NEW YORK, March 29, 2017 (GLOBE NEWSWIRE) --
Seth Lederman, M.D., president and chief executive officer of Tonix, will provide a corporate update and an overview of Tonix’s posttraumatic stress disorder (PTSD) clinical program. TNX-102 SL* was recently granted Breakthrough Therapy designation by the U.S. Food and Drug Administration (FDA) for the treatment of PTSD. This month, Tonix dosed the first patient for the “HONOR” study, a 12-week placebo-controlled Phase 3 clinical study evaluating TNX-102 SL 5.6 mg, in military-related PTSD. The interim analysis of the HONOR study is expected in the first half of 2018 and topline results are expected in the second half of 2018. Additional details of the HONOR study are available at
In his podium presentation, Dr. Lederman will also provide details of Tonix’s recently expanded therapeutic pipeline in PTSD and the new development program in a potential smallpox-preventing vaccine containing a live form of horsepox virus (HPXV).
The presentation will be webcast live and remain available for...