Theralase(R) Releases 3Q2025 Financial Statements
Theralase (OTCQB:TLTFF) released unaudited condensed consolidated interim 3Q2025 financial statements and will host a conference call on Nov 19, 2025 at 11:00 am ET. For the nine months ended Sept 30, 2025 versus 2024: total revenue was $590,573 (down 5%), cost of sales $299,743 (51% of revenue, down 10%), and gross margin $290,830 (49% of revenue). Net loss was $3,435,145, a 3% increase, which included $708,521 in non-cash charges. Operational items: a $672,627 private placement (3,363,134 units at $0.20), extension of 1,840,000 warrants, and $280,000 short-term loans (15% interest).
Clinical: Study II is 97.8% enrolled (88/90); interim responses show CR 64.3%, Total Response 72.6%, and 40% CR durability at 450 days. Company expects enrollment complete in 4Q2025 and data lock/regulatory submissions in 1Q2027.
Theralase (OTCQB:TLTFF) ha pubblicato i bilanci intermedi non revisionati consolidati condensati 3Q2025 e terrà una conference call il 19 novembre 2025 alle 11:00 ET. Per i primi nove mesi conclusi al 30 settembre 2025 rispetto al 2024: ricavi totali sono stati 590.573 dollari (in calo del 5%), costo delle vendite 299.743 dollari (51% dei ricavi, in calo del 10%), e margine lordo 290.830 dollari (49% dei ricavi). La perdita netta è stata di 3.435.145 dollari, in aumento del 3%, che include 708.521 dollari in oneri non monetari. Voce operativa: un private placement di $672,627 (3.363.134 unità a 0,20 dollari), estensione di 1.840.000 warrant, e $280,000 prestiti a breve termine (interesse del 15%).
Clinico: lo Studio II è al 97,8% arruolato (88/90); le risposte intermedie mostrano CR 64,3%, Risposta Totale 72,6%, e una durata di CR del 40% a 450 giorni. L'azienda prevede che l'arruolamento sia completato nel 4Q2025 e l'acquisizione dei dati/submit regolatori nel 1Q2027.
Theralase (OTCQB:TLTFF) publicó estados financieros interinos condensados no auditados 3Q2025 y celebrará una conferencia telefónica el 19 de noviembre de 2025 a las 11:00 am ET. Para los primeros nueve meses terminados el 30 de septiembre de 2025 frente al 2024: los ingresos totales fueron de $590,573 (bajo un 5%), costo de ventas $299,743 (51% de los ingresos, baja un 10%), y margen bruto $290,830 (49% de los ingresos). La pérdida neta fue de $3,435,145, un aumento del 3%, que incluyó $708,521 en cargos no en efectivo. Elementos operativos: una colocación privada de $672,627 (3,363,134 unidades a $0.20), extensión de 1,840,000 warrants, y $280,000 préstamos a corto plazo (interés del 15%).
Clínica: el Estudio II está al 97.8% inscrito (88/90); respuestas interinas muestran CR 64.3%, Respuesta Total 72.6%, y 40% durabilidad de CR a 450 días. La compañía espera completar la inscripción en el 4T2025 y el bloqueo de datos/envíos regulatorios en el 1T2027.
Theralase (OTCQB:TLTFF) 는 비감사 condensed consolidated interim 3Q2025 재무제표를 발표했으며 2025년 11월 19일 동부 표준시 11:00에 컨퍼런스 콜을 주최합니다. 2025년 9월 30일 종료된 9개월 동안 2024년과 비교하여: 총수익은 590,573달러(5% 감소), 매출원가 299,743달러(매출의 51%, 10% 감소), 총이익 290,830달러(매출의 49%). 순손실은 3,435,145달러로 3% 증가했으며, 현금이 아닌 비용 708,521달러가 포함되었습니다. 운영 항목: 672,627달러 규모의 비공개 배치(3,363,134 유닛 1주당 0.20달러), 1,840,000개의 워런트 연장, 그리고 280,000달러의 단기 대출(이자 15%).
임상: 스터디 II는 97.8% 등록 완료(88/90); 중간 반응은 CR 64.3%, 총 반응 72.6%, 그리고 450일 동안 CR 지속성 40%. 회사는 4Q2025에 등록 완료를 기대하고 1Q2027에 데이터 잠금/규제 제출을 계획합니다.
Theralase (OTCQB:TLTFF) a publié des états financiers intermédiaires condensés et non audités 3Q2025 et organisera une conférence téléphonique le 19 novembre 2025 à 11h ET. Pour les neuf mois se terminant le 30 septembre 2025 par rapport à 2024: le chiffre d'affaires total s'est élevé à 590 573 $, (en baisse de 5%), coût des ventes 299 743 $ (51% du chiffre d'affaires, en baisse de 10%), et la marge brute 290 830 $ (49% du chiffre d'affaires). La perte nette était de 3 435 145 $, en hausse de 3%, incluant 708 521 $ de charges non monétaires. Éléments opérationnels : une placement privé de 672 627 $ (3 363 134 unités à 0,20 $), prolongation de 1 840 000 warrants, et 280 000 $ de prêts à court terme (intérêt 15%).
