Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
INO-4212 is a polyvalent DNA-based vaccine developed for the prevention and treatment of Ebola virus infections. It consists of two optimized SynCon DNA plasmids (INO-4201 and INO-4202) encoding the glycoprotein antigen from various circulating Ebola strains between 1975 and 2014. The vaccine is designed to stimulate both T cell and antibody immune responses against Ebola virus. In clinical studies, it has demonstrated safety, tolerability, and robust immunogenicity in healthy volunteers. Preclinical studies showed that INO-4212 provided complete protection against lethal Ebola challenge in animal models with long-lasting immune responses detectable for at least one year after vaccination. The vaccine can be administered intramuscularly or intradermally followed by electroporation using a specialized device to enhance cellular uptake of the DNA[1][2][4][5].
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 INO-4212.