Phase 3 clinical trial for compound that shows promise in treatment of Rett syndrome is pleased to share that Neuren Pharmaceuticals, today, after meeting with the FDA, will conduct a Phase 3 clinical trial for trofinetide, a compound that shows great promise in the treatment of Rett syndrome, in children and adults. This critical Phase 3 trial will be the final clinical step before FDA approval to become a prescribable drug. has worked tirelessly with Neuren Pharmaceuticals, trofinetide's manufacturer, to conduct two separate Phase 2 clinical trials, both of which achieved significant clinical benefit. Trial results for females ages five through 45 largely showed strong evidence of improvement in Rett syndrome symptoms of breathing, hand wringing, and mood. Neuren Pharmaceuticals measured these results utilizing the Rett Syndrome Behavior Questionnaire as well as two other efficacy measures.

For many families, these improvements will revolutionize their child's quality of life. Phase 2 results also provided strong evidence of potential disease modification rather than simply addressing symptoms in isolation. The successful completion of Phase 3 will provide a treatment that is an integral part of's comprehensive research strategy to correct the biology and reset neurologic function.

Phase 3 will be a double-blind, randomized, placebo-controlled trial and will test one active dose group with a treatment duration of 6 months. The dosing regimen has been designed to achieve consistent drug exposure in subjects regardless of their weight.'s Chief Science Officer, Steve Kaminsky, PhD, shares "This news is incredibly motivating as and Neuren now embark on the first phase 3 trial with a drug designed to change Rett biology and improve the lives of those affected."

Neuren's Executive Chairman, Dr. Richard Treagus, comments "We are pleased to have held a very constructive meeting with the FDA Division of Neurology Products. It has provided necessary confirmation on the key issues relating to our proposed Phase 3 trial in Rett syndrome. We are now able to progress the final stages of development with full confidence." is relentless in our pursuit of the first-ever prescribable treatment for Rett syndrome.​


The opinions expressed here are the views of the writer and do not necessarily reflect the views and opinions of News Medical.
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