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What to Expect in 2026 and Beyond Here are plausible scenarios: Best-case: Phase 3 trials conclude by 2025, regulatory submission in 2026, FDA approval and U.S

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Counterfeit GLP-1 drugs have become, as Katherine Eban wrote in a Vanity Fair investigation, a hot commodity among transnational crime groups, homegrown counterfeiters, rogue compounders, shady middlemen, unscrupulous doctors, and medi-spas of dubious legality. By February, Eban reported, illegal pharmacies in the US were filling more than 734,000 GLP-1 prescriptions per month, according to data compiled by Translucent DataLab, which scrutinizes illegal online pharmacies, and IQVIA, a major data and clinical research company

"Insulin requirements are often lower in individuals with type 1 using a GLP-1 receptor agonist," said Dr