The reversal comes just two days after the company announced its launch and highlights the intensifying scrutiny surrounding compounded glucagon-like peptide-1 (GLP-1) therapies as both regulators and branded manufacturers continue to push back against copycat alternatives marketed alongside FDA-approved drugs
Participants were randomly assigned to receive either once-daily oral semaglutide (maximum dose of 14 mg) or a placebo, in addition to standard care
Right now, the momentum behind GLP-1s is real
Could it cause excessive sedation or paradoxically reduce benzodiazepine effectiveness
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