|Event:||22 nd Annual BIO-Europe International Partnering Conference|
|Date:||Wednesday, November 9, 2016|
|Time:||11:15am (Central European Time)|
|Location:||KoelnMesse - Congress Center North, Cologne, Germany|
NEW YORK, Nov. 02, 2016 (GLOBE NEWSWIRE) -- Tonix Pharmaceuticals Holding Corp. (Nasdaq:TNXP) (Tonix), which is developing a next-generation treatment for posttraumatic stress disorder (PTSD), announced today that it will present at the 22 nd Annual BIO-Europe International Partnering Conference being held November 7-9, 2016 in Cologne, Germany. Seth Lederman, M.D., president and chief executive officer of Tonix, will provide a corporate update and an overview of Tonix's PTSD clinical program. Tonix recently held a successful End-Of-Phase 2 meeting with the U.S. Food and Drug Administration (FDA) based on positive data from its 12-week randomized, double-blind, placebo-controlled Phase 2 AtEase clinical trial evaluating TNX-102 SL* in military-related PTSD. Tonix intends to commence a 12-week Phase 3 study evaluating TNX-102 SL, 5.6 mg, in military-related PTSD in the first quarter of 2017.
*TNX-102 SL (cyclobenzaprine HCl sublingual tablets) is an Investigational New Drug and has not been approved for any indication. About Tonix Pharmaceuticals Holding Corp. Tonix is developing next-generation medicines for common disorders of the central nervous system, with its lead program focusing on posttraumatic stress disorder. This disorder is characterized by chronic disability, inadequate treatment options, high utilization of healthcare services, and significant economic burden. This press release and further information about Tonix can be found at www.tonixpharma.com.