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Theralase(R) Releases Q2 2026 Financial Statements
Theralase(R) Provides Updates on its Phase II Bladder Cancer Clinical Study and Oncology Pipeline
August 28, 2026 4:36 PM EDT | Source:
Theralase Technologies Inc.
Toronto, Ontario--(Newsfile Corp. - August 28, 2026) - Theralase® Technologies Inc.
(TSXV: TLT) (OTCQB: TLTFF)
("
Theralase®
" or the "
Company
"), a clinical-stage pharmaceutical company dedicated to the research and development of energy-activated small molecules for the safe and effective destruction of various cancers, bacteria and viruses, has released the Company's unaudited interim consolidated financial statements for the six-month period ended June 30th, 2026 ("
Financial Statements
").
Theralase® will be hosting a conference call on
September 3rd
at
11:00 am ET
, which will include a presentation of the financial and operational results for the quarter ended June 30th, 2026.
To ensure Theralase® has time to address questions during the call, please e-mail them in advance to
mperraton@theralase.com
.
Zoom Meeting Link:
https://us02web.zoom.us/j/89698954744
Conference Call in:
Webinar ID:
896 9895 4744
- 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An archived version will be available on the website following the conference call.
Table 1:
Financial Summary for the Six-Month Period Ended June 30
th
To view an enhanced version of this graphic, please visit:
https://images.newsfilecorp.com/files/2786/311984_96140ebca497fa6e_001full.jpg
Financial Highlights:
For the six-month period ended June 30th, 2026 (All funds in Canadian Dollars):
Total revenue decreased to $296,927 from $310,933 for the same period in 2025, a 5% decrease.
Cost of sales for the six-month period ended June 30th, 2026, was $146,981 (50% of revenue), resulting in a gross margin of $149,946 (50% of revenue). In comparison, cost of sales for the same period in 2025 was $178,966 (58% of revenue), resulting in a gross margin of $131,967 (42% of revenue).
Selling expenses remained essentially unchanged at $138,811, compared with $139,011 for the same period in 2025.
Administrative expenses for the six-month period ended June 30th, 2026 increased to $1,003,798 from $995,333 for the same period in 2025, a 1% increase. The increase was primarily attributable to higher professional fees, investor relations, administrative salaries and amortization and depreciation allocation, partially offset by lower stock-based compensation.
Net research and development expenses for the six-month period ended June 30th, 2026 decreased to $1,101,126 from $1,460,447 for the same period in 2025, a 25% decrease. The decrease was primarily attributable to lower Study II patient enrollment and treatment costs. Research and development expenses represented 49% of the Company's operating expenses and reflect continued investment in the research and development of the Company's Drug Division.
The net loss for the six-month period ended June 30th, 2026 was $2,093,926, which included $287,146 of net non-cash expenses (amortization, stock-based compensation and interest accretion on lease liabilities). This compared with a net loss of $2,423,234 for the same period in 2025, which included $485,865 of net non-cash expenses. The Drug Division represented $1,684,924 (80%) of the loss. The 14% decrease in net loss was primarily due to reduced research and development spending on Study II.
Cash was $5,260,832 as of June 30th, 2026, compared with $182,914 as of December 31st, 2025. Subsequent to quarter-end, on August 24th, 2026, the Company closed a brokered private placement under the listed issuer financing exemption for aggregate gross proceeds of $3,555,000.
Operational Highlights:
Collaborative Clinical Development Agreement
On January 12
th
, 2026, the Company announced that it had entered into a collaborative clinical development agreement dated January 9
th
, 2026 with Ferring Pharmaceuticals, expanding the Company's existing Phase II NMIBC clinical program (NCT03945162) through the addition of a new cohort evaluating Ruvidar® (TLD-1433) in combination with Adstiladrin® (nadofaragene firadenovec-vncg) for adult patients diagnosed with high-risk Bacillus Calmet