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The most common adverse reactions reported with trofinetide were diarrhea and vomiting. 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. The product, which received FDA approval in March 2023, was approved based on data from the randomized, how to get velcade prescription double-blind, placebo-controlled phase 3 LAVENDER study (ClinicalTrials. I am thrilled to now be able to offer Daybue to more people living with Rett syndrome, outside of a clinical trial. Daybue is supplied as a strawberry-flavored oral solution containing 200 mg of trofinetide per mL.
I am thrilled to now be able to offer Daybue to more 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.
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