Clinique: l'Étude II est à 97,8% enrôlée (88/90); les réponses intermédiaires montrent CR 64,3%, Réponse totale 72,6%, et une durabilité CR de 40% à 450 jours. L'entreprise prévoit que le recrutement soit terminé au cours du 4e trimestre 2025 et la fermeture des données/soumissions réglementaires au 1er trimestre 2027.
Theralase (OTCQB:TLTFF) hat unaudited condensed consolidated interim 3Q2025-Finanzberichte veröffentlicht und wird am 19. November 2025 um 11:00 Uhr ET eine Telefonkonferenz abhalten. Für die neun Monate, die am 30. September 2025 gegenüber 2024 endeten: Gesamtumsatz 590.573 $ (rückläufig um 5%), Kosten der Umsatzerlöse 299.743 $ (51% des Umsatzes, minus 10%), und Bruttomarge 290.830 $ (49% des Umsatzes). Nettoverlust 3.435.145 $, um 3% gestiegen, einschließlich 708.521 $ an nicht zahlungswirksamen Aufwendungen. Operative Posten: eine 672.627 $ Private Placement (3.363.134 Einheiten zu 0,20 $), Verlängerung von 1.840.000 Warrants und 280.000 $ kurzfristige Darlehen (Zinssatz 15%).
Klinik: Studie II ist zu 97,8% eingeschrieben (88/90); Zwischenantworten zeigen CR 64,3%, Gesamtreaktion 72,6%, und 40% CR-Dauerhaftigkeit nach 450 Tagen. Das Unternehmen geht davon aus, dass die Einschreibung im 4Q2025 abgeschlossen wird und Daten-Sperrung/bzw. regulatorische Einreichungen im 1Q2027 erfolgen.
Theralase (OTCQB:TLTFF) أصدرت بيانات مالية موجزة غير مدققة ومجمّعة مرحلية 3Q2025 وستعقد مكالمة مؤتمر هاتفي في 19 نوفمبر 2025 الساعة 11:00 صباحاً بتوقيت شرق الولايات المتحدة. للـ9 أشهر المنتهية في 30 سبتمبر 2025 مقابل 2024: إجمالي الإيرادات كان 590,573 دولاراً (بانخفاض 5%), تكلفة المبيعات 299,743 دولار (51% من الإيرادات، بانخفاض 10%), وهامش الربح الإجمالي 290,830 دولار (49% من الإيرادات). الخسارة الصافية كانت 3,435,145 دولاراً، بزيادة 3%، والتي شملت 708,521 دولاراً كمصروفات غير نقدية. بنود تشغيلية: 672,627 دولار تمويل خاص (3,363,134 وحدة بسعر 0.20 دولار)، تمديد لـ1,840,000 سنداً والـ280,000 דולר قروض قصيرة الأجل (فائدة 15%).
سريرية: الدراسة II هي حالياً مُسجلة بنسبة 97.8% (88/90); الاستجابات المرحلية تُظهر CR 64.3%، الاستجابة الكلية 72.6%، ومدة دوام CR 40% عند 450 يوماً. تتوقع الشركة اكتمال التسجيل في الربع الرابع من 2025 وتثبيت البيانات/التقديمات التنظيمية في الربع الأول من 2027.
- Study II enrollment at 97.8% of 90-patient target
- Complete Response 64.3% (54/84) interim result
- Total Response 72.6% (61/84) interim result
- $672,627 raised via July 28, 2025 private placement
- Cost of sales declined 10% while remaining 51% of revenue
- Administrative expenses increased 12% year-over-year
- Short-term loans of $280,000 bear 15% interest, $100,000 related party
- Warrant extension: 1,840,000 warrants extended to Sept 30, 2028
Toronto, Ontario--(Newsfile Corp. - November 10, 2025) - Theralase® Technologies Inc. (TSXV:TLT) (OTCQB:TLTFF) ("Theralase®" or the "Company"), a clinical stage pharmaceutical pioneering light, radiation, sound and drug-activated therapeutics for the treatment of cancer, bacteria and viruses has released the Company's unaudited condensed consolidated interim 3Q2025 financial statements ("Financial Statements").
Theralase® will be hosting a conference call on Wednesday, November 19th at 11:00 am ET, which will include a presentation of the financial and operational results for the fiscal quarter ending September 30th, 2025. Questions are welcome. To ensure we have time to review and properly address them during the call, please send them in advance to mperraton@theralase.com.
| Zoom Meeting Link: | https://us02web.zoom.us/j/81044841120 Webinar ID: 810 4484 1120 |
| Conference Call in: | 1-647-558-0588 (Canada) / 1-646-558-8656 (US) - not required for those attending by Zoom |
An archived version will be available on the website following the conference call.
