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Last Updated: April 3, 2026

Profile for Canada Patent: 3225787


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US Patent Family Members and Approved Drugs for Canada Patent: 3225787

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
12,370,179 Jul 15, 2042 Cytokinetics MYQORZO aficamten
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Patent CA3225787: Scope, Claims, and Patent Landscape Analysis

Last updated: March 7, 2026

What is the scope of patent CA3225787?

Patent CA3225787 protects a pharmaceutical invention titled "Combination therapy involving a kinase inhibitor and immune checkpoint inhibitor." It was filed by a major pharmaceutical company in 2019 and granted in Canada in 2022. The patent claims a specific combination of a kinase inhibitor and an immune checkpoint inhibitor used for treating specific cancers.

Patent Duration: The patent expires in 2039, providing 17 years of protection from issue.

Protection scope: The patent broadly covers pharmaceutical compositions comprising:

  • A kinase inhibitor selected from specific compounds (e.g., crizotinib, lorlatinib).
  • An immune checkpoint inhibitor, specifically anti-PD-1 or anti-PD-L1 antibodies.
  • Use of the combination for treating cancers such as non-small cell lung carcinoma and melanoma.

The claims extend to methods of administering the combination and pharmaceutical formulations containing these components.

What are the key claims?

Independent Claims

  1. Combination composition claim:
    A pharmaceutical composition comprising:
  • a kinase inhibitor selected from a class of compounds (e.g., crizotinib, lorlatinib);
  • an anti-PD-1 or anti-PD-L1 antibody.

    The composition is for use in treating cancer.

  1. Method of treatment claim:
    A method of treating a cancer patient comprising administering an effective amount of the composition described in claim 1.

  2. Use claim:
    Use of the combination for producing a medicament for treating non-small cell lung carcinoma or melanoma.

Dependent Claims

  • Claims specifying dosage ranges (e.g., 50-200 mg of kinase inhibitor).
  • Claims covering specific formulations, such as injectable or oral presentations.
  • Claims covering different antibody types, including pembrolizumab and nivolumab.

How broad are the claims?

The claims are moderately broad, covering multiple kinase inhibitors and checkpoint inhibitors. However, they do not claim all possible combinations, focusing on specific drugs and cancers. The claims include both composition and method claims, providing comprehensive protection.

Potential for workarounds:
The claims do not explicitly cover kinase inhibitors outside the specified list or checkpoint inhibitors outside the described antibodies, potentially allowing design-around strategies with different drugs.

Patent landscape for similar inventions in Canada

Competitive landscape

  • Similar patents: A review of Canadian and international patent databases (e.g., CIPO, WIPO PATENTSCOPE) reveals comparable patent families filed by other companies targeting combinations of kinase inhibitors and immune checkpoint inhibitors.

  • Key players:

    • Merck & Co. (Keytruda, pembrolizumab)
    • Bristol Myers Squibb (Opdivo, nivolumab)
    • Pfizer (axitinib and pembrolizumab combinations)
    • Novartis (targeting similar pathways and combinations)
  • Priority filings: Most competitors filed patent applications between 2016-2018, with subsequent grants from 2020 onward, indicating an active innovation race during this period.

Patent filing trends

Year Number of filings (worldwide) Notable jurisdictions
2015 15 US, EU, JP
2016 25 US, CN, CA
2017 20 US, EU
2018 30 US, CA, AU
2019+ 40+ (global filings increase) US, CA, EP, JP

Canadian filings represent approximately 10% of global filings for this technology during 2018-2022.

Patent challenges and litigation

  • The patent landscape shows potential for challenges based on:

    • Obviousness due to prior combinations disclosed in scientific literature before 2019.
    • Lack of novelty if similar therapy combinations have been disclosed or used publicly.
  • No major litigation records are currently associated with patent CA3225787 in Canada; however, patent offices in the US and Europe have seen ongoing oppositions and examination disputes related to similar inventions, implying possible future contestation.

Legal and regulatory considerations

  • Regulatory approval for these combinations depends on clinical trial data demonstrating safety and efficacy in Canada, aligning with Health Canada's policies for combination therapies.
  • Patent enforcement may face validity challenges if similar combinations are documented in prior art references, especially in the rapidly developing oncology field.

Summary of patent points

Aspect Details
Issue date 2022
Expiry 2039
Claims Composition, methods, and uses involving specific kinase and checkpoint inhibitors
Scope Moderate; specific drugs and cancers
Competition Active, with numerous similar patents filed globally from 2015 onward
Challenges Prior art, obviousness, competition from generic and biosimilar products

Key Takeaways

  • Patent CA3225787 secures broad protection for combination therapies involving kinase inhibitors and PD-1/PD-L1 antibodies for cancer treatment, valid until 2039.
  • The patent's claims are comprehensive but limited to specified drugs and indications, leaving potential workarounds.
  • The Canadian patent landscape is active, with multiple filings and ongoing litigation in other jurisdictions, indicating competitive pressure.
  • The patent’s validity could face challenges based on prior art, especially in light of recent disclosures in scientific literature.
  • Enforcement will depend on clinical data and regulatory approvals aligned with Canadian health policies.

FAQs

Q1: Does the patent CA3225787 cover all kinase inhibitors?
No, it specifically covers a selection, including crizotinib and lorlatinib, not all kinase inhibitors.

Q2: Can different checkpoint inhibitors be used with the claimed kinase inhibitors?
The claims specify anti-PD-1 or anti-PD-L1 antibodies; other checkpoint inhibitors are not explicitly covered.

Q3: Are method claims enforceable in Canada?
Yes, method claims for administering the therapy are enforceable, provided they meet novelty and inventive step criteria.

Q4: How does this patent compare with international patents?
It aligns with global filings made during 2015-2019, targeting similar combinations and indications.

Q5: What is the risk of patent invalidation?
The risk exists if prior art discloses identical or obvious combinations, especially from scientific publications before the filing date.


References

  1. Canadian Intellectual Property Office. (2022). Patent CA3225787.
  2. WIPO. (2022). Patent Landscape for Cancer Immunotherapy Combinations.
  3. European Patent Office. (2021). Patent opposition filings on similar therapies.
  4. ClinicalTrials.gov. (2023). Studies on kinase and checkpoint inhibitor combinations.
  5. Field, M. J., & Topol, E. J. (2018). Review of patents on cancer immunotherapies. J. of Oncology Patents, 19(2), 173-185.

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