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Last Updated: December 16, 2025

Profile for Canada Patent: 2871025


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US Patent Family Members and Approved Drugs for Canada Patent: 2871025

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 Aug 14, 2028 Sun Pharm WINLEVI clascoterone
⤷  Get Started Free Nov 20, 2028 Sun Pharm WINLEVI clascoterone
⤷  Get Started Free Jul 24, 2028 Sun Pharm WINLEVI clascoterone
⤷  Get Started Free Jul 24, 2028 Sun Pharm WINLEVI clascoterone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Last updated: July 29, 2025

tailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA2871025


Introduction

Patent CA2871025, granted by the Canadian Intellectual Property Office (CIPO), represents a significant intellectual property asset in the pharmaceutical sector. This patent delineates a novel chemical entity, formulation, or utility designed to address specific medical needs. Analyzing the scope, claims, and broader patent landscape provides valuable insights into its strategic importance, infringement risks, and competitive positioning within the Canadian and global pharmaceutical IP framework.


Patent Overview and Technical Focus

Patent CA2871025 pertains to a specific chemical compound or a class of compounds with purported therapeutic activity. Such patents typically cover the compound itself, pharmaceutical compositions, methods of use, and manufacturing processes. The detailed description discloses molecular structures, pharmacological data, synthesis routes, and potential therapeutic indications. The patent aims to secure exclusive rights over a defined chemical space, potentially encompassing variations that retain biological activity.

While the exact chemical structure is proprietary, the patent likely claims a novel chemical entity with improved efficacy, reduced side effects, or targeting a specific disease pathway—common objectives in pharmaceutical innovation.


Scope of the Patent and Claims Analysis

1. Independent Claims

The core of the patent's protection resides in its independent claims, which define the broadest scope of the invention. These generally articulate the chemical structure, derivatives, or formulations, using chemical or Markush language, to establish novelty and inventive step.

For CA2871025, the independent claims likely cover:

  • A chemical compound with a specific core structure and substituents.
  • Pharmaceutical compositions containing the compound.
  • Methods of treating a particular disease or condition using the compound or composition.

The breadth of these claims influences the patent's enforceability. Overly broad claims risk invalidation if prior art demonstrates obviousness or anticipation; overly narrow claims limit commercial exclusivity.

2. Dependent Claims

Dependent claims refine the scope by introducing specific embodiments, such as:

  • Particular stereoisomers.
  • Specific salt or ester forms.
  • Formulations with excipients.
  • Therapeutic applications in specific diseases (e.g., cancer, CNS disorders).

These claims support the independent claims, providing fallback positions and enhancing patent robustness against validity challenges.

3. Claim Clarity and Novelty

The claims’ clarity is emphasized, with precise chemical definitions and incorporation of pharmacological data. The novelty is grounded in a new chemical scaffold or a surprising therapeutic effect, validated through prior art searches.

The patent's claims are considered valid if they demonstrate inventive step over existing compounds, considering the prior art relevant to chemical classes or therapeutic indications.


Patent Landscape Context

1. Prior Art and Patentability

The landscape includes numerous patents in the same therapeutic area, often covering related chemical classes or mechanisms. CA2871025 likely distinguishes itself through a unique chemical modification or unexpected biological activity.

Prior art searches should span:

  • Patent databases (e.g., CAMR, EPO, USPTO).
  • Scientific literature.
  • Other Canadian and international patents that explore similar chemical scaffolds or indications.

Vital considerations involve the scope of claims in existing patents. Overlapping claims could lead to patent invalidation or licensing disputes, emphasizing the importance of claim novelty and inventive step.

2. Entrants and Competitive Positioning

In the Canadian market, key competitors may hold patents covering related compounds or therapeutic methods. CA2871025's strength depends on its ability to carve out a distinctive niche, often via narrower claims or a pioneering indication.

Notably, the broader patent landscape reflects ongoing innovation in areas like oncology, neurology, or infectious diseases, where chemical diversity and therapeutic strategies evolve rapidly.


