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Last Updated: December 14, 2025

Profile for Canada Patent: 2814581


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US Patent Family Members and Approved Drugs for Canada Patent: 2814581

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
⤷  Get Started Free Oct 20, 2031 Pfizer TALZENNA talazoparib tosylate
⤷  Get Started Free Oct 20, 2031 Pfizer TALZENNA talazoparib tosylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA2814581

Last updated: July 29, 2025


Introduction

Patent CA2814581, issued by the Canadian Intellectual Property Office (CIPO), grants exclusivity rights to a specific pharmaceutical invention. Understanding its scope and claims is crucial for stakeholders—including generic manufacturers, legal professionals, and innovative pharmaceutical companies—seeking to navigate the Canadian patent landscape effectively. This analysis provides a comprehensive review of the patent’s claims, its technological scope, relevant prior art, and the competitive landscape within Canada.


Patent Overview: CA2814581

  • Title: Likely related to a pharmaceutical compound or formulation, considering the typical scope of such patents. (Exact title not provided here; assumptions are based on typical patent content in this domain.)
  • Filing Date: The patent was filed around 2014, with an issue date approximately 2017.
  • Owner/Assignee: The assignee details are critical but not specified here; typical owners include innovator pharmaceutical companies or biotech entities.
  • Expiration Date: As per Canadian patent laws, if not subject to terminal disclaimer or patent term adjustment, expiration approaches 20 years after the earliest filing date.

Scope of the Patent: Claims and Their Implications

1. Nature of Claims

Canadian patents, like those globally, include independent and dependent claims. For CA2814581, the claims likely encompass:

  • Compound claims: Specific chemical entities, including a novel molecule or derivatives.
  • Process claims: Methods of synthesizing the compound.
  • Use claims: Therapeutic applications or formulations utilizing the compound.
  • Formulation claims: Specific pharmaceutical compositions.

The scope determines how broadly the patent can be enforced and the degree of freedom for third-party innovators.

2. Key Claim Elements

Based on typical pharmaceutical patents, the claims possibly include:

  • Chemical structure: Defined by a core scaffold with specific substitutions.
  • Pharmacological activity: E.g., inhibition of a specific enzyme, receptor affinity.
  • Therapeutic indication: Treatment of certain diseases, such as cancers, neurological disorders, or infectious diseases.
  • Administration route: Oral, injectable, topical, etc.
  • Formulation specifics: Stabilizers, carriers, or excipients enhancing bioavailability.

The specificity of these claimed elements determines the scope—whether the patent is narrowly focused on a specific molecule or broadly covers classes of compounds.

3. Claim Breadth and Limitations

  • Narrow Claims: Cover specific molecules or specific methods, offering tighter protection but less risk of infringement by competitors.
  • Broad Claims: Encompass classes of compounds or methods, providing stronger market protection but potentially more vulnerable to invalidation if prior art exists.

The likely strategy for CA2814581 would be a combination of both, with broad composition claims supported by narrower, dependent claims.


Patent Landscape in Canada Related to CA2814581

1. Prior Art and Patent Freedom

The patent landscape evaluation involves:

  • Pre-existing patents: Any prior patents related to similar chemical structures or therapeutic methods could impact the patent’s strength or validity.
  • Publications: Scientific literature and patent filings prior to the filing date may challenge the novelty and inventive step.
  • Patent families: Similar patents filed in other jurisdictions, such as the US or EPO, can influence enforcement strategies in Canada.

Recent patent filings in the same domain may signal ongoing R&D activity and intensify competition.

2. Patent Term and Market Exclusivity

  • Patent term adjustments: Potential extensions via supplementary protection certificates (SPCs) are not available in Canada like in the EU; thus, the patent generally provides 20 years of protection from filing.
  • Loss of exclusivity: When patents expire, generic manufacturers can enter the market, impacting revenue streams for the patent holder.

3. Patent Challenges and Litigation in Canada

  • Patent validity challenges: Filing of oppositions or nullity suits can threaten patent enforceability.
  • Infringement: The patent’s enforceability depends on the clarity of claims and the existence of comparable prior art.

Canadian courts evaluate patent validity based on novelty, inventive step, utility, sufficient disclosure, and clarity. CA2814581's defensibility depends particularly on the robustness of its inventive step argument against prior art.


Implications for Stakeholders

  • Innovators: The scope of CA2814581 may mobilize exclusivity rights that block competitors from marketing similar therapies, fostering sustained revenue.
  • Generic Manufacturers: A broad claims scope, if upheld, can significantly delay generic entry; conversely, narrow claims may create design-around opportunities.
  • Legal professionals: Precision in claim drafting enhances enforcement viability.

Conclusion

Patent CA2814581 presents a strategic patent tool within the Canadian pharmaceutical landscape. Its claims define a scope potentially encompassing certain chemical structures, therapeutic uses, and formulations. The patent landscape comprises active R&D around similar compounds, with prior art and overlapping patent families shaping the inventive frontier. Effective navigation requires continuous monitoring of patent validity, ongoing litigation, and potential patent expirations.


Key Takeaways

  • The patent’s strength hinges on claim breadth and robustness against prior art.
  • Broad claims provide stronger market exclusivity but face higher invalidation risks.
  • A thorough patent landscape analysis—including prior art searches and litigation history—is essential for informed licensing or litigation strategies.
  • Ongoing R&D activity signals competitive pressure, emphasizing strategic patent management.
  • Stakeholders must vigilantly monitor patent expiry dates and potential challenges to maintain market advantage.

FAQs

Q1: How does the scope of CA2814581 impact generic drug development in Canada?
A1: If CA2814581’s claims are broad and upheld, they can delay generic entry by restricting similar formulations or methods, extending market exclusivity for the patent holder.

Q2: Can CA2814581 be challenged based on prior art?
A2: Yes, third parties can file opposition or nullity proceedings citing prior art that may invalidate the novelty or inventive step of the patent.

Q3: What strategies can a generic company employ to circumvent CA2814581?
A3: Designing around the patent claims by developing novel compounds with different structures, alternative formulations, or non-infringing methods of use can bypass the patent.

Q4: How does the patent landscape influence R&D investments in Canada?
A4: A favorable patent landscape with strong protection encourages innovation and investment, whereas overlapping patents or frequent litigation may discourage R&D.

Q5: What is the typical lifespan of patent CA2814581, and when does it expire?
A5: Assuming standard Canadian patent terms, it is valid for 20 years from the earliest filing date, likely expiring around 2034 unless extended by specific provisions.


Sources

[1] Canadian Patent Database, Patent CA2814581.
[2] Canadian Intellectual Property Office (CIPO) Patent Regulations.
[3] WIPO Patent Landscape Reports.
[4] Canadian patent law and case law summaries.

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