Condition: Measles · Measles-Mumps-Rubella+Chickenpox Vaccine · Sponsor: GlaxoSmithKline
This study is evaluating the immunogenicity and safety of intramuscular administration of the investigational MMRVNS vaccine compared to intramuscular administration of the MMRV (Merck's measles, mumps, rubella and varicella) vaccine (ProQuad) that is already licensed for this route, when administered as a second dose in children 15 months to 6 years of age who were previously primed with a first dose of any combination of measles, mumps, rubella and varicella-containing vaccine(s).
This description comes directly from the study's public registry record.
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| GSK Investigational Site | Birmingham, Alabama, United States | Recruiting |
| GSK Investigational Site | Walnut Creek, California, United States | Recruiting |
| GSK Investigational Site | Miami, Florida, United States | Recruiting |
| GSK Investigational Site | Miami, Florida, United States | Recruiting |
| GSK Investigational Site | Atlanta, Georgia, United States | Recruiting |
| GSK Investigational Site | Chicago, Illinois, United States | Recruiting |
| GSK Investigational Site | Farmington Hills, Michigan, United States | Recruiting |
| GSK Investigational Site | Dayton, Ohio, United States | Recruiting |
| GSK Investigational Site | Simpsonville, South Carolina, United States | Recruiting |
| GSK Investigational Site | Spartanburg, South Carolina, United States | Recruiting |
| GSK Investigational Site | Frisco, Texas, United States | Recruiting |
| GSK Investigational Site | Houston, Texas, United States | Recruiting |
+ 5 more locations — full list on the registry record.
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Source record: clinicaltrials.gov/study/NCT07406360