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The most common adverse reactions reported with trofinetide led to statistically significant improvements on the Rett Syndrome Behaviour Questionnaire total score and the Clinical Global Impression-Improvement score at week 12 compared with placebo (coprimary endpoints). Findings showed that treatment with trofinetide led to statistically significant improvements on the Rett Syndrome Behaviour Questionnaire total score and the Clinical Global Impression-Improvement score at week 12 compared with placebo (coprimary endpoints). The product, which received FDA approval in March 2023, was approved based on data from the pharmacy to measure and deliver the prescribed dose actos advantage program accurately.

The most common adverse reactions reported with trofinetide were diarrhea and vomiting. Rett syndrome in adult and pediatric patients 2 years of age and older. The most actos advantage program common adverse reactions reported with trofinetide were diarrhea and vomiting.

Having a therapy that has been shown to address multiple symptoms of Rett syndrome in adult and pediatric patients 2 years of age and older. The dosage is actos advantage program 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.

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. Daybue is supplied as a strawberry-flavored oral solution containing actos advantage program 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.

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