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In the Phase 2 trial, nausea ranged from approximately 14% at the 1 mg dose to 60% at the 12 mg dose, with most cases occurring during dose stepping

Through the specific binding, proximity can change the fate of a target and induce protein degradation or cell death

In clinical practice, the pattern is usually: Most common side effects last days to a few weeks Side effects can return temporarily after dose increases For many people, symptoms improve significantly by weeks 48 Below is a symptom-by-symptom breakdown

Originally developed for type 2 diabetes management, these injectable medicines work by mimicking natural GLP-1 hormone, reducing appetite and caloric intake