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SCB-2019/Clover
SCB-2019 is a recombinant protein vaccine candidate designed to stimulate immune responses against SARS-CoV-2 by presenting the spike protein receptor-binding domain.
SCB-2019 is a recombinant protein vaccine candidate designed to stimulate immune responses against SARS-CoV-2 by presenting the spike protein receptor-binding domain. Used for COVID-19 prevention in adults.
At a glance
| Generic name | SCB-2019/Clover |
|---|---|
| Sponsor | D'Or Institute for Research and Education |
| Drug class | Recombinant protein vaccine |
| Target | SARS-CoV-2 spike protein receptor-binding domain (RBD) |
| Modality | Biologic |
| Therapeutic area | Immunology / Infectious Disease |
| Phase | Phase 3 |
Mechanism of action
SCB-2019 is a subunit vaccine consisting of the receptor-binding domain (RBD) of the SARS-CoV-2 spike protein produced in mammalian cells and formulated with an adjuvant. It is designed to elicit both humoral and cellular immune responses to provide protection against COVID-19 infection and severe disease.
Approved indications
- COVID-19 prevention in adults
Common side effects
- Injection site pain or erythema
- Fatigue
- Headache
- Myalgia
- Fever
Key clinical trials
- Safety and Immunogenicity Dose-finding Study of Adjuvanted SCB-2020S Vaccine in Adults (PHASE1)
- Assessment of Immunogenicity, Safety and Reactogenicity of a Booster Dose of Various COVID-19 Vaccine Platforms in Individuals Primed With Several Regimes. (PHASE3)
- An Observer-blind, Cohort Randomized, Exploratory Phase 3 Study to Evaluate the Safety and Immunogenicity of Recombinant Covid-19 Vaccine, mRNA Covid-19 Vaccine and Recombinant SARS-CoV-2 Trimeric S-protein Subunit Vaccine as 4th Dose in Individuals Primed/ Boosted With Various Regimens (PHASE3)
- Immunogenicity and Safety of Heterologous and Homologous Boosting With ChAdOx1-S and CoronaVac or a Formulation of SCB-2019 (COVID-19) (PHASE2)
- Immunogenicity and Safety of Adjuvanted SCB-2020S Vaccines in Adults (PHASE2)
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |