Kintara Therapeutics Announces Fiscal 2024 First Quarter Financial Results and Provides Corporate Update
- None.
- The suspension of VAL-083 development may impact the company's pipeline and future revenue potential.
RECENT CORPORATE DEVELOPMENTS
- Announced that preliminary topline results from the Glioblastoma Adaptive Global Innovative Learning Environment (GBM AGILE) study showed that VAL-083 did not perform better than the current standards of care in glioblastoma. These topline results included preliminary safety data for VAL-083 that was similar to that of the current standards of care used to treat glioblastoma. With this study outcome, Kintara is suspending the development of VAL-083 and turning its focus to its second program, REM-001. In addition to focusing on its REM-001 program, Kintara will evaluate a wide range of strategic options aimed at potentially maximizing shareholder value. (October 2023)
- Awarded a
Small Business Innovation Research (SBIR) grant from the National Institutes of Health (NIH) to support the clinical development of REM-001, a second-generation photodynamic therapy (PDT) photosensitizer agent for the treatment of cutaneous metastatic breast cancer (CMBC). (June 2023)$2.0 million
"We are looking forward to enrolling the first patient in our 15 patient REM-001 study for cutaneous metastatic breast cancer, a disease with little or no current treatment options" commented Robert E. Hoffman, Kintara's President and Chief Executive Officer. "The majority of study expenses will be covered by the
SUMMARY OF FINANCIAL RESULTS FOR FISCAL YEAR 2023 FIRST QUARTER ENDED SEPTEMBER 30, 2023
As of September 30, 2023, Kintara had cash and cash equivalents of approximately
For the three months ended September 30, 2023, Kintara reported a net loss of approximately
Selected Balance Sheet Data (in thousands) | ||||||||
September 30, 2023 | June 30, | |||||||
$ | $ | |||||||
Cash and cash equivalents | 216 | 1,535 | ||||||
Working capital (deficiency) | (2,553) | 188 | ||||||
Total assets | 1,477 | 3,979 | ||||||
Total stockholders' equity (deficiency) | (2,026) | 731 |
Selected Statement of Operations Data (in thousands, except per share data)
| |||||||||
September 30, | June 30, | ||||||||
2023 | 2023 | ||||||||
$ | $ | ||||||||
Research and development | 1,859 | 3,171 | |||||||
General and administrative | 1,103 | 1,475 | |||||||
Other income | - | (50) | |||||||
Net loss for the period | (2,962) | (4,596) | |||||||
Series A Preferred cash dividend | (2) | (2) | |||||||
Series C Preferred stock dividend | (173) | (362) | |||||||
Net loss for the period attributable to common stockholders | (3,137) | (4,960) | |||||||
Basic and fully diluted weighted average number of shares | 1,718 | 1,464 | |||||||
Basic and fully diluted loss per share | (1.83) | (3.39) | |||||||
Kintara's financial statements as filed with the
ABOUT KINTARA
Located in
Kintara has a proprietary, late-stage photodynamic therapy platform that holds promise as a localized cutaneous, or visceral, tumor treatment as well as in other potential indications. REM-001 Therapy, which consists of the laser light source, the light delivery device, and the REM-001 drug product, has been previously studied in four Phase 2/3 clinical trials in patients with CMBC who had previously received chemotherapy and/or failed radiation therapy. In CMBC, REM-001 has a clinical efficacy to date of
For more information, please visit www.kintara.com or follow us on X at @Kintara_Thera, Facebook and Linkedin.
SAFE HARBOR STATEMENT
Any statements contained in this press release that do not describe historical facts may constitute forward-looking statements as that term is defined in the Private Securities Litigation Reform Act of 1995, including statements regarding the status of the Company's clinical trials; the topline results of the GBM AGILE Study; and the Company's review of strategic alternatives. Any forward-looking statements contained herein are based on current expectations but are subject to a number of risks and uncertainties. The factors that could cause actual future results to differ materially from current expectations include, but are not limited to, risks and uncertainties relating to the Company's ability to develop, market and sell products based on its technology; the status of the Company's clinical trials; the topline results of the GBM AGILE Study; the expected benefits and efficacy of the Company's products and technology; the availability of substantial additional funding for the Company to continue its operations and to conduct research and development, clinical studies and future product commercialization; the Company's business, research, product development, regulatory approval, marketing and distribution plans and strategies; and global unrest. These and other factors are identified and described in more detail in the Company's filings with the SEC, including the Company's Annual Report on Form 10-K for the year ended June 30, 2023, the Company's Quarterly Reports on Form 10-Q, and the Company's Current Reports on Form 8-K.
CONTACTS
Investors
Robert E. Hoffman
Kintara Therapeutics
rhoffman@kintara.com
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SOURCE Kintara Therapeutics
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