Moderna and Johnson & Johnson on Tuesday said that US regulators should authorise booster shots of their COVID-19 vaccines, citing data that showed waning effectiveness of both over time.
The comments were released in briefing documents by the companies ahead of a meeting of the FDA's outside expert advisers on Thursday and Friday to discuss booster doses of the vaccines.
Moderna cited data supporting the public health benefit of a booster dose and made a case for a US authorisation of the shot in adults aged 65 and over as well as high-risk individuals.
The Pfizer/BioNTech vaccine is currently offered as a booster dose in the United States and available to people aged 65 and older as well as to those who are at high risk of severe disease or are regularly exposed to the virus.
Johnson & Johnson on Tuesday underscored the benefits of a booster and said its data suggested the shot could benefit high-risk individuals if administered two months after the original dose and after six months for lower-risk Americans.
The meeting will discuss Moderna's booster shot on Thursday, followed by a discussion around the J&J booster dose on Friday.
Briefing documents from the regulator's scientists were expected to be released later on Tuesday.
Kenya tourist helicopter crash kills seven
US, South Korea to cut length, scope of military drills after Trump order
Central African Republic gold mine collapse kills at least 100
Israeli airstrike kills nine Palestinians at Gaza police station
Thai schools hold shooting response drills after deadly school attack
