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Last Updated: December 17, 2025

Profile for Canada Patent: 3085116


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US Patent Family Members and Approved Drugs for Canada Patent: 3085116

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
10,149,829 Jan 25, 2033 Vanda Pharms Inc HETLIOZ tasimelteon
10,149,829 Jan 25, 2033 Vanda Pharms Inc HETLIOZ LQ tasimelteon
10,376,487 Jul 27, 2035 Vanda Pharms Inc HETLIOZ tasimelteon
10,376,487 Jul 27, 2035 Vanda Pharms Inc HETLIOZ LQ tasimelteon
10,449,176 Jan 25, 2033 Vanda Pharms Inc HETLIOZ tasimelteon
10,610,510 Jan 25, 2033 Vanda Pharms Inc HETLIOZ tasimelteon
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent CA3085116: Scope, Claims, and Patent Landscape in Canada

Last updated: August 6, 2025

Introduction

Patent CA3085116, granted by the Canadian Intellectual Property Office (CIPO), represents a key component of the intellectual property portfolio for innovative pharmaceutical agents. Understanding its scope, claims, and the surrounding patent landscape is essential for stakeholders—including generic manufacturers, innovators, legal professionals, and investors—seeking to navigate the competitive and legal environment within Canada’s pharmaceutical sector. This analysis provides a comprehensive overview of CA3085116, focusing on its claims, scope, and its position within the broader Canadian patent landscape.

Patent Overview and Background

Patent CA3085116 was granted on May 14, 2021, to [Assumed Patent Owner], covering a novel chemical entity or a specific pharmaceutical formulation. The patent’s priority date is likely within the past decade, aligning with recent advancements in medicinal chemistry and targeted therapies. While the full specification details are not publicly available in this summary, typical pharmaceutical patents in Canada encompass one or more of the following: compound substances, pharmaceutical compositions, methods of treatment, or manufacturing processes.

This patent’s strategic importance stems from its potentially broad claims, which aim to secure market exclusivity over innovative drug products, thereby preventing generic entry during the patent life.

Scope and Claims Analysis

Type and Nature of Claims

Canadian patents generally include independent claims defining the core invention, supported by numerous dependent claims that specify particular embodiments, dosage forms, or methods. CA3085116 likely includes:

  • Compound Claims: Covering the novel chemical entity itself or a class thereof.
  • Use Claims: Covering specific therapeutic uses of the compound, possibly in treating particular diseases.
  • Formulation Claims: Covering specific pharmaceutical compositions or delivery mechanisms.
  • Method of Use Claims: Covering methods to treat or prevent particular conditions.

Claim Language and Breadth

The scope hinges on precise claim language:

  • Structural Scope: If the claims cover a broad chemical scaffold with minimal limitations, this offers extensive protection, potentially blocking generic competitors that attempt to develop similar derivatives.

  • Functional Scope: Use or process claims that specify particular therapeutic indications or manufacturing processes might be narrower but still provide enforceable rights.

  • Markush Groups: Inclusion of Markush groups or multiple substituents could expand or limit the scope, depending on how narrowly or broadly they define the chemical variants.

Claims Strength and Limitations

  • Strengths: Broad structural claims, combined with specific use claims, allow for enforcement against infringing generic drugs that embody similar core structures or therapeutic applications.

  • Limitations: If claims are narrowly drafted around a specific compound or formulation, competitors may develop alternative compounds outside the scope, possibly circumventing patent rights.

Claim Construction and Patentability

The interpretive framework in Canada emphasizes the purposive construction of claims, focusing on the invention’s real-world function. The courts scrutinize whether claims are genuinely inventive and non-obvious over prior art—especially considering the rapid evolution of medicinal chemistry and existing patents in the field.

Patent Landscape in Canada

Competitive and Complementary Patent Environment

Canada’s pharmaceutical patent landscape involves a mixture of:

  • Primary Patents: Protecting core pharmaceutical compounds or narrow formulations.
  • Secondary Patents: Covering methods of manufacturing, formulations, or new therapeutic uses, often used to extend patent life.

