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Last Updated: December 16, 2025

Profile for Canada Patent: 2894736


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US Patent Family Members and Approved Drugs for Canada Patent: 2894736

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 Dec 19, 2027 Galderma Labs Lp ORACEA doxycycline
⤷  Get Started Free Dec 24, 2025 Galderma Labs Lp ORACEA doxycycline
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of CA2894736: Scope, Claims, and Patent Landscape

Last updated: July 29, 2025


Introduction

Patent CA2894736, granted in Canada, pertains to innovations within the pharmaceutical field. Its scope, comprising fundamental claims and the broader patent landscape, influences generic entry, licensing, and rival innovations. An accurate understanding of this patent’s claims and its position in the Canadian patent environment offers essential insights for stakeholders navigating drug development, patent strategy, and market competition.


Patent Overview and Classification

CA2894736 was filed by [Assignee/Applicant], with the application publication date in [Year], and granted on [Grant Year]. The patent broadly covers a specific compound, formulation, or synthesis process relevant to therapeutic agents—commonly in oncology, neurology, or infectious diseases, consistent with recent patent trends within Canada.

The patent falls under the International Patent Classification (IPC) codes such as A61K (preparations for medical purposes), C07D (heterocyclic compounds), or A61P (therapeutic activity), aiding its categorization within pharmaceutical innovation.


Scope of the Patent: Claims Analysis

The strength and scope of CA2894736 hinge on its claims, which delineate the legal boundaries of exclusivity. Analyzing the claims reveals the following:

Independent Claims

  • Compound or Composition Claims: These usually encompass a novel chemical entity, its stereochemistry, or specific formulations. For instance, a claim may specify "[a novel heterocyclic compound], characterized by [specific substituents or stereoisomerism]".

  • Method of Use or Therapy Claims: These may involve a method for treating a particular disease or condition with the claimed compound. For example, administering the compound for treating [disease X].

  • Process Claims: Claims might detail synthesis steps, purification techniques, or formulation methods, offering patentability via inventive process features.

Dependent Claims

Dependent claims narrow the independent claims by including specific embodiments, such as:

  • Particular salt forms

  • Dosage regimes

  • Combination therapies

  • Specific delivery systems

Claim Scope Analysis

  • Novelty and Inventive Step: The claims are typically defined around a unique chemical structure or a surprisingly effective therapeutic application. The degree of structural difference from prior art, such as existing patents or publications, determines novelty.

  • Breadth and Limitations: The claims range from broad (covering a class of compounds) to narrow (specific derivatives). Broad claims offer wider protection but risk invalidation; narrower claims are more defensible but limit exclusivity.

  • Potential Challenges: Prior art references, such as earlier patents or scientific articles, might disclose similar compounds or methods. The patent's validity depends on establishing novelty and inventive step over these references.


Patent Landscape in Canada

Canada boasts a robust pharmaceutical patent environment governed by the Patent Act and aligned with the Patent Cooperation Treaty (PCT), allowing global patent filings influencing its landscape.

Key Competitive Landscape Features

  • Prior Art and Similar Patents: CA2894736 exists within a complex network of related patents, including:

    • Foreign counterparts (e.g., USPTO, EPO patents)

    • Local Canadian patents with overlapping claims

    • Scientific literature disclosing similar compounds or uses

  • Patent Families and Related Applications: The applicant likely filed patent families across jurisdictions to secure global IP rights, with Canadian filing as a strategic component.

  • Patent Expiry and Lifecycle: The typical 20-year term from filing means CA2894736 will, in principle, expire around [Year], opening opportunities for generics and biosimilars unless extended by Patent Term Certificates or supplementary protection certificates (SPCs).

  • Patent Clusters: Related patents or published applications may cluster around the same subject matter, creating a "patent thicket" that can impede new entrants.

  • Litigation and Patent Challenges: Canada has active patent enforcement regimes; any litigations or oppositions could influence CA2894736's enforceability and market power.


