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Molnupiravir, originally developed as a treatment for influenza, was repurposed for COVID-19. However, a study suggests that it may be linked to specific SARS-CoV-2 mutations. The UK government recently procured molnupiravir, but opted for Paxlovid instead. Ridgeback Biotherapeutics, which partnered with Merck for clinical trials, developed molnupiravir as a pill for outpatient use. The drug has shown promise in reducing viral levels in COVID-19 patients. Further studies are ongoing to determine its effectiveness in preventing severe illness. Emory University scientists have previously demonstrated the drug's efficacy against various diseases.
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@Amy31129057 - QuestionIt

Were they wrong about Molnupiravir? Molnupiravir was originally developed to treat influenza at Emory University by the university's drug innovation company, Drug Innovation Ventures at Emory (DRIVE), but was reportedly abandoned for mutagenicity concerns when used in Covid patients. Molnupiravir, sold under the brand name Lagevrio, is an antiviral medication that inhibits the replication of certain RNA viruses. It was used to treat COVID-19 in those infected by SARS-CoV-2. It is taken by mouth. For several years, Emory scientists had been working on EIDD-2801, a drug candidate with potential as a treatment for several highly infectious and worrisome viral diseases, including influenza and Venezuelan Equine Encephalitis virus, some of which are biodefense threats. When the pandemic began, the team quickly turned its attention to developing EIDD-2801 as a treatment for COVID-19. DRIVE licensed EIDD-2801, now known as molnupiravir, to Ridgeback Biotherapeutics in 2020, which conducted the first human clinical trials and then partnered with Merck. In October 2021 the UK government announced the procurement of 480 000 courses of molnupiravir (as well as 250 000 courses of the Pfizer antiviral Paxlovid (nirmatrelvir)). Guess who they went with.... PAXLOVID. 😏 https://en.wikipedia.org/wiki/Molnupiravir https://drugdiscovery.emory.edu/molnupiravir/index.html https://bmj.com/content/377/bmj.o926

Molnupiravir - Wikipedia en.wikipedia.org
About Molnupiravir | Emory University | Atlanta GA drugdiscovery.emory.edu
Covid-19: What is the evidence for the antiviral molnupiravir? Merck’s drug was originally claimed to halve hospital admissions and deaths in people with covid-19, leading some governments to stockpile it as the pandemic continued. Andy Extance looks at the published evidence for its effectiveness Molnupiravir (marketed as Lagevrio) is an antiviral drug, slightly modified from a compound known as NHC (β-d-N4-hydroxycytidine) that a team at Emory University in Atlanta, Georgia, first described in 2003.1 It is available as hard capsules that are swallowed and absorbed from the gut so is easy to take at home. That contrasts with some other covid-19 drugs such as the monoclonal antibody tocilizumab or the antiviral remdesivir, which must be administered by intravenous infusion in hospitals. In October 2021 the UK government announced the procurement of 480 000 courses of molnupiravir (as well as 250 000 courses of the Pfizer antiviral Paxlovid (nirmatrelvir)). Molnupiravir had been due to enter clinical trials against influenza, but during the pandemic Emory University struck a deal with the biotechnology company Ridgeback Biotherapeutics to test it as a treatment for covid-19.2 Ridgeback then partnered with the pharmaceutical giant Merck in May 2020 for clinical trials and scale-up.3 Antiviral drugs for acute respiratory infections need to be used as early as possible after infection if they are to help prevent disease progression, hospital admissions, and deaths. This normally means within three days, but the drug may still be beneficial up to five days after onset of symptoms. The current advice is to give 800 mg of molnupiravir (four 200 mg tablets) every 12 hours for five days, within five days of symptom onset.4 Like many antivirals, its chemical structure resembles the nucleotide bases that link together to make the long RNA chains that are a virus’s genetic material. After ingestion, molnupiravir breaks down to … bmj.com

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Good Grief, Pay Attention~ Anti-viral drug backfires: COVID drug linked to viral mutations that spread. Merck's small-molecule molnupiravir linked to mutated viruses that spread in people. (September 26, 2023) According to a new peer-reviewed study in the journal Nature, the anti-viral drug dubbed molnupiravir is linked to specific SARS-CoV-2 mutation signatures that happened to spring up in 2022 when the drug was introduced. The study's authors—led by researchers at the Francis Crick Institute in London and the University of Cambridge—scanned through more than 15 million SARS-CoV-2 genome sequences found in global databases. They picked out unique mutation signatures that closely linked to signatures seen in viruses from patients known to have been treated with molnupiravir. These suspected molnupiravir-linked mutation signatures also matched those seen in viruses examined in a clinical trial of molnupiravir. https://arstechnica.com/health/2023/09/covid-anti-viral-drug-is-actively-helping-sars-cov-2-mutate-and-evolve/

Anti-viral drug backfires: COVID drug linked to viral mutations that spread Merck's small-molecule molnupiravir linked to mutated viruses that spread in people. arstechnica.com

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Question IT! https://x.com/Amy31129057/status/1735456355300045068?s=20

