This is the Weekend Edition of Bloomberg Opinion Today, a roundup of the most popular stories Bloomberg Opinion publishes each week based on web readership. New subscribers can sign up here; follow us on Bluesky, TikTok, Instagram, LinkedIn and Threads. Some 10,000 federal health workers lost their jobs earlier this month — among them, a group of regulators who help new medicines get approved. If Health and Human Services Secretary Robert F. Kennedy Jr. doesn’t reverse course, American patients will suffer, and half a century of US leadership in pharmaceutical innovation could come to a precipitous end. Three decades ago, the US lagged Europe in access to new medications. Pressured to narrow the disparity, Congress passed a law in 1992 to speed up drug approvals. The new framework allowed regulators to collect fees from drug companies, which vastly increased resources at the FDA for reviews. Today, Americans have access to three-quarters of new medicines, and the US has become a world leader in some of the most advanced treatments, including cell and gene therapies. The promise of such innovations — which can, among other medical miracles, target and destroy cancer cells, potentially reverse hearing loss, and enable sickle-cell patients to live without debilitating pain — can hardly be overstated. Yet US dominance in such medicine shouldn’t be taken for granted.
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