Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
ZIP1642 is a lipid nanoparticle-formulated, dual-antigen self-amplifying RNA (saRNA) vaccine candidate for COVID-19 developed by Ziphius Vaccines. It encapsulates two separate saRNA constructs encoding the SARS-CoV-2 spike receptor-binding domain (S-RBD) and nucleocapsid (N) protein in a single LNP, enabling in situ amplification of RNA and prolonged antigen expression at low doses. Preclinical studies in mice and hamsters have shown that intramuscular prime-boost immunization with ZIP1642 elicits high titers of neutralizing antibodies against multiple SARS-CoV-2 variants (including Wuhan-like, Beta, Delta, and reduced but detectable responses to Omicron), as well as robust Th1-biased CD4+ and CD8+ T cell responses specific for both S and N antigens, leading to reduced viral loads, lung pathology, and inflammatory markers after challenge. ZIP1642 is positioned as a next-generation multi-antigen saRNA COVID-19 vaccine, but to date its development has remained in the preclinical stage.
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 ZIP1642.