drugset / Trial / NCT05158140
Safety, Tolerability, and Immunogenicity of V110 or V114 Co-administered With a Booster Dose of mRNA-1273 in Healthy Adults (V110-911)
RandomizedParallel-groupDouble-blindPrevention
Summary
The purpose of this study is to evaluate the concomitant and non-concomitant use of messenger ribonucleic acid (mRNA) mRNA-1273, the nucleoside-modified mRNA vaccine for active immunization to prevent coronavirus disease (COVID-19) caused by severe acute respiratory syndrome coronavirus (SARS-CoV-2), with a 23-valent pneumococcal polysaccharide vaccine (V110) for the prevention of pneumococcal disease, or a 15-valent pneumococcal conjugate vaccine (V114) indicated for the prevention of invasive pneumococcal disease.
Timeline
- Start
- 2022-01-12
- Primary completion
- 2023-02-21
- Completion
- 2023-02-21
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Elasomeran | Messenger RNA (mRNA) | 50 ug | Intramuscular |
| Subject | Pneumovax 23 | Vaccine | 0.5 ml | Intramuscular |
| Subject | V114 | Vaccine | 0.5 ml | Intramuscular |