Tonix Pharmaceuticals (NASDAQ: TNXP), a fully integrated biopharmaceutical company with marketed products and a pipeline of development candidates, participated in this month’s Annual European Congress of Rheumatology (“EULAR”) event. The gathering was held June 12–15, 2024, in Vienna, Austria. According to the announcement, the company presented a poster during the four-day international event. According to the announcement, the poster indicated that treatment with Tonix’s Tonmya(TM) (TNX-102 SL, sublingual cyclobenzaprine HCl) in a phase 3 RESILIENT study resulted in significantly reduced daily pain while also showing broad fibromyalgia symptom improvement.
“People suffering with fibromyalgia tend to struggle with daily activities, have impaired quality of life and are frequently disabled,” said Tonix Pharmaceuticals CEO Seth Lederman, MD, in the press release. “We believe the activity of Tonmya on pain, sleep quality, fatigue cognitive dysfunction and depression are indicative of the broad-spectrum activity of Tonmya, suggesting Tonmya treats fibromyalgia at a syndromal level. We are excited by the prospect of offering this patient population its potential first new therapy option in more than a decade.”
To view the poster, visit https://ibn.fm/6r02J
To view the full press release, visit https://ibn.fm/UV4ds
About Tonix Pharmaceuticals Holding Corp.
Tonix is a biopharmaceutical company focused on developing, licensing and commercializing therapeutics to treat and prevent human disease and alleviate suffering. Tonix’s development portfolio is focused on central nervous system (“CNS”) disorders. Tonix’s priority is to submit a New Drug Application (“NDA”) to the U.S. Food and Drug Administration in the second half of 2024 for Tonmya, a product candidate for which two positive phase 3 studies have been completed for the management of fibromyalgia. TNX-102 SL is also being developed to treat acute stress reaction as well as fibromyalgia-type Long COVID. Tonix’s CNS portfolio includes TNX-1300 (cocaine esterase), a biologic designed to treat cocaine intoxication with Breakthrough Therapy designation. Tonix’s immunology development portfolio consists of biologics to address organ-transplant rejection, autoimmunity and cancer, including TNX-1500, which is a humanized monoclonal antibody targeting CD40-ligand (“CD40L” or “CD154”) being developed for the prevention of allograft rejection and for the treatment of autoimmune diseases. Tonix also has product candidates in development in the areas of rare disease and infectious disease. Tonix Medicines, the company’s commercial subsidiary, markets Zembrace(R) SymTouch(R) (sumatriptan injection) 3 mg and Tosymra(R) (sumatriptan nasal spray) 10 mg for the treatment of acute migraine with or without aura in adults. For more information about the company, please visit www.TonixPharma.com.
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