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发表于 2016-10-2 13:51 |只看该作者 |倒序浏览 |打印
80% of data in Chinese clinical trials have been fabricated

Oh crap.
FIONA MACDONALD
1 OCT 2016
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A Chinese government investigation has revealed that more than 80 percent of the data used in clinical trials of new pharmaceutical drugs have been "fabricated".

The report uncovered fraudulent behaviour at almost every level, and showed that some pharmaceutical companies had hidden or deleted records of potentially adverse side effects, and tampered with data that didn't meet their desired outcomes.

In light of the findings, 80 percent of current drug applications, which were awaiting approval for mass production, have now been cancelled.

The investigation, led by the Chinese State Food and Drug Administration (SFDA), looked at data from 1,622 clinical trials for new pharmaceutical drugs currently awaiting approval. The applications in question were all for Western medicine, not traditional Chinese medicine.

The SFDA found that the more than 80 percent of the data failed to meet analysis requirements, were incomplete, or totally non-existent.

Not only did the report find that many of the 'new' drugs awaiting approval were actually a combination of existing drugs, they also showed that many clinical trial outcomes were written before the trials had actually taken place, and the data had been simply manipulated to match what companies wanted to find.

Worst of all, it wasn't just a few scientists or pharma companies doing the dirty work. The report found that pretty much everyone involved was guilty of some kind of malpractice of fraud.

Perhaps most worryingly, even third party independent investigators tasked with inspecting clinical trial facilities are mentioned in the report as being "accomplices in data fabrication due to cut-throat competition and economic motivation".

In other words, China's pharmaceutical industry has a really, really big problem - and the SFDA now has to worry about all the other new drugs approved as "safe" based on potentially unreliable clinical trials.

The problem isn't regulation - Chinese clinical trials have similar guidelines in place as the Western world, with three phases required to test for safety, efficiency, and whether or not the new drug is better than the existing treatment.

Those guidelines are all well-communicated and inspected by third parties, but there's clearly a "lack of adherence to them", explains Ben Hargreaves from PharmaFile.

The SFDA report was released by the state-owned Economic Information Daily Newspaper, and, as yet, there's no English version available online to go over with a fine-toothed comb, so for now, we're taking the Chinese media's word for it.

But as shocking as it all sounds, Economic Information Daily Newspaper also cites unnamed industry insiders who weren't surprised in the slightest at the revelations.

"Clinical data fabrication was an open secret even before the inspection," the paper quoted an unnamed hospital chief as saying, reports Radio Free Asia.

According to Luo Liang, a Chinese healthcare professional, the problem stems from the fact that local pharmaceutical companies trying to produce Western drugs struggle to turn a profit.

"The domestic market for Western pharmaceuticals in China is either confined to very straightforward generic products that have been around for a long time ... or revolves around joint-venture pharmaceutical manufacture with foreign companies," Liang told Sing Man for Radio Free Asia.

"Either that, or Chinese pharmaceutical factories get hold of the formula for certain drugs whose patents have expired," he added. "There are no new drugs in development in the same way that there are overseas ... I don't think that the 80 percent figure is overstated."

While traditional Chinese medicine wasn't covered by this investigation, some think even worse practices are going on in that industry, but are less likely to be uncovered because they're "harder to regulate".

"It's not just the medicines," he said. "In China, everything is fake, and if there's a profit in pharmaceuticals, then someone's going to fake them too."

As damning as this problem is for China's scientists, they aren't the only ones that are under more and more pressure to publish positive and "groundbreaking" results in order to keep their jobs.

A study published earlier this month revealed that the enormous pressure on academics is acting like a form of natural selection, and evolving science into something "shoddy and unreliable".

Let's just hope reports like this serve as a wake-up call to show what's really at stake when we can't trust researchers anymore - because that's a pretty scary reality to consider.

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发表于 2016-10-2 13:51 |只看该作者
在中国的临床试验数据的80%,已经制造了
中国的临床试验80%的数据伪造
哦,废话。
FIONA MACDONALD
2016年10月1日
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中国政府的调查显示,在新药品的临床试验中使用的数据的80%以上已经被“捏造”。

该报告揭露欺诈行为,几乎所有层面,并表明,一些制药公司已经隐藏或删除潜在的不良副作用的记录,并与没有达到他们想要的结果的数据被篡改。

在调查结果,80%的目前的药物应用,正等待批准大规模生产的光,现在已经取消了。

经查,被中国国家食品药品监督管理局(SFDA)的带领下,检查了数据从目前正在等待批准的新药品1622临床试验。有问题的应用程序都是为西药,不是传统意义上中国中药。

