The U.S. Patent and Trademark Office Grants BioMark Patent That Expands Its Claims Covering Its Legacy Liquid Biopsy Assay
BioMark Diagnostics Inc. (CSE: BUX, FSE: 20B, OTC Pink: BMKDF) has been granted U.S. Patent No. 17/895.69 by the USPTO, strengthening its liquid biopsy technology for cancer management. The patent protects BioMark's SAT1 legacy assay platform for assessing tumor velocity and treatment response in glioblastoma (GBM) and triple-negative breast cancer (TNBC) patients with specific genetic mutations.
Key points:
- GBM market size estimated at $2.80 billion in 2024, expected to reach $4.60 billion by 2029 (CAGR 8%)
- TNBC accounts for 15% of all breast cancers
- BioMark plans to launch a preclinical study for TNBC patients with BRCA mutations
- The patent enhances BioMark's position in developing cancer management solutions
BioMark Diagnostics Inc. (CSE: BUX, FSE: 20B, OTC Pink: BMKDF) ha ottenuto il brevetto statunitense n. 17/895.69 dall'USPTO, rafforzando la sua tecnologia di biopsia liquida per la gestione del cancro. Il brevetto protegge la piattaforma di test SAT1 legacy di BioMark per la valutazione della velocità del tumore e della risposta al trattamento nei pazienti con glioblastoma (GBM) e cancro al seno triplo negativo (TNBC) con specifiche mutazioni genetiche.
Punti chiave:
- Dimensione del mercato GBM stimata in $2,80 miliardi nel 2024, si prevede raggiunga $4,60 miliardi entro il 2029 (CAGR 8%)
- Il TNBC rappresenta il 15% di tutti i tumori al seno
- BioMark prevede di avviare uno studio preclinico per pazienti TNBC con mutazioni BRCA
- Il brevetto migliora la posizione di BioMark nello sviluppo di soluzioni per la gestione del cancro
BioMark Diagnostics Inc. (CSE: BUX, FSE: 20B, OTC Pink: BMKDF) ha recibido la patente de EE. UU. n. 17/895.69 por parte de la USPTO, fortaleciendo su tecnología de biopsia líquida para la gestión del cáncer. La patente protege la plataforma de ensayo SAT1 legacy de BioMark para evaluar la velocidad del tumor y la respuesta al tratamiento en pacientes con glioblastoma (GBM) y cáncer de mama triplemente negativo (TNBC) con mutaciones genéticas específicas.
Puntos clave:
- Tamaño del mercado de GBM estimado en $2.80 mil millones en 2024, se espera que alcance $4.60 mil millones para 2029 (CAGR 8%)
- El TNBC representa el 15% de todos los cánceres de mama
- BioMark planea lanzar un estudio preclínico para pacientes de TNBC con mutaciones BRCA
- La patente mejora la posición de BioMark en el desarrollo de soluciones para la gestión del cáncer
BioMark Diagnostics Inc. (CSE: BUX, FSE: 20B, OTC Pink: BMKDF)는 USPTO에 의해 미국 특허 제 17/895.69호를 획득하여 암 치료를 위한 액체 생검 기술을 강화했습니다. 이 특허는 특정 유전자 변이가 있는 신경교종(GBM) 및 삼중 음성 유방암(TNBC) 환자의 종양 속도 및 치료 반응을 평가하기 위한 BioMark의 SAT1 레거시 검사 플랫폼을 보호합니다.
핵심 사항:
- GBM 시장 규모는 2024년에 28억 달러로 예상되며, 2029년까지 46억 달러에 이를 것으로 보임 (연평균 성장률 8%)
- TNBC는 모든 유방암의 15%를 차지합니다.
- BioMark는 BRCA 변이가 있는 TNBC 환자를 위한 전임상 연구를 시작할 계획입니다.
- 특허는 BioMark가 암 관리 솔루션 개발에서의 입지를 강화합니다.
