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The US targets 15 high-cost drugs, including Biktarvy and Xeljanz, for price negotiations, a move that could reshape global pharmaceutical economics and R&D priorities.

The U.S. government has opened a new front in its battle against high drug prices, releasing a list of 15 medicines targeted for aggressive price negotiations in 2028. The list includes blockbuster treatments for HIV and arthritis, signaling a crackdown on medications that lack generic competition and drain billions from the public purse.
Among the high-profile targets are Gilead’s HIV powerhouse Biktarvy and Pfizer’s arthritis drug Xeljanz. The selection was driven by data showing these 15 drugs alone cost the Medicare program $27 billion in the year leading up to October 2025. Enabled by the Inflation Reduction Act, these negotiations allow the government to use its massive purchasing power to dictate terms, a practice standard in Europe and Canada but revolutionary in the American market.
While this is a U.S. domestic policy, the implications are global. The U.S. market typically subsidizes drug development profits; squeezed margins there could lead pharmaceutical giants to rethink their pricing strategies worldwide. For patients relying on Biktarvy—a daily pill that has revolutionized HIV care by combining three powerful antivirals—the move raises questions about the future landscape of innovation.
"The era of unlimited pricing power for pharma is ending," notes a healthcare economist. "When the world's most profitable market starts clamping down, companies will look to protect their bottom line. We might see shifts in R&D priorities away from chronic conditions managed by pills toward acute therapies like gene editing."
For the millions of seniors in the U.S. struggling with copays, the negotiations promise relief. But for the global health ecosystem, the recalibration of drug economics adds a layer of uncertainty. As the U.S. government tightens its belt, the shockwaves will be felt in boardrooms and research labs from Basel to Boston.
The 2028 deadline sets the stage for a high-stakes poker game between Washington regulators and corporate executives, with the health of millions—and the future of drug discovery—hanging in the balance.
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