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

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(Neutral)
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earnings date

Tonix Pharmaceuticals (Nasdaq: TNXP) announced it will host a conference call and webcast to report its second quarter 2026 financial results and operational highlights on Monday, August 10, 2026, at 8:30 a.m. ET. Investors can access the live call and webcast via advance registration links, with a replay available under “IR Events” in the Investors section of the company’s website.

Tonix is a fully integrated, commercial-stage biotechnology company focused on CNS disorders, infectious diseases, immunology, and rare diseases. Its portfolio includes TONMYA for fibromyalgia, acute migraine products Zembrace SymTouch and Tosymra, and multiple clinical-stage candidates such as TNX-102 SL, TNX-4800, TNX-801, TNX-1500, and TNX-2900.

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Positive

  • None.

Negative

  • None.

Market Context

Insider context showed Net Buying across 3 transactions. That platform signal adds governance contex...
Analysis

Insider context showed Net Buying across 3 transactions. That platform signal adds governance context to the scheduled second-quarter 2026 report; no financial figures are provided, leaving the upcoming disclosure's result detail as the main watchpoint.

Key Figures

Reporting period: Q2 2026 Reporting date: August 10, 2026 Conference time: 8:30 a.m. ET +5 more
8 metrics
Reporting period Q2 2026 Financial results and operational highlights
Reporting date August 10, 2026 Conference call and webcast
Conference time 8:30 a.m. ET August 10, 2026 conference call and webcast
Fibromyalgia treatment gap >15 years TONMYA described as the first treatment for fibromyalgia in more than 15 years
TONMYA dosage 2.8 mg Cyclobenzaprine HCl sublingual tablets
Zembrace dosage 3 mg Sumatriptan injection
Tosymra dosage 10 mg Sumatriptan nasal spray
Clinical study phase Phase 2 TNX-102 SL studies in major depressive disorder and acute stress disorder

Historical Context

5 past events · Latest: Jul 15 (Positive)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Jul 15 Preclinical data publication Positive +5.0% Published preclinical mpox data in the peer-reviewed Journal of Virology
Jul 13 Payer coverage agreement Positive -6.6% Announced managed Medicare coverage agreement adding approximately 9 million lives
Jun 29 Phase 2 enrollment Positive -3.6% Enrolled first patient in Phase 2 HORIZON study for depression
Jun 11 Investor meeting attendance Neutral -2.8% Announced attendance at BTIG Infectious Disease Day 2026 investor meetings
Jun 08 Payer coverage agreement Positive +5.8% Signed second commercial payer agreement expanding TONMYA coverage to 52 million lives

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

TNXP's recent positive company announcements produced mixed reactions, with three of five events diverging from the announcement sentiment.

Key Terms

cns, phase 2 clinical studies, monoclonal antibody, investigational new drugs or biologics
4 terms
cns medical
"focused on central nervous system (CNS) disorders"
CNS stands for the central nervous system, the brain and spinal cord that control thought, movement and bodily functions. For investors, CNS-focused products and research matter because therapies aimed at this “delicate wiring” are scientifically challenging, often carry higher development and regulatory risk, and can take longer to prove safe and effective — but successful treatments also tend to command large markets and premium pricing.
phase 2 clinical studies medical
"extending the science behind TONMYA in Phase 2 clinical studies"
Phase 2 clinical studies are mid-stage research trials that test a drug or medical treatment in a larger group of patients to assess whether it works as intended and to further evaluate safety and dosing. Think of them as the prototype testing phase where researchers look for evidence of benefit and manageable side effects; results help investors gauge whether a therapy has real commercial potential and a clearer path toward late-stage trials and regulatory review.
monoclonal antibody medical
"including monoclonal antibody TNX-4800"
A monoclonal antibody is a laboratory-made protein designed to recognize and attach to a specific target in the body, such as a disease-causing substance or cell. It functions like a highly precise lock-and-key tool, helping to treat or detect illnesses. For investors, companies developing monoclonal antibodies can represent promising opportunities in the healthcare sector, especially as these treatments often address unmet medical needs.
investigational new drugs or biologics regulatory
"are investigational new drugs or biologics"
Medicines or biological products that are not yet approved for general use and are being tested in humans under a regulator's permission; they include experimental drugs, vaccines, gene therapies, and other biologic treatments that have passed initial lab and animal studies. Think of them as prototypes being tested in controlled trials to assess safety and effectiveness; for investors, their status signals development stage, regulatory risk, potential future market value, and the near-term costs and milestones tied to approval progress.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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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
deborah.elson@tonixpharma.com
investor.relations@tonixpharma.com  

Brian Korb (Investors)
astr partners
(917) 653-5122
brian.korb@astrpartners.com

Andrea Cohen (Media)
Sam Brown Inc.
(917) 209-7163
andreacohen@sambrown.com


FAQ

When will Tonix Pharmaceuticals (TNXP) report its Q2 2026 financial results?

Tonix Pharmaceuticals plans to report its Q2 2026 financial results on August 10, 2026, at 8:30 a.m. ET. According to Tonix, the update will be delivered via a conference call and webcast that also cover operational highlights.

How can investors access the Tonix Pharmaceuticals (TNXP) Q2 2026 earnings conference call and webcast?

Investors can access the Tonix Q2 2026 earnings call and webcast by registering through the provided online links. According to Tonix, a replay will be posted under “IR Events” in the Investors section of its website after the event.

Will a replay be available for the Tonix Pharmaceuticals (TNXP) August 10, 2026 earnings call?

Yes, a replay of the August 10, 2026 Tonix earnings call will be available. According to Tonix, investors can access the replay under the “IR Events” area in the Investors section of the company’s website following the live presentation.

What therapeutic areas does Tonix Pharmaceuticals (TNXP) focus on as it reports Q2 2026 results?

Tonix focuses on central nervous system disorders, infectious diseases, immunology, and rare diseases. According to Tonix, its portfolio spans marketed products for fibromyalgia and acute migraine and multiple investigational candidates in depression, stress disorders, Lyme disease, transplant rejection, and Prader-Willi syndrome.

What are the key marketed products of Tonix Pharmaceuticals (TNXP) ahead of its Q2 2026 report?

Tonix’s marketed products include TONMYA for fibromyalgia and acute migraine treatments Zembrace SymTouch and Tosymra. According to Tonix, these products are supported by its CNS commercial infrastructure while it advances multiple investigational clinical programs.

Which Tonix Pharmaceuticals (TNXP) pipeline candidates are highlighted alongside the Q2 2026 earnings announcement?

Tonix highlights TNX-102 SL for major depressive and acute stress disorders, TNX-4800 for Lyme disease prevention, TNX-801 for mpox and smallpox, TNX-1500 for kidney transplant rejection, and TNX-2900 for Prader-Willi syndrome. According to Tonix, these remain investigational.