U.S., Dec. 16 -- ClinicalTrials.gov registry received information related to the study (NCT07282795) titled 'Post-marketing Surveillance Study for the Safety of Efluelda(R) Pre-filled Syringe' on Dec. 02.

Brief Summary: To objective of this study is to investigate the incidence of adverse events (AEs) and adverse drug reactions (ADRs) occurred following administration of Efluelda(R) in adults aged 65 years or older under routine clinical practice, as per approved indications This is an open-label, multi-center, observational active safety surveillance study, designed to be conducted under standard healthcare setting of the Republic of Korea, in accordance with "Regulation on the Operation of Risk Management Plans".

The study duration of e...