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FDA awarded NT102 the title of orphan drug for the treatment of Dravet syndrome

 Last Update: 2021-11-12
 Source: Internet
 Author: User

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Dravet syndrome is a rare childhood syndrome that affects 1 in 15,700 babies born in the United States and is characterized by encephalopathy and epilepsy
.

It is difficult to diagnose because many symptoms are not obvious in the first year after the child is born

Children's Epilepsy Diagnostic Fund

Have normal or near-normal cognitive and motor development before epileptic seizure

Neuroene Therapeutics recently announced that the FDA has granted the company's proprietary compound NT102 the orphan drug designation
.

NT102 was developed as a mitochondrial and neuroprotective substance for the treatment of neurological diseases, such as drug-resistant epilepsy

FDA NT102 has a wide range of seizure protection in a variety of preclinical animal models, especially for the epileptic seizures of Dravet syndrome (a rare childhood syndrome characterized by severe encephalopathy and epilepsy)

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