Alpha Tau Medical Announces Third Quarter 2024 Financial Results and Provides Corporate Update
- Alpha DaRT$(R)$ accepted into the prestigious Total Product Life Cycle Advisory Program $(TAP)$ of the FDA, to accelerate market access to the Alpha DaRT(R) for patients with recurrent glioblastoma multiforme (GBM) -
- First patient treated in Recurrent Lung Cancer study in Israel, which will assess the safety and feasibility of delivering Alpha DaRT(R) sources into the lung using an endobronchial ultrasound procedure -
- FDA approval of an Investigational Device Exemption $(IDE)$ application to initiate a multi-center study for the treatment of recurrent cutaneous squamous cell carcinoma (cSCC) in immunocompromised patients using the Alpha DaRT(R) -
- Cash, cash equivalents & deposits balance of $68.4 million, with runway of at least two years -
JERUSALEM, Nov. 19, 2024 (GLOBE NEWSWIRE) -- Alpha Tau Medical Ltd. ("Alpha Tau", or the "Company") (NASDAQ: DRTS, DRTSW), the developer of the innovative alpha-radiation cancer therapy Alpha DaRT(R) , reported third quarter 2024 financial results and provided a corporate update.
"Alpha Tau has continued to make great progress during 2024, with a number of important trials moving ahead and continued generation of data across superficial tumors and cancers of internal organs," said Alpha Tau Chief Executive Officer Uzi Sofer. "Our decision to use the ReSTART pivotal trial to explore our implementation of the Alpha DaRT(R) treatment with community clinicians such as Mohs surgeons continues to bear fruit. We look forward to releasing important data in internal organ cancers in the coming months and giving our stakeholders a deeper look at the future we envision for the Alpha DaRT(R) ," stated Alpha Tau CEO Uzi Sofer.
Recent Corporate Highlights:
-- In October, Alpha Tau announced its acceptance into FDA's Total Product
Life Cycle Advisory Program $(TAP.AU)$ to accelerate market access to Alpha
DaRT(R) for patients with recurrent glioblastoma multiforme (GBM). TAP's
primary goal is to expedite and enable patient access to innovative and
highly promising medical devices which are not currently on the market by
providing frequent, and strategic communications with the FDA, and by
facilitating engagement with other key parties for developers of devices
of public health importance, working toward reducing the time, cost and
uncertainty of patient access through reimbursement and commercial
adoption following FDA authorization.
-- In October, the first patient with recurrent lung cancer was treated in a
clinical trial at Hadassah Medical Center in Jerusalem, Israel. The study
will assess safety and feasibility of delivering Alpha DaRT(R) sources
into the lung using an endobronchial ultrasound (EBUS) procedure,
including the rate of successful source placement and any
treatment-related adverse events. For more information, please see here:
https://www.clinicaltrials.gov/study/NCT05632913
-- In September, the FDA approved and Investigational Device Exemption (IDE)
application to initiate a multi-center study for the treatment of
recurrent cutaneous Squamous Cell Carcinoma (cSCC) in immunocompromised
patients using the Alpha DaRT(R). The clinical study, which is an
investigator-initiated study led by the Winship Cancer Institute of Emory
University in Atlanta, has been approved to enroll up to 28 U.S. patients
at up to 8 institutions in the U.S., and will focus on patients with
recurrent cSCC who have a weakened immune system due to any primary or
secondary immunodeficiencies, excluding diabetes. For more information,
please see here:
https://www.clinicaltrials.gov/study/NCT06615635
Upcoming Milestones:
-- Anticipating response from PMDA in Japan in Q1 2025 for pre-market
approval for Alpha DaRT in patients with recurrent head and neck cancer.
-- Planned release of data from pancreatic cancer trials in Canada and
Israel in Q1 2025.
-- Targeting completion of patient recruitment in the ReSTART pivotal U.S.
multi-center trial in recurrent cutaneous squamous cell carcinoma in H1
2025. For more information, please see here:
https://www.clinicaltrials.gov/study/NCT05323253
-- Targeting release of data from combination trial of Alpha DaRT with
pembrolizumab (Keytruda(R)) in H1 2025. For more information, please see
here: https://www.clinicaltrials.gov/study/NCT05047094
-- Targeting first brain cancer treatment in H1 2025.
