drugset / Trial / NCT04742738
Safety and Immunogenicity Study of SARS-CoV-2 Nanoparticle Vaccine (GBP510) Adjuvanted With Aluminum Hydroxide (COVID-19)
Phase 1/2
Completed
260 enrolled
SK Bioscience Co., Ltd.
Coalition for Epidemic Preparedness Innovations · collab
RandomizedParallel-groupQuadruple-blindPrevention
Summary
This is a first-in-human, Phase I/II, randomized, placebo-controlled, observer-blinded, age-escalating study to assess the safety, reactogenicity and immunogenicity of a SK SARS-CoV-2 recombinant protein nanoparticle vaccine (GBP510) adjuvanted with Alum in healthy younger and older adults.
Timeline
- Start
- 2021-01-20
- Primary completion
- 2021-07-30
- Completion
- 2022-07-07
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | GBP510 | Vaccine | 10 ug | Intramuscular |
| Subject | GBP510 | Vaccine | 25 ug | Intramuscular |
Indications
No indication recorded.