FDA hits pause on one of the first US human clinical trials to use CRISPR

FDA hits pause on one of the first US human clinical trials to use CRISPR
One of the first CRISPR human trials in the United States has been paused by the FDA before it had even begun
One of the first CRISPR human trials in the United States has been paused by the FDA before it had even begun
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One of the first CRISPR human trials in the United States has been paused by the FDA before it had even begun
One of the first CRISPR human trials in the United States has been paused by the FDA before it had even begun

The CRISPR-Cas9 genome editing system has inarguably revolutionized medical research, promising a future where scientists can treat a vast array of human illnesses from cancer to blindness. But since its discovery in 2012, progress towards human trials has been slow. Now, another setback has appeared with the FDA pausing one of the first human trials using the technique in the United States before it even begins.

The proposed treatment to be trialed is called CTX001, and in the US it was set to be investigated for patients suffering from sickle cell disease. The treatment isolates stem cells from a patient's blood and then uses CRISPR to make a single genetic change designed to raise levels of fetal hemoglobin in red blood cells.

The Phase 1/2 human clinical trial in the US was set to commence later this year until a recent announcement from CRISPR Therapeutics, the company developing the treatment, revealed the US Food and Drug Administration (FDA) has just placed a clinical hold on the trial. At this stage the only details released by the company state that the hold on the trial is pending "the resolution of certain questions that will be provided by the FDA as part of its review of the IND [Investigational New Drug Application]."

No information has been revealed clarifying exactly what the FDA's enquiries are, but upon announcement of the clinical trial hold CRISPR Therapeutics stocks tumbled by nearly 19 percent.

The US trial was set to run in conjunction with a European trial targeting a condition called beta-thalassemia using the same treatment. The status of the European trial is reportedly unaffected by this FDA decision and still on track to be initiated later in 2018, making it the first CRISPR human trial to take place in Europe.

The sickle cell CTX001 trial was set to be one of the first two CRISPR trials to commence in the US in 2018. The other trial, being run out of the University of Pennsylvania, targets three types of cancer: multiple myeloma, sarcoma, and melanoma. It is still reportedly on track for commencement very soon, although its clinical trial status is still labeled as "recruiting."

This roadblock is yet another affirmation of the challenges scientists are facing in translating this momentous technological advance into safe and effective human treatments. The only current human trials using the CRISPR technique are reportedly underway in China, but there have been concerns that the country may be racing forward in its trials too quickly.

While the last few years have undeniably proved exciting as CRISPR has made sophisticated gene editing a reality, the next couple of years are set to show us just how easy or difficult it will be to translate revolutionary technology into safe human clinical treatments.

Source: CRISPR Therapeutics

I am certain the medical cartels are fighting hard to make sure this never reaches the market, at least in the United States. When there is no clear indicator on why something like this was stalled in the approval process, if you dig deep enough it's probably some "deep pockets" that are blocking things.
No risk, no gain! Another reason China will ultimately outstrip the USA in research and results in most fields...
The FDA, proudly killing Americans for the last 112 years. Their approval process has little to do with drug safety and benefits to the public and more to do with helping Big Pharma line their pockets. The are thousands of people who die everyday because it takes up to 2-3 years for a drug to go through their procedures. How many drugs and medical products went through the FDA's stringent and convoluted approval system and still ended with lawsuit generating injuries and deaths. I've recently seen half a dozen ads on TV from lawyer groups, requesting injured parties to contact them for a class action lawsuit for drugs with serious side effects and medical devices that have failed.
@Fabian: The "deep pockets" are actually the ones funding CRISPR Tx and its love child with Bayer Pharma (one of the world's largest Pharma/chemical companies): Casebia Therapeutics. Same thing with Allogene, Intellia, Editas, Spark, Juno, Kite, Bellicum, etc. It's all being funded directly by Big Pharma, Big Biotech and VC companies. I'm deeply involved with helping scientists and MD's use CRISPR editing to make ex-vivo and in-vivo gene therapies so I'm speaking from literally first-hand knowledge.
I know the conspiracy theory logic says that Big Pharma blocks cures, but it's absolutely not the case here. Whereas a small drug or biologic can lead to sustained revenue over the mid to long term, cures such as the ones mentioned in the article offer almost immediate payments of between $500k and $1 million per patient. In today's corporate culture where only short term quarter-over-quarter results matter, cures now look extremely promising. Yes from a financial standpoint, but also from a core mission statement that most of these companies have: curing disease and enabling longer life-spans with a higher quality of living.
And just a heads-up, the HSPC autologous therapies mentioned in the article above are the very tippy top of a massive ice berg that's coming in the next 20 years to transform healthcare as we know it. Side effects, chronic treatments, death from 100's of cancers, genetic defects that lead to early death. All curable. We've entered the golden age of biotech and the future looks extremely bright.