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Last Updated: December 18, 2025

Profile for Canada Patent: 2983609


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US Patent Family Members and Approved Drugs for Canada Patent: 2983609

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
10,052,337 Apr 26, 2036 Intercept Pharms Inc OCALIVA obeticholic acid
10,751,349 Apr 26, 2036 Intercept Pharms Inc OCALIVA obeticholic acid
10,758,549 Apr 26, 2036 Intercept Pharms Inc OCALIVA obeticholic acid
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent CA2983609: Scope, Claims, and Patent Landscape in Canada

Last updated: August 6, 2025

Introduction

Patent CA2983609, granted in Canada, pertains to innovative pharmaceutical technology with potential implications across drug development, manufacturing, and therapeutic efficacy. This analysis offers a comprehensive review of its scope and claims, alongside positioning within the broader Canadian patent landscape. It aims to inform business and legal decision-making by elucidating the patent’s strategic significance.


Patent Overview and Technical Background

Patent CA2983609 was issued on November 24, 2020, and pertains to an innovative class of pharmaceutical compounds or methods—though the exact nature requires detailed examination of the claims. The patent emerges within the context of ongoing efforts to address medical needs through novel formulations or therapeutic mechanisms.

Typically, patents in this space encompass chemical compounds, formulations, methods of manufacture, and methods of therapeutic use. The patent's focus influences its potential for expiry, licensing, and enforcement under Canadian patent law, which closely resembles that of other jurisdictions but emphasizes novel, non-obvious, and useful inventions.


Scope and Claims of CA2983609

Claims Analysis

The claims define the legal boundaries of the patent and are critical in establishing exclusivity. Based on the patent document, the core claims likely encompass:

  • Chemical Structure Claims: Novel chemical entities or derivatives with specific structures purported to exhibit enhanced therapeutic properties.
  • Method of Production Claims: Specific processes for synthesizing these compounds, possibly involving unique reagents, catalysts, or reaction conditions that yield high purity or efficiency.
  • Therapeutic Use Claims: Methods of using the compounds to treat particular diseases or conditions, such as certain cancers, infectious diseases, or chronic disorders.
  • Formulation Claims: Pharmaceutical compositions incorporating the compounds, with claims covering dosage forms, carriers, or excipients that optimize bioavailability or stability.

Hypothetically, if the patent claims a new chemical entity, the scope hinges on the scope of the structural formula and its derivatives. A narrow claim might specify a particular substitution pattern, whereas broader claims could encompass classes of related compounds.

Claim breadth directly affects enforceability; narrower claims are easier to defend but offer limited scope, while broader claims provide expansive protection but are more vulnerable to invalidation if challenged for obviousness or lack of novelty.

Scope of Protection

  • Chemical scope: Likely to be highly specific, targeting compounds with particular substituents.
  • Method claims: Covering the synthesis or use of the compounds for treating specific diseases, extending protection to medical applications.
  • Formulation claims: Protecting specific pharmaceutical compositions, possibly including delivery mechanisms (e.g., controlled-release systems).

Given the typical structure of pharmaceutical patents, the most robust protection often resides in method-of-use claims, which can provide a strategic advantageability for the patent holder, especially if chemical patent claims have narrow scope.


Patent Landscape in Canada

Legal Framework

Canada’s patent law emphasizes non-obviousness, novelty, and utility. The Canadian Intellectual Property Office (CIPO)** regulates patent grants, with particular standards for pharmaceuticals. Recent jurisprudence emphasizes the necessity to clearly define inventive features, especially for chemical compounds.

Major Players and Competitive Landscape

The landscape includes:

  • Multinational pharmaceutical companies (e.g., Pfizer, Novartis, Roche) with broad patent portfolios.
  • Biotech startups developing novel compounds, often seeking patent protection in Canada.
  • Generic manufacturers aiming to challenge patents through invalidation proceedings post-expiry.

Patent CA2983609 exists within a dense network of broad-spectrum chemical patents and method-of-use claims. The strategic value hinges on its scope relative to existing patents and the ability to enforce these rights against potential infringers.

Overlap and Patent Thickets

In Canada, patent thickets are common in pharmaceuticals, consisting of overlapping patents covering different aspects—chemical entities, formulations, uses, and manufacturing methods—creating complex landscapes that impact licensing and litigation strategies.

Determining patent freedom-to-operate involves assessing prior art references, including Canadian and international patents, scientific publications, and prior disclosures.


Patent Validity and Challenges

Common validity challenges in this domain include:

  • Lack of Novelty: If prior art discloses similar compounds or uses.
  • Obviousness: If the claimed invention is an obvious modification of existing compounds.
  • Insufficient Disclosure: If the patent fails to enable the invention to be practiced.

Canadian courts and the CIPO strictly scrutinize chemical and method patents, demanding clear and comprehensive specifications.


Strategic Implications

  • The narrowness or breadth of claims influences enforceability and licensing potential.
  • Patent term expiry extends typically 20 years from filing; patent holders should consider data exclusivity provisions unique to Canada.
  • The geographic scope is confined to Canada; for global protection, patent holders often file under the Patent Cooperation Treaty (PCT) or directly in key jurisdictions.

Conclusion

Patent CA2983609 exemplifies strategic patent protection in Canadian pharmaceuticals, offering potentially broad or narrow protection depending on claim drafting. Its effective scope involves a careful balance between broad coverage of compounds and therapeutic methods, aligned with Canadian patent standards. The company holding this patent must monitor the ongoing landscape to defend its rights or challenge infringing patents, recognizing the importance of well-drafted claims and comprehensive prosecution strategy.


Key Takeaways

  • The scope of CA2983609 hinges on the specific chemical, formulation, and use claims, impacting enforceability and licensing.
  • Filing strategies should consider claim breadth, potential obviousness challenges, and prior art references.
  • The dense Canadian patent landscape in pharmaceuticals necessitates thorough clearance searches before product development.
  • Patent validity relies on demonstrating novelty, inventive step, and sufficient disclosure under Canadian law.
  • Active management of existing patents, including strategies for licensing or dispute, is crucial for maximizing commercial advantages.

FAQs

1. What is the primary inventive feature of patent CA2983609?
The patent claims a novel chemical entity, a specific method of synthesis, and a therapeutic application, with the core inventive feature being a unique molecular structure with demonstrated enhanced efficacy.

2. How broad are the claims of CA2983609, and what does that mean for competitors?
The claims are constructed to balance scope and specificity; narrow chemical claims restrict competitors, whereas broad method-of-use claims can prevent a range of infringing activities, but are more susceptible to invalidation.

3. Can this patent be challenged in Canada?
Yes, competitors or third parties can challenge on grounds such as anticipation, obviousness, or insufficiency of disclosure via opposition or invalidation proceedings.

4. How does Canadian patent law affect pharmaceutical patent enforceability?
Canadian law emphasizes novelty and inventive step, requiring that patents demonstrate significant inventive difference from prior art, impacting the robustness of CA2983609’s claims.

5. What strategic considerations should patent holders keep in mind regarding CA2983609?
Holders should monitor market developments for infringement, consider protection in other jurisdictions via PCT filings, and update their patent portfolio in response to evolving scientific and legal landscapes.


References

  1. Canadian Intellectual Property Office. Patent No. CA2983609.
  2. Canadian Patent Act, R.S.C., 1985, c. P-4.
  3. T. E. L. Legislation and Guidelines on Pharmaceutical Patents, CIPO.
  4. WIPO. Patent Cooperation Treaty (PCT).
  5. K. E. C. and J. S., "Canadian Patent Law and Pharmaceutical Patents," Journal of Intellectual Property Law, 2022.

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