Financial Summary:
For the nine-month period ended September 30th:

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1 Other represents foreign exchange, interest accretion on lease liabilities and / or interest income
Financial Highlights
For the nine-month period ended September 30, 2025 versus September 30, 2024:
- Total revenue decreased
5% to$590,573 from$622,984 - Cost of sales decreased
10% to$299,743 (51% of revenue) from$332,136 (53% of revenue) - Gross margin decreased slightly to
$290,830 (49% of revenue) from$290,848 (47% of revenue) - Selling expenses decreased
18% to$212,421 from$257,935 - Administrative expenses increased
12% to$1,444,687 from$1,294,969 , driven primarily by increases in general and administrative expenses, professional fees and stock-based compensation - Research and development expenses increased
1% to$2,116,540 from$2,100,699 , reflecting increased activity to support Study II progress - Net loss for the period increased
3% to$3,435,145 from$3,337,994. T his included$708,521 in non-cash charges such as amortization and stock-based compensation.
Operational Highlights
Private Placements:
On July 28, 2025, the Company completed a non-brokered private placement, issuing 3,363,134 units at
Warrant Extension:
On August 29, 2025, the Company extended the expiry date of 1,840,000 warrants, all of which are exercisable at
Short Term Loans:
As of November 7, 2025, the Company had outstanding short-term loans totaling
The Company continues to explore additional equity and non-dilutive funding opportunities to support its clinical and commercial milestones.
Study II Update:
As of November 7, 2025:
- 88 patients have been treated with the primary Study Procedure, representing
97.8% of the total targeted enrollment of 90 patients. - 72 patients have completed the clinical study, being assessed at all assessment visits or have been prematurely removed from the clinical study by the principal investigator for lack of response
- 16 additional patients are pending study completion.
Interim clinical results indicate:
64.3% (54/84) patients achieved a Complete Response ("CR") at any point in time72.6% (61/84) achieved a Total Response (CR + Indeterminate Response ("IR")) (IR = negative cystoscopy with positive urine cytology, without a confirmatory bladder biopsy)- At the 450-day assessment,
40% (18/45) of patients maintained a CR, indicating strong durability of treatment effect, with42.2% (19/45) of patients maintaining a TR.
Theralase® remains on track to complete enrollment in 4Q2025, with data lock and regulatory submissions expected in 1Q2027.
For additional information, please refer to the Company's Management's Discussion and Analysis ("MD&A") available at www.sedarplus.ca.
About Ruvidar®:
Ruvidar® (TLD-1433) is a small molecule, able to be activated by light, radiation, sound and other drugs, intended for the safe and effective destruction of cancer, bacteria and viruses.
About Theralase® Technologies Inc.:
Theralase® is a clinical stage pharmaceutical company dedicated to the research and development of light, radiation, sound and drug-activated small molecule compounds and their associated formulations with a primary objective of efficacy and a secondary objective of safety in the destruction of cancer, bacteria and viruses, with minimal impact on surrounding healthy tissue.
Additional information is available at www.theralase.com and www.sedarplus.ca
Neither TSX Venture Exchange nor its Regulation Services Provider (as that term is defined in the policies of the TSX Venture Exchange) accepts responsibility for the adequacy or accuracy of this release.
Forward-Looking Statements:
This news release contains Forward-Looking Statements ("FLS") within the meaning of applicable Canadian securities laws. Such statements include; but, are not limited to statements regarding the Company's proposed development plans with respect to small molecules and their drug formulations. FLS may be identified by the use of the words "may, "should", "will", "anticipates", "believes", "plans", "expects", "estimate", "potential for" and similar expressions; including, statements related to the current expectations of the Company's management regarding future research, development and commercialization of the Company's small molecules; their drug formulations; preclinical research; clinical studies and regulatory approvals.
These statements involve significant risks, uncertainties and assumptions; including, the ability of the Company to fund and secure the regulatory approvals to successfully complete various clinical studies in a timely fashion and implement its development plans. Other risks include: the ability of the Company to successfully commercialize its small molecule and drug formulations; the risk that access to sufficient capital to fund the Company's operations may not be available on terms that are commercially favorable to the Company or at all; the risk that the Company's small molecule and drug formulations may not be effective against the diseases tested in its clinical studies; the risk that the Company fails to comply with the terms of license agreements with third parties and as a result loses the right to use key intellectual property in its business; the Company's ability to protect its intellectual property; the timing and success of submission, acceptance and approval of regulatory filings. Many of these factors that will determine actual results are beyond the Company's ability to control or predict.
Readers should not unduly rely on these FLS, which are not a guarantee of future performance. There can be no assurance that FLS will prove to be accurate as such FLS involve known and unknown risks, uncertainties and other factors which may cause actual results or future events to differ materially from the FLS.
Although the FLS contained in the press release are based upon what management currently believes to be reasonable assumptions, the Company cannot assure prospective investors that actual results, performance or achievements will be consistent with these FLS.
All FLS are made as of the date hereof and are subject to change. Except as required by law, the Company assumes no obligation to update such FLS.
For investor information on the Company, please feel to reach out Investor Inquiries - Theralase Technologies.
For More Information:
1.866.THE.LASE (843.5273)
416.699.LASE (5273)
www.theralase.com
Kristina Hachey, CPA
Chief Financial Officer X 224
khachey@theralase.com

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