BioMark Diagnostics Inc. (CSE: BUX, FSE: 20B, OTC Pink: BMKDF) a obtenu le brevet américain n° 17/895.69 de l'USPTO, renforçant sa technologie de biopsie liquide pour la gestion du cancer. Le brevet protège la plateforme de test hérité SAT1 de BioMark pour évaluer la vitesse de la tumeur et la réponse au traitement chez les patients atteints de glioblastome (GBM) et de cancer du sein triple négatif (TNBC) présentant des mutations génétiques spécifiques.
Points clés :
- Taille du marché du GBM estimée à 2,80 milliards de dollars en 2024, avec une prévision d'atteindre 4,60 milliards de dollars d'ici 2029 (TAC 8%)
- Le TNBC représente 15 % de tous les cancers du sein
- BioMark prévoit de lancer une étude préclinique pour les patients TNBC avec des mutations BRCA
- Le brevet renforce la position de BioMark dans le développement de solutions de gestion du cancer
BioMark Diagnostics Inc. (CSE: BUX, FSE: 20B, OTC Pink: BMKDF) hat vom USPTO das US-Patent Nr. 17/895.69 erhalten, welches die Flüssigbiopsie-Technologie zur Krebsbehandlung stärkt. Das Patent schützt die SAT1 Legacy-Testplattform von BioMark zur Bewertung der Tumorgeschwindigkeit und des Ansprechens auf die Behandlung bei Glioblastom (GBM) und dreifach-negativem Brustkrebs (TNBC) bei Patienten mit spezifischen genetischen Mutationen.
Wichtige Punkte:
- Marktgröße für GBM wird auf 2,80 Milliarden USD im Jahr 2024 geschätzt und soll bis 2029 auf 4,60 Milliarden USD anwachsen (CAGR 8%)
- TNBC macht 15% aller Brustkrebsfälle aus
- BioMark plant, eine präklinische Studie für TNBC-Patienten mit BRCA-Mutationen zu starten
- Das Patent stärkt die Position von BioMark in der Entwicklung von Lösungen zur Krebsbehandlung
- Granted U.S. Patent No. 17/895.69, expanding BioMark's IP portfolio in liquid biopsy technology
- Patent protects SAT1 legacy assay platform for assessing tumor velocity and treatment response in GBM and TNBC patients
- Glioblastoma Multiforme Treatment Market expected to grow from $2.80 billion in 2024 to $4.60 billion by 2029 (CAGR 8%)
- Planned preclinical study to evaluate effectiveness of adjuvant treatments in TNBC patients with BRCA mutations
- None.
The new patent granted by the USPTO strengthens and expands BioMark's global IP portfolio in liquid biopsy, enhancing cancer management solutions.
Vancouver, British Columbia--(Newsfile Corp. - July 31, 2024) - BioMark Diagnostics Inc., (CSE: BUX) (FSE: 20B) (OTC Pink: BMKDF) ("BioMark" or the "Company"), a leading developer of liquid biopsy tests for early detection of hard-to-detect and treat cancers, is pleased to announce the issuance of U.S. Patent No. 17/895.69 by the U.S. Patent and Trademark Office (USPTO). This patent protects the company's Spermidine/spermine N(1)-acetyltransferase 1 (SAT1) legacy assay platform for assessing tumor velocity and treatment response, particularly in glioblastoma patients (GBM) and triple-negative breast cancer (TNBC) patients with specific genetic mutations.
"We are thrilled to announce the issuance of this new patent, underscoring our commitment to advancing liquid biopsy technology for patients with especially challenging cancers," said Rashid Bux, CEO and President of BioMark. "By expanding our patent estate and initiating new research initiatives, we are positioning BioMark as a leading player in the fight against cancer. The successful outcome of these developments will enhance our role in delivering needed solutions in cancer management, ultimately aiming to save lives and improve the quality of patient care."
Glioblastoma Multiforme (GBM)
- Glioblastoma multiforme (GBM) is the most common type of primary brain tumor in adults. As a grade IV astrocytoma, GBM is highly invasive and aggressive. Current treatments, including surgical resection, radiation, and chemotherapy, yield a median survival time of 15 months. There is a pressing need to develop novel strategies for treating GBM, quickly assess tumor velocity, and effectively monitor treatment response.
