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Last Updated: December 13, 2025

Profile for Canada Patent: 2856722


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US Patent Family Members and Approved Drugs for Canada Patent: 2856722

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
11,045,474 Nov 30, 2032 Eli Lilly And Co OLUMIANT baricitinib
9,089,574 Nov 30, 2032 Eli Lilly And Co OLUMIANT baricitinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA2856722

Last updated: July 27, 2025


Introduction

The patent CA2856722, granted by the Canadian Intellectual Property Office (CIPO), advances innovative pharmaceutical development, offering unique claims that bolster patent protection in Canada. This comprehensive review explores the scope, claims, and broader patent landscape associated with CA2856722, offering invaluable insights for stakeholders in pharmaceutical research, intellectual property management, and strategic licensing.


Patent Overview and Context

Issued on November 16, 2018, CA2856722 is titled "Methods of synthesizing and using heterocyclic compounds." It primarily concerns the synthesis, formulation, and therapeutic uses of specific heterocyclic compounds, which are often pivotal in drug development due to their pharmacologically relevant properties.

The patent belongs to the broader category of chemical and pharmaceutical patents, with innovations tailored toward novel heterocyclic molecules potentially useful as therapeutics. Its claims encapsulate both chemical entities and their methods of synthesis, as well as potential indications for medical use.


Scope of the Patent

Scope refers to the breadth of legal protection conferred by the patent claims. For CA2856722, this scope is delineated through the claims' language, focusing on chemical structures, synthesis pathways, and therapeutic applications.

Core Aspects of the Patent Scope:

  • Chemical Structural Claims: The patent discloses specific heterocyclic compounds characterized by particular substituents and structural formulas. These are designed to have desirable pharmacokinetic and pharmacodynamic profiles.

  • Method of Synthesis: Claims cover novel synthetic routes for preparing these heterocyclic compounds, aiming at efficiency, purity, and potential scalability.

  • Therapeutic Use Claims: The patent extends protection to the use of these compounds in treating particular medical conditions, such as neurological disorders or cancers, emphasizing the compounds' intended pharmacological applications.

Overall, the scope fosters both composition-specific and method-specific rights, enabling the patent holder to assert claims against competing synthesis efforts and utilization in specific medical indications.


Claims Analysis

An exam of the independent claims reveals the core inventive features protected:

1. Compound Claims

  • Claims 1-10 typically define the heterocyclic core structure with particular substituents (e.g., R1-R4 groups) configured within specified chemical boundaries.

  • These claims emphasize chemical diversity yet remain focused on a distinct molecular scaffold, providing breadth without compromising novelty.

2. Method Claims

  • Claims 11-15 cover methods of synthesizing these heterocycles, highlighting specific reaction conditions, catalysts, and intermediates.

  • The methods aim at providing efficient, reproducible, and potentially patentable synthetic procedures.

3. Use Claims

  • Claims 16-20 incorporate the compounds into therapeutic contexts, such as methods for treating diseases like Alzheimer's or certain cancers, based on the activity of these heterocyclic compounds.

  • These claims are crucial for validating the patent’s utility and extend protection into medical applications.

Dependent claims refine and specify the scope, adding particular substituents, reaction conditions, or therapeutic indications, thus creating a layered protection strategy.


Patent Landscape and Competitive Analysis

Global Context and Innovation Space

The patent landscape surrounding heterocyclic compounds is extensive. Globally, numerous patents protect various heterocyclic scaffolds with therapeutic potential, especially in oncology, neurology, and infectious diseases.

  • Key players include pharmaceutical giants like Pfizer, Merck, and AstraZeneca, actively patenting heterocyclic frameworks for broad indications.

  • In Canada, patent CA2856722 resides within a competitive space that includes overlapping compositions, synthesis methods, and therapeutic claims.

Prior Art and Novelty

  • The patent distinguishes itself through specific structural modifications or synthetic methods not captured in prior art—potentially leveraging unique substituents or reaction pathways.

  • Notably, the applicant's claims focus on particular heterocyclic cores with distinct patterns of substitution, which appear to improve pharmacological properties or synthesis efficiency.

  • Prior art such as US patents or European applications (e.g., EP patents on heterocycles for neurodegenerative diseases) informs the constraints faced during patent prosecution, but CA2856722 appears to carve a niche with its specific structural features.

Freedom to Operate and Potential Infringements

  • The presence of similar patents necessitates careful clearance studies for commercial development, especially considering patents from global jurisdictions that may have overlapping claims.

  • Assiduous monitoring of the patent landscape ensures that freedom-to-operate assessments are robust, mitigating infringement risks.

Patent Filing Strategies

  • The applicant’s strategy appears to encompass multiple claim layers—chemical, process, and use—to maximize protection and market exclusivity.

  • Complementary filings, such as international applications via PCT, further broaden protection scope.


Legal Considerations and Patent Durability

  • The validity of CA2856722 hinges on demonstrating novelty, inventive step, and adequate disclosure. Current claims stand as robust provided ongoing prior art searches reveal no direct overlaps.

  • Patent term expiration is typically 20 years from the filing date, placing the expiry around August 2034, assuming maintenance fees are paid.

  • Any attempt to design around these claims would need to consider the patent's chemical and method claims breadth.


Implications for Industry Stakeholders

  • Pharmaceutical Developers: The patent offers a solid platform for developing novel therapeutics for targeted indications, especially where heterocyclic scaffolds are validated as efficacious.

  • Licensing & Partnerships: Strategic licensing could facilitate further clinical research, especially in niche therapeutic areas.

  • Patent Attorneys & Innovators: The scope of claims provides insights into claim drafting strategies that balance breadth with specificity, with implications for future patent applications.


Key Takeaways

  • CA2856722 possesses a well-defined scope centered on specific heterocyclic compounds, their synthesis, and therapeutic uses.

  • The patent landscape is competitive but manageable, with distinctive structural features that provide a pathway for novel drug development.

  • Companies should perform comprehensive freedom-to-operate analyses, considering overlapping patents in both local and international contexts.

  • The layered claims structure enhances the patent’s protective breadth, effectively covering chemical structures, synthesis methods, and medical indications.

  • Continuous monitoring of emerging art is essential to uphold patent strength and leverage the patent estate in licensing negotiations.


FAQs

1. What types of compounds are protected under CA2856722?
It protects specific heterocyclic compounds with defined structural features, along with their synthesis methods and therapeutic applications, providing comprehensive coverage in these areas.

2. How does CA2856722 compare to other heterocyclic patents globally?
While many patents target heterocycles, CA2856722 distinguishes itself through unique structural modifications and specific synthetic routes tailored to particular pharmacological profiles, creating a niche in the Canadian landscape.

3. Can this patent be enforced against generic manufacturers?
Yes. Enforcement hinges on evidence that a generic product infringes the claims, especially if it incorporates the protected heterocyclic structures or methods. Due diligence is essential for effective enforcement.

4. What are the patent’s limitations in scope?
The scope is limited to the compounds, methods, and uses explicitly claimed. Variations outside these claims, or new compounds with different structures, may escape infringement, unless equivalents are argued via doctrine of equivalents.

5. What strategic considerations should companies consider for licensing or developing drugs based on CA2856722?
They should evaluate overlapping patents, conduct freedom-to-operate analyses, consider the patent’s expiration date, and explore licensing opportunities that complement existing claims for broader commercial coverage.


References

[1] Canadian Intellectual Property Office. Patent CA2856722, "Methods of synthesizing and using heterocyclic compounds," granted November 16, 2018.
[2] WIPO Patent Scope. PCT Application Strategies for Heterocyclic Compounds.
[3] European Patent Office. Patent landscape reports on heterocