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If a drug demonstrates evidence of effectiveness and an acceptable safety profile in Phase 2 evaluations, Phase 3 trials are undertaken to obtain the additional information about clinical efficacy and safety in a larger number of patients, typically at geographically dispersed clinical trial sites, to permit the FDA to evaluate the overall benefit-risk relationship of the drug and to provide adequate information for the labeling of the drug
GLP-1 side effects (nausea, appetite loss) are unrelated to Lipo C and typically resolve within weeks
60 The study demonstrated GLP1s ability to prevent atrial electrical and structural remodelling, crucial in new-onset and established AF
2019;11:e10293
Recognizing these causes can help you respond the right way instead of feeling concerned
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