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The most common adverse effect related to skin are site injection reactions, effluvium, and allergic reactions including acute urticaria and angioedema [5]

Myint, M

Research efforts must continue with the ultimate goal of preventing neuronal damage and preserving normal cognitive functioning

DOSING USED IN PHASE 3 STUDIES In the most recent studies from the TRIUMPH programme (Phase 3) , retatrutide was administered as follows: Route: Subcutaneous Frequency: Once weekly Study duration: Approximately 68 weeks Phase 3 Schedule Recommended Dosage (Clinical Research Escalation Model) Retatrutide is administered once weekly using a gradual dose escalation to improve tolerability

Berry C, La Vecchia C, Nicotera P

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