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The ability to target Alzheimers disease before significant cognitive impairment sets in would mark a major advancement in how the medical community approaches the condition

The SURMOUNT-1 trial protocol allowed one dose de-escalation for intolerable side effects, which underscores that slower titration is acceptable and sometimes preferred

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The July 2024 interim report found that PBM and brand drug manufacturer rebate contracts are expressly conditioned on limiting access to potentially lower-cost generic and biosimilar competitors [1]