The FDA has delayed the PDUFA date for Moderna’s RSV vaccine, the company announced Friday morning.
The delay likely won’t push the decision past the end of May, according to Moderna’s press release, and regulators have not raised any concerns about “vaccine safety, efficacy or quality” preventing the shot’s approval. Rather, the FDA cited “administrative constraints” for the delay, and the shot is still on track to be reviewed at the CDC’s June ACIP meeting, when the agency will make its recommendations for the upcoming RSV vaccine season.
Unlock this article instantly by becoming a free subscriber.
You’ll get access to free articles each month, plus you can customize what newsletters get delivered to your inbox each week, including breaking news.