U.S., Oct. 30 -- ClinicalTrials.gov registry received information related to the study (NCT07222059) titled 'Phase 3 Single Arm, Open Study on vYF in Adults' on Oct. 27.
Brief Summary: The purpose of this study is to assess the safety and immunogenicity of vYF in adults aged 18 years and over in Japan.
Study details include:
* The study duration will be up to approximately 1 month.
* One single dose of vYF will be administrated subcutaneously at the 1st visit.
* The visit frequency will be Day 01 (Visit 01) and Day 29 (Visit 02). One telephone call (TC) will be planned at Day 15.
Number of Participants:
A total of 254 participants is expected to be included in the study with the aim to obtain a total of 203 evaluable participants.
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