Condition: Pneumococcal Infection · Sponsor: Merck Sharp & Dohme LLC
The purpose of this study is to evaluate the safety, tolerability, and immunogenicity of V116 compared to PPSV23 in children and teenagers 2 through 17 years of age, who had completed routine pneumococcal vaccine as infants/toddlers. Researchers want to learn if V116 is as good as, or is better than the PPSV23 vaccine in terms of the antibody immune response. V116 and PPSV23 will be studied in children and teenagers who have a higher risk of getting pneumococcal disease (PD).
This description comes directly from the study's public registry record.
No contact information is available for this study as per the public registry record.
Always discuss trial participation with your own doctor first.
| Central Research Associates ( Site 0145) | Birmingham, Alabama, United States | — |
| Velocity Clinical Research, Phoenix ( Site 0122) | Phoenix, Arizona, United States | — |
| Madera Family Medical Group ( Site 0120) | Madera, California, United States | — |
| Optumcare Colorado Springs, LLC ( Site 0113) | Colorado Springs, Colorado, United States | — |
| Accel Research Sites Network- Nona Pediatric Center ( Site 0109) | Orlando, Florida, United States | — |
| University of South Florida-Department of Pediatrics ( Site 0110) | Tampa, Florida, United States | — |
| Velocity Clinical Research at Primary Pediatrics, Macon ( Site 0128) | Macon, Georgia, United States | — |
| Bingham Memorial Hospital ( Site 0149) | Blackfoot, Idaho, United States | — |
| Clinical Research Prime ( Site 0105) | Idaho Falls, Idaho, United States | — |
| Clinical Research Prime Rexburg ( Site 0104) | Rexburg, Idaho, United States | — |
| University of Louisville, Norton Children's Research Institute ( Site 0148) | Louisville, Kentucky, United States | — |
| Velocity Clinical Research, Lafayette ( Site 0103) | Lafayette, Louisiana, United States | — |
+ 80 more locations — full list on the registry record.
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