Emergency Use Of Molnupiravir Tablet For COVID Seeks Government Permission

Emergency Use Of Molnupiravir Tablet For COVID Seeks Government Permission

Merck & Co. announced on Friday that it will seek government clearance for the emergency use of molnupiravir, a novel antiviral tablet that has been shown in a clinical study to reduce the risk of hospitalization or death in greater patients infected with COVID-19.

Emergency Use Of Molnupiravir Tablet For COVID Seeks Government Permission

A new drug is one of many antiviral tablets now being studied, and scientists believe they will provide doctors with a strong new tool to combat the infection.

Emergency Use Of Molnupiravir Tablet For COVID Seeks Government Permission

More tools and therapies are desperately required to combat the COVID-19 epidemic, which has become a leading cause of mortality and remains to severely harm patients, families, and societies, as well as burden health care systems all over the world, according to Merck CEO and President Robert Davis. they are confident that molnupiravir will become an essential medication in the worldwide battle against the pandemic as a result of these encouraging 


According to Daria Hazuda, VP of infectious diseases and vaccine research at Merck, “We’ve long felt that antivirals, particularly an oral antiviral, would be critical in combating the pandemic. Given the development of variations and the virus’s continuing evolution, keeping patients out of the hospital is critical.”

Specialists in infectious diseases reacted positively to the news.

Dr. Robert Shafer, an allergy specialist and preventive treatment expert at Stanford University, told The New York Times, “I believe that will translate into many thousands of lives being saved overseas, where there is less available to monoclonal antibodies, and in our country, too.”

Antiviral tablets, according to Angela Rasmussen, a virologist and research scientist at the University of Saskatchewan’s Vaccine and Infectious Disease Organization, can reach more individuals than time-consuming antibody therapies.

The Times stated that late-stage research findings for two other antiviral tablets, one produced by Pfizer and the other by Atea Pharmaceuticals and Roche, are anticipated in the coming months.

Molnupiravir was given twice a day for five days in the Merck study, which was not peer-reviewed or published.

Because the drug’s advantages to patients were so clear, an independent board of specialists evaluating the trial’s data advised that the trial be terminated early, according to Merck. The decision has been approved by the US Food and Drug Administration, according to the firm.

The research has enlisted 775 volunteers in the U.s. And abroad by early August. The tablets have to be taken within five days of being infected. Compared to those who got placebo tablets, participants who received the medication had a 50% lower chance of being hospitalized or dying, with no negative side effects, according to Merck.

In the antiviral pill group, only 7% of participants were hospitalized, and none of those patients died, contrasted to a 14 percent hospitalizations rate and eight fatalities in the placebo group.

According to the Post, lab and animal tests indicate that the tablet may also work against the Delta version. Unlike vaccinations or antibodies, which target particular proteins on the virus’s surface, molnupiravir causes nonsense mutations in the coronavirus’s genetic code, preventing it from replicating. That suggests it might work against other coronaviruses or RNA viruses as well.

According to the New York Times, the Merck pill’s effectiveness was lower than that of monoclonal antibody therapies, which imitate antibodies produced naturally by the immune system when needed.

These medicines have recently been in great demand, but they are costly and time-consuming to give due to their intravenous delivery. According to the New York Times, research has found that they cut hospitalizations and fatalities in high-risk individuals by 70 percent to 85 percent.

People who are eligible for monoclonal antibody therapies, perhaps elderly persons, and those with medical problems that place them at high risk of adverse consequences from COVID-19 infection may be included in this group at first. According to the New York Times, scientists believe the medication will eventually be used in many patients who test positive for the virus.


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