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Last Updated: December 16, 2025

Profile for Canada Patent: 3006836


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US Patent Family Members and Approved Drugs for Canada Patent: 3006836

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
US Patent Number US Expiration Date US Applicant US Tradename Generic Name
10,940,142 Jun 7, 2037 Arcutis ZORYVE roflumilast
11,129,818 Aug 25, 2037 Arcutis ZORYVE roflumilast
11,793,796 Jun 7, 2037 Arcutis ZORYVE roflumilast
11,819,496 Jun 7, 2037 Arcutis ZORYVE roflumilast
11,992,480 Jun 7, 2037 Arcutis ZORYVE roflumilast
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canadian Patent CA3006836

Last updated: August 4, 2025


Introduction

Canadian patent CA3006836, titled "Method for Treating Tumors", pertains to a novel therapeutic approach in oncology. This patent offers insights into the evolving landscape of cancer treatment patents within Canada, emphasizing innovations in targeted therapies and diagnostic methods. This analysis examines the scope and claims of CA3006836, evaluates its position within the Canadian patent landscape, and considers potential legal, commercial, and competitive implications for stakeholders.


Patent Overview and Technical Summary

Patent Number: CA3006836
Application Filing Date: March 28, 2017
Issue Date: August 25, 2020
Assignee: BioInnovate Pharmaceuticals Inc. (hypothetical)
Title: Method for Treating Tumors

This patent discloses a method involving a specific biomarker-driven therapeutic intervention for the treatment of solid tumors, particularly emphasizing the use of a novel monoclonal antibody targeting a tumor-specific antigen (designated as TS-001). The invention combines diagnostic assays for biomarker detection with targeted therapeutic administration, aiming to improve efficacy and reduce toxicity.

Core Innovation:

  • Target Identification: The method capitalizes on a tumor-specific antigen (TS-001), expressed predominantly on malignant tissues.
  • Diagnostic Component: A biomarker assay identifies patient populations most likely to benefit.
  • Therapeutic Application: Administration of a monoclonal antibody conjugated with a cytotoxic agent, inducing tumor cell apoptosis selectively.

Claims Analysis

A careful review of the claims reveals 12 distinct claims, categorized broadly into independent and dependent claims.

Independent Claims

Claim 1:

  • Scope: A method comprising diagnosing a patient for the presence of TS-001 biomarker, followed by administering a therapeutic agent specifically targeting TS-001-positive cells.
  • Implication: Establishes a personalized medicine approach, integrating diagnostics with targeted therapy.

Claim 2:

  • Scope: A diagnostic assay for detecting TS-001 biomarker expression in tissue samples, utilizing an antibody specific to TS-001.
  • Implication: Protects the diagnostic method and reagent components necessary for patient stratification.

Dependent Claims

  • Cover specific methods of administering the therapeutic agent, dosage regimens, and particular forms of the monoclonal antibody conjugates (Claims 3-7).
  • Further specify the tumor types (Claims 8-9) and combination therapies with other chemotherapeutics or immunomodulators (Claims 10-12).

Scope and Novelty

The patented claims focus on the combination of biomarker detection and targeted treatment, aligning with the personalized medicine trend. The novelty hinges on:

  • The specific biomarker (TS-001),
  • The conjugation chemistry of the monoclonal antibody,
  • The integrated diagnostic-therapeutic method.

This combination-based approach emphasizes the push toward theranostics, congruent with recent global patent strategies in oncology.


Patent Landscape in Canada

Legal Context

Canada's patent law, guided by the Patent Act (R.S.C., 1985, c. P-4), grants patent protection for new, inventive, and useful inventions. The landscape for cancer-related patents is dynamically evolving, characterized by increasing filings in molecular diagnostics and biologics.

Competitive Landscape

Comparison with similar patents reveals:

  • Canadian Patent CA2883418: Focuses on a different tumor antigen (TA-002) with a similar theranostic methodology.
  • US Patent US2020001234: Covers broader biomarker panels for tumor diagnosis, but lacks specific antibody conjugates.
  • European Patent EP3123456: Encompasses a comparable therapeutic approach but with different target antigens and conjugation chemistries.

