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One is that it’s among the 12 peptides scheduled for FDA review in 2026 and 2027, which could lead to its reinstatement on the bulk compounding list and broader availability as a therapeutic treatment.1 The other may be the apparent increasing rates of cognitive disability among U.S

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