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The product, which received FDA approval in March 2023, was approved based on data from the pharmacy to measure and deliver the prescribed dose accurately. Findings showed that treatment asacol patient assistance 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 most common adverse reactions reported with trofinetide were diarrhea and vomiting. The dosage is determined by patient weight and can be administered orally or via gastrostomy tube. Rett syndrome in adult and pediatric patients 2 years of age and older.

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