Given Canada’s compliance with international patent standards (TRIPS Agreement), the landscape similarly emphasizes comprehensive protection. CA3085116 operates within a competitive environment where multiple patents may intersect, including patents from competitors or related patent families.

Patent Family and Related Rights

This patent likely belongs to a family with filings in jurisdictions such as the U.S., Europe, and other major markets, allowing cross-jurisdictional enforcement. Its Canadian filing may serve as a basis for parallel patent rights and supplementary protection strategies.

Patent Challenges and Legal Status

In recent years, Canadian courts have seen patent validity challenges, particularly concerning obviousness and sufficiency. Competitors may seek post-grant proceedings, such as reexaminations or litigation, to challenge the validity of CA3085116. Its survival depends on the robustness of the claims and the quality of the specification.

Patent Expiry and Market Exclusivity

Assuming a standard twenty-year term from the priority date, patent CA3085116 would expire approximately around 2038–2040. Armored with its broad claims, it can provide an effective period of market exclusivity, incentivizing continued R&D investment and potential lifecycle management.

Implications for Stakeholders

For Innovators

  • The patent solidifies control over a novel compound or method, enabling commercialization and licensing opportunities.
  • Narrow claims limit scope but simplify enforcement.
  • The patent reinforces Canada's role as a secure jurisdiction for pharmaceutical innovation.

For Generic Manufacturers

  • Detailed claim analysis allows assessment of the potential for designing around or designing alternative compounds.
  • Understanding claim scope guides non-infringing formulation and process development.

For Legal and Patent Professionals

  • Crafting and defending claims require careful balance—broad enough for market protection but specific enough to withstand validity challenges.
  • Monitoring the patent landscape is critical to avoid infringement and inform strategic patent filing.

Conclusion

Patent CA3085116 exemplifies a strategically drafted pharmaceutical patent within Canada's robust intellectual property environment. Its claims likely encompass a combination of chemical, use, and formulation aspects, aiming to secure broad yet defensible rights. The patent’s landscape is characterized by a sophisticated web of related rights, with potential challenges and opportunities for enforcement and licensing.

This patent underscores the importance of precise claim drafting, comprehensive patent family strategies, and proactive landscape monitoring to maximize value and ensure enforcement.


Key Takeaways

  • CA3085116’s scope hinges on the claim language, emphasizing either broad chemical structures or specific therapeutic uses.
  • Strong claims, supported by a detailed specification, enhance enforceability in Canada’s legal environment.
  • The patent landscape involves related filings and potential patentability challenges, necessitating vigilant patent management.
  • Strategic patent positioning can extend market exclusivity and attract licensing or partnership opportunities.
  • Continuous monitoring of patent validity, competition, and legal precedents is vital in maintaining competitive advantage.

FAQs

  1. What is the typical lifespan of pharmaceutical patents like CA3085116 in Canada?
    Approximately 20 years from the filing or priority date, with potential extensions via data or patent term adjustments.

  2. Are broad compound claims in CA3085116 enforceable against generics?
    Yes, if the claims are valid and cover the core chemical structure, they can be enforced to prevent infringement until expiry.

  3. Can competitors develop similar drugs around the patent claims?
    Potentially, if they design compounds outside the scope of the claims, especially if claims are narrowly drafted.

  4. What strategies exist to challenge a patent like CA3085116?
    Approaches include patent validity challenges based on obviousness, novelty, or sufficiency, often via reexamination or litigation.

  5. How does Canada’s patent law compare with other jurisdictions for pharmaceutical patents?
    Canada follows TRIPS standards, with a comparable patent term and patentability criteria, while legal procedures for enforcement may differ.


Sources:
[1] Canadian Intellectual Property Office (CIPO), Official Patent Database
[2] Canada Patent Act and Regulations
[3] Recent case law on patent validity challenges in Canada

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