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U.K. regulators approved a CRISPR-based medicine to treat both sickle cell disease and beta thalassemia, making it the world’s first therapy built on the revolutionary gene-editing technology and ushering in a new era of genetic medicine, STAT reports. The authorization of the therapy, from Vertex Pharmaceuticals and CRISPR Therapeutics, is itself not a surprise. Studies have shown the one-time treatment enabled many sickle cell patients to live free of debilitating pain crises and relieved thalassemia patients of needing regular blood transfusions, raising hopes they have been effectively cured. But it also stands as a major achievement, coming just over a decade after the first lab experiments that showed CRISPR’s potential as a gene-editing tool were published.

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Panels in both the U.S. House and U.S. Senate passed restrictions on pharmacy benefit manager practices, increasing the chances the measures will be included in future government spending bills, STAT says. The policies are not identical, but at least three PBM reforms have been passed by panels in both chambers. One would replace PBM fees tied to a percentage of drug prices with flat fees. Another would require Medicare to create standard performance measures on which PBMs base pharmacy payments. A third would require PBMs to report data about drug costs, savings, beneficiary out-of-pocket costs, payments to pharmacies, and the amount of business directed to PBM-owned pharmacies.

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