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In its brief opposing the preliminary injunction, the FDA defends its data-driven conclusion that "Lilly's supply is currently exceeding demand and will meet or exceed projected demand across all strengths of Mounjaro and Zepbound." The FDA's determination relied heavily on confidential data provided by Lilly

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New delivery routes including sublingual, intranasal, and inhaled formulations have attracted patent interest [9, 33, 34] and some scientific attention [35], though market signals remain limited