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This process typically takes several years from the point of Phase 3 trial completion, and no specific timeline for retatrutide approval should be assumed

Event Phase 2 Rate (12 mg group) Phase 2 Rate (Placebo) Nausea 45.8% 11.6% Diarrhea 33.3% 9.3% Vomiting 22.2% 2.3% Constipation 16.7% 7.0% Decreased appetite 22.2% 2.3% The nausea incidence at the highest dose a nausea percentage of roughly 46% makes it the single most reported adverse event in retatrutide clinical trials 2026 data

Where Can You Get Retatrutide

Customer support answered me on a Sunday afternoon