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FDA authorizes change in how monkeypox vaccine is given, stretching supply amid high demand

FDA authorizes change in how monkeypox vaccine is given, stretching supply amid high demand
today, the biden Harris administration is making key announcements after conversations over the past several days with key federal partners, the infectious disease community and Bavarian nordic. Today, the FDA has issued an emergency use authorization or EU *** allowing healthcare providers to use an alternative dosing regimen of the genius vaccine. This will increase the total number of doses available for use by up to five fold. The EU *** also allows for use of the vaccine and individuals younger than 18 years of age determined to be at high risk of monkeypox infection in these individuals. Geniuses administered by subcutaneous injection. As dr calif described this strategy would change the method of administration for the genius vaccine from subcutaneous to intradermal to allow vaccine providers to use an existing one dose vial of the vaccine to administer *** total of up to five separate doses. Intradermal injections are often used for TB skin tests and have been used for other types of vaccines before. Some health care providers may not be as familiar with intradermal administration where you deliver the vaccine into the layer of skin just underneath the top layer compared to the more traditional subcutaneous administration, which goes into the fat layer underneath the skin. For this reason, CDC will be providing information and educational materials to vaccine providers to help ensure this new strategy can be implemented quickly and as seamlessly as possible. Today. Just laid out is *** game changer when it comes to our response and our ability to get ahead of the virus. It's safe. It's effective and it will significantly scale the volume of vaccine doses available for communities across the country. As secretary, Becerra mentioned, we distributed over 670,000 vials of vaccine already to jurisdictions across the country, and we have 400,000 vials in the strategic national stockpile that have been allocated jurisdictions ready to be ordered when jurisdictions use 90% of their current supply. With today's announcement, those 400,000 vials have the potential to provide up to two million doses to Americans. We encourage jurisdictions to utilize the alternative dosing method as quickly as possible, and we'll be your partner in this step every step of the way.
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FDA authorizes change in how monkeypox vaccine is given, stretching supply amid high demand
The U.S. Food and Drug Administration issued an emergency use authorization Tuesday that allows health care providers to change how the Jynneos monkeypox vaccine is administered, stretching out the supply amid high demand.The vaccine can now be given to high-risk adults intradermally, meaning between the layers of the skin, rather than subcutaneously, or under the skin, as it has been given up till now. This will allow providers to get five doses out of a standard one-dose vial.The new EUA also allows subcutaneous vaccination in people under 18 who are at high risk of infection."In recent weeks the monkeypox virus has continued to spread at a rate that has made it clear our current vaccine supply will not meet the current demand," FDA Commissioner Dr. Robert M. Califf said in a statement. "The FDA quickly explored other scientifically appropriate options to facilitate access to the vaccine for all impacted individuals. By increasing the number of available doses, more individuals who want to be vaccinated against monkeypox will now have the opportunity to do so."The move comes less than a week after the Biden administration declared monkeypox a public health emergency, which gives the FDA and other government health agencies more flexibility to fight the spread of the virus.Earlier Tuesday, U.S. Department of Health and Human Services Secretary Xavier Becerra issued a determination to pave the way for the FDA's move."Last week, I declared monkeypox to be a public health emergency to unlock additional tools that will help us contain and end this outbreak and to signal to the American people that we are taking our response to the next level," Becerra said in a statement. "Today's action will allow FDA to exercise additional authorities that may increase availability of vaccines to prevent monkeypox while continuing to ensure the vaccine meets high standards for safety, effectiveness and manufacturing quality."As of Monday, the U.S. government has shipped 617,693 doses of Jynneos to states and jurisdictions. The U.S. Centers for Disease Control and Prevention has estimated that at least 1.5 million people in the U.S. are eligible for monkeypox vaccination.As of Monday evening, the CDC reports 8,934 probable or confirmed monkeypox cases in 49 states, Puerto Rico and the District of Columbia.With an intradermal vaccination, "basically, you're staying in the skin; you're not going through the skin," said Dr. Daniel Griffin, an infectious disease specialist at Columbia University.Using a smaller dose with intradermal injection has been done with vaccines for flu and rabies, epidemiologist Dr. Jay Varma told CNN in an email."The skin has special cells that are very good at helping a vaccine stimulate the body's immune system," he wrote.These cells, called dendritic cells, are better able to produce an immune response, Griffin said."They live in the skin, and they're better at teaching the immune system what they need to respond to," he said."If you're able to give the monkeypox vaccine intradermally, you can give a smaller dose. ... They just would need to have some sort of demonstration that you get the same immune response," he said.

The U.S. Food and Drug Administration issued an emergency use authorization Tuesday that allows health care providers to change how the Jynneos monkeypox vaccine is administered, stretching out the supply amid high demand.

The vaccine can now be given to high-risk adults intradermally, meaning between the layers of the skin, rather than subcutaneously, or under the skin, as it has been given up till now. This will allow providers to get five doses out of a standard one-dose vial.

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The new EUA also allows subcutaneous vaccination in people under 18 who are at high risk of infection.

"In recent weeks the monkeypox virus has continued to spread at a rate that has made it clear our current vaccine supply will not meet the current demand," FDA Commissioner Dr. Robert M. Califf said in a . "The FDA quickly explored other scientifically appropriate options to facilitate access to the vaccine for all impacted individuals. By increasing the number of available doses, more individuals who want to be vaccinated against monkeypox will now have the opportunity to do so."

The move comes less than a week after the Biden administration declared monkeypox a public health emergency, which gives the FDA and other government health agencies more flexibility to fight the spread of the virus.

Earlier Tuesday, U.S. Department of Health and Human Services Secretary Xavier Becerra issued a determination to pave the way for the FDA's move.

WEST HOLLYWOOD, CALIFORNIA - AUGUST 03: A pharmacist prepares a dose of the Jynneos monkeypox vaccine at a pop-up vaccination clinic opened today by the Los Angeles County Department of Public Health at the West Hollywood Library on August 3, 2022 in West Hollywood, California. California Governor Gavin Newsom declared a state of emergency on August 1st over the monkeypox outbreak which continues to grow globally. (Photo by Mario Tama/Getty Images)
Mario Tama
A pharmacist prepares a dose of the Jynneos monkeypox vaccine at a pop-up vaccination clinic opened today by the Los Angeles County Department of Public Health at the West Hollywood Library on August 3, 2022 in West Hollywood, California.

"Last week, I declared monkeypox to be a public health emergency to unlock additional tools that will help us contain and end this outbreak and to signal to the American people that we are taking our response to the next level," Becerra said in a . "Today's action will allow FDA to exercise additional authorities that may increase availability of vaccines to prevent monkeypox while continuing to ensure the vaccine meets high standards for safety, effectiveness and manufacturing quality."

As of Monday, the U.S. government has shipped 617,693 doses of Jynneos to states and jurisdictions. The U.S. Centers for Disease Control and Prevention has estimated that at least 1.5 million people in the U.S. are eligible for monkeypox vaccination.

As of Monday evening, the CDC 8,934 probable or confirmed monkeypox cases in 49 states, Puerto Rico and the District of Columbia.

With an intradermal vaccination, "basically, you're staying in the skin; you're not going through the skin," said Dr. Daniel Griffin, an infectious disease specialist at Columbia University.

Using a smaller dose with intradermal injection has been done with vaccines for flu and rabies, epidemiologist Dr. Jay Varma in an email.

The Biden administration is preparing to move forward with a plan to stretch the limited supply of monkeypox vaccine doses that would allow providers to use one-fifth as much per shot, two people familiar with the plans said.
CNN
The Biden administration is preparing to move forward with a plan to stretch the limited supply of monkeypox vaccine doses that would allow providers to use one-fifth as much per shot, two people familiar with the plans said.

"The skin has special cells that are very good at helping a vaccine stimulate the body's immune system," he wrote.

These cells, called dendritic cells, are better able to produce an immune response, Griffin said.

"They live in the skin, and they're better at teaching the immune system what they need to respond to," he said.

"If you're able to give the monkeypox vaccine intradermally, you can give a smaller dose. ... They just would need to have some sort of demonstration that you get the same immune response," he said.