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Tonix Pharmaceuticals Sets Nov. 9 Date for Q3 2026 Financial Results and Operational Update

By FisherVista•
Tonix Pharmaceuticals will report third-quarter 2026 financial results and operational highlights on Nov. 9, 2026, a disclosure that matters because it will give investors a fresh look at the commercial rollout of its newly approved fibromyalgia drug TONMYA and the progress of its CNS and immunology pipeline.
Tonix Pharmaceuticals Sets Nov. 9 Date for Q3 2026 Financial Results and Operational Update

Tonix Pharmaceuticals (NASDAQ: TNXP), a fully integrated, commercial-stage biotechnology company, will host a conference call and webcast on Monday, Nov. 9, 2026, at 8:30 a.m. ET to report its third-quarter 2026 financial results and operational highlights.

The timing of the announcement is significant for investors and patients alike. Tonix is at a pivotal stage: it is commercializing TONMYA(TM) (cyclobenzaprine HCl sublingual tablets 2.8mg), which the company describes as the first new treatment for fibromyalgia in more than 15 years. The quarterly update will be the first since the company began marketing that flagship medicine, and it will offer Wall Street its clearest view yet of how quickly the product is reaching patients and generating revenue.

Tonix’s CNS commercial infrastructure also supports its marketed acute migraine products, Zembrace(R) SymTouch(R) and Tosymra(R), giving the company multiple revenue streams in neurology. Beyond the commercial portfolio, Tonix is maximizing the science behind TONMYA in Phase 2 clinical trials to evaluate its potential in major depressive disorder and acute stress disorder. Those studies could eventually expand the drug’s label well beyond fibromyalgia, a possibility that carries substantial long-term value if the data hold up.

The company’s pipeline extends further. Its CNS portfolio includes TNX-2900, which is Phase 2 ready for the treatment of Prader-Willi syndrome, a rare disease. Tonix is also advancing 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 cautions that its product development candidates are investigational new drugs or biologics and that their efficacy and safety have not been established and they have not been approved for any indication.

Investors and interested parties can register to participate in the conference call or view the webcast through the company. A replay will be available under “IR Events” in the Investors section of the Tonix website. The full press release is available at https://nnw.fm/va44Q, and the latest news and updates relating to TNXP are available in the company’s newsroom at https://nnw.fm/TNXP.

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FisherVista

FisherVista

@fishervista