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Defence Therapeutics Receives USPTO Allowance for Patent Application Covering Next-Gen ADC Technology

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Defence Therapeutics (DTCFF) has received USPTO Notice of Allowance for patent application 18/351,291 covering next-generation antibody-drug conjugate (ADC) technology. The patent, valid until 2043, includes composition-of-matter claims for therapeutically active ADCs and their use in treating diseases like cancer. The company's Accum-based ADCs have shown enhanced intracellular delivery and cytotoxic activity in preclinical cancer models compared to conventional ADCs. The technology features antibodies conjugated to innovative constructs with bile acid and nuclear localization signal from RPS17. This adds to Defence's existing patent portfolio, which includes granted patents in the US, Japan, Australia, and Israel, marking their eighth U.S. patent overall.
Defence Therapeutics (DTCFF) ha ricevuto la Notifica di Concessione dall'USPTO per la domanda di brevetto 18/351,291 riguardante la tecnologia di anticorpi coniugati a farmaci (ADC) di nuova generazione. Il brevetto, valido fino al 2043, include rivendicazioni sulla composizione di ADC terapeuticamente attivi e il loro utilizzo nel trattamento di malattie come il cancro. Gli ADC basati su Accum dell'azienda hanno dimostrato una maggiore capacità di consegna intracellulare e attività citotossica in modelli preclinici di cancro rispetto agli ADC convenzionali. La tecnologia prevede anticorpi coniugati a costrutti innovativi contenenti acido biliare e un segnale di localizzazione nucleare derivato da RPS17. Questo si aggiunge al portafoglio brevetti esistente di Defence, che include brevetti concessi negli Stati Uniti, Giappone, Australia e Israele, segnando l'ottavo brevetto statunitense complessivo.
Defence Therapeutics (DTCFF) ha recibido el Aviso de Aprobación de la USPTO para la solicitud de patente 18/351,291 que cubre la tecnología de conjugados anticuerpo-fármaco (ADC) de próxima generación. La patente, válida hasta 2043, incluye reivindicaciones sobre la composición de ADCs terapéuticamente activos y su uso en el tratamiento de enfermedades como el cáncer. Los ADCs basados en Accum de la compañía han demostrado una mayor entrega intracelular y actividad citotóxica en modelos preclínicos de cáncer en comparación con los ADCs convencionales. La tecnología presenta anticuerpos conjugados a construcciones innovadoras que incluyen ácido biliar y una señal de localización nuclear derivada de RPS17. Esto se suma al portafolio de patentes existente de Defence, que incluye patentes otorgadas en EE. UU., Japón, Australia e Israel, marcando su octava patente estadounidense en total.
Defence Therapeutics(DTCFF)는 차세대 항체-약물 접합체(ADC) 기술을 다루는 특허 출원 18/351,291에 대해 미국 특허청(USPTO)으로부터 허가 통지를 받았습니다. 이 특허는 2043년까지 유효하며, 치료용 활성 ADC의 조성물 및 암과 같은 질병 치료에의 사용을 포함하는 청구항을 포함합니다. 회사의 Accum 기반 ADC는 기존 ADC에 비해 전임상 암 모델에서 세포 내 전달 및 세포독성 활성이 향상된 것으로 나타났습니다. 이 기술은 담즙산과 RPS17의 핵 위치 신호를 포함하는 혁신적인 구조물에 결합된 항체를 특징으로 합니다. 이는 미국, 일본, 호주, 이스라엘에서 승인된 특허를 포함하는 Defence의 기존 특허 포트폴리오에 추가되어, 총 8번째 미국 특허가 되었습니다.
Defence Therapeutics (DTCFF) a reçu un avis d'acceptation de l'USPTO pour la demande de brevet 18/351,291 couvrant une technologie de conjugués anticorps-médicaments (ADC) de nouvelle génération. Le brevet, valable jusqu'en 2043, comprend des revendications sur la composition de matières des ADC thérapeutiquement actifs et leur utilisation dans le traitement de maladies telles que le cancer. Les ADC basés sur Accum de la société ont montré une meilleure délivrance intracellulaire et une activité cytotoxique accrues dans des modèles précliniques de cancer par rapport aux ADC conventionnels. La technologie comprend des anticorps conjugués à des structures innovantes avec un acide biliaire et un signal de localisation nucléaire provenant de RPS17. Cela s'ajoute au portefeuille de brevets existant de Defence, qui comprend des brevets délivrés aux États-Unis, au Japon, en Australie et en Israël, marquant ainsi leur huitième brevet américain au total.
Defence Therapeutics (DTCFF) hat vom USPTO die Mitteilung über die Zulassung für die Patentanmeldung 18/351,291 erhalten, die eine Technologie der nächsten Generation für Antikörper-Wirkstoff-Konjugate (ADC) abdeckt. Das Patent, gültig bis 2043, umfasst Zusammensetzungsansprüche für therapeutisch aktive ADCs und deren Einsatz zur Behandlung von Krankheiten wie Krebs. Die auf Accum basierenden ADCs des Unternehmens zeigten in präklinischen Krebsmodellen eine verbesserte intrazelluläre Abgabe und zytotoxische Aktivität im Vergleich zu herkömmlichen ADCs. Die Technologie umfasst Antikörper, die an innovative Konstrukte mit Gallensäure und einem Kernlokalisationssignal von RPS17 gekoppelt sind. Dies ergänzt das bestehende Patentportfolio von Defence, zu dem bereits erteilte Patente in den USA, Japan, Australien und Israel gehören, und markiert das insgesamt achte US-Patent.
Positive
  • Patent protection until 2043 provides long-term market exclusivity for ADC technology
  • Enhanced preclinical performance compared to conventional ADCs in cancer models
  • Broad patent coverage including composition-of-matter claims and therapeutic applications
  • Expanding patent portfolio across multiple jurisdictions strengthens IP position
Negative
  • Technology still in preclinical stage, requiring significant development before commercialization
  • Pending patent applications in key markets like Canada and Europe create uncertainty

