍奇淋巴瘤患者病情完全缓解。

好不容易扳回一局。今天,据朱诺报道,本周早些时候,CAR-T免疫疗法JCAR015临床II期试验又导致两人脑水肿,其中一人已经于昨晚死亡,至于另一人,用朱诺的话说,「没有恢复的希望。」

四个月前,FDA叫停JCAR015临床II期试验的时候,朱诺称,导致患者死亡的主要原因是化疗药物氟达拉滨,在后续的研究中他们会改进化疗的方法,死亡案例应该不会再出现。

但是还是出现了同样的现象。这一次朱诺没有等FDA叫停,他主动终止了JCAR015临床II期试验。朱诺表示,他们已经通知FDA,并正在与FDA和数据与安全监测委员会合作,以确定JCAR015下一步该如何走。

JCAR015是朱诺的主要候选疗法,朱诺一直希望JCAR015能在明年获得FDA的上市批准,但这一时间表在第一次导致死亡之后被取消,目前看来更是遥遥无期。

此消息一出,朱诺的股价重挫30%以上。

原始出处:

【1】Siemers ER, Sundell KL, Carlson C, Case M, Sethuraman G, et al. 2016. Phase 3 solanezumab trials: Secondary outcomes in mild Alzheimer’s disease patients. Alzheimer’s & Dementia: The Journal of the Alzheimer’s Association 12:110-20

【2】Turtle CJ, Hanafi L-A, Berger C, Hudecek M, Pender B, et al. 2016. Immunotherapy of non-Hodgkin’s lymphoma with a defined ratio of CD8 and CD4 CD19-specific chimeric antigen receptor-modified T cells. Science Translational Medicine 8:355ra116-355ra116

【3】http://www.fiercebiotech.com/biotech/juno-car-t-study-put-hold-again-after-cerebral-edemas-and-fatality-again

【4】https://investor.lilly.com/releasedetail.cfm?ReleaseID=1000871

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    2017-03-01 juliusluan78
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    2017-07-05 仁者大医
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  4. 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    2016-12-05 Jackie Li

    收藏

    0

  5. 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    2016-11-30 mswert122

    总觉得前沿科学家很牛

    0

  6. 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  7. 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  8. 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channel=null, level=null, likeNumber=60, replyNumber=0, topicName=null, topicId=null, topicList=[TopicDto(id=97761, encryptionId=60ca9e761ce, topicName=阿尔兹海默)], attachment=null, authenticateStatus=null, createdAvatar=, createdBy=be952422716, createdName=habb, createdTime=Sun Nov 27 05:08:00 CST 2016, time=2016-11-27, status=1, ipAttribution=), GetPortalCommentsPageByObjectIdResponse(id=1594468, encodeId=e000159446859, content=<a href='/topic/show?id=b317956200' target=_blank style='color:#2F92EE;'>#III期#</a>, beContent=null, objectType=article, channel=null, level=null, likeNumber=48, replyNumber=0, topicName=null, topicId=null, topicList=[TopicDto(id=9562, encryptionId=b317956200, topicName=III期)], attachment=null, authenticateStatus=null, createdAvatar=, createdBy=a12645, createdName=智智灵药, createdTime=Sun Nov 27 05:08:00 CST 2016, time=2016-11-27, status=1, ipAttribution=), GetPortalCommentsPageByObjectIdResponse(id=158250, encodeId=fe3515825081, content=献给研究的前沿科学家, beContent=null, objectType=article, channel=null, level=null, likeNumber=69, replyNumber=0, topicName=null, topicId=null, topicList=[], attachment=null, authenticateStatus=null, createdAvatar=null, createdBy=1cdf1948157, createdName=Peter程, createdTime=Sat Nov 26 09:53:06 CST 2016, time=2016-11-26, status=1, ipAttribution=), GetPortalCommentsPageByObjectIdResponse(id=158148, encodeId=e8c815814890, content=看来得另辟蹊径了, beContent=null, objectType=article, channel=null, level=null, likeNumber=64, replyNumber=0, topicName=null, topicId=null, topicList=[], attachment=null, authenticateStatus=null, createdAvatar=, createdBy=445f1740270, createdName=meiliwuxian, createdTime=Fri Nov 25 20:14:03 CST 2016, time=2016-11-25, status=1, ipAttribution=), GetPortalCommentsPageByObjectIdResponse(id=158119, encodeId=601d15811921, content=股票市场好现实,呵呵, beContent=null, objectType=article, channel=null, level=null, likeNumber=95, replyNumber=0, topicName=null, topicId=null, topicList=[], attachment=null, authenticateStatus=null, createdAvatar=https://wx.qlogo.cn/mmopen/vi_32/Q0j4TwGTfTKDtuWHtWxToIW0ZEvbHgDb4ibqQ1xaDQxcsHC5NIc2RJUxQgHJOLGEg8OUT345rDPmka4icU0WHPgw/0, createdBy=379f1941464, createdName=艳阳天2016, createdTime=Fri Nov 25 15:42:46 CST 2016, time=2016-11-25, status=1, ipAttribution=)]
    2016-11-26 Peter程

