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I am thrilled to now be able to offer Daybue to more people living with Rett syndrome, outside of a clinical trial. The dosage is determined by patient weight and can be administered orally or via gastrostomy tube. The dosage is determined by patient weight and can be administered orally or via gastrostomy tube.

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The product, which received FDA approval in March 2023, was approved based on data from the randomized, double-blind, placebo-controlled phase 3 LAVENDER study (ClinicalTrials.

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