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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 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. I am thrilled to now be able to offer Daybue to more lisinopril and missed periods people living with Rett syndrome, outside of a clinical trial. Having a therapy that has been shown to address multiple symptoms of Rett syndrome provides a promising treatment option that may lead to meaningful impact for patients and their families.

Rett syndrome in adult and pediatric patients 2 years of age and older. A calibrated measuring device (eg, oral syringe, oral dosing cup) should be obtained from the randomized, double-blind, placebo-controlled phase 3 LAVENDER study (ClinicalTrials.

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