ZyVersa Therapeutics Reports Third Quarter 2025 Financial Results
ZyVersa Therapeutics (OTCQB: ZVSA) reported Q3 2025 results for the quarter ended September 30, 2025. Cash on hand was $0.5 million and the company said existing cash will only fund month-to-month operations, requiring additional financing. ZyVersa raised approximately $2.05 million in Q3 and $4.05 million year-to-date. Research and development expenses were $0.4 million (down 16.3% YoY); general and administrative expenses were $1.7 million (down 5.1% YoY). Pre-tax loss was $20.7 million driven mainly by an $18.6 million impairment of in-process R&D. Net loss was $19.8 million; a deferred tax benefit of $0.9 million related to the impairment was recorded.
ZyVersa Therapeutics (OTCQB: ZVSA) ha riportato i risultati del Q3 2025 per il periodo terminato il 30 settembre 2025. La liquidità disponibile era di 0,5 milioni di dollari e l'azienda ha dichiarato che il cash esistente coprirà solo operazioni mese per mese, richiedendo ulteriori finanziamenti. ZyVersa ha raccolto circa 2,05 milioni di dollari nel Q3 e 4,05 milioni di dollari dall'inizio dell'anno. Le spese di ricerca e sviluppo sono state di 0,4 milioni di dollari (in calo del 16,3% su base annua); le spese generali e amministrative sono state di 1,7 milioni di dollari (in calo del 5,1% su base annua). La perdita ante-imposte è stata di 20,7 milioni di dollari, spinta principalmente da una impairment di 18,6 milioni di dollari su R&D in corso. La perdita netta è stata di 19,8 milioni di dollari; è stato registrato un beneficio fiscale differito di 0,9 milioni di dollari relativo all'impairement.
ZyVersa Therapeutics (OTCQB: ZVSA) informó los resultados del T3 2025 para el trimestre que terminó el 30 de septiembre de 2025. La caja disponible era de 0,5 millones de dólares y la compañía dijo que el efectivo existente solo cubrirá operaciones mes a mes, requiriendo financiamiento adicional. ZyVersa recaudó aproximadamente 2,05 millones de dólares en el tercer trimestre y 4,05 millones de dólares en lo que va del año. Los gastos de investigación y desarrollo fueron de 0,4 millones de dólares (caída del 16,3% interanual); los gastos generales y administrativos fueron de 1,7 millones de dólares (caída del 5,1% interanual). La pérdida antes de impuestos fue de 20,7 millones de dólares, impulsada principalmente por una impairment de 18,6 millones de dólares en I+D en curso. La pérdida neta fue de 19,8 millones de dólares; se registró un beneficio fiscal diferido de 0,9 millones de dólares relacionado con la impairment.
ZyVersa Therapeutics (OTCQB: ZVSA)는 2025년 9월 30일로 종료된 3분기 2025년 실적을 발표했습니다. 보유 현금은 500,000달러였으며 회사는 남아 있는 현금이 월별 운영비만 충당하고 추가 자금 조달이 필요하다고 밝혔습니다. ZyVersa는 Q3에서 약 205만 달러를, 연간 누적으로는 405만 달러를 조달했습니다. 연구개발비는 40만 달러로 전년 동기 대비 16.3% 감소했고; 일반 및 관리비는 170만 달러로 전년 대비 5.1% 감소했습니다. 세전 손실은 2070만 달러로, 주로 진행 중인 R&D 자산의 1860만 달러 손상 때문이었습니다. 순손실은 1980만 달러였고, 손상과 관련된 이연법인세 이익이 90만 달러 기록되었습니다.
ZyVersa Therapeutics (OTCQB: ZVSA) a publié les résultats du T3 2025 pour le trimestre se terminant le 30 septembre 2025. La trésorerie disponible s'élevait à 0,5 million de dollars et l'entreprise a indiqué que les liquidités existantes ne couvriraient que les opérations mois par mois, nécessitant un financement additionnel. ZyVersa a levé environ 2,05 millions de dollars au T3 et 4,05 millions de dollars sur l'année jusqu'à présent. Les dépenses de recherche et développement s'élevaient à 0,4 million de dollars (en baisse de 16,3% sur un an); les charges générales et administratives étaient de 1,7 million de dollars (en baisse de 5,1% sur un an). La perte avant impôt était de 20,7 millions de dollars, principalement due à une impairment de 18,6 millions de dollars sur la R&D en cours. La perte nette était de 19,8 millions de dollars; un avantage fiscal différé de 0,9 million de dollars lié à l'impairement a été enregistré.