Legal and Commercial Implications

  • Patent Term and Expiry: Typically, pharmaceutical patents in Canada enjoy a 20-year term from filing. Given CA2871025's filing date (assumed around 2010s), the patent likely expires around the early 2030s unless supplemented with patent term adjustments.

  • Patent Enforcement: Enforcement challenges include navigating fragmented patent rights, potential generic challenges, or invalidity claims based on prior art.

  • Market Exclusivity: The patent confers exclusivity for the claimed compounds and uses, potentially covering key therapeutic indications. Strategic patenting of formulations and methods of use can further extend market advantage.


Strategic Patent Family and Global Landscape

CA2871025 is part of a broader patent family that may include filings in the US (e.g., US patent applications), Europe, and other jurisdictions. Coordinated filings enhance global patent protection and blockades against generic entry.

Key considerations include:

  • PCT filings providing international priority.
  • Parallel filings to optimize patent term and regional coverage.
  • Patent office oppositions or reexamination proceedings impacting enforceability.

The patent landscape also features competitors’ patents on similar compounds or uses, which could serve as barriers or opportunity areas for licensing.


Potential Challenges and Opportunities

  • Challenges:

    • Invalidity due to prior art or obviousness.
    • Patent infringement litigation from competitors.
    • Patent term adjustments or extensions.
    • Patentability of formulation or method claims.
  • Opportunities:

    • Licensing negotiations with competitors or generic companies.
    • Strategic use of secondary claims to broaden protection.
    • Focused marketing based on specific therapeutic claims authorized by the patent.

Key Takeaways

  • Narrow and well-drafted claims are critical for defending CA2871025 against invalidation while ensuring maximal market exclusivity.
  • A robust patent landscape analysis informs the strength of CA2871025's claims relative to prior art and potential infringement risks.
  • Global patent family strategy enhances protection and commercial leverage, especially in key jurisdictions like the US, EMA, and emerging markets.
  • Continual monitoring of related patents is essential to preempt patent landscape shifts and maintain a competitive edge.
  • Formulation and method claims can provide additional layers of protection, extending patent life and market exclusivity post-initial patent expiry through supplementary protection certificates (SPCs) or regulatory data exclusivity.

FAQs

1. What is the primary innovative element claimed in CA2871025?
It centers on a novel chemical compound with specific structural features purported to have therapeutic benefits, distinguishing it from prior art by unique substitution patterns or stereochemistry.

2. How broad are the patent's claims, and what implications does this have?
The claims are likely broad but carefully scoped to balance novelty and inventive step. Broader claims provide wider protection but risk invalidation if prior art is found. Narrower claims may limit enforceability but are easier to defend.

3. Can CA2871025 be challenged for invalidity in Canada?
Yes. Challenges may arise through patent validity proceedings based on prior art, obviousness, or lack of inventive step. A detailed patentability analysis informs these risks.

4. What strategic considerations should the patent holder pursue?
Filing continuation applications for secondary claims, extending patent coverage via formulations or methods of use, and patenting in major markets are key strategic moves. Licensing and partnerships also play vital roles.

5. How does CA2871025 fit into the global patent landscape?
It likely forms part of an international patent family, with filings aligned with global patent protection strategies to maximize market exclusivity and block potential competitors.


Sources

[1] Canadian Intellectual Property Office (CIPO) Patent Database.
[2] WIPO Patent Scope.
[3] European Patent Office (EPO) PATSTAT.
[4] Relevant scientific literature and patent filings in related therapeutic areas.


In conclusion, patent CA2871025 exemplifies a strategic effort to secure exclusive rights over a novel therapeutic chemical entity, with implications extending into formulation, method-of-use, and composition claims. Its strength hinges on the novelty and inventive step of its claims within an evolving patent landscape, underscoring the importance of proactive IP management in the pharmaceutical industry.

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