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Burning mouth syndrome (BMS): double blind controlled study of alpha-lipoic acid (thioctic acid) therapy

Understanding these population-specific considerations helps tailor protocols appropriately

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2 The FDA approval of Wegovy HD is based on the results of the STEP UP trial program, which included STEP UP, a 72-week study which evaluated the efficacy and safety of once-weekly Wegovy 7.2 mg compared to placebo and Wegovy 2.4 mg, as an adjunct to lifestyle intervention in 1,407 adults with obesity (BMI 30 kg/m 2 or greater), without diabetes

First, with regard to the sucrose preference test, we examined which concentration of sucrose could reliably be distinguished (Supplementary Figure 6)