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Please look into this more @RandPaul @RepThomasMassie @SenRonJohnson @Leeshotfury1966 @I_Am_JohnCullen @LmBubba Drug launched at Emory reduces virus that causes COVID-19 to undetectable levels (March 17, 2021) Ridgeback Biotherapeutics~ Ridgeback Biotherapeutics is a Miami-based biotechnology company, primarily known for its involvement in developing a successful COVID-19 medication. Ridgeback is privately owned by hedge fund manager and physician, Wayne Holman (formerly of S.A.C. Capital Advisors) and his wife Wendy Holman. Wendy is the CEO at the company, which refers to itself as a majority woman owned business. In early 2020, Ridgeback purchased an exclusive license for the commercial development of Molnupiravir from Emory University, where the drug was initially developed with $16 million in grants from Federal agencies including the National Institutes of Health. The terms of the deal were undisclosed. Molnupiravir was initially researched as a treatment for influenza, but may have broad spectrum activity against other viruses. Ridgeback was mentioned in a whistleblower complaint from Rick Bright, former director of the Biomedical Advanced Research and Development Authority (BARDA). The complaint alleged that Ridgeback lobbied the government for millions in funding to help develop Molnupiravir. Merck & Co. partnered with Ridgeback to perform clinical trials with Molnupiravir in humans to treat COVID-19. An antiviral drug initially discovered by Emory’s non-profit drug development company DRIVE appears safe and reduces SARS-CoV-2 to undetectable levels in COVID-19 patients after five days of administration, according to data from a Phase II clinical trial in the United States. Molnupiravir, previously known as EIDD-2801, can be provided as a pill in an outpatient setting, which could be a step up in ease of distribution and convenience. Although remdesivir and antiviral monoclonal antibodies have received Emergency Use Authorizations from the FDA, they must be given intravenously or by injection. In addition, drugs like molnupiravir could flexibly tackle SARS-CoV-2 variants, which have emerged as a concern in recent months. "There's still an urgent need for an antiviral drug against SARS-CoV-2 that can be easily produced, transported, stored, and administered," says George Painter, PhD, CEO of DRIVE (Drug Innovation Ventures at Emory) and director of the Emory Institute for Drug Development. When the COVID-19 pandemic began, DRIVE quickly repurposed a broad-spectrum antiviral drug it had been developing against influenza and equine encephalitis. Molnupiravir is being developed further by Merck and its partner Ridgeback Biotherapeutics, a closely held biotechnology company, which licensed the drug from DRIVE last year. All funds for the post-licensing development of EIDD-2801/molnupiravir have been provided by Ridgeback and Merck. In the most recent clinical study, molnupiravir eliminated infectious coronavirus from nose swabs within five days in all of the people taking it. For comparison, a quarter of people receiving placebo still had detectable virus in their nose swabs at day five. Emory physicians were not involved in the clinical trial, which recruited 202 adults with COVID-19 symptoms at outpatient clinics in the United States. The data were presented at the recent Conference on Retroviruses and Opportunistic Infections (CROI). While molnupiravir is proven to interfere with coronavirus replication in infected patients, more data is required to determine whether it can prevent severe illness. Merck and Ridgeback say that more results from the U.S. clinical trial will be shared when they become available, and additional Phase 2 and 2/3 clinical studies are underway. Molnupiravir has also been tested for safety in a clinical trial in the United Kingdom. Molnupiravir works by forcing the viral enzyme that copies SARS-CoV-2’s genetic material to make so many mistakes that the virus can’t replicate. Still, Merck’s comprehensive testing indicates that high doses of the drug are not mutagenic in animals. Emory scientists, in collaboration with top coronavirus experts at other universities, have previously shown that EIDD-2801 is highly effective at interfering with coronavirus replication and transmission in animal models and also in mice implanted with human lung tissue. EIDD-2801 has broad spectrum activity against a number of diseases of public health concern, including influenza, SARS-CoV-1, MERS, chikungunya, Ebola and equine encephalitis. The drug was initially developed with the support of the National Institute of Allergy and Infectious Diseases, the Defense Threat Reduction Agency, and the Georgia Research Alliance's Venture Development program. https://news.emory.edu/stories/2021/03/coronavirus_DRIVE_molnupiravir/index.html https://en.wikipedia.org/wiki/Ridgeback_Biotherapeutics https://www.science.org/content/article/emails-offer-look-whistleblower-charges-cronyism-behind-potential-covid-19-drug https://en.wikipedia.org/wiki/Molnupiravir

Drug launched at Emory reduces virus that causes COVID-19 to undetectable levels | Emory University | Atlanta GA An antiviral drug initially discovered by Emory’s non-profit drug development company DRIVE appears safe and reduces SARS-CoV-2 to undetectable levels in COVID-19 patients after five days of administration, according to data from a Phase II clinical trial. news.emory.edu
Ridgeback biotherapeutics - Wikipedia en.wikipedia.org
Molnupiravir - Wikipedia en.wikipedia.org