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Description

Serious adverse events in the Phase 2 trial were low

By week 36, this weight loss effect was even more pronounced, increasing from 9.4% to 14.7%, while the placebo group saw a reduction of only 2.3%

Minimizing concentration-dependent adverse events: Evaluate whether dose-splitting might reduce peak-related gastrointestinal symptoms based on pharmacokinetic modeling

Rosemary Daly, D.O., DABPM r