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Kalshi will allow bets on selected clinical trial results and full FDA decisions, starting with Phase 3 studies from established companies. The FDA separately approved Merck's Lipfendra cholesterol pill based on studies showing up to 60% LDL reduction.
news.ycombinator.comKalshi plans to launch prediction markets allowing bets on clinical trial outcomes and FDA regulatory approvals. The exchange is partnering with AppliedXL to select and monitor the markets. Initially, Kalshi will allow bets only on Phase 3 trial outcomes run by established drug companies and on full FDA approval decisions.
The U.S. Food and Drug Administration approved Merck’s Lipfendra pill for lowering cholesterol. Lipfendra is a once-daily pill intended to reduce LDL cholesterol beyond what statins alone achieve. Approval was based on studies showing up to 60% reduction in LDL cholesterol over six months in adults with or at risk for atherosclerotic cardiovascular disease.
Analysts project Lipfendra peak annual sales exceeding $5 billion.
These outlets didn't split into competing frames — coverage was uniform.
theepochtimes.comThe Food and Drug Administration approved enlicitide, sold as Lipfendra, on Thursday. The daily pill inhibits PCSK9 and carries a lower list price than existing injectable treatments.
The IndependentThe Joint Committee on Vaccination and Immunisation advised adding a teenage booster dose to the national schedule. The change follows an outbreak in Kent that killed two teenagers earlier in 2026.
indianexpress.comEli Lilly will pay $2.8 billion in cash to acquire AtaiBeckley, a developer of psychedelic treatments for mental health conditions. The deal includes up to $1 billion in additional milestone payments. It adds the target’s compounds to Lilly’s neuroscience programs.