Intellia’s second CRISPR therapy reduces swelling attacks by 95% in hereditary angioedema
An experimental CRISPR therapy has dramatically lowered levels of an inflammation-promoting protein and reduced bouts of harmful swelling by 95% in patients with an inherited condition, Intellia Therapeutics announced Sunday at a medical conference in Germany.
A Phase I clinical trial tested three dose levels of a gene editing therapy in 10 patients with hereditary angioedema, a rare, genetic disease that leaves people prone to sudden inflammation and swelling. The attacks can be disfiguring when beneath the skin, painful when they occur in the gut, and deadly when they block breathing in the airways.
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