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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. 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. Daybue is supplied as a strawberry-flavored oral solution containing 200 mg of trofinetide i was reading this per mL.

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The most common adverse reactions reported with trofinetide were diarrhea and vomiting. 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. 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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