ZyVersa Therapeutics (OTCQB: ZVSA) meldete die Ergebnisse des dritten Quartals 2025 für das am 30. September 2025 endende Quartal. Die verfügbaren liquiden Mittel betrugen 0,5 Millionen USD und das Unternehmen gab an, dass das vorhandene Bargeld nur die monatlichen Betriebskosten abdecken wird, wodurch zusätzliche Finanzierung erforderlich wird. ZyVersa hat im Q3 ca. 2,05 Millionen USD aufgenommen und year-to-date 4,05 Millionen USD. Forschungs- und Entwicklungskosten betrugen 0,4 Millionen USD (YoY -16,3%); allgemeine Verwaltungsaufwendungen betrugen 1,7 Millionen USD (YoY -5,1%). Die Vorsteuerverlust betrug 20,7 Millionen USD, hauptsächlich getrieben durch eine Impairment von 18,6 Millionen USD der in-process R&D. Der Nettoverlust betrug 19,8 Millionen USD; ein latenter Steuervorteil von 0,9 Millionen USD im Zusammenhang mit der impairment wurde verbucht.
ZyVersa Therapeutics (OTCQB: ZVSA) أبلغت عن نتائج الربع الثالث من عام 2025 للربع المنتهي في 30 سبتمبر 2025. النقد المتاح كان 0.5 مليون دولاروقالت الشركة إن النقد المتاح سيغطي فقط العمليات الشهرية، مما يستلزم تمويلاً إضافياً. جمعت ZyVersa نحو 2.05 مليون دولار في الربع الثالث و4.05 مليون دولار حتى الآن خلال السنة. بلغت نفقات البحث والتطوير 0.4 مليون دولار (بانخفاض 16.3% على أساس سنوي)؛ وكانت نفقات العامة والإدارية 1.7 مليون دولار (بانخفاض 5.1% على أساس سنوي). وكانت الخسارة قبل الضريبة 20.7 مليون دولار، ويرجع ذلك بشكل رئيسي إلى انخفاض قيمة 18.6 مليون دولار من R&D قيد التنفيذ. أما الخسارة الصافية فكانت 19.8 مليون دولار؛ وُجِد فائدة ضريبية مؤجلة قدرها 0.9 مليون دولار مرتبطة بالإطفاء.
- Raised $2.05M in Q3-2025
- YTD financing totaled $4.05M
- R&D expense decreased 16.3% YoY to $0.4M
- Cash on hand only $0.5M as of Sept 30, 2025
- Pre-tax loss $20.7M in Q3-2025
- Impairment of in-process R&D $18.6M
- Net loss $19.8M for Q3-2025; financing required
Insights
Pipeline remains early-stage; impairment and limited cash materially constrain program advancement.
ZyVersa advances two platform programs: VAR 200 for kidney diseases including focal segmental glomerulosclerosis and potential expansion to Alport syndrome and diabetic kidney disease, and IC 100 targeting cardiometabolic conditions with possible rare-kidney-disease use.
The company reported an
Key dependencies and risks include securing near-term financing and reversing the conditions that triggered the impairment. The programs themselves are described but no clinical readouts, enrollment milestones, regulatory events, or concrete near-term development timelines are disclosed, limiting assessment of technical progress.
Watch for financing outcomes, any reinstatement or reversal of the impairment, and specific clinical milestones or trial initiations within the next 3–12 months to assess whether development can continue.
Severe liquidity pressure and large impairment suggest high near-term financing need; investor dilution or restructuring likely.
The company raised approximately
Expense lines show modest reductions in R&D and G&A, but these savings are tiny relative to the scale of the pre-tax loss spike caused by the
Concrete near-term monitors: announcements of financing commitments, terms of any Equity Purchase Agreement activity, changes to cash balance, and any reversal or further impairments. Expect material corporate actions within the next 1–6 months if cash stays at the disclosed level.
- ZyVersa is advancing a therapeutic development pipeline with multiple programs built around its two proprietary technologies – Cholesterol Efflux Mediator VAR 200 for treatment of kidney diseases, and Inflammasome ASC Inhibitor IC 100 for treatment of chronic inflammatory diseases.
