Condition: Respiratory Syncytial Virus Infections · Sponsor: GlaxoSmithKline
The study will evaluate the immune response of the RSVPreF3 OA investigational vaccine in Chinese adults 18 to 59 years of age (YOA) who are at increased risk of respiratory syncytial virus (RSV) disease, in comparison with the immune response generated in older adults 60 YOA and above from the 219815 (RSV OA=ADJ-021; NCT06551181) study following a single dose of the RSVPreF3 OA vaccine. In addition, the safety and reactogenicity of the vaccine will also be assessed.
This description comes directly from the study's public registry record.
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| GSK Investigational Site | Beijing, Beijing Municipality, China | Recruiting |
| GSK Investigational Site | Xiangtan, Hunan, China | Recruiting |
| GSK Investigational Site | Nanjing, Jiangsu, China | Recruiting |
| GSK Investigational Site | Chengdu, Sichuan, China | Recruiting |
| GSK Investigational Site | Chengdu, China | Recruiting |
| GSK Investigational Site | Chongqing, China | Recruiting |
| GSK Investigational Site | Chongqing, China | Recruiting |
| GSK Investigational Site | Guangzhou, China | Recruiting |
| GSK Investigational Site | Guangzhou, China | Recruiting |
| GSK Investigational Site | Jiujiang, China | Recruiting |
| GSK Investigational Site | Kunming, China | Recruiting |
| GSK Investigational Site | Nanning, China | Recruiting |
+ 3 more locations — full list on the registry record.
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Source record: clinicaltrials.gov/study/NCT07220109