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Tag: Molnupiravir

Is The Virus That Has Turned Our World Upside Down Able To Be Solved With a Pill?

The scientific method of developing a hypothesis, testing the hypothesis, collecting the data and presenting the data to other scientists has led the world to many of its greatest scientific accomplishments. As we face greater and greater scientific problems each year, it is necessary to continue this method to find the best treatments for the world’s diseases. Covid-19 and its variants will continue to be at the top of the world’s problems since we see that vaccines don’t stop the spread of the disease and we just don’t know what new variants will do. To solve this, scientists are working hard to create new drug solutions to treat this deadly virus once a patient has been infected. The most recent being the Merck and Pfizer’s pills: Molnupiravir and Paxlovid. Both of these drugs are to be ingested soon after noticing symptoms. Both have shown promising results, but if we want this pandemic to be over with so we can get back to normal, we need assurances that these pills work now and for the coming variants.

Pfizer tested their antiviral combination Paxlovid pill and found that their pill works with an astonishing 89% decrease in hospitalization given in a 3 day symptom onset. When given within 5 days it was slightly less, yet still an improvement from our current numbers. Their research found three of the 389 people with Covid-19 (.08%) were hospitalized, compared to a 27 out of 385 (7%) in the placebo group. The pill is a protease inhibitor, just like the ones used to help stop the spread of HIV. It stops the action of protease, which halts the ability of the virus to replicate. Paxlovid uses a decades-old HIV drug, called ritonavir, that accelerates the protease inhibitor. With this data, the FDA approved Paxlovid just before Christmas.

Pfizer (2021)

Merck partnered with Ridgeback Therapeutics to produce their molnupiravir pill. It is a nucleoside analog, meaning it is an artificial building block of RNA, this introduces errors into the DNA of the Covid virus so it can’t replicate. The early trial stages gave a 48% reduction of the chances of hospitalization or death. The trial stopped once these results were revealed in hopes that it would be distributed to the public early. It was approved by the FDA one day after the Pfizer drug, but can’t be used in kids because of side effects. The effective success rate of the drug later dropped to 30%, so much lower than the Pfizer drug. After staying at a 30% success rate, there were more problems that arose. Due to it being a nucleoside analog, it was shown to be able to potentially harm human RNA in pregnant women. There were animal tests completed that showed both growth problems which would make it impossible to give the pill to pregnant women, children, or adolescents. Lindsay Baden, an infectious disease doctor who was apart of the FDA’s advisory committee said the drug might be helpful for “the right patient population, the right virus at the right time.” Ridgeback and Merck recently decided to let developing, poor countries make molnupiravir so that the drug can help countries that can’t usually afford expensive medicine we buy in the USA.

Merck & Co

Although a lot of the world is desperate for a swift end to the virus that has changed our lives over the past 2 years, these studies have shown how difficult this virus is to prevent and treat. Paxlovid looks like the most usable and safe drug to take when it is compared to molnupiravir.

Understanding Merck’s Molnupiravir

Since the beginning of the pandemic, research of antiviral medicines and drugs have only become more specific with combating the Coronavirus. Merck’s new drug, Molnupiravir, was a result of pharmaceuticals amplifying research on Covid. The foreshadowing of this drug shows a bright future and an end to Covid-19 once and for all.

Merck applied for authorization first in October and many praised the new drug as a potential game-changer. Pfizer submitted their version of medication called Paxlovid in November. The Food and Drug Administration has provided emergency use authorizations for pills from both Merck and Pfizer while scientists continue to study the real-world effectiveness of both. Molnupiravir is administered as four 200 milligram capsules taken orally every 12 hours for five days, for a total of 40 capsules. It is not authorized for use for longer than five consecutive days where its use seems to be feasible to all users.

Molnupiravir works by introducing errors into the SARS-CoV-2 virus’ genetic code where it prevents the virus from further replicating. Dr. Shaw, a Yale Medicine infectious diseases specialist, explains when the drug enters your bloodstream, it blocks the ability of the SARS-CoV-2 virus to replicate, a Yale Medicine infectious diseases specialist, Dr. Shaw explains. The coronavirus uses RNA as its genetic material. The structure of Molnupiravir resembles the nucleosides (or chemical building blocks) used to make the virus’s RNA. The drug works by incorporating itself into the RNA as it’s being synthesized where it “results in many mutations, or changes in the RNA genetic code, introduced into the viral RNA,” says Dr. Shaw. “And when this RNA is translated into viral proteins, these proteins contain too many mutations for the virus to function.” If this disables replication and RNA’s ability to infect our cells, we will not be as sick from Covid no longer.

An early report showed the Merck drug cut the risk of hospitalization and death to 50% in patients who had mild-to-moderate cases. Results from the Molnupiravir clinical trial, conducted in the U.S. and other countries, suggested the drug would be effective against CDC “variants of concern,” including the Delta, Gamma, and Mu mutations. Scientists are still studying how well the drug works to treat Omicron and are optimistic since its application is the same with Omicron’s RNA.

While this is exciting news, the vaccine many researchers, scientist, and doctors say is still our first line of defense. Some are even concerned that the attention on Molnupiravir will “draw attention away from vaccination,” says Dr. Meyer. “Some people might say, ‘I’m not getting vaccinated because I’ll have access to these medications’—to this pill or to remdesivir or other treatments. But you can’t trade one for the other. If you haven’t done so already, the most important thing is still to get the vaccine.”

Should Scientists Continue With the Production of Merck’s Covid-19 Pill?

In a recent clinical trial to test Merck’s Covid-19 pill, Scientists have found that the drug showed early signs of preventing hospitalization and death from the coronavirus in people at high risk of severe disease. Merck’s Covid-19 pill would be taken orally to prevent the replication of certain RNA viruses to prevent the spread of coronavirus. The drug molnupiravir was the driving factor of this pill that would allow it to show such high results. The antiviral medication works by making mutations in viral RNA so that viruses are rendered noninfectious. Such mutations happen throughout the virus’s genetic genome.

Pill 3

A 48 percent reduction in the relative risk of hospitalization or death. Despite this, on November 26, Merck announced in a news release that when all the available data from the trial was in, the relative reduction risk fell to 30 percent. After being reviewed by the FDA, the scientists determined that the placebo group and the molnupiravir group were too similar to declare the drug effective. They came to a 13-10 split decision vote about whether the drug should be immediately sent out for emergency use. The vote and debate reflected a storm of uncertainty about the drug’s efficacy and who should use it. Not only was there a debate, but the panel also queried whether the drug could lead to an even more dangerous version of the coronavirus and whether it can cause growth delays in children or mutation in human DNA. The drug is an artificial RNA building block, a nucleotide, that can mimic cytosine and uracil bases. Some enzymes in human cells might convert those RNA subunits to a DNA building block, which may lead to mutations in human DNA, especially in blood cells.

“The potential for this drug to drive some very challenging variants into the public is of major, major concern,” said James Hildreth, an immunologist, and president of Meharry Medical College in Nashville. Merck representatives noted that it is doubtful because infectious viruses were no longer detected after five days of taking the drug dosage. In one of their studies, the company found seven patients who had changes in the coronavirus’s spike protein after taking molnupiravir. Still, there was no evidence that the viruses spread to other people.

The question of whether Merck’s Covid-19 Pill will work is still very unknown due to the symptoms it may cause and the side effects that come along with it. The question may never be answered due to the progressively changing varients of the coronavirus. We should continue testing this drug and modifying it to have the best outcome and the least amount of side effects. What do you think about these new drugs? What next steps should scientists take to make it available to the public? Should we release it to the public?

New Covid-19 Pill! Will it work?

Pill 2

In a study conducted by Tina Saey, she looked at Merck’s Covid- 19 pill Molnupiravir and how it is affecting hospitalization rates of Covid-19. Molnupiravir, “an antiviral drug that can be taken at home” is the first medicine that can be taken orally that is approved to help fight off Covid-19. The drug is typically administered to patients who have mild to moderate Covid within five days of their symptoms appearing. Molnupiravir has been tested several times and is now waiting on the FDA for formal approval. This new pill could be a game-changer, but will it really be as great as it seems?

