A team of a dozen executives at drugmaker Gilead Sciences Inc. meets
daily to discuss the coronavirus epidemic in China and the company’s
cross-continental scramble to develop the first drug for the new
disease.
If the company’s drug succeeds in studies in China, it could become
the first treatment proven to work against a respiratory virus that has
killed more than 1,000 people and infected some 42,600 in fewer than
three months.
There are some positive albeit preliminary signs, notably the
recovery of a 35-year-old man in Washington state whose condition
rapidly improved after receiving the drug and who was recently
discharged from the hospital.
“We’ve done this long enough that we know it could be an antidote,”
says Gilead’s chief medical officer, Merdad Parsey, cautioning that the
result could be a false positive and that the drug could fail in broader
testing.
Gilead has been sprinting to ramp up manufacturing of the drug,
called remdesivir, to meet a surge in demand if it proves effective, and
provide the medicine to two clinical trials of 760 Chinese patients and
a handful of patients requesting emergency use.
The Foster City, Calif., drug maker is among several companies
developing treatments targeting the coronavirus. AbbVie Inc. and Johnson
& Johnson have shipped HIV drugs to China to see if the agents work
against the virus.
Gilead, a longtime maker of treatments for viruses like HIV and
hepatitis C, had been monitoring the outbreak since late December when
the first reports of an unexplained pneumonia outbreak emerged from
China.
The company accelerated its push to study remdesivir after Chinese
scientists said Jan. 9 that they had identified the source of the
outbreak as a coronavirus, a family of diseases common in animals that
can cause severe respiratory illness when transmitted to humans.
Gilead invented remdesivir several years ago and first developed it
to treat Ebola, a virus that has ravaged parts of eastern and central
Africa. The drug was less effective than rival drugs in a study of Ebola
patients in Congo last year.
Yet Gilead had reason to think remdesivir might work in
coronaviruses. Company researchers working with academic scientists
found that remdesivir was effective in treating mice infected with
another coronavirus known as Middle East respiratory syndrome, or MERS.
The work was partially funded with $3.8 million in grants from the
National Institutes of Health. The mice studies were far from definitive
but suggested the drug had promise against the new coronavirus. The
data were published in the journal Nature Communications on Jan. 10.
“The attention level went up dramatically when we found out it was a
coronavirus, and that was the turning point,” Dr. Parsey says. “That’s
when we got mobilized and formed a team across the company to see what
we could do here.”
Gilead was soon exchanging information about the virus with officials
from the Chinese Center for Disease Control and Prevention, the World
Health Organization and the U.S. Centers for Disease Control and
Prevention. They discussed how to determine if remdesivir might be
effective at treating the outbreak.
By Jan. 20, Gilead was in talks with Beijing pulmonologist Cao Bin, a
prominent researcher deployed to Wuhan to help lead the medical care of
patients. With input from the U.S. Food and Drug Administration and the
WHO, Gilead worked with Dr. Cao’s team to design the studies, says
Gilead’s Diana Brainard, senior vice president for HIV and emerging
viral infections.
The trials are being conducted at several hospitals in Wuhan, according to Chinese news reports.
Last week, Gilead shipped the last batch of remdesivir needed to
supply the two studies, the first in patients with mild-to-moderate
disease and the second in patients with severe disease. The studies are
expected to be completed in early April.
“We’re all tracking the number of infections and deaths, and we really want to help,” says Dr. Brainard.
The company’s “coronavirus response team” now numbers about 100
employees across the company and includes executives from all major
departments.
Gilead employees in the U.S., along with many of the 400 employees it
has in Beijing and Shanghai, have worked hundreds of extra hours since
the mobilization began, juggling 3 a.m. conference calls, late-night
text messages and 7 a.m. office meetings to keep up with colleagues in
different time zones, Dr. Brainard says.
In addition to supplying remdesivir to the China trials, Gilead has
provided doses for individuals in countries including the U.S. and
France. Typically companies supply experimental drugs only in clinical
testing, though they can make exceptions in life-threatening situations
if the FDA gives approval.
CDC officials told the medical team treating the infected man in
Washington about remdesivir after his condition worsened. The company
got a compassionate-use request for the drug on Jan. 25. Within 36
hours, the FDA approved the request, and Gilead shipped the drug to
Washington.
Gilead’s stock rose 9% last week following a report in the New
England Journal of Medicine detailing the Washington patient’s recovery.
Yet some analysts express doubts that remdesivir will become a
money-maker anytime soon, even if it is shown to work against the novel
coronavirus.
If approved in China, Gilead may be able to charge only as little as
$260 per treatment course in the country, according to Morgan Stanley
estimates, far less than what a similar drug would cost in the U.S. Some
analysts say Gilead might not even make that much, if China decides to
bypass the company and authorize manufacturing of generic versions.
China could grant a patent to a state-run Chinese research institute,
which last week applied for a patent covering use of remdesivir against
the coronavirus. China also could invoke a World Trade Organization
“compulsory license” rule that allows countries to manufacture generic
copies of patented drugs in order to protect public health, some
analysts have said. Gilead would likely get paid royalties in either
scenario.
Gilead says it applied for a patent on remdesivir use in coronaviruses in 2016, and the application is pending in China.
Despite the uncertainty, Gilead has been building manufacturing
capacity. Over the past month, Gilead began coordinating with contract
manufacturers to start producing the drug again in North America and
halted production of an approved product at one of its own facilities in
North America so it could start making remdesivir itself, Dr. Parsey
says.
https://www.marketscreener.com/GILEAD-SCIENCES-4876/news/Gilead-Sciences-Scrambles-to-Supply-Experimental-Coronavirus-Drug-29987102/
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