    献给研究的前沿科学家

    0

  9. 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authenticateStatus=null, createdAvatar=https://wx.qlogo.cn/mmopen/vi_32/Q0j4TwGTfTKDtuWHtWxToIW0ZEvbHgDb4ibqQ1xaDQxcsHC5NIc2RJUxQgHJOLGEg8OUT345rDPmka4icU0WHPgw/0, createdBy=379f1941464, createdName=艳阳天2016, createdTime=Fri Nov 25 15:42:46 CST 2016, time=2016-11-25, status=1, ipAttribution=)]
    2016-11-25 meiliwuxian

    看来得另辟蹊径了

    0

  10. 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authenticateStatus=null, createdAvatar=https://wx.qlogo.cn/mmopen/vi_32/Q0j4TwGTfTKDtuWHtWxToIW0ZEvbHgDb4ibqQ1xaDQxcsHC5NIc2RJUxQgHJOLGEg8OUT345rDPmka4icU0WHPgw/0, createdBy=379f1941464, createdName=艳阳天2016, createdTime=Fri Nov 25 15:42:46 CST 2016, time=2016-11-25, status=1, ipAttribution=)]
    2016-11-25 艳阳天2016

    股票市场好现实,呵呵

    0

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真的已经找阿尔兹海默症可以传播的新证据了?

上周的Nature期刊发表了一篇题为Evidence for human transmission of amyloid-β pathology and cerebral amyloid angiopathy的研究论文,作者们声称他们找到了阿尔兹海默症可以传播的新证据。随后有很多媒体进行了后续报道。例如,英国的每日镜报报道为“爆炸性的新的研究表明,阿尔兹海默病可以传播,就像朊病毒可通过输血、

Acta Neuropathol:新药或可改善阿尔兹海默症或其他脑部疾病

神经病理学中心的Armin Giese教授和研究人员分析了一种新的物质,可以作为一个原型发展的药物来治疗阿尔茨海默氏症和其他脑部疾病。该物质被称为“anle138b”,这种物质可以改善小鼠疾病症状并提高它们的认知。科学家们报告这些发现在《Acta Neuropathologica》杂志上。 “我们已经发现,这种物质能防止tau蛋白的聚合。此聚合是阿尔茨海默氏症和其他脑部疾病的典型的表现,被称

新型工程化蛋白或可扼杀阿尔兹海默氏症

图片来源:medicalxpress.com 最近,一项来自瑞典皇家理工学院(kth royal institute of technology)的最新研究指出,一种工程化的新型蛋白可以成功抑制携带人类阿尔兹海默氏症基因的小鼠患痴呆症,相关研究或为开发治疗相关疾病的疗法提供希望。文章中研究者开发了一种可以靶向作用淀粉样β蛋白多肽的结合性蛋白,淀粉样β蛋白和阿尔兹海默氏症发病直接相关。 当同

Genome Biol:用于揭示阿尔兹海默氏症早期发病的基因特性

来自伦敦国王学院的科学家近日通过研究发现,一种用于特殊的基因特性或可帮助预测某些疾病的早期发病情况,比如阿尔兹海默氏症,相关研究刊登于国际杂志Genome Biology上。该研究中研究者旨在在65岁的老年个体机体中定义一些和健康老化相关的基因特性,而利用分子特性研究者常常可以进行年龄相关疾病早期风险的判断,这就可以帮助寻找指示疾病的新型指示器。 研究者James Timmons教授表示,我

PNAS:科学家筛选可以保护机体抵御痴呆症的新基因

优胜劣汰,适者生存是生物学界最容易被误解的术语,近日,刊登在国际杂志PNAS上的一项研究报告中,来自加利福尼亚大学的研究人员通过研究表示,对于人类而言,自然选择或许更倾向于使得祖父母获得遗传保护而抵御痴呆症的发生,老年阶段维持较好的认知和记忆能力或许会促进老年人传播他们的智慧,并且关爱子孙们,同时痴呆症的老年人却跟需要照顾自己。 这种外祖母的假设更契合于亲属选择(血缘淘汰)的规则,也就是说,个人

Lancet Neurol:健康老年人群中临床和认知功能轨迹研究 (AIBL)

已知的在认知功能正常的老年人群中(年龄60岁或以上)有50-60%会出现脑淀粉样β蛋白(Aβ)沉积和神经退行性变。尚不清楚出现阿尔兹海默病病理变化和神经退行性变对认知功能的长期影响,以及他们是否独立或协同影响了认知功能。此研究的目的在于使用两种标记(阿尔兹海默病病理和神经退行性变)的影像构建健康老年人群的认知功能轨迹。 2006年11月3日到2014年11月25日,墨尔本,珀斯,澳大利亚57

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