Exposure-Response models using predicted exposure of deutetrabenazine’s active metabolites following BID and QD formulation administration, and therapeutic responses in the phase 3 TD and HD studies of the BID formulation were leveraged to predict changes in clinical efficacy endpoints following QD formulation administration in patients.
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This study estimated proportions of patients with TD at risk of DDIs with valbenazine/deutetrabenazine in real-world practice.