Tonix Pharmaceuticals (NASDAQ: TNXP), a fully integrated, commercial-stage biopharmaceutical company, announced the appointment of George Lederman, Ph.D., as executive vice president of strategy and transformation, effective Oct. 30, 2026. In his new role, Lederman will lead artificial intelligence (“AI”) initiatives aimed at improving operational efficiency and reducing costs, while overseeing business development efforts, including potential partnerships and licensing opportunities to advance the company’s clinical programs and share development expenses.
Lederman joins Tonix from Aliaxis, where he served as vice president of global strategy, leading corporate and portfolio strategy initiatives and supporting operational restructuring efforts. Previously, he was an associate partner at McKinsey & Company, where he helped develop the firm’s digitization practice and advised clients on AI, machine learning and advanced analytics. His appointment comes as Tonix advances its commercial portfolio, including an approved fibromyalgia treatment, and investigational programs in Lyme disease prevention and immunology. Lederman is the son of Tonix President, CEO and Chairman Seth Lederman, M.D. His appointment and compensation were reviewed and approved by independent board members and the appropriate committees under the company’s related-party transaction policies.
To view the full press release, visit https://ibn.fm/byGIq
Tonix Pharmaceuticals Holding Corp.
Tonix Pharmaceuticals is a fully-integrated, commercial-stage biotechnology company focused on central nervous system (CNS) and immunology treatments in areas of high unmet medical need. TONMYA(TM) (cyclobenzaprine HCl sublingual tablets 2.8mg), the Company’s recently approved flagship medicine, is the first new treatment for fibromyalgia in more than 15 years. Tonix’s CNS commercial infrastructure supports its marketed products, including its acute migraine products, Zembrace(R) SymTouch(R) and Tosymra(R). Tonix is maximizing the science behind TONMYA in Phase 2 clinical trials to evaluate its potential in major depressive disorder and acute stress disorder. In addition, the company’s CNS portfolio includes TNX-2900, which is Phase 2 ready for the treatment of Prader-Willi syndrome, a rare disease. Tonix is also advancing a pipeline of immunology programs, including monoclonal antibody TNX-4800 for Lyme disease prophylaxis and TNX-1500, a third-generation CD40 ligand inhibitor for the prevention of kidney transplant rejection.
Tonix’s product development candidates are investigational new drugs or biologics; their efficacy and safety have not been established and have not been approved for any indication.
NOTE TO INVESTORS: The latest news and updates relating to TNXP are available in the company’s newsroom at https://ibn.fm/TNXP
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