Study met primary and all key secondary efficacy endpoints
Participants receiving DT120 ODT achieved a statistically significant reduction in Hamilton Anxiety Rating Scale (HAM-A) score, with a placebo-adjusted change of 5.4 points from baseline at Week 12 (p<0.0001, Cohen’s d=0.81)
DT120 ODT was generally well tolerated, with a safety profile consistent with prior clinical experience
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