Bexobrutideg works by recruiting the body's own protein-destruction machinery to break down Bruton's tyrosine kinase, or BTK, an enzyme whose signaling activity drives the growth and survival of certain blood cancer cells. Unlike conventional BTK inhibitors, which block the protein's activity, bexobrutideg degrades the protein itself, the company said. The drug has shown responses in early clinical studies in chronic lymphocytic leukemia patients who progressed on other therapies, including those with resistance mutations to existing BTK inhibitors.