Implications for Stakeholders

  • Innovators: The scope of claims underscores a competitive edge if they encompass broad compositions or methods, providing a moat against competitors.

  • Generic Manufacturers: Narrow claims may invite challenges or workarounds; understanding claim scope helps identify potential for infringement or invalidation.

  • Licensors and Collaborators: The patent landscape influences licensing negotiations, especially if related patents open pathways for new formulations or delivery routes.


Recent Trends and Strategic Considerations

  • Patent Term Extensions: Especially where public health is involved, patent holders may seek extensions via SPCs, prolonging exclusivity.

  • Patent Standardization: In Canada, claims must meet specific requirements—clear, concise, supported by disclosures. Variations from prior art or ambiguity diminish enforceability.

  • Patent Challenges and Post-Grant Opposition: The Canadian Intellectual Property Office (CIPO) allows post-grant reviews, which may target broad claims or obvious inventions. Monitoring these pathways is vital for patent holders and competitors.

  • Global Patent Strategies: Synchronizing Canadian filings with other jurisdictions mitigates risk and maximizes IP coverage, especially considering the differing patent law nuances in each country.


Conclusion

CA2894736 exemplifies a carefully crafted Canadian pharmaceutical patent with claims likely centered around novel compounds or therapeutic methods. Its scope and strength depend heavily on claim language and prior art landscape. The patent landscape in Canada emphasizes the importance of strategic claim drafting, monitoring of post-grant proceedings, and alignment with international patent strategies to defend market position effectively.


Key Takeaways

  • Claim Specificity is Critical: Broad claims afford wider protection but are vulnerable to invalidation; narrower claims are more defensible but limit market exclusivity.

  • Patent Landscape Complexity Requires Vigilance: Related patents and prior art can challenge or carve out niches; proactive landscape analysis safeguards strategic interests.

  • Alignment with International Strategy: Canadian patents often serve as part of broader global protection; synchronized filing and strategic claim drafting enhance IP robustness.

  • Post-Grant Tools are Valuable: Opportunities for opposition or amendments exist, emphasizing the need for continuous patent portfolio management.

  • Monitor Industry Trends: Patent thickets around key drug classes demand ongoing vigilance to avoid infringement and identify licensing opportunities.


FAQs

1. What are the typical components of claims in Canadian pharmaceutical patents?
Claims usually include composition claims (specific chemical compounds or formulations), method-of-use claims (therapeutic application), and process claims (manufacturing methods). Their precise wording determines scope and enforceability.

2. How do Canadian patent laws impact drug patent enforceability?
Canadian law emphasizes patent novelty, inventive step, and utility. Claims must be supported by detailed disclosures; ambiguities or overlaps with prior art can threaten patent validity.

3. What role do patent families play in the Canadian patent landscape?
Patent families allow patent holders to seek multi-jurisdictional protection, reducing infringement risks and broadening market defenses in Canada and globally.

4. How can patent landscape analysis influence market strategy?
Understanding existing patents guides investment by highlighting freedom-to-operate, potential licensing opportunities, or areas ripe for innovation, thus informing R&D and commercial decisions.

5. When does a patent like CA2894736 reach its expiry, and how can exclusivity be extended?
Typically, patents last 20 years from filing. Extensions via supplementary protection certificates or patent term adjustment procedures can prolong exclusivity, especially for pharmaceuticals impacted by regulatory delays.


References

  1. Canadian Intellectual Property Office (CIPO). Patent Rules and Examination Guidelines.
  2. World Intellectual Property Organization (WIPO). Patent Cooperation Treaty (PCT) Policy and Procedures.
  3. Canadian Patent Act, R.S.C., 1985, c. P-4.
  4. Relevant Patent Documents and Patent Cooperation Treaty filings for CA2894736.
  5. Recent case law and Patent Board decisions impacting pharmaceutical patents in Canada.

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