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FDA advisers vote to recommend authorization of COVID-19 pill from Merck

FDA advisers vote to recommend authorization of COVID-19 pill from Merck
PILL SHOWS THE TREATMENT CAN REDUCEHE T RISKF O COVID-19 HOSPITALIZATIONS AND DEATHS BY AS MUCH AS 30% THAT바카라 게임 웹사이트™ AS DROP FROM A PREVIOUS STUDY TT HASAID THE DRUG COULD DO AS MUCH AS HALF. IT바카라 게임 웹사이트™S DISAPPOINTING, BUT IT바카라 게임 웹사이트™LL STILL PROVIDE A GOOD TOOL IN THE ARSENAL TO HELP LIMIT SEVERE DISEASE JOHNS HOPKINS VIROLOGIST, DR. ANDREW PECOS YSSA THE DATA IS STILL PROMISING THOUGH TESTED IN OVER 1400 PATIENTS MANY WITH A LIKELIHOOD TO HAVE SEVERE. DUMPS THE PILL IS SAID TO INSERT MUTATIONS INTO THE VIRUS바카라 게임 웹사이트™S GENETIC CODE PREVENTING MORE REPRODUCTION. IT CERTAINLY WON바카라 게임 웹사이트™T BE AVAILABLE TO CHILDREN BECAUSE THERE HAS BEEN NO CLINICAL STUDY YET TO LOOK AT DOSING OR EFFICACY IN ANYBODY UNDER THE AGE OF 18. FOR CHILDREN PREGNANT WOMEN DR. PECASH SAYS THE DATA IS NOT THERE YET. BUT GOOD NEWS WITH WHAIST KNOWN A MEANSO T FIGHT THE VIRUS AND IT바카라 게임 웹사이트™S VARIANCE TAKING OVERHE T COURSE OF FIVE DAYS WITH AS MUCH AS 40 PILLS. THIS DRUG HAS ACTUALLY BEEN UNRDE INVESTIGATION FOR SOME TIME NOW. IT바카라 게임 웹사이트™S BEEN TESTED IN THE LABORATORY VERY EXTENSIVELY. THIS WAS A GOOD CLINICAL TRIAL IN TERMS OFHE T NUMBER OF PEOPLE THE FDA IS EXPECTED TO MEET NEXT TUESDAY TO HEAR FROM HEALTH EXPERTS ON THE MEDICATION FOR NOW WHAT바카라 게임 웹사이트™S CLEAR ACCORDING TO DR. PECOSH. IT IS NOT A REPLACEMENT FOR THE VACCINEHA TT PREVENTS MEOR SPREAD AND DEATH. THE VACCINE IS STILL GONNA WORK BETTER. THIS IS ANOTHER LAY OERF PROTECTION THAT WE CAN GIVE THE POPULATION TO LIMIT SEVERE DISEASE. SO NOT A REPLACEMENT FOR VACCINES, BUT AN ADDITIONAL TOOL TO VACCINES TO HELP US DEAL WITH THIS DISEASE. AND PFIZER ALSO IS WORKING ON ITS OWN VERSIONF O A COVID-19 ORAL PLIL WHICH HAD DATA THAT SAID IT WAS9% 8 EFFECTIVE IN PREVENTING THOSE HOSPITALIZATIONS AND DEATHS IF THE FDA VOTES TO APPROVE THE MERC PILL, DR. PECOSH SAYS WE COULD SEE PUBLICSE U AS EARLY AS XTNE YEAR
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FDA advisers vote to recommend authorization of COVID-19 pill from Merck
A panel of U.S. health advisers on Tuesday narrowly backed a closely watched COVID-19 pill from Merck, setting the stage for a likely authorization of the first drug that Americans could take at home to treat the coronavirus.A Food and Drug Administration panel voted 13-10 that the drug바카라 게임 웹사이트™s benefits outweigh its risks, including potential birth defects if used during pregnancy.The recommendation came after hours of debate about the drug바카라 게임 웹사이트™s modest benefits and potential safety issues. Experts backing the treatment stressed that it should not be used by anyone who is pregnant and called on FDA to recommend extra precautions before the drug is prescribed, including pregnancy tests for women of child-bearing age.The vote specifically backed the drug for adults with mild-to-moderate COVID-19 who face the greatest risks, including older people and those with conditions like obesity and asthma. Most experts also said the drug shouldn't be used in vaccinated patients, who weren't part of the study and haven't been shown to benefit.The FDA isn바카라 게임 웹사이트™t bound by the panel바카라 게임 웹사이트™s recommendation and is expected to make its own decision before year바카라 게임 웹사이트™s end. The pill is already authorized in the U.K.The drug, molnupiravir, could provide a much-needed weapon against the virus as colder