Tonix Pharmaceuticals to Present at Two Upcoming January Investor Conferences
07 January 2025 - 11:00PM
Tonix Pharmaceuticals Holding Corp. (Nasdaq: TNXP) (Tonix or the
Company), a biopharmaceutical company with marketed products and a
pipeline of development candidates, announced today that Tonix
management will present and host investor meetings at the following
January investor conferences:
8th Annual
Neuroscience Innovation Forum by Sachs Associates
Company Presentation |
Presenter: |
Seth Lederman,
M.D., President and Chief Executive Officer of Tonix
Pharmaceuticals |
Date: |
Sunday, January 12, 2025 |
Place: |
Marines Memorial Club, San Francisco, Calif. |
Time: |
11:15 a.m. PT |
Room: |
Track A – Room Rosenberg |
Panel |
Participant: |
Seth Lederman,
M.D., President and Chief Executive Officer of Tonix
Pharmaceuticals |
Title: |
Revolutionizing Neuropsychiatric Treatments: Novel Approaches
Panel |
Date: |
Sunday, January 12, 2025 |
Place: |
Marines Memorial Club, San Francisco, Calif. |
Time: |
1:15 p.m. PT |
2025 Biotech Showcase |
Presenter: |
Seth Lederman,
M.D., President and Chief Executive Officer of Tonix
Pharmaceuticals |
Date: |
Tuesday, January 14, 2025 |
Place: |
Hilton San Francisco Union Square, San Francisco, Calif. |
Time: |
10:00 a.m. PT |
Room: |
Yosemite C (Ballroom level) |
Investors interested in arranging a meeting with
the Company's management during these conferences should contact
the respective conference coordinators. Replays of both webcasts of
the Company’s presentations at the Neuroscience Innovation Forum
and the 2025 Biotech Showcase will be available under the IR Events
tab of the Tonix website at www.tonixpharma.com following each
presentation.
Tonix Pharmaceuticals Holding
Corp.*
Tonix is a fully integrated biopharmaceutical
company focused on transforming therapies for pain management and
vaccines for public health challenges. Tonix’s development
portfolio is focused on central nervous system (CNS) disorders.
Tonix’s priority is to advance TNX-102 SL, a product candidate for
the management of fibromyalgia, for which an NDA was submitted
based on two statistically significant Phase 3 studies for the
management of fibromyalgia and for which a PDUFA (Prescription Drug
User Fee act) goal date of August 15, 2025 has been assigned for a
decision on marketing approval. The FDA has also 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’s 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’s 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’s 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® SymTouch® (sumatriptan injection) 3
mg and Tosymra® (sumatriptan nasal spray) 10 mg for the treatment
of acute migraine with or without aura in adults.
* 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.
Zembrace SymTouch and Tosymra are registered
trademarks of Tonix Medicines. All other marks are property of
their respective owners.
This press release and further information about
Tonix can be found at www.tonixpharma.com.
Forward Looking Statements
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 “anticipate,”
“believe,” “forecast,” “estimate,” “expect,” and “intend,” 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 “SEC”) 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.
Investor Contact
Jessica MorrisTonix
Pharmaceuticalsinvestor.relations@tonixpharma.com (862)
904-8182
Peter VozzoICR Healthcarepeter.vozzo@icrhealthcare.com (443)
213-0505
Media Contact
Ray JordanPutnam Insightsray@putnaminsights.com(949)
245-5432
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