US FDA authorises Bavarian Nordic’s Jynneos for emergency use against monkeypox
The authorisation will increase the total number of doses available for use by up to five-fold and also allows for use of the vaccine in individuals younger than 18 years of age determined to be at high risk of monkeypox infection by subcutaneous injection
The US Food and Drug Administration (FDA) yesterday authorised Bavarian Nordic’s Jynneos vaccine for emergency use via intradermal injection in individuals aged 18 years and older who are determined to be at high risk for monkeypox infection.
The authorisation will increase the total number of doses available for use by up to five-fold and also allows for use of the vaccine in individuals younger than 18 years of age determined to be at high risk of monkeypox infection by subcutaneous injection.
“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,” said Robert M Califf, Commissioner, FDA.
Edits by EP News Bureau
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