Breakdown | ||||
Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|
Income Statement | Total Revenue | |||
10.09M | 7.77M | 0.00 | 0.00 | 0.00 | Gross Profit |
2.33M | 3.03M | -112.09M | -92.31M | -50.51M | EBIT |
-136.70M | -118.38M | -112.09M | -92.31M | -50.51M | EBITDA |
-71.73M | -114.09M | -110.84M | -92.26M | -50.48M | Net Income Common Stockholders |
-130.04M | -116.66M | -116.88M | -92.29M | -52.17M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | |||
98.78M | 24.95M | 120.23M | 178.66M | 77.07M | Total Assets |
162.89M | 154.46M | 225.69M | 240.90M | 98.18M | Total Debt |
8.12M | 9.81M | 760.00K | 956.00K | 1.31M | Net Debt |
-90.66M | -15.13M | -119.47M | -177.70M | -75.76M | Total Liabilities |
23.33M | 48.93M | 18.51M | 22.18M | 10.54M | Stockholders Equity |
139.56M | 105.53M | 207.18M | 218.72M | 87.65M |
Cash Flow | Free Cash Flow | |||
-61.05M | -109.90M | -146.20M | -110.86M | -57.13M | Operating Cash Flow |
-60.92M | -102.00M | -98.05M | -75.56M | -48.57M | Investing Cash Flow |
-120.00K | -29.07M | -48.15M | -35.31M | -8.56M | Financing Cash Flow |
134.87M | 36.52M | 87.84M | 212.49M | 123.11M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
53 Neutral | $5.14B | 3.03 | -43.89% | 2.83% | 16.75% | -0.06% | |
52 Neutral | $89.86M | 5.55 | 0.51% | ― | -34.58% | -62.19% | |
52 Neutral | $108.78M | ― | -58.55% | ― | 825.97% | 38.32% | |
51 Neutral | $135.61M | ― | -140.82% | ― | -48.37% | -44.70% | |
50 Neutral | $193.37M | ― | -91.44% | ― | -2.04% | -478.87% | |
46 Neutral | $122.83M | ― | -189.46% | ― | -3.24% | 31.00% | |
34 Underperform | $137.89M | ― | -44.50% | ― | ― | 52.54% |
On May 21, 2025, Tonix Pharma announced the dosing of the first patient in the Phase 2 OASIS trial, which aims to evaluate the TNX-102 SL product candidate for reducing acute stress reaction and disorder. Sponsored by the University of North Carolina Institute for Trauma Recovery and supported by a $3 million grant from the U.S. Department of Defense, the trial will involve approximately 180 motor vehicle collision trauma survivors in the U.S., assessing the safety and efficacy of TNX-102 SL compared to a placebo.
The most recent analyst rating on (TNXP) stock is a Buy with a $4.00 price target. To see the full list of analyst forecasts on Tonix Pharma stock, see the TNXP Stock Forecast page.
On May 14, 2025, Tonix Pharmaceuticals announced the appointment of Joseph Hand as General Counsel and Executive Vice President of Operations, effective immediately. This strategic leadership change is expected to impact the company’s operations and potentially strengthen its industry positioning.
The most recent analyst rating on (TNXP) stock is a Buy with a $4.00 price target. To see the full list of analyst forecasts on Tonix Pharma stock, see the TNXP Stock Forecast page.
On May 8, 2025, Tonix Pharma held its annual shareholder meeting where seven proposals were approved. Key decisions included the election of eight board members, ratification of EisnerAmper LLP as the accounting firm, and authorization for potential reverse stock splits. Additionally, shareholders approved amendments to the stock incentive plan, the 2025 Employee Stock Purchase Plan, and executive compensation, with a decision to hold executive compensation votes every three years.
On April 28, 2025, Tonix Pharmaceuticals presented promising data at the AACR Annual Meeting, demonstrating that their fusion protein mTFF2-MSA, combined with an anti-PD1 antibody, effectively activates cancer-killing CD8+ T Cells and reduces immunosuppression in tumor microenvironments in animal models. This development highlights Tonix’s potential impact in cancer treatment, particularly with their TNX-1700 candidate, which is in preclinical stages for gastric and colorectal cancers.
On April 23, 2025, Tonix Pharmaceuticals presented promising preclinical data at the World Vaccine Congress in Washington. Their TNX-801 vaccine candidate showed efficacy in protecting animals against mpox and rabbitpox, including in immunocompromised subjects, indicating potential for future development and market opportunities.
On March 24, 2025, Tonix Pharmaceuticals announced that the FDA will not require an Advisory Committee meeting for the New Drug Application of TNX-102 SL, a product candidate for fibromyalgia management. This development could streamline the approval process, potentially accelerating the product’s market entry and impacting the company’s operations and market positioning positively.
On March 10, 2025, Tonix Pharmaceuticals announced receiving a $50,000 grant from the Medical CBRN Defense Consortium to support the development of its TNX-801 vaccine candidate for mpox and smallpox. The grant will aid in creating a commercialization plan for TNX-801, which has shown promising results, including being significantly less virulent than traditional smallpox vaccines and providing durable protection in animal models.
On February 27, 2025, Tonix Pharma Limited, a subsidiary of Tonix Pharmaceuticals Holding Corp., signed an employment agreement with Siobhan Fogarty, the Chief Technical Officer. The agreement includes an annual salary, bonus eligibility, and equity compensation, with a 180-day notice period for termination, reflecting standard industry practices.
On March 3, 2025, Tonix Pharmaceuticals presented data at the 7th International Congress on Controversies in Fibromyalgia, highlighting the effectiveness of their transmucosal sublingual cyclobenzaprine (TNX-102 SL) in reducing pain associated with fibromyalgia through improved non-restorative sleep. This presentation underscores Tonix’s commitment to addressing fibromyalgia and strengthens its position in the pharmaceutical industry by showcasing successful results from two Phase 3 studies.