Mar 6, 2020 - The British AI start-up, owned by Google's parent company Alphabet, ... can take months but the use of machine learning could speed up that ... Scientists racing to create a potent vaccine against the virus need as ... It comes as the number of cases of coronavirus across the world ... Use our tool to find out ...
Mar 23, 2020 - How AI can help develop a drug to treat coronavirus ... In recent weeks, researchers at London-based BenevolentAI have been ... The likes of Sanofi, the French pharmaceutical giant, are now rolling out clinical trials for Covid-19 ... "The opportunity for AI to speed up the discovery of vaccines, drugs and ...
Mar 21, 2020 - AI is speeding up drug research. At the end of the day, the war on the novel coronavirus is not over until we develop a vaccine that can immunize ...
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Mar 27, 2020 - The technology is being used to speed up the development of testing kits and ... AI experts to develop new data mining techniques that can help the scientific ... “We need to come together as companies, governments, and scientists ... drugs that could be used to treat coronavirus patients before a vaccine ... ............................................................................................................................
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The Food and Drug Administration issued an emergency approval Tuesday
for a serological testing kit produced by Bodysphere Inc. that can
detect a positive or negative result for COVID-19 in two minutes.
Why it matters: Access to testing has improved in the U.S. thanks to
commercial labs, but the average wait time for a patient's results is
four to five days — with some reports of it taking more than a week. These antibody tests could help people know if they are able to go
back to work, as well as aid researchers in tracking the scale and
death rate of the disease — key data for current and future pandemic
policies. They're especially useful for determining whether
health care workers have some immunity and are at lower risk if they go
back to work.
Yes, but: The
Bodysphere two-minute test can only detect the coronavirus in people
who have had the infection for several days, meaning the test can't be
used too early on when the body hasn't produced enough antibodies. The big picture: The FDA has been rushing to approve tests from companies that promise quicker results.
Abbott Laboratories received emergency authorization last week to
produce portable coronavirus tests, which the company indicates can
detect the virus within five minutes.
A blister pack of Hydroxychloroquine sulfate pills is displayed on March 26, 2020, in London.
John Phillips/Getty ImagesUpdated: 3/31/20 at 7:45 p.m. PST Topline:
The Food and Drug Administration on Sunday issued an emergency
authorization for experimental coronavirus treatments using chloroquine
and hydroxychloroquine, anti-malaria drugs touted by President Donald
Trump despite inconclusive clinical proof of their efficacy.
The Department of Health and Human Services said Sunday hydroxychloroquine and chloroquine products can be distributed and prescribedby doctors through the Strategic National Stockpile “to hospitalized teen and adult patients with COVID-19, as appropriate, when a clinical trial is not available or feasible.”
HHS said Germany’s
Sandoz has already given 30 million doses of hydroxychloroquine to the
Strategic National Stockpile, the federal government’s inventory of
medical supplies for public health emergencies, while Bayer has donated a
million doses of chloroquine.
The agency is fast-tracking a process that usually takes years while the FDA conducts clinical trials in New York, a hot spot for the virus.
HHS said the emergency
authorization was issued because the potential benefits of the product
outweigh the risks and acknowledged that “anecdotal reports suggest that
these drugs may offer some benefit in the treatment of hospitalized
COVID-19 patients,” but cautioned that “clinical trials are needed to
provide scientific evidence that these treatments are effective.”
Trump had falsely claimed that the FDA had approved the drugs for coronavirus treatment before Sunday.
Confusion over their
use has led some Americans to seek over-the-counter replacements, such
as an Arizona man who bought a nonpharmaceutical form of chloroquine
phosphate, a common chemical used to clean fish tanks, which killed him and landed his now-widow in intensive care.
The CDC warns
against taking nonpharmaceutical chloroquine phosphate without a
prescription and the supervision of a healthcare provider because it
“can cause serious health consequences, including death.”
Chief critic: Some in the scientific community are concerned there hasn’t been enough testing of the drugs. “It’s a difficult issue
because it’s an emotional issue. With people having no other options
available, it’s hard to say that if there’s something that seems like it
may work, they should be denied the option to try it. The part that
makes this more complicated is that there was an irresponsible, in my
opinion, expression that this actually is effective when there is no
real scientific evidence that it is,” Dr. Kenneth Kaitin, director of the Tufts Center for the Study of Drug Development, told Forbes.
Key background:
Trump continues to praise the anti-malarial drugs in daily press
briefings, Fox News has devoted segments to the drugs’ potential
benefits, and others, including the president’s personal lawyer Rudy Giuliani and Turning Points USA founder Charlie Kirk,
have promoted chloroquine and hydroxychloroquine as coronavirus cures.