Financial results for quarter ended September 30, 2024
R&D expenses for the nine months ended September 30, 2024 were $19.5 million, compared to $18.9 million for the same period in 2023, due to increased employee compensation and benefits, including share-based compensation, increased costs of raw materials, reduced government grants, and increased travel expenses related to our U.S. multi-center pivotal trial, offset by lower third-party contractor expenses.
Marketing expenses for the nine months ended September 30, 2024 were $1.7 million, compared to $1.5 million for the same period in 2023, due to increased employee compensation and benefits.
G&A expenses for the nine months ended September 30, 2024 were $4.6 million, compared to $5.3 million for the same period in 2023, primarily due to decreased professional fees (including D&O insurance and legal expenses), offset by increased travel expenses and increased employee compensation and benefits, including share-based compensation.
Financial income, net, for the nine months ended September 30, 2024 was $3.5 million, compared to $4.0 million for the same period in 2023, due to changes in foreign exchange rates, a decrease in interest from bank deposits, and an increase in interest on long-term loan.
For the nine months ended September 30, 2024, the Company had a net loss of $22.3 million, or $0.32 per share, compared to a net loss of $21.8 million, or $0.31 per share, in the nine months of 2023.
Balance Sheet Highlights
As of September 30, 2024, the Company had cash and cash equivalents, short-term deposits and restricted deposits in the amount of $68.4 million, compared to $84.9 million at December 31, 2023. The Company expects that this cash balance will be sufficient to fund anticipated operations for at least two years.
About Alpha DaRT(R)
Alpha DaRT(R) (Diffusing Alpha-emitters Radiation Therapy) is designed to enable highly potent and conformal alpha-irradiation of solid tumors by intratumoral delivery of radium-224 impregnated sources. When the radium decays, its short-lived daughters are released from the sources and disperse while emitting high-energy alpha particles with the goal of destroying the tumor. Since the alpha-emitting atoms diffuse only a short distance, Alpha DaRT(R) aims to mainly affect the tumor, and to spare the healthy tissue around it.
About Alpha Tau Medical Ltd.
Founded in 2016, Alpha Tau is an Israeli oncology therapeutics company that focuses on research, development, and potential commercialization of the Alpha DaRT(R) for the treatment of solid tumors. The technology was initially developed by Prof. Itzhak Kelson and Prof. Yona Keisari from Tel Aviv University.
Forward-Looking Statements
This press release includes "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995. When used herein, words including "anticipate," "being," "will," "plan," "may, " "continue," and similar expressions are intended to identify forward-looking statements. In addition, any statements or information that refer to expectations, beliefs, plans, projections, objectives, performance or other characterizations of future events or circumstances, including any underlying assumptions, are forward-looking. All forward-looking statements are based upon Alpha Tau's current expectations and various assumptions. Alpha Tau believes there is a reasonable basis for its expectations and beliefs, but they are inherently uncertain. Alpha Tau may not realize its expectations, and its beliefs may not prove correct. Actual results could differ materially from those described or implied by such forward-looking statements as a result of various important factors, including, without limitation: (i) Alpha Tau's ability to receive regulatory approval for its Alpha DaRT technology or any future products or product candidates; (ii) Alpha Tau's limited operating history; (iii) Alpha Tau's incurrence of significant losses to date; (iv) Alpha Tau's need for additional funding and ability to raise capital when needed; (v) Alpha Tau's limited experience in medical device discovery and development; (vi) Alpha Tau's dependence on the success and commercialization of the Alpha DaRT technology; (vii) the failure of preliminary data from Alpha Tau's clinical studies to predict final study results; (viii) failure of Alpha Tau's early clinical studies or preclinical studies to predict future clinical studies; (ix) Alpha Tau's ability to enroll patients in its clinical trials; (x) undesirable side effects caused by Alpha Tau's Alpha DaRT technology or any future products or product candidates; (xi) Alpha Tau's exposure to patent infringement lawsuits; (xii) Alpha Tau's ability to comply with the extensive regulations applicable to it; (xiii) the ability to meet Nasdaq's listing standards; (xiv) costs related to being a public company; (xv) changes in applicable laws or regulations; and the other important factors discussed under the caption "Risk Factors" in Alpha Tau's annual report filed on form 20-F with the SEC on March 7, 2024, and other filings that Alpha Tau may make with the United States Securities and Exchange Commission. These and other important factors could cause actual results to differ materially from those indicated by the forward-looking statements made in this press release. Any such
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