Landmark gene-editing therapy approved: here’s what you need to know
The FDA approved the landmark treatment on Friday. It’s expected to cost more than $1 million.
The FDA approved the landmark treatment on Friday. It’s expected to cost more than $1 million.
The FDA approved the landmark treatment on Friday. It’s expected to cost more than $1 million.
The FDA approved the landmark treatment on Friday. It’s expected to cost more than $1 million.
The FDA approved the landmark treatment on Friday. It’s expected to cost more than $1 million.
The FDA approved the landmark treatment on Friday. It’s expected to cost more than $1 million.
The FDA approved the landmark treatment on Friday. It’s expected to cost more than $1 million.
Now the CDC’s vaccine expert panel will review for recommendation to the CDC director.
Now the CDC’s vaccine expert panel will review for recommendation to the CDC director.
Now the CDC’s vaccine expert panel will review for recommendation to the CDC director.
Now the CDC’s vaccine expert panel will review for recommendation to the CDC director.
Now the CDC’s vaccine expert panel will review for recommendation to the CDC director.
Now the CDC’s vaccine expert panel will review for recommendation to the CDC director.
Advisers signaled interest in making available a vaccine made with a technology different from the messenger RNA shots that have dominated the U.S. immunization arsenal against the disease.
Advisers signaled interest in making available a vaccine made with a technology different from the messenger RNA shots that have dominated the U.S. immunization arsenal against the disease.
Advisers signaled interest in making available a vaccine made with a technology different from the messenger RNA shots that have dominated the U.S. immunization arsenal against the disease.
Advisers signaled interest in making available a vaccine made with a technology different from the messenger RNA shots that have dominated the U.S. immunization arsenal against the disease.
The committee found that the vaccine has largely been safe for that population of children, with incidents of myocarditis and other rare adverse events lower compared to older kids.
The committee found that the vaccine has largely been safe for that population of children, with incidents of myocarditis and other rare adverse events lower compared to older kids.
The committee found that the vaccine has largely been safe for that population of children, with incidents of myocarditis and other rare adverse events lower compared to older kids.
The committee found that the vaccine has largely been safe for that population of children, with incidents of myocarditis and other rare adverse events lower compared to older kids.
The company is aiming to produce at least 2 billion doses of its vaccine in 2022, of which the U.S. has ordered 100 million.
The company is aiming to produce at least 2 billion doses of its vaccine in 2022, of which the U.S. has ordered 100 million.
The company is aiming to produce at least 2 billion doses of its vaccine in 2022, of which the U.S. has ordered 100 million.
Independent advisers to the FDA endorsed the pill, molnupiravir, in an unusually tight 13-10 vote this week after airing concerns about its low efficacy rate and potential safety risks to pregnant people.
Independent advisers to the FDA endorsed the pill, molnupiravir, in an unusually tight 13-10 vote this week after airing concerns about its low efficacy rate and potential safety risks to pregnant people.
Independent advisers to the FDA endorsed the pill, molnupiravir, in an unusually tight 13-10 vote this week after airing concerns about its low efficacy rate and potential safety risks to pregnant people.
The CDC’s vaccine advisers are scheduled to meet Tuesday to evaluate the shot, and are expected to vote in favor of its use
The CDC’s vaccine advisers are scheduled to meet Tuesday to evaluate the shot, and are expected to vote in favor of its use
The CDC’s vaccine advisers are scheduled to meet Tuesday to evaluate the shot, and are expected to vote in favor of its use
The CDC’s vaccine advisers are scheduled to meet Tuesday to evaluate the shot, and are expected to vote in favor of its use