Montreal, Quebec--(Newsfile Corp. - June 9, 2025) - Defence Therapeutics Inc. (CSE: DTC) (OTCQB: DTCFF) (FSE: DTC) ("Defence" or the "Company"), a leading biotechnology company specializing in drug delivery technologies, is pleased to announce that the United States Patent and Trademark Office (USPTO) has issued a Notice of Allowance for its U.S. patent application covering one of its next-generation antibody-drug conjugate (ADC) technologies. The allowance of U.S. patent application no. 18/351,291 ('291) includes valuable composition-of-matter claims broadly covering therapeutically active ADCs - not limited to individual diseases or therapeutic targets - as well as claims covering the use of ADCs for treating or diagnosing diseases such as cancer.

Defence's Accum®-based ADCs have demonstrated enhanced intracellular delivery and cytotoxic activity in multiple preclinical cancer models compared to conventional ADCs. Upon grant, the '291 patent application will provide the Company with potential market exclusivity until 2043 for its proprietary second-generation Accum®-based ADCs, which include antibodies conjugated to innovative new constructs featuring a bile acid conjugated to a nuclear localization signal (NLS) derived from the ribosomal protein eS17 (RPS17).

This milestone builds on Defence's established patent portfolio for its foundational Accum® technology, which includes granted patents in the United States (US 11,352,437), Japan (JP 7,126,956), Australia (AU 2017233725), and Israel (IL 261765), with applications currently pending in Canada and Europe.

"Second-generation Accum®-based ADCs represent a significant advancement in both oncotherapy and targeted drug delivery," said Sébastien Plouffe, CEO and Founder of Defence Therapeutics. "This recent allowance underscores the innovation and versatility embedded in our ADC platform technology and reflects our commitment to developing novel, effective cancer treatments that push the boundaries of current ADC technologies."

This newly allowed U.S. patent application is poised to become the eighth granted U.S. patent in Defence's expanding portfolio, which now comprises seven published patent families.

About Defence:

Defence Therapeutics is a publicly-traded clinical-stage biotechnology company developing and engineering the next generation of ADC products using its proprietary platform. The core of Defence Therapeutics platform is the ACCUM® technology, which enables precision delivery of ADCs in their intact form to target cells. As a result, increased efficacy and potency can be reached against cancer.

For further information:
Sebastien Plouffe, President, CEO and Director
P: (514) 947-2272
Splouffe@defencetherapeutics.com
www.defencetherapeutics.com

Cautionary Statement Regarding "Forward-Looking" Information

This release includes certain statements that may be deemed "forward-looking statements". All statements in this release, other than statements of historical facts, that address events or developments that the Company expects to occur, are forward-looking statements. Forward-looking statements are statements that are not historical facts and are generally, but not always, identified by the words "expects", "plans", "anticipates", "believes", "intends", "estimates", "projects", "potential" and similar expressions, or that events or conditions "will", "would", "may", "could" or "should" occur. Although the Company believes the expectations expressed in such forward-looking statements are based on reasonable assumptions, such statements are not guarantees of future performance and actual results may differ materially from those in the forward-looking statements. Factors that could cause the actual results to differ materially from those in forward-looking statements include regulatory actions, market prices, and continued availability of capital and financing, and general economic, market or business conditions. Investors are cautioned that any such statements are not guarantees of future performance and actual results or developments may differ materially from those projected in the forward-looking statements. Forward-looking statements are based on the beliefs, estimates and opinions of the Company's management on the date the statements are made. Except as required by applicable securities laws, the Company undertakes no obligation to update these forward-looking statements in the event that management's beliefs, estimates or opinions, or other factors, should change.

Neither the CSE nor its market regulator, as that term is defined in the policies of the CSE, accepts responsibility for the adequacy or accuracy of this release.

To view the source version of this press release, please visit https://www.newsfilecorp.com/release/254853

FAQ

What is the significance of Defence Therapeutics' (DTCFF) new patent allowance?

The patent allowance provides market exclusivity until 2043 for Defence's next-generation ADC technology, covering both composition-of-matter and therapeutic applications for cancer treatment.

How does Defence Therapeutics' Accum-based ADC technology perform compared to conventional ADCs?

According to preclinical studies, Defence's Accum-based ADCs demonstrate enhanced intracellular delivery and superior cytotoxic activity compared to conventional ADCs in multiple cancer models.

What is the current patent portfolio status of Defence Therapeutics (DTCFF)?

Defence has granted patents in the US, Japan, Australia, and Israel, with this new allowance becoming their eighth US patent. Applications are pending in Canada and Europe.

What unique features does Defence Therapeutics' new ADC technology include?

The technology features antibodies conjugated to innovative constructs containing bile acid and a nuclear localization signal derived from the ribosomal protein eS17 (RPS17).

When will Defence Therapeutics' (DTCFF) new ADC patent expire?

The patent will provide market exclusivity until 2043, protecting Defence's proprietary second-generation Accum-based ADC technology.
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