Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
SCTV01E is a tetravalent recombinant protein-based COVID-19 vaccine developed to provide broad protection against multiple SARS-CoV-2 variants, specifically Alpha, Beta, Delta, and Omicron BA.1. The vaccine consists of the trimeric spike extracellular domain (S-ECD) proteins from these four variants formulated with a squalene-based oil-in-water adjuvant (SCT-VA02B). It is designed to induce balanced and broad-spectrum neutralizing antibody responses as well as T cell immunity against both ancestral and emerging SARS-CoV-2 strains. Clinical trials have demonstrated that SCTV01E is safe, well tolerated, and highly immunogenic in adults and children. In phase 3 studies, it showed efficacy rates of approximately 80% in preventing symptomatic COVID-19 infection. The vaccine has been authorized for emergency use in China for adults aged 18 years and older[1][2][3][4][6].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on SCTV01E.