In an open letter, Gilead (NASDAQ:GILD)
CEO Daniel O’Day says he expects to have initial data about the
potential of remdesivir to combat coronavirus “in the coming weeks.”
“When the news of the coronavirus first emerged,
Gilead immediately began to investigate the potential of remdesivir, a
medicine we had been studying for many years as part of our extensive
research in antivirals. Remdesivir had never been approved for use but
based on what we had learned to date, we knew it might have potential
with the novel coronavirus. Since then, we have been working with the
greatest sense of urgency and responsibility to determine whether
remdesivir does indeed work against COVID-19,” he writes.
“Multiple studies are ongoing, and we are on track
to have initial data in the coming weeks. If it is approved, we will
work to ensure affordability and access so that remdesivir is available
to patients with the greatest need.
“In the meantime, we have made the investigational
medicine available for severely ill patients who cannot enroll in a
trial. This ‘compassionate use’ program is typically reserved for a
small number of individual cases but there is nothing typical about this
crisis and to date we have provided remdesivir to more than 1,000
patients.
“With expanded access, hospitals or physicians can
apply for emergency use of remdesivir for multiple severely ill
patients at a time. While it will take some time to build a network of
active sites, this approach will ultimately accelerate emergency access
for more people.”
Last week, Gilead dropped
its orphan drug designation for remdesivir, a status granted by the FDA
that would have extended monopoly rights for the drug if it came on the
market.
https://seekingalpha.com/news/3556087-gilead-ceo-on-track-to-initial-data-in-coming-weeks
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