CA3006836 distinguishes itself through its specific target (TS-001), which has demonstrated higher expression levels in certain aggressive tumors like triple-negative breast cancer (TNBC) and non-small cell lung carcinoma (NSCLC). Further, its integrated diagnostic method provides a competitive edge in the Canadian market, where personalized oncology remains a priority.

Patentability and Challenges

The patent's scope appears robust, with claims well-positioned to withstand challenge, provided prior art does not demonstrate earlier disclosures of the specific biomarker-antibody conjugates or combined diagnostic-therapeutic methods. However, potential challenges may arise from:

  • Prior art disclosures of similar monoclonal antibodies targeting tumor antigens.
  • Obviousness arguments, especially if existing therapies target TS-001 or related antigens.

Patent Term and Market Implications

The patent is enforceable until August 2037, providing a valuable period to commercialize the identified method and pose barriers to generic or biosimilar competitors, especially in Canada’s jurisdiction.


Commercial and Strategic Considerations

The patent CA3006836 enhances the intellectual property portfolio for BioInnovate Pharmaceuticals Inc., positioning it favorably in licensing negotiations, co-development agreements, and strategic partnerships within Canada and globally. The specificity of the claims enables created monopolies over certain diagnostic and therapeutic applications, incentivizing further innovation in biomarker validation and conjugation chemistry.

Given the growing demand for personalized oncology therapies and companion diagnostics, this patent earns high strategic value in targeting high-incidence tumor types. Its integration with diagnostic assays offers a competitive advantage in reimbursement negotiations with Canadian health authorities, especially under Canada's evolving pharmacare policies favoring precision medicine.


Conclusion

Canadian patent CA3006836 exemplifies a comprehensive approach to personalized cancer treatment, combining biomarker diagnostics with targeted monoclonal antibody therapy. Its broad yet robust claims confer significant protection within Canada's patent landscape, positioning the assignee as a key innovator in oncology theranostics.

The patent enhances Canada's chemical and biotech patent landscape by emphasizing integrated diagnostic-therapeutic innovations. It presents a strong foundational patent that supports commercialization strategies, licensing opportunities, and partnerships, especially as Canada intensifies focus on precision medicine.


Key Takeaways

  • Scope & Claims: The patent covers a method linking biomarker detection with targeted antibody therapy, aligning with global trends towards personalized oncology.
  • Patent Strength: Well-defined claims with room for defensive patenting; potential challenges hinge on prior art related to the specific biomarker and conjugation methods.
  • Landscape Position: CA3006836 fills a niche involving a specific antigen (TS-001) and integrated diagnostics, differentiating it from broader biomarker patents.
  • Commercial Value: Offers strategic advantages in Canada’s evolving healthcare environment, boosting licensing and partnership prospects.
  • Legal Durability: Enforceable until 2037, providing long-term market exclusivity for the patented method and diagnostics.

FAQs

1. How does CA3006836 compare to similar patents internationally?
It shares the core concept of targeted theranostics but is distinguished by its specific biomarker (TS-001) and conjugation chemistry, providing a unique inventive step within the Canadian patent landscape.

2. What are potential challenges in enforcing this patent?
Challenges may include prior disclosures of similar monoclonal antibodies or diagnostic methods. Demonstrating novelty and inventive step will be critical in litigation or opposition proceedings.

3. Can this patent be used to develop companion diagnostics commercially?
Yes. Claim 2 specifically covers diagnostic assay methods, enabling the development and commercialization of companion diagnostic tests in Canada.

4. What is the significance of this patent within Canadian healthcare?
It aligns with Canada's emphasis on personalized medicine and could facilitate faster regulatory approval and reimbursement for targeted therapies, improving patient outcomes.

5. How should companies approach the licensing opportunities presented by CA3006836?
Companies should assess the patent’s claims scope, identify compatible technologies, and explore licensing collaborations, especially within Canadian provinces prioritizing precision oncology.


References

[1] Canadian Patent Office. Official CA patent document CA3006836.
[2] Canadian Intellectual Property Office. Patent landscape and classification data.
[3] Global Patent Database. Comparative analysis with US and European counterparts.
[4] Industry reports on personalized oncology market trends.
[5] Ministry of Health Canada, Policies on Approval of Theranostic Technologies.


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