Tacere is focused on the most devastating of public health threats, infectious diseases for which there are currently neither cures nor effective treatments. Using internal expertise in research and development coupled with its extensive academic and clinical alliances, Tacere remains at the forefront of RNAi therapeutic development.
RNA interference is a natural mechanism that exists in every cell of the human body and can be redirected to silence genes and genetic elements, including viruses such as HCV. Unlike small molecule drugs, RNAi drugs target and eliminate the underlying genetic basis for the disease using cellular machinery that is catalytic and ever-present.
Capturing the full potential of RNAi, the scientific and management team of Tacere has pioneered the development of a multi-targeting approach that allows multiple regions of a disease-causing agent to be attacked simultaneously, creating a “cocktail in one drug.”
By harnessing the advances of gene medicine and using a delivery method for macromolecules that has demonstrated safety in clinical trials, TT-033 can be administered via peripheral IV, yet selectively penetrates hepatocytes, the liver cell in which HCV replicates. The target sites of the HCV virus are conserved across multiple genotypes, making TT-033 effective for a far broader patient population.
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