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Trump administration advances plan for peptide drugs favored by RFK Jr.

The advisers backed compounding access despite FDA scientists citing limited human data and possible liver damage, allergic reactions and tumor growth.

  • On Thursday, the Department of Health and Human Services submitted an "interim access policy" to the White House, aiming to allow specialty pharmacies to produce certain experimental peptides.
  • Earlier this year, Health and Human Services Secretary Robert F. Kennedy Jr. directed the FDA to reconsider restrictions, prompting a July advisory panel vote to ease regulations on six compounds, including BPC-157 and TB-500.
  • FDA staff scientists warned the substances lack clinical evidence and pose risks like liver toxicity, contradicting proponents who characterize the access push as a matter of "medical freedom."
  • Reports from users like Dylan Meetze and Dominik E. include severe adverse effects—migraines, fatigue, and muscle spasms—after taking peptides that influencers promote as safe for "body optimization."
  • Major telehealth providers like Hims & Hers and Noom plan to offer these peptides if access is eased, entering a market Wall Street analysts estimate could be worth $3 billion.
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The Washington Post broke the news in Washington, United States on Tuesday, October 13, 2026.
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