Twitter eventually removed a Giuliani tweet that falsely said
“hydroxychloroquine has been shown to have a 100% effective rate
treating COVID-19.” There is no proven cure or vaccine for the
coronavirus. News peg:
Scientists hope chloroquine and hydroxychloroquine—decades-old drugs
that are used to treat malaria, lupus and rheumatoid arthritis—may be
used to treat the coronavirus, but early studies have providedmixedevidence proving their effectiveness and the drugs may entail risks such as vision problems
or cardiac arrest. The frenzy surrounding the treatment has caused some
doctors to hoard hydroxychloroquine—which is sold under the brand name
Plaquenil—by writing prescriptions for themselves or for their families.
Some state pharmacy boards have issued rules limiting prescriptions,
including Texas, Louisiana, Ohio and North Carolina.
March 30, 2020 - The FDA has authorized a coronavirus test that the manufacturer says can tell if someone is infected with the virus within 5 minutes.
The test is meant to be used in places like a doctor's
office, emergency room, or urgent care center. The test will provide
results through a platform currently used by many of those locations for
tests like flu and strep, instead of sending the throat or nasal swab
to a lab for analysis.
The FDA's emergency use authorization (EUA), issued on
Friday, does not mean that the FDA has approved the test, but that it is
allowing its use because of the coronavirus outbreak.
In a news release,
Abbott Diagnostics Scarborough in Illinois said the test can tell if a
person has the coronavirus in as little as 5 minutes and tell if someone
doesn't have the virus in 13 minutes.
A shortage of tests has hindered efforts to contain the
virus in the U.S, which leads the world with more than 100,000 cases of
COVID-19. Testing has been focused on priority groups, such as
hospitalized patients and health care professionals with symptoms,
according to CDC guidelines.
Abbott said it will make the tests available to health care
providers next week and work with the government to send the tests to
areas where they're most needed.
5 days ago - Most 3D printers today are best suited to making plastic parts, not cloth or filters used in face masks. Based in Redwood City, California, Carbon is ...
5 days ago - HP 3D Printed Masks for COVID-19 response; Designed by research institute CIIRC CVUT ... A single print can produce 300 test swabs at a time enabling ... frequently reviewing 3Dprinters and sharing his technical expertise.
Mar 20, 2020 - Manufacturers such as Vauxhall and Airbus are planning to repurpose their factories and utilize 3D-printing technology to create parts for ventilators to treat patients with the coronavirus. Prime Minister Boris Johnson appealed to companies to help in a “wartime” effort to ...
1 day ago - In one week, the group designed, made, tested, and are now distributing 3D-printed COVID-19 test swabs. Northwell's eight 3D printers are now ...
3 days ago - 3D Printer Crowdsourcing for COVID-19 public spreadsheet; Useful 3D Files; Cad Crowd's 3D Printing Challenge. Update 3/27. As the global 3D ...
3 days ago - The brand's Covid-19 masks consist of a visor that is worn across the forehead and secured behind the ears with elastic. Clear plastic film is ...
5 days ago - HP 3D Printing Covid-19. (Image credit: HP). HP has revealed plans on how it is using its 3D printers and expertise to help fight coronavirus, ...
How 3D printing can affect your broken supply chain during the crisis caused by the Covid-19 outbreak? 3D printing VS coronavirus. Worldwide pandemic ...
3 days ago - The additive manufacturing and 3D printing community has many members keen to assist during the COVID-19 pandemic. This is a summary of ...
3 days ago - 3D printing in support of COVID-19 containment efforts. Producing critical parts to help meet urgent needs. Materials on these pages are being ...
1 day ago - Top 1: COVID-19, how is 3D printing helping the fight? Given the current health crisis, the 3D printing community has mobilized to curb the ...
A medical worker screening people for COVID-19 in Jammu and Kashmir (representational image) | Photo: ANI
Text Size:
New Delhi: With the novel coronavirus going from
‘regional crisis’ to ‘pandemic’ status, researchers and pharmaceutical
giants are scrambling to find a cure.
The World Health
Organization (WHO) has launched global clinical trials to test possible
treatments for COVID-19 across 10 countries as a “solidarity trial”.
Some of the treatments to be tested are drugs already being used for other illnesses like HIV, Ebola and malaria.
Top drugs under trial include anti-malarial medicine chloroquine,
anti-viral drug remdesivir, a combination of HIV drugs lopinavir and
ritonavir, as well as a combination of the latter two drugs infused with
Interferon beta.
The popular anti-parasitic medication which treats malaria has been
around since the 1940s. US President Donald Trump Thursday called it a “game changer”, and proposed its use for COVID-19 cases.
However, American drug regulator, Food and Drug Administration (FDA), said “the agency is currently looking at widespread clinical trials of the drug, but it is not yet approved for that use”.
Biotech investor and doctor Mike Pellini was the first to use chloroquine as a possible cure for coronavirus.
