Posted on 04/09/2020 11:40:11 AM PDT by nickcarraway
Slated for human trials, EIDD-2801 could become the first pill for COVID-19
An oral medicine was able to hinder the coronavirus behind COVID-19 as it attempted to replicate itself in human lung cells in test tubes, scientists reported Monday. It also hampered closely related coronaviruses from reproducing in mice for several days and improved their lung functions.*
The drug, called EIDD-2801, interferes with a key mechanism that allows the SARS-CoV-2 virus to reproduce in high numbers and cause infections, the researchers explained in the journal Science Translational Medicine. Human trials have not yet been done, but if the effect is similar in people, the drug would be the first pill available to help with the COVID-19 pandemic, which has resulted in more than 1.3 million cases and about 76,400 deaths worldwide. An oral medication would be a boon, because it would be easier to give to more people than an intravenous injection.
The study was done by a team at Emory University, the University of North Carolina at Chapel Hill and Vanderbilt University Medical Center in Nashville, Tenn. A company that has licensed the drug, Ridgeback Biotherapeutics, has just been granted permission from the U.S. Food and Drug Administration to begin 10 patient trials of the antiviral pill in the next few months.
The same university collaboration had already found that Gilead Sciences experimental medicine remdesivir was effective in shutting down replication of the coronaviruses that caused the original SARS and MERS epidemics. Remdesivir has received attention because it entered clinical trials against SARS-CoV-2 in March, and the first results may come by late April. The findings announced yesterday indicate that EIDD-2801 was possibly even more successful in disrupting coronavirus replication than the Gilead drug. On March 20 the researchers investigating EIDD-2801, co-led by Tim Sheahan of Chapel Hill, posted the results of their animal studies on the preprint server bioRxiv while submitting them for peer review. Given the current COVID-19 crisis, it was important to share, says George Painter, a professor of chemistry and executive director of the Emory Institute for Drug Development, which first produced the drug.
Back in 2018 Painter and the labs he leads identified EIDD-2801s activity during a search for a universal influenza medicine. Last October, before the pandemic hit, the Emory program got $15.9 million from the National Institute of Allergy and Infectious Diseases to perform human tests of the drug against the flu virus that was likely to be circulating later in the year. When SARS-CoV-2 emerged, Painters group immediately shifted focus.
EIDD-2801 inhibits the coronaviruss self-copying operations in a manner that is different from remdesivir. While remdesivir brings that replication process to a full stop, EIDD-2801 introduces mutationsmistakesinto the viruss RNA as it makes copies so that the viral RNA becomes so damaged that it cannot infect cells. Another feature of the drug is that it is able to work against a host of other RNA viruses. Thus, it could serve as a multipurpose antiviral, much in the way some antibiotics can work against a wide variety of bacteria. In several preclinical studies, researchers from multiple labs have shown that EIDD-2801 was effective against several strains of influenza, as well as the viruses for respiratory syncytial virus and the viruses for chikungunya, Venezuelan equine encephalitis and Eastern equine encephalitisall microbes that intermittently pop up in different parts of the world and produce widespread sickness in their wake.
The compound may be initially beneficial as a prophylaxis [that] health care workers can take to prevent an infection, says Wayne Holman, co-founder of Miami-based Ridgeback Biotherapeutics, which has licensed the drug from Emorys nonprofit biotech company Drug Innovation Ventures at Emory (DRIVE). Another potential use of EIDD-2801 might be to protect uninfected nursing home residents and workers if an outbreak occurs inside a facility. Holman says the wider goal is to have an oral pill that can be taken twice a day by patients at home early in the course of the disease to prevent it from progressing to hospitalization, mechanical ventilation or death.
In addition to planning clinical trials in the U.S., Ridgeback has also asked U.K. authorities to start tests there as well. Weve done three to four years of development work in just the past three to four weeks in response to the new pandemic, Holman says.
Read more about the coronavirus outbreak here.
*Editors Note (4/7/20): This paragraph was edited after posting to correct the description of the studys findings. Only coronaviruses related to SARS-CoV-2 were tested in mice, not SARS-CoV-2 itself.
“Doesn’t halt replication, but induces errors in replication...”
— Dr. Eldon Tyrell, to Roy Baty, in “Blade Runner”
Chloroquine does the same thing, that’s been known more than ten years.
This drug is being developed now?
Why didn’t Fauci focus on developing a drug like this, or determining efficacy of chloroquine over the past 15 years?
36 years and he has done nothing.
And the cost will be what.....$1,000.00 per pill?
"the drug would be the first pill available to help with the COVID-19 pandemic"Bring Out Your Deaduh huh...
Post to me or FReep mail to be on/off the Bring Out Your Dead ping list.
The purpose of the Bring Out Your Dead ping list (formerly the Ebola ping list) is very early warning of emerging pandemics, as such it has a high false positive rate.
The false positive rate was 100%.
At some point we may well have a high mortality pandemic, and likely as not the Bring Out Your Dead threads will miss the beginning entirely.
*sigh* Such is life, and death...
If a quarantine saves just one child's or one old farts life, it's worth it.
This drug supposedly causes mutations in viral RNA. What about our own cellular RNA? What can possibly go wrong?
The development of EIDD-2801 has been funded in whole or in part with Federal funds from the National Institute of Allergy and Infectious Diseases (NIAID), under contract numbers HHSN272201500008C and 75N93019C00058, and from the Defense Threat Reduction Agency (DTRA), under contract numbers HDTRA1-13-C-0072 and HDTRA1-15-C-0075, for the treatment of Influenza, coronavirus, chikungunya, and Venezuelan Equine Encephalitis Virus.
About Ridgeback
Headquartered in Miami, Florida, Ridgeback Biotherapeutics is a privately held, majority woman owned biotechnology company focused on orphan and infectious diseases. Initial funding for Ridgeback Biotherapeutics originated from Wayne and Wendy Holman; two individuals committed to investing in and supporting technologies that will make the world a better place.
Ridgeback has exclusively licensed DRIVE's EIDD-2801
Ridgeback Biotherapeutics will be responsible for advancing this promising therapeutic through clinical development and ensuring that EIDD-2801 is available during the current pandemic.
So Ridgeback is responsible for "ensuring that the drug will be available during the current pandemic." Do they have the resources and capability to actually DO that?
there are multiple promising clinical trials with several different drugs and also convalescent plasma
chloroquine does not do the same thing. It is not the magic bullet some think it is
“chloroquine does not do the same thing. It is not the magic bullet some think it is”
This in response to my saying choloquine does the same thing referring to this statement in the article: “An oral medicine was able to hinder the coronavirus behind COVID-19 as it attempted to replicate itself in human lung cells in test tubes”.
Chloroquine has been know for more than ten years stop viral proliferation in vitro, which is what this statement describes.
I can give you multiple references to chloroquine’s effectiveness in vitro if you want.
Re “magic bullet”’ no duh. There are no panaceas and magic bullets but nice of you to set up a strawman.
Re “an oral medicine”. It just shows how sloppy the writing us, even in Scientific Anerican wherein it is being developed as an oral drug, the in vitro studies are certainly not oral. Just messy writing.
Two years ago my son in Puerto Rico told me the PR Gov. was recommending Vitamin C to fight Zika and Chikungunya. He said VItamin C was disappearing from store shelves.
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