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B. Riley says Novavax Nuvaxovid approval removes regulatory overhang

The FDA approved the biologics license application for Nuvaxovid for active immunization to prevent coronavirus disease 2019 caused by severe acute respiratory syndrome coronavirus 2 in adults 65 years and older and individuals 12 through 64 years who have at least one underlying condition that puts them at high risk for severe outcomes from COVID-19. B.Riley said it views the approval as the removal of an important regulatory overhang for Novavax (NVAX) partner Sanofi (SNY). The firm added that this milestone unlocks $200M in milestone payments for Novavax from Sanofi. B. Riley told investors that the approval letter does note a relatively narrower label relative to peers. B. Riley reiterated a Buy rating and $18 price target on shares of Novavax.

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