Tech entrepreneur Elon Musk also tweeted that chloroquine was “maybe worth considering” as a potential treatment.
Chloroquine works by increasing the levels
of haem or heme — a substance toxic to the malarial parasite — in the
blood. This kills the parasite and stops the infection from spreading.
According to some earlier studies, “chloroquine has strong antiviral effects on SARS-CoV infection of primate cells”. One study showed
that chloroquine interferes with “terminal glycosylation of the
cellular receptor, angiotensin-converting enzyme 2”, which may
negatively influence the virus-receptor binding and abrogate the
infection.
Chloroquine is widely available in India, and is manufactured by
several local companies including Ipca Laboratories, Alembic
Pharmaceutricals and Cadila Pharmaceuticals.
If the drug works as a cure for the novel coronavirus, scaling up production won’t be difficult.
Foreign drug makers like Abbott, Bayer and Leo Pharmaceuticals also sell this drug in India.
Another drug in the spotlight is remdesivir — an anti-viral developed
by drugmaker Gilead, which specialises in manufacturing anti-HIV drugs. According to the WHO, remdesivir may have the best shot at treating COVID-19.
Remdesivir is an investigational broad-spectrum anti-viral drug,
which was developed to fight the Ebola virus. It is currently undergoing
clinical trials on coronavirus patients in China. WHO expects the trial
data to be available within weeks, according to media reports.
At a press briefing
in Beijing, WHO assistant director-general Bruce Aylward said: “There
is only one drug right now that we think may have real efficacy, and
that’s remdesivir.”
It was previously tested on humans with the Ebola virus disease, and has shown promise
in animal models for treating Middle East Respiratory Syndrome (MERS)
and Severe Acute Respiratory Syndrome (SARS), which are caused by other
coronaviruses. Also read:Govt sets up science and tech core team to coordinate efforts against coronavirus
Japanese flu pill favipiravir
According to a report in The Guardian
which, in turn, quoted a Japanese media report, “medical authorities in
China have said a drug used in Japan to treat new strains of influenza
appeared to be effective in coronavirus patients”.
The reports said doctors in Japan are using the drug in clinical
studies on COVID-19 patients with mild to moderate symptoms. However,
the drug has not shown great results on patients with severe symptoms.
The reports quoted Zhang Xinmin, an official in China’s science and
technology ministry, as saying: “Favipiravir, developed by a subsidiary
of Fujifilm with brand name Avigan, had produced encouraging outcomes in
clinical trials in Wuhan and Shenzhen involving 340 patients.
“It has a high degree of safety and is clearly effective in treatment,” Xinmin said.
The use of favipiravir showed definite improvements in lung condition
in 91 per cent of the patients treated with it, compared to 62 per cent
of those treated without the drug. Also read:One coronavirus patient infects 1.7 people in India, much lower than in China, Italy: Study
Plasma therapy
The US FDA is currently evaluating
therapies such as convalescent plasma and hyperimmune globulin. These
are antibody-rich blood products are taken from the blood donated by
people who have recovered from COVID-19. Research is going on to check
if these products “could shorten the length, or lessen the severity, of
the illness”.
Japanese drugmaker Takeda Pharmaceutical is also developing a therapy against the coronavirus using blood plasma. Bloombergreported
that with its background in manufacturing immunoglobulin-based products
approved by top regulating bodies across the globe, including the US
FDA, “the Japanese pharmaceutical company could have an edge because the
treatment involves a process that already has approval from
regulators”.
However, Takeda has not yet tested the therapy on any COVID-19 patients. Also read:No new cases in China to clean Venice waters — the latest on COVID-19
Combination of HIV drugs
Several patients across the globe have reported benefits from
treatment with a combination of HIV drugs — lopinavir and ritonavir.
Lopinavir, which acts against the viral 3CL protease, has modest
anti-viral activity against SARS-CoV-2 (the novel coronavirus),
according to an study published in The New England Journal of Medicine (NEJM).
“Together with ritonavir, which increases drug bioavailability, it is
in clinical trials, along with the immunomodulator interferon beta-1b,
for the treatment of Middle East Respiratory Syndrome (MERS),” the
article stated.
In India, the Union health ministry has also recommended the use of
anti-HIV drug combinations for high-risk groups of patients, but there
is no current evidence from randomised controlled trials to recommend a
specific treatment.
However, according to another study published in the NEJM,
these drugs have failed to cure COVID-19. A clinical trial in Beijing
tested the lopinavir-ritonavir combination on people who were severely
ill, but the outcomes of 94 people who received them were no different
from 100 patients who received standard care, the study stated. However,
it drew an open-ended conclusion.
“In hospitalised adult patients with severe COVID-19, no benefit was
observed with lopinavir-ritonavir treatment beyond standard care. Future
trials in patients with severe illness may help to confirm or exclude
the possibility of a treatment benefit,” the study said.