- GBM is relatively rare, with an incidence of about 3.2 per 100,000 people globally each year, translating to approximately 13,000 new cases annually in the United States alone (National Brain Tumor Society).
- The Glioblastoma Multiforme Treatment Market size is estimated at USD 2.80 billion in 2024 and is expected to reach USD 4.60 billion by 2029, growing at a CAGR of
8% . *
*Source: https://www.mordorintelligence.com/industry-reports/glioblastoma-multiforme-treatment-market.
Triple-Negative Breast Cancer (TNBC)
- Approximately 1 in 8 women in Canada and the US will be diagnosed with breast cancer in their lifetime. TNBC, the deadliest breast cancer subtype, accounts for about
15% of all breast cancers. Standard treatment is limited to untargeted chemotherapy, though the recent approval of adjuvant-targeted Olaparib for high-risk HER2-negative breast cancer offers an additional option for patients with germline BRCA mutations. - Metastatic TNBC patients have a median survival of 2 years. Early detection and effective treatment response assessment can provide clinicians with critical information for therapy decisions.
- BioMark plans to launch a preclinical study to evaluate the effectiveness of specific adjuvant treatments in TNBC patients with BRCA mutations using its SSAT1 liquid biopsy. This research aims to generate critical data for future clinical trials and potentially offer clinicians a valuable tool for early treatment response assessment.
"We continue to expand our patent estate related to our legacy assay with additional candidates selected to improve our signal-to-noise ratio linked to our assay performance. This is a timely announcement for BioMark as we set our sights on expanding clinical trials with partners in the US interested in developing molecular assays that can assess response to treatment effectiveness and tumor velocity in both GBM and TNBC patients who harbor specific mutations that make treatment difficult," says Rashid Bux.
BioMark's extensive portfolio of patents covering key products in this market creates shareholder value by providing the company with both the freedom to operate and significant product differentiation.
About Spermidine/spermine N(1)-acetyltransferase 1 (SAT1)
It is an enzyme involved in the polyamine catabolic pathway, playing a critical role in the regulation of polyamine levels within cells. Elevated activity of SAT1 has been associated with increased sensitivity to certain types of cancer treatments, including radiation therapy.
About BioMark Diagnostics Inc.
BioMark is a liquid biopsy company developing a molecular diagnostic technology platform that leverages the power of metabolomics and machine learning algorithms to bring new cancer diagnostics to market and improve cancer prognosis by allowing physicians to detect carcinomas in the presymptomatic stages. The technology can also be used for measuring response to treatment and potentially for serial monitoring of cancer survivors. While the Company current focus is on the commercialization of its liquid biopsy test for early detection of lung, it has plans to expand into other hard-to-detect and treat cancers such as brain, ovarian, and pancreatic.
Further information about BioMark is available under its profile on the SEDAR+ website www.sedarplus.ca and the CSE website https://thecse.com/.
For further information on BioMark, please Contact:
Rashid Ahmed Bux
President & CEO
BioMark Diagnostics Inc.
Tel. 604-370-0779
Email: info@biomarkdiagnostics.com
Forward-Looking Information:
This press release may include forward-looking information within the meaning of Canadian securities legislation, concerning the business of BioMark. Forward-looking information is based on certain key expectations and assumptions made by the management of BioMark. Although BioMark believes that the expectations and assumptions on which such forward-looking information is based are reasonable, undue reliance should not be placed on the forward-looking information because BioMark can give no assurance that they will prove to be correct. Forward-looking statements contained in this press release are made as of the date of this press release. BioMark disclaims any intent or obligation to update publicly any forward-looking information, whether as a result of new information, future events, or results or otherwise, other than as required by applicable securities laws.
The CSE has not reviewed, approved, or disapproved the content of this press release.
To view the source version of this press release, please visit https://www.newsfilecorp.com/release/218289
FAQ
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