Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
RQ3013 is an mRNA-based COVID-19 vaccine developed to encode a chimeric spike protein containing mutations from both the Alpha (B.1.1.7) and Beta (B.1.351) variants of SARS-CoV-2, with some sources also indicating inclusion of Omicron variant mutations[5][6]. The vaccine uses pseudouridine-modified messenger RNA encapsulated in lipid nanoparticles to deliver the genetic instructions for spike protein expression, thereby inducing an immune response[1][2][5]. Preclinical studies demonstrated that RQ3013 elicits robust neutralizing antibody responses against multiple SARS-CoV-2 variants in animal models[4][6]. In clinical trials as a heterologous booster following three doses of inactivated vaccines, RQ3013 showed superior immunogenicity and acceptable safety compared to other boosters such as Ad5-nCoV and ZF2001, with relative efficacy against symptomatic infection ranging from 62% to 69%[1][2]. The vaccine is being developed by Walvax and RNAcure.
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 RQ3013.