weather pushes case counts higher and U.S. officials brace for the arrival of the new omicron variant. Merck hasn바카라 게임 웹사이트™t specifically tested its drug against the new variant but said it should have some potency based on its effectiveness against other strains of coronavirus.But that uncertainty frustrated many panelists as they grappled with whether to back the treatment for millions of Americans."With no data saying it works with new variants I really think we need to be careful about saying that this is the way to go," said Dr. David Hardy of Charles Drew University School of Medicine and Science, who ultimately voted to back the drug.The panel바카라 게임 웹사이트™s narrow-but-positive recommendation came despite new data from Merck that paint a less compelling picture of the drug바카라 게임 웹사이트™s effectiveness than just a few weeks earlier.Last week, Merck said final study results showed molnupiravir reduced hospitalization and death by 30% among adults infected with the coronavirus, when compared with adults taking a placebo. That effect was significantly less than the 50% reduction it first announced based on incomplete results.That smaller-than-expected benefit amplified experts' concerns about the drug's toxicity for fetuses.FDA scientists told the panelists earlier Tuesday that company studies in rats showed the drug caused toxicity and birth defects when given at very high doses. Taken together, FDA staffers concluded the data "suggest that molnupiravir may cause fetal harm when administered to pregnant individuals."FDA is weighing a blanket restriction against any use in pregnant women or allowing it in rare cases. Some panelists said the option should be left open for pregnant mothers who have high-risk COVID-19 and may have few other treatment options.Dr. Janet Cragan, who backed the drug, said that even with tight restrictions some pregnant women would inevitably take the drug."I don바카라 게임 웹사이트™t think you can ethically tell a woman with COVID-19 that she can바카라 게임 웹사이트™t have the drug if she바카라 게임 웹사이트™s decided that바카라 게임 웹사이트™s what she needs," a panel member and staffer with the Centers for Disease Control and Prevention. "I think the final decision has to come down to the individual woman and her provider."Merck's drug uses a novel approach to fight COVID-19: It inserts tiny errors into the coronavirus바카라 게임 웹사이트™ genetic code to stop it from reproducing. That genetic effect has raised concerns that the drug could spur more virulent strains of the virus. But FDA regulators said Tuesday that risk is theoretical and seems unlikely.While Merck and its partner Ridgeback Biotherapeutics were the first to submit their COVID-19 pill to the FDA, rival drugmaker Pfizer is close behind with its own pill under review.Pfizer바카라 게임 웹사이트™s drug is part of a decades-old family of antiviral pills known as protease inhibitors, a standard treatment for HIV and hepatitis C. They work differently than Merck바카라 게임 웹사이트™s pill and haven바카라 게임 웹사이트™t been linked to the kind of mutation concerns raised with Merck바카라 게임 웹사이트™s drug.Pfizer said this week that its drug shouldn바카라 게임 웹사이트™t be affected by the omicron variant바카라 게임 웹사이트™s mutations.The U.S. government has agreed to purchase 10 million treatment courses of Pfizer바카라 게임 웹사이트™s drug, if it바카라 게임 웹사이트™s authorized. That바카라 게임 웹사이트™s more than three times the government바카라 게임 웹사이트™s purchase agreement with Merck for 3.1 million courses of molnupiravir.Both drugs require patients to take multiple pills, twice a day for five days.

A panel of U.S. health advisers on Tuesday narrowly backed a closely watched COVID-19 pill from Merck, setting the stage for a likely authorization of the first drug that Americans could take at home to treat the coronavirus.

A Food and Drug Administration panel voted 13-10 that the drug바카라 게임 웹사이트™s benefits outweigh its risks, including potential birth defects if used during pregnancy.

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The recommendation came after hours of debate about the drug바카라 게임 웹사이트™s modest benefits and potential safety issues. Experts backing the treatment stressed that it should not be used by anyone who is pregnant and called on FDA to recommend extra precautions before the drug is prescribed, including pregnancy tests for women of child-bearing age.

The vote specifically backed the drug for adults with mild-to-moderate COVID-19 who face the greatest risks, including older people and those with conditions like obesity and asthma. Most experts also said the drug shouldn't be used in vaccinated patients, who weren't part of the study and haven't been shown to benefit.

The FDA isn바카라 게임 웹사이트™t bound by the panel바카라 게임 웹사이트™s recommendation and is expected to make its own decision before year바카라 게임 웹사이트™s end. The pill is already authorized in the U.K.

The drug, molnupiravir, could provide a much-needed weapon against the virus as colder weather pushes case counts higher and U.S. officials brace for the arrival of the new omicron variant.

Merck hasn바카라 게임 웹사이트™t specifically tested its drug against the new variant but said it should have some potency based on its effectiveness against other strains of coronavirus.

But that uncertainty frustrated many panelists as they grappled with whether to back the treatment for millions of Americans.

"With no data saying it works with new variants I really think we need to be careful about saying that this is the way to go," said Dr. David Hardy of Charles Drew University School of Medicine and Science, who ultimately voted to back the drug.

The panel바카라 게임 웹사이트™s narrow-but-positive recommendation came despite new data from Merck that paint a less compelling picture of the drug바카라 게임 웹사이트™s effectiveness than just a few weeks earlier.

Last week, Merck said final study results showed molnupiravir reduced hospitalization and death by 30% among adults infected with the coronavirus, when compared with adults taking a placebo. That effect was significantly less than the 50% reduction it first announced based on incomplete results.

That smaller-than-expected benefit amplified experts' concerns about the drug's toxicity for fetuses.

FDA scientists told the panelists earlier Tuesday that company studies in rats showed the drug caused toxicity and birth defects when given at very high doses. Taken together, FDA staffers concluded the data "suggest that molnupiravir may cause fetal harm when administered to pregnant individuals."

FDA is weighing a blanket restriction against any use in pregnant women or allowing it in rare cases. Some panelists said the option should be left open for pregnant mothers who have high-risk COVID-19 and may have few other treatment options.

Dr. Janet Cragan, who backed the drug, said that even with tight restrictions some pregnant women would inevitably take the drug.

"I don바카라 게임 웹사이트™t think you can ethically tell a woman with COVID-19 that she can바카라 게임 웹사이트™t have the drug if she바카라 게임 웹사이트™s decided that바카라 게임 웹사이트™s what she needs," a panel member and staffer with the Centers for Disease Control and Prevention. "I think the final decision has to come down to the individual woman and her provider."

Merck's drug uses a novel approach to fight COVID-19: It inserts tiny errors into the coronavirus바카라 게임 웹사이트™ genetic code to stop it from reproducing. That genetic effect has raised concerns that the drug could spur more virulent strains of the virus. But FDA regulators said Tuesday that risk is theoretical and seems unlikely.

While Merck and its partner Ridgeback Biotherapeutics were the first to submit their COVID-19 pill to the FDA, rival drugmaker Pfizer is close behind with its own pill under review.

Pfizer바카라 게임 웹사이트™s drug is part of a decades-old family of antiviral pills known as protease inhibitors, a standard treatment for HIV and hepatitis C. They work differently than Merck바카라 게임 웹사이트™s pill and haven바카라 게임 웹사이트™t been linked to the kind of mutation concerns raised with Merck바카라 게임 웹사이트™s drug.

Pfizer said this week that its drug shouldn바카라 게임 웹사이트™t be affected by the omicron variant바카라 게임 웹사이트™s mutations.

The U.S. government has agreed to purchase 10 million treatment courses of Pfizer바카라 게임 웹사이트™s drug, if it바카라 게임 웹사이트™s authorized. That바카라 게임 웹사이트™s more than three times the government바카라 게임 웹사이트™s purchase agreement with Merck for 3.1 million courses of molnupiravir.

Both drugs require patients to take multiple pills, twice a day for five days.