国家药监局发现,超过80%的数据未能达到分析的要求,不完整,或完全不存在。

不仅该报告发现,许多“新”的药物正在等待批准的实际上是现有药物的组合,他们也表明,许多临床试验的成果被写入之前的审判已经实际发生,而且数据已经简单地操纵符合哪些公司希望能找到。

最糟糕的是,它不只是一个几位科学家或医药公司做肮脏的工作。该报告发现,几乎每个人都参与犯有某种欺诈的弊端的。

也许最令人担忧的是,随着检查的临床试验设施的任务,即使第三方独立调查报告中被提及为“数据制作的帮凶,由于恶性竞争和经济动机”。

换句话说,中国的医药行业有一个非常,非常大的问题 - 与国家药监局现在要担心所有批准基于对潜在不可靠的临床试验“安全的”等新型毒品。

问题不在于调控 - 中国临床试验也有类似的指引到位作为西方世界,与需要分三个阶段进行测试的安全,效率,以及新的药物是否比现有治疗更好。

这些准则都是良好的沟通和第三方检查,但显然有一个“缺乏坚持他们”,从PharmaFile本哈格里夫斯说。

国家药监局报告是由国有经济信息日报发布,并且,迄今为止,有可上网用细齿梳去在没有英文版本,所以现在,我们走的是中国媒体的话吧。

但令人震惊,因为它所有的声音,经济信息日报还援引谁没有丝毫的惊讶启示不愿透露姓名的业内人士。

“临床数据制作是一个公开的秘密,甚至在检查前,”该报援引一位不愿透露姓名医院院长的话说,报道自由亚洲电台。

据罗亮,中国的医疗专业人士,这个问题的原因是,本土制药企业试图生产西药很难扭亏为盈茎。

“国内市场对中国医药西部要么仅限于非常简单的通用产品已经存在了很长一段时间......或周围合资药品生产与国外公司围绕”亮告诉星人对自由亚洲电台。

“如果不是这样,还是中国药厂获得公式某些药物,其专利已经过期的话,”他补充说。 “有在以同样的方式发展没有新的药物,有海外...我不认为80%的数字被夸大了。”

虽然没有包括在本研究中国传统医学,有些人认为更糟糕的做法在业内是怎么回事,但不太可能被发现,因为他们是“难以监管”。

“这不仅仅是药品,”他说。 “在中国,一切都是假的,以及是否有药品利润,那么别人的要假的他们。”

作为确凿的,因为这问题对于中国的科学家,他们不是唯一的是在越来越大的压力来发布,以正和“突破性”结果,以保住自己的饭碗。

本月初公布的一项研究表明,在学术上的巨大压力,表现得像自然选择的一种形式,并不断发展的科学到的东西“伪劣和不可靠的”。

我们只是希望这样的报告作为一个警钟,显示岌岌可危什么是真正的时候,我们不能信任的研究人员了 - 因为这是一个非常可怕的现实考虑。

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发表于 2016-10-2 14:58 |只看该作者
这报道造谣,之前讨论过了
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发表于 2016-10-2 16:24 |只看该作者

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发表于 2016-10-2 18:34 |只看该作者
本帖最后由 smilingcloud 于 2016-10-2 18:57 编辑

http://www.sda.gov.cn/WS01/CL008 ... ne&isappinstalled=0
国家食品药品监督管理总局关于开展药物临床试验数据自查核查工作的公告(2015年第117号)


1622个药物临床试验数据自查品种1184种主动撤回,占80%


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发表于 2016-10-2 20:05 |只看该作者
StephenW 发表于 2016-10-2 16:24
回复 MP4 的帖子

来自: http://www.sciencealert.com/



不用出处了,肯定是造谣
首先这总数是SFDA下查的名单,不是所有
其次主动撤回是企业经常有的事,不能把撤回说造假。
分母和分子都不会,数据肯定错。
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发表于 2016-10-2 20:06 |只看该作者
smilingcloud 发表于 2016-10-2 18:34
http://www.sda.gov.cn/WS01/CL008 ... ne&isappinstalled=0
国家食品药品监督管理总局关于开展药物临床试 ...

谣狗你好
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发表于 2016-10-2 20:29 |只看该作者



http://www.sda.gov.cn/WS01/CL0051/128084.html

”本次药物临床试验自查涉及1622个品种。其中,申请人提交自查资料的注册申请为1094个,占 67%;主动撤回的注册申请317个,占20%;申请减免临床试验等不需要提交的注册申请193个,占12%”
欢迎收看肝胆卫士大型生活服务类节目《乙肝勿扰》,我们的目标是:普度众友,收获幸福。
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发表于 2016-10-2 21:01 |只看该作者
造假不是新闻,不造假才是新闻
头像被屏蔽

元帅

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发表于 2016-10-2 21:03 |只看该作者
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