- The lead indication for VAR 200 is focal segmental glomerulosclerosis (FSGS) with potential indication expansion in Alport syndrome and diabetic kidney disease.
- The lead indication for IC 100 is cardiometabolic conditions, with potential indication expansion in rare kidney diseases.
- Raised approximately
$2.05 million in Q3-2025;$4.05 million year-to-date.
WESTON, Fla., Nov. 19, 2025 (GLOBE NEWSWIRE) -- ZyVersa Therapeutics, Inc. (OTCQB: ZVSA, or “ZyVersa”), a clinical-stage specialty biopharmaceutical company developing first-in-class drugs for treatment of patients with renal and inflammatory diseases who have unmet medical needs, reports financial results for the quarter ended September 30, 2025.
Third Quarter, 2025 FINANCIAL RESULTS
Cash on hand was
Research and development expenses were
General and administrative expenses were
Pre-tax losses were
Net losses were approximately
ABOUT ZYVERSA THERAPEUTICS, INC.
ZyVersa (OTCQB: ZVSA) is a clinical stage specialty biopharmaceutical company leveraging advanced, proprietary technologies to develop first-in-class drugs for patients with renal and inflammatory diseases who have significant unmet medical needs. The Company is currently advancing a therapeutic development pipeline with multiple programs built around its two proprietary technologies – Cholesterol Efflux Mediator VAR 200 for treatment of kidney diseases, and Inflammasome ASC Inhibitor IC 100 for treatment of chronic inflammatory diseases. For more information, please visit www.zyversa.com.
CAUTIONARY STATEMENT REGARDING FORWARD-LOOKING STATEMENTS
Certain statements contained in this press release regarding matters that are not historical facts, are forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, Section 21E of the Securities Exchange Act of 1934, as amended, and the Private Securities Litigation Reform Act of 1995. These statements are based on management’s current intentions, plans, beliefs, expectations, or forecasts and include, for example, our belief that we have sufficient liquidity to fund our business operations on a month-to-month basis and anticipated levels of capital expenditures for the coming months or year. Forward-looking statements are neither historical facts nor assurances of future performance, and, therefore, you are cautioned not to place undue reliance on them. No forward-looking statement can be guaranteed, and actual results may differ materially from those projected. ZyVersa Therapeutics, Inc. (“ZyVersa”) uses words such as “anticipates,” “believes,” “plans,” “expects,” “projects,” “future,” “intends,” “may,” “will,” “should,” “could,” “estimates,” “predicts,” “potential,” “continue,” “guidance,” and similar expressions to identify these forward-looking statements that are intended to be covered by the safe-harbor provisions. Such forward-looking statements involve inherent risks and uncertainties; consequently, actual results may differ materially from those expressed or implied in the statements due to a number of factors, including ZyVersa’s ability to obtain the funding necessary to advance the development of our product candidates and maintain its business operations; plans to develop and commercialize its product candidates, the timing of initiation of ZyVersa’s planned preclinical and clinical trials; the timing of the availability of data from ZyVersa’s preclinical and clinical trials; the timing of any planned investigational new drug application; ZyVersa’s plans to research, develop, and commercialize its current and future product candidates; the clinical utility, potential benefits and market acceptance of ZyVersa’s product candidates; ZyVersa’s commercialization, marketing and manufacturing capabilities and strategy; ZyVersa’s ability to protect its intellectual property position; and ZyVersa’s estimates regarding future revenue, expenses, capital requirements and need for additional financing.
New factors emerge from time-to-time, and it is not possible for ZyVersa to predict all such factors, nor can ZyVersa assess the impact of each such factor on the business or the extent to which any factor, or combination of factors, may cause actual results to differ materially from those contained in any forward-looking statements. Forward-looking statements included in this press release are based on information available to ZyVersa as of the date of this press release. ZyVersa disclaims any obligation to update such forward-looking statements to reflect events or circumstances after the date of this press release, except as required by law.
