Full Press Release Details
OS Therapies Reports
Third Quarter 2024 Financial Results and Provides Business Update
New York, NY, November 15, 2024 -
OS Therapies, Inc. (NYSE-A: OSTX) ("OS Therapies" or "the Company"), a clinical-stage cancer immunotherapy
and antibody drug conjugate biotechnology company, today reported financial results for the third quarter of 2024 ended September 30,
2024 and provided a business update.
"The third quarter was pivotal for OS
Therapies as we completed our initial public offering and finished dosing the final patient enrolled in our Phase 2b clinical trial of
OST-HER2 in resected, recurrent osteosarcoma," said Paul Romness, MHP, Chairman & CEO of OS Therapies. "We are now looking
forward to releasing topline data in December and then engaging with the FDA regarding getting this potentially life-saving cancer immunotherapy
to patients that have no other potential treatment options as quickly as possible."
OS Therapies' lead product candidate,
OST-HER2, is a cancer immunotherapy biologic drug candidate comprised of HER2 bioengineered form of the bacteria Listeria monocytogenes
(Lm) that infects HER2 presenting cancer cells and triggers a strong immune response against cancer cells expressing HER2. This off-the-shelf
treatment is designed to prevent metastasis, delay recurrence, kill primary tumors expressing HER2 and increase overall survival. The
Company has fully enrolled and finished treating all patients in a potentially pivotal Phase IIb clinical trial in recurred, resected
osteosarcoma, dosing 41 patients with OST-HER2 at 21 clinical trial sites across the United States. OST-HER2 has received Rare Pediatric
Disease Designation (RPDD) from the Food and Drug Administration (FDA), and Fast Track and Orphan Drug Designations by the FDA and European
Medicines Agency (EMA). OS Therapies is in active discussions with FDA regarding Breakthrough Therapy Designation for OST-HER2. Upon any
Biologics Licensing Authorization (BLA) from the FDA for OST-HER2 in osteosarcoma, the Company will be granted a Priority Review Voucher
based upon the RPDD. OST HER2 has also completed a Phase 1 clinical trial primarily in breast cancer patients, in addition to strong preclinical
data demonstrating efficacy on a standalone basis and in combination with HER2-targeting therapeutic antibodies such as Herceptin .
Third Quarter Corporate Highlights:
Financial Highlights for the Third Quarter:
The Company is a pre-revenue biotechnology
company. The Company anticipates beginning to generate revenue through the sale of a priority review voucher it expects to be issued by
FDA upon approval of its rare pediatric disease designated drug candidate OST-HER2 and licensing rights to its products and product candidates
as they achieve upcoming de-risking clinical and regulatory milestones.
Loss from Operations:
The Company recorded a net operating loss
of $2.875 million in the third quarter of 2024 compared to an operating loss of $2.006 million in the third quarter of 2023. The increase
in net loss was largely due to the expenses associated with the initial public offering. Net loss per share in the third quarter of 2024
was $0.18 on 15.897 million weighted average shares outstanding compared to the third quarter of 2023 where the Company delivered a loss
of $0.38 per share on 5.340 million weighted average shares outstanding.
This press release shall not constitute an
offer to sell or the solicitation of an offer to buy any securities.
For more information, please see the Company's
website at www.ostherapies.com
OS Therapies is a clinical stage oncology
company focused on the identification, development and commercialization of treatments for Osteosarcoma (OS) and other solid tumors. OST-HER2,
the Company's lead asset, is an immunotherapy leveraging the immune-stimulatory effects of Listeria bacteria to initiate a strong
immune response targeting the HER2 protein. The Company has completed enrollment for a 41-patient Phase 2b clinical trial of OST-HER2
in resected, recurrent osteosarcoma, with results expected in the fourth quarter of 2024. OST-HER2 has completed a Phase 1 clinical study
primarily in breast cancer patients, in addition to showing strong preclinical efficacy data in various models of breast cancer. OST-HER2
has been conditionally approved by the U.S. Department of Agriculture for the treatment of canines with osteosarcoma. In addition, OS
Therapies is advancing its next generation Antibody Drug Conjugate (ADC) platform, known as tunable ADC (tADC), which
features tunable, tailored antibody-linker-payload candidates. This platform leverages the Company's proprietary silicone linker
technology, enabling the delivery of multiple payloads per linker. For more information, please visit www.ostherapies.com.
Forward-Looking Statements
Statements in this press release about future
expectations, plans and prospects, as well as any other statements regarding matters that are not historical facts, may constitute forward-looking
statements within the meaning of the federal securities laws. These forward-looking statements and terms such as "anticipate,"
"expect," "intend," "may," "will," "should" or other comparable terms involve
risks and uncertainties because they relate to events and depend on circumstances that will occur in the future. OS Therapies' drug
development efforts, clinical trial results, patient enrollments, FDA regulatory approvals, designations, and intellectual property protections.
Prospective investors are cautioned that any such forward-looking statements are not guarantees of future performance and involve risks
and uncertainties, including those described under the caption "Risk Factors" and elsewhere in the prospectus filed with the
SEC relating to the offering and that actual results may differ materially from those indicated by such forward-looking statements. Any
forward-looking statements contained in this press release speak only as of the date hereof, and, except as required by the federal securities
laws, OS Therapies specifically disclaims any obligation to update any forward-looking statement, whether as a result of new information,
future events or otherwise.
Corporate and Media Contact: