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The FDA requires extensive safety monitoring for all weight loss medications, and manufacturers must report adverse events, including cancer diagnoses

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For IP strategy teams at other biologic manufacturers, the Humira playbook has three translatable elements: build secondary patents on clinically meaningful formulation attributes, proactively negotiate biosimilar licensing timelines to control entry sequencing, and invest in rebate competitiveness modeling that extends through the post-LOE period, not just up to it

Diabetic Medicine