Post Traumatic Stress Drug Candidate Gets Breakthrough Therapy Status

DECEMBER 19, 2016
Gale Scott
The US Food and Drug Administration (FDA) has granted breakthrough therapy designation to a drug candidate for post-traumatic stress disorder (PTSD).  

The product is cyclobenzaprine HCl sublingual tablets, known as TNX-102 SL, the product is made by Tonix Pharmaceuticals. According to the drug company, the approval was granted on the basis of a phase 2 study known as AtEase in subjects who have PTSD associated with their military service.The trial was a 12-week, randomized controlled study.

A phase 3 study will begin in the first quarter of 2017, the company said.

The evidence of the phase 2 trial showed the drug "may demonstrate substantial improvement over existing therpies one or more clincally significant endpoints," the company said in a news release.

An estimated eight million people in the US have episodes of PTSD, the company said.  

Current treatment is generally with selective serotonin reuptake inhibitors or serotonin-norepinephrine reuptake inhibitors.

Tonix Pharmaceuticals Holding Company is based in Manhattan.


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