{"id":61077,"date":"2024-10-29T12:06:46","date_gmt":"2024-10-29T12:06:46","guid":{"rendered":"https:\/\/english.saigonbiz.com.vn\/2024\/10\/29\/tonix-pharmaceuticals-to-present-at-bio-europe-2024\/"},"modified":"2024-10-29T12:06:46","modified_gmt":"2024-10-29T12:06:46","slug":"tonix-pharmaceuticals-to-present-at-bio-europe-2024","status":"publish","type":"post","link":"https:\/\/english.saigonbiz.com\/vn\/tonix-pharmaceuticals-to-present-at-bio-europe-2024\/","title":{"rendered":"Tonix Pharmaceuticals to Present at BIO-Europe\u00ae 2024"},"content":{"rendered":"
\n

CHATHAM, N.J., Oct. 29, 2024 (GLOBE NEWSWIRE) — Tonix Pharmaceuticals Holding Corp. (Nasdaq: TNXP) (Tonix or the Company), a fully-integrated biopharmaceutical company with marketed products and a pipeline of development candidates, announced today that Seth Lederman, M.D., Chief Executive Officer of Tonix Pharmaceuticals, will present at BIO-Europe\u00ae<\/sup>, being held November 4-6, 2024, in Stockholm, Sweden. The presentation will take place on Monday, November 4, 2024, at 1:00 p.m. CET.<\/p>\n

To schedule a meeting with the Company\u2019s management at the conference, please submit a meeting request through the partneringOne<\/a> system or contact brandon.weiner@westwicke.com<\/a>.<\/p>\n

Tonix Pharmaceuticals Holding Corp.<\/strong>*
<\/strong><\/sup>Tonix is a fully integrated biopharmaceutical company focused on transforming therapies for pain management and modernizing solutions for public health challenges. Tonix\u2019s development portfolio is focused on central nervous system (CNS) disorders, and its priority is to progress TNX-102 SL, a product candidate for which an NDA was submitted based on two statistically significant Phase 3 studies for the management of fibromyalgia. The FDA has granted Fast Track designation to TNX-102 SL for the management of fibromyalgia. TNX-102 SL is also being developed to treat acute stress reaction and acute stress disorder under a Physician-Initiated IND at the University of North Carolina in the OASIS study funded by the U.S. Department of Defense (DoD). Tonix\u2019s CNS portfolio includes TNX-1300 (cocaine esterase), a biologic in Phase 2 development designed to treat cocaine intoxication that has FDA Breakthrough Therapy designation and its development is supported by a grant from the U.S. National Institute of Drug Abuse and Addiction. Tonix\u2019s immunology development portfolio consists of biologics to address organ transplant rejection, autoimmunity and cancer, including TNX-1500, which is an Fc-modified 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, including TNX-2900 for Prader-Willi syndrome, and infectious disease, including a vaccine for mpox, TNX-801. Tonix recently announced a contract with the U.S. DoD\u2019s Defense Threat Reduction Agency (DTRA) for up to $34 million over five years to develop TNX-4200, small molecule broad-spectrum antiviral agents targeting CD45 for the prevention or treatment of infections to improve the medical readiness of military personnel in biological threat environments. Tonix owns and operates a state-of-the art infectious disease research facility in Frederick, MD. Tonix Medicines, our commercial subsidiary, markets Zembrace\u00ae<\/sup> SymTouch\u00ae<\/sup> (sumatriptan injection) 3 mg and Tosymra\u00ae<\/sup> (sumatriptan nasal spray) 10 mg for the treatment of acute migraine with or without aura in adults.<\/p>\n

* Tonix\u2019s 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.<\/p>\n

Zembrace SymTouch and Tosymra are registered trademarks of Tonix Medicines. All other marks are property of their respective owners.<\/p>\n

This press release and further information about Tonix can be found at www.tonixpharma.com<\/u><\/a>.<\/p>\n

Forward Looking Statements
<\/strong>Certain statements in this press release are forward-looking within the meaning of the Private Securities Litigation Reform Act of 1995. These statements may be identified by the use of forward-looking words such as \u201canticipate,\u201d \u201cbelieve,\u201d \u201cforecast,\u201d \u201cestimate,\u201d \u201cexpect,\u201d and \u201cintend,\u201d among others. These forward-looking statements are based on Tonix’s current expectations and actual results could differ materially. There are a number of factors that could cause actual events to differ materially from those indicated by such forward-looking statements. These factors include, but are not limited to, risks related to the failure to obtain FDA clearances or approvals and noncompliance with FDA regulations; risks related to the failure to successfully market any of our products; risks related to the timing and progress of clinical development of our product candidates; our need for additional financing; uncertainties of patent protection and litigation; uncertainties of government or third party payor reimbursement; limited research and development efforts and dependence upon third parties; and substantial competition. As with any pharmaceutical under development, there are significant risks in the development, regulatory approval and commercialization of new products. Tonix does not undertake an obligation to update or revise any forward-looking statement. Investors should read the risk factors set forth in the Annual Report on Form 10-K for the year ended December 31, 2023, as filed with the Securities and Exchange Commission (the \u201cSEC\u201d) on April 1, 2024, and periodic reports filed with the SEC on or after the date thereof. All of Tonix’s forward-looking statements are expressly qualified by all such risk factors and other cautionary statements. The information set forth herein speaks only as of the date thereof.<\/p>\n

Investor Contact
<\/strong>Jessica Morris
Tonix Pharmaceuticals
investor.relations@tonixpharma.com<\/u><\/a>
<\/a><\/u>(862) 904-8182<\/p>\n

Peter Vozzo
ICR Westwicke
peter.vozzo@westwicke.com<\/u><\/a>
(443) 213-0505<\/p>\n

Media Contact
<\/strong>Ray Jordan
Putnam Insights
ray@putnaminsights.com
(949) 245-5432<\/p>\n

<\/div>\n","protected":false},"excerpt":{"rendered":"

CHATHAM, N.J., Oct. 29, 2024 (GLOBE NEWSWIRE) — Tonix Pharmaceuticals Holding Corp. (Nasdaq: TNXP) (Tonix or the Company), a fully-integrated biopharmaceutical company with marketed products and a pipeline of development candidates, announced today that Seth Lederman, M.D., Chief Executive Officer of Tonix Pharmaceuticals, will present at BIO-Europe\u00ae, being held November 4-6, 2024, in Stockholm, Sweden. 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