Patented multivalent RNAi platform for multi-gene suppression and viral treatment
Target multiple disease genes simultaneously with MV-RNA; Deliver RNAi therapeutics to specific organs using programmable shells; Suppress SARS-2 viral expression in infected cells with AmpliVIR RNA; Develop nasal spray or inhalation treatments for early-stage viral infections; Design RNA nanoparticles for targeted delivery to liver, kidney, brain, or other tissues
Pivoting research toward SARS-2 treatment with AmpliVIR RNA; Patented multivalent RNAi platform; Focus on programmable nanoparticle delivery; Early-stage development in RNA delivery and biopharmaceuticals; Research collaboration opportunities with scientists and institutions