Ms. Saey states that “finding an early treatment hasn’t been easy”, so when Molnupiravir came around experts praised its development. Initially, the pill showed great signs of preventing hospitalizations and death from Covid-19. The results were so promising, a 48% decrease in hospitalizations, that the trial ended early so that the pill might become available to the public faster. However, when all the data was collected and analyzed the reduction in hospitalization rate dropped to 30%. The unexplained decrease happened when participants in the placebo group were no longer experiencing severe symptoms. Due to the decrease in reported effectiveness, the FDA’s antimicrobial drugs advisory committee came to a split 13-10 decision on whether the drug should be available for emergency use. 

The main concern for authorizing Molnupiravir is that the pill could create even more dangerous versions of the Covid- 19 coronavirus. The drug works by making mutations in the RNA. This is when a change occurs that affects nucleic acids, the building blocks of RNA. A handful of these mutations could land in the spike protein. Spike proteins interact with the cell receptors located on the host cell; in terms of Covid-19 it helps the coronavirus break into cells. The spike protein could also burst into other proteins making the virus more transmittable. James Hildreth, an immunologist stated that, “the potential for this drug to drive some very challenging variants into the public is of major, major concern.” Although this is a possibility it seems unlikely because, after five days of usage, infectious viruses in participants taking Molnupiravir were no longer detectable. 

SARS-CoV-2 without background

Spike Protein

Overall, there is much promise but also notable concerns to the new drug Molnupiravir. I believe that this new medicine, even with its downsides, could save hundreds of thousands of lives. As Ms. Saey states, “a 30 percent reduction in hospitalizations and deaths is worth giving the drug temporary authorization.”

The Potential End To COVID-19: How An Antiviral Pill Could Decrease Death Rates

When will the world return back to normal? In recent years, people have questioned the longevity of the COVID-19 outbreak. While concentrating on vaccine delivery and vaccination capabilities, a pill has been developed in the hopes of preventing future COVID variations. Hopefully, the pill will eventually be administered to patients; this would make it the first oral treatment for the virus.

A current study on molnupiravir, an antiviral pill, has published data demonstrating that the medicine has the ability to lower hospitalization and fatality rates as a result of COVID-19. The study dealt with two groups of people. One group of 377 people were given a placebo, and the other group of 385 people were given molnupiravir to examine how the antiviral affected patients with COVID-19. The findings were substantial. Within 29 days of starting the trial, 14.1 percent of the group given the placebo were hospitalized. Fortunately, of the individuals who were given molnupiravir, only 7.3 percent of them were hospitalized.

Molnupiravir is a prodrug of N4-hydroxycytidine (NHC), a nucleoside analog (meaning that it contains a sugar and a nitrogenous base). Molnupiravir metabolism

Molnupiravir is similar to the genetic coding of the coronavirus’s RNA, as is remdesivir (a FDA-approved medication). By interfering with the polymerase enzyme, the “fake” basic elements impair the coronavirus’s RNA synthesis, preventing the virus from replicating. Despite the fact that the two medications serve the same goal, they serve different actions. Remdesivir penetrates a growing RNA strand, slowing and ultimately blocking the polymerase enzyme. Unlike the COVID-19 vaccine, the structure of molnupiravir gives it the ability to target the polymerase enzyme instead of the virus’s spike protein. Molnupiravir enters the cell and is transformed into RNA-like building components. The active medication binds to the genome of RNA viruses, setting off a chain of mutations; this process is known as viral error catastrophe. In simpler terms, it disrupts how the virus replicates RNA.

Molnupiravir could theoretically be administered as soon as a patient receives a positive COVID-19 test, thereby preventing floods of COVID-19 patients from overburdening medical systems while the highly infectious delta variant continues to spread. Although the side effects of the drug remain unknown, it has been reported that the side effects of COVID-19 are much worse than those of molnupiravir. The antiviral drug has the potential to save lives, but the primary concern is about the long-term repercussions. When contemplating molnupiravir, the fear of birth abnormalities or cancer comes into play because it is a mutagenic medication. In response, the drug’s creator, Merck, stated that there is no indication of the possibility for mutagenicity. Although the manufacturer is confident in the treatment and believes that the long-term consequences are insignificant, it is logical that parents might have concerns about molnupiravir.

Ultimately, if patients receive the vaccination that targets the spike protein and are also able to take molnupiravir, hospitalization and mortality rates may dramatically reduce.

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