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Gama tpica de investigacin: de 200 a 500 mcg de la mezcla combinada por aplicacin Por va subcutnea De 1 a 3 veces al da, segn el protocolo del estudio Conservar la solucin reconstituida refrigerada y utilizar en un plazo de 30 das

Discontinuation Rates Discontinuation rates due to adverse events in the Phase 2 trial were dose-dependent, ranging from approximately 6% in the 1 mg arm to 16% in the 12 mg arm

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This pattern is common in clinical trials of GLP1based therapies, where weight loss progresses most rapidly at the start before leveling off