The 2 primary endpoints assessing change in HQ-CT and CY-BOCS for the 9.6-mg carbetocin arm showed numeric improvements vs placebo that did not reach statistical significance; therefore, the trial did not meet its primary endpoint and all other statistical analyses are considered nominal.
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Intranasal Carbetocin Reduces Hyperphagia, Anxiousness, and Distress in Prader-Willi Syndrome: CARE-PWS Phase 3 Trial.
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The sentences
The primary endpoints showed numeric improvements in both HQ-CT and CY-BOCS which were not statistically significant; however, the 3.2-mg arm showed nominally significant improvements in HQ-CT, PADQ, and CGI-C scores vs placebo.