Kintara Therapeutics Announces Fiscal 2023 Third Quarter Financial Results and Provides Corporate Update
RECENT CORPORATE DEVELOPMENTS
- Case study data from two abstracts was presented by MD Anderson Cancer Center from the VAL-083 expanded access program at the American Association for Cancer Research (AACR) Annual Meeting (April):
- RELA fusion-positive ependymoma and diffuse midline glioma treated with VAL-083 under expanded access - case reports. The abstract described two patient case reports, one with ependymoma and one with diffuse midline glioma, treated with VAL-083 under an expanded access program. The cases highlighted that VAL-083 may be a treatment option for recurrent RELA fusion-positive ependymoma and diffuse midline glioma refractory to other treatments.
- VAL-083 in patients with recurrent glioblastoma treated under expanded access program. The abstract reported on background characteristics, and safety and efficacy measures, from 24 patients with recurrent GBM treated with VAL-083 under an expanded access program. The posters illustrated that the use of VAL-083 continued to show benefit in the treatment of GBM patients who had multiple recurrences and have limited therapeutic options.
"We are encouraged by the recent progress of our lead asset in brain cancer, VAL-083, including data presented at the AACR Annual Meeting, and look forward to announcing top-line data in the international registrational GBM AGILE Study before the end of calendar 2023," commented Robert E. Hoffman, Kintara's President and Chief Executive Officer. "We continue to be optimistic about the future of our REM-001 program for treating cutaneous metastatic breast cancer and our team is more committed than ever to bringing this innovative therapy to patients in need."
SUMMARY OF FINANCIAL RESULTS FOR FISCAL YEAR 2023 THIRD QUARTER ENDED MARCH 31, 2023
As of March 31, 2023, Kintara had cash and cash equivalents of approximately
For the three months ended March 31, 2023, Kintara reported a net loss of approximately
Selected Balance Sheet Data (in thousands) | ||||||||
March 31, 2023 | June 30, | |||||||
$ | $ | |||||||
Cash and cash equivalents | 3,045 | 11,780 | ||||||
Working capital | 3,226 | 9,268 | ||||||
Total assets | 6,740 | 15,948 | ||||||
Total stockholders' equity | 3,786 | 11,795 | ||||||
Selected Statement of Operations Data (in thousands, except per share data) | ||||||||||
For the three months ended | ||||||||||
March 31, | March 31, | |||||||||
2023 | 2022 | |||||||||
$ | $ | |||||||||
Research and development | 2,005 | 3,474 | ||||||||
General and administrative | 1,297 | 1,884 | ||||||||
Other income | (38) | (2)) | ||||||||
Net loss for the period | (3,264) | (5,356) | ||||||||
Series A Preferred cash dividend | (2) | (2) | ||||||||
Net loss for the period attributable to common stockholders | (3,266) | (5,358) | ||||||||
Basic and fully diluted weighted average number of shares | 1,681 | 983 | ||||||||
Basic and fully diluted loss per share | (1.94) | (5.45) | ||||||||
For the nine months ended | ||||||||||
March 31, | March 31, | |||||||||
2023 | 2022 | |||||||||
$ | $ | |||||||||
Research and development | 7,235 | 11,169 | ||||||||
General and administrative | 4,212 | 6,055 | ||||||||
Other income | (133) | (9) | ||||||||
Net loss for the period | (11,314) | (17,215) | ||||||||
Series A Preferred cash dividend | (6) | (6) | ||||||||
Series C Preferred stock dividend | (362) | (2,462) | ||||||||
Net loss for the period attributable to common stockholders | (11,682) | (19,683) | ||||||||
Basic and fully diluted weighted average number of shares | 1,596 | 879 | ||||||||
Basic and fully diluted loss per share | (7.32) | (22.39) | ||||||||
Kintara's financial statements as filed with the
ABOUT KINTARA
Located in
VAL-083 is a 'first-in-class', small-molecule chemotherapeutic with a novel mechanism of action that has demonstrated clinical activity against a range of cancers, including central nervous system, ovarian and other solid tumors (e.g., NSCLC, bladder cancer, head and neck) in
Kintara also 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 Twitter 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 and the GBM AGILE Study. 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 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; global unrest; and the continued impact of the COVID-19 pandemic. 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, 2022, the Company's Quarterly Reports on Form 10-Q, and the Company's Current Reports on Form 8-K.
CONTACTS
Investors
LifeSci Advisors
Mike Moyer, Managing Director
617.308.4306
mmoyer@lifesciadvisors.com
Media Inquiries
David Schull or Ignacio Guerrero-Ros, Ph.D.
Russo Partners
858.717.2310
646.942.5604
david.schull@russopartnersllc.com
ignacio.guerrero-ros@russopartnersllc.com
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SOURCE Kintara Therapeutics