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Retatrutide's Phase 2 trial reported nausea in approximately 45 to 58% of participants at the 8 mg and 12 mg doses, with vomiting in 20 to 30%
Understanding the dose-response relationship is essential for designing appropriate research protocols [9]
Both methods were compared to the conventional design, which calculates chronic GFR slope from the first on-treatment visit to the end of treatment
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