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CBS News Establishing protocols: If the FDA requires ongoing data collection or formal clinical pathways to maintain compounding access, it will incentivize structured research into dosing, bioavailability, and long-term toxicity rather than relying solely on anecdotal claims

There are some dramatic left-tail-risk scenariosfor example, if all people with above-average body mass index take GLP-1 medications and stick to the prescribed regimen for a prolonged period, this could drive a decline in food consumption of more than 10%

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Continued treatment with tirzepatide for maintenance of weight reduction in adults with obesity or overweight: The SURMOUNT-4 randomized clinical trial