Press Releases July 27, 2026 07:00 AM

Tonix Pharmaceuticals to Report Second Quarter 2026 Financial Results on August 10, 2026

Tonix Pharmaceuticals announces Q2 2026 financial results release and webcast for August 10, 2026

By Leila Farooq
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Tonix Pharmaceuticals Holding Corp., a commercial-stage biotech focused on CNS, infectious diseases, immunology, and rare diseases, will report their Q2 2026 financial results on August 10, 2026. The company markets several CNS products including TONMYA® for fibromyalgia and migraine treatments, while advancing a diverse pipeline featuring therapies for Lyme disease, mpox, kidney transplant rejection, and Prader-Willi syndrome. Investors are invited to the webcast and conference call for insights on recent progress and financial performance.

Tonix Pharmaceuticals to Report Second Quarter 2026 Financial Results on August 10, 2026
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Key Points

  • Tonix will report Q2 2026 financial results on August 10, 2026, including operational highlights.
  • The company markets TONMYA® for fibromyalgia, and acute migraine products Zembrace® SymTouch® and Tosymra®.
  • Research and development programs include treatments for Lyme disease prevention, mpox and smallpox vaccines, kidney transplant rejection, and rare diseases such as Prader-Willi syndrome.
  • Sectors impacted include biotechnology, pharmaceuticals, CNS disorders, infectious diseases, immunology, and rare diseases.

BERKELEY HEIGHTS, N.J., July 27, 2026 (GLOBE NEWSWIRE) -- Tonix Pharmaceuticals Holding Corp. (Nasdaq: TNXP) (“Tonix” or the “Company”), a fully integrated, commercial-stage biotechnology company, today announced that it will host a conference call and webcast to report second quarter 2026 financial results and operational highlights on Monday, August 10, 2026, at 8:30 a.m. ET.

To listen to the conference call, register at this link. To view the webcast, register at this link.

A replay will be available under “IR Events” in the Investors section of the Company’s website at https://ir.tonixpharma.com/news-events/ir-events.

Tonix Pharmaceuticals Holding Corp.
Tonix Pharmaceuticals* is a fully integrated, commercial-stage biotechnology company focused on central nervous system (CNS) disorders, infectious diseases, immunology conditions, and rare diseases where there exists high unmet medical need. TONMYA® (cyclobenzaprine HCl sublingual tablets 2.8mg), the Company’s flagship internally conceived and developed medicine, is the first treatment for fibromyalgia in more than 15 years. Tonix’s CNS commercial infrastructure supports its marketed products, including its acute migraine products, Zembrace® SymTouch® (sumatriptan injection 3 mg) and Tosymra® (sumatriptan nasal spray 10 mg). Tonix is extending the science behind TONMYA in Phase 2 clinical studies to evaluate the potential of TNX-102 SL in major depressive disorder and acute stress disorder/acute stress reaction. Tonix is also advancing a pipeline of infectious disease programs, including monoclonal antibody TNX-4800 (anti-OspA mAb) for Lyme disease prevention in the U.S. and TNX-801 (horsepox, live virus vaccine), a vaccine in development for the prevention of mpox and smallpox. Within immunology, Tonix is developing TNX-1500 (anti-CD40L mAb), a third-generation CD40 ligand inhibitor for the prevention of kidney transplant rejection. Finally, the Company’s rare disease portfolio includes TNX-2900 for the treatment of Prader-Willi syndrome. To learn more, visit www.tonixpharma.com.

*Tonix’s product development candidates, including TNX-102 SL for new, unapproved indications, are investigational new drugs or biologics. Their efficacy and safety have not been established and have not been approved for any indication.

Zembrace SymTouch and Tosymra are registered trademarks of Tonix Medicines. TONMYA is a registered trademark of Tonix Pharma Limited. All other marks are property of their respective owners.

Forward Looking Statements

Certain statements in this press release are forward-looking within the meaning of the Private Securities Litigation Reform Act of 1995 including those relating to the completion of the offering, the satisfaction of customary closing conditions, the intended use of proceeds from the offering and other statements that are predictive in nature. These statements may be identified by the use of forward-looking words such as “anticipate,” “believe,” “forecast,” “estimate,” “expect,” and “intend,” among others. 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 successfully launch and commercialize TONMYA® and any of our approved products; risks related to the failure to obtain FDA clearances or approvals and noncompliance with FDA regulations; 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 in the Company’s Annual Report on Form 10-K for the year ended December 31, 2025, as filed with the SEC on March 12, 2026, and periodic reports filed with the SEC on or after the date thereof. Tonix does not undertake an obligation to update or revise any forward-looking statement. 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.

Contacts
Deborah Elson (Investors/Media)
Tonix Pharmaceuticals
[email protected]
[email protected]  

Brian Korb (Investors)
astr partners
(917) 653-5122
[email protected]

Andrea Cohen (Media)
Sam Brown Inc.
(917) 209-7163
[email protected]


Risks

  • Potential failure to successfully launch and commercialize approved and pipeline products including TONMYA®.
  • Regulatory risks including obtaining FDA clearances and compliance with FDA regulations.
  • Financial risks including need for additional financing to support ongoing clinical development and commercialization efforts.

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