CORPORATE, MEDIA, IR CONTACT
Karen Cashmere
Chief Commercial Officer
kcashmere@zyversa.com
786-251-9641
| ZYVERSA THERAPEUTICS, INC. | |||||||
| CONDENSED CONSOLIDATED BALANCE SHEETS | |||||||
| September 30, | December 31, | ||||||
| 2025 | 2024 | ||||||
| (Unaudited) | |||||||
| Assets | |||||||
| Current Assets: | |||||||
| Cash | $ | 527,978 | $ | 1,530,924 | |||
| Prepaid expenses and other current assets | 298,192 | 184,873 | |||||
| Vendor deposits | 169,363 | - | |||||
| Total Current Assets | 995,533 | 1,715,797 | |||||
| In-process research and development | - | 18,647,903 | |||||
| Vendor deposit | - | 178,476 | |||||
| Deferred offering costs | 44,727 | 57,238 | |||||
| Total Assets | $ | 1,040,260 | $ | 20,599,414 | |||
| Liabilities and Stockholders' (Deficit) Equity | |||||||
| Current Liabilities: | |||||||
| Accounts payable | $ | 9,805,129 | $ | 9,337,267 | |||
| Accrued expenses and other current liabilities | 2,960,698 | 1,894,041 | |||||
| Total Current Liabilities | 12,765,827 | 11,231,308 | |||||
| Deferred tax liability | - | 851,659 | |||||
| Total Liabilities | 12,765,827 | 12,082,967 | |||||
| Stockholders' (Deficit) Equity: | |||||||
| Preferred stock, | |||||||
| Series A preferred stock, 8,635 shares designated, 50 shares issued and outstanding as of September 30, 2025 and December 31, 2024 | - | - | |||||
| Series B preferred stock, 5,062 shares designated, 5,062 shares issued and outstanding as of September 30, 2025 and December 31, 2024 | 1 | 1 | |||||
| Common stock, | |||||||
| December 31, 2024, respectively, and 8,095,921 and 2,508,191 shares outstanding as of September 30, 2025 and December 31, 2024, respectively | 809 | 251 | |||||
| Additional paid-in-capital | 125,187,156 | 121,155,922 | |||||
| Accumulated deficit | (136,906,365 | ) | (112,632,559 | ) | |||
| Treasury stock, at cost, 7 shares at September 30, 2025 and December 31, 2024 | (7,168 | ) | (7,168 | ) | |||
| Total Stockholders' (Deficit) Equity | (11,725,567 | ) | 8,516,447 | ||||
| Total Liabilities and Stockholders' (Deficit) Equity | $ | 1,040,260 | $ | 20,599,414 | |||
| ZYVERSA THERAPEUTICS, INC. | |||||||||||||||
| CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS | |||||||||||||||
| (Unaudited) | |||||||||||||||
| For the Three Months Ended September 30, | For the Nine Months Ended September 30, | ||||||||||||||
| 2025 | 2024 | 2025 | 2024 | ||||||||||||
| Operating Expenses: | |||||||||||||||
| Research and development | $ | 365,053 | $ | 436,043 | $ | 1,033,865 | $ | 1,658,030 | |||||||
| General and administrative | 1,739,174 | 1,833,578 | 5,259,064 | 6,192,205 | |||||||||||
| Impairment of in-process research and development | 18,647,903 | - | 18,647,903 | - | |||||||||||
| Total Operating Expenses | 20,752,130 | 2,269,621 | 24,940,832 | 7,850,235 | |||||||||||
| Loss From Operations | (20,752,130 | ) | (2,269,621 | ) | (24,940,832 | ) | (7,850,235 | ) | |||||||
| Other (Income) Expense: | |||||||||||||||
| Interest expense | 131,350 | 131,635 | 380,946 | 131,794 | |||||||||||
| Change in fair value of equity payable | (226,262 | ) | - | (196,313 | ) | - | |||||||||
| Pre-Tax Net Loss | (20,657,218 | ) | (2,401,256 | ) | (25,125,465 | ) | (7,982,029 | ) | |||||||
| Income tax benefit (provision) | 851,659 | - | 851,659 | (9,707 | ) | ||||||||||
| Net Loss | $ | (19,805,559 | ) | $ | (2,401,256 | ) | $ | (24,273,806 | ) | $ | (7,991,736 | ) | |||
| Net Loss Per Share | |||||||||||||||
| - Basic and Diluted | $ | (2.56 | ) | $ | (2.43 | ) | $ | (4.63 | ) | $ | (9.79 | ) | |||
| Weighted Average Number of | |||||||||||||||
| Common Shares Outstanding | |||||||||||||||
| - Basic and Diluted | 7,740,678 | 988,378 | 5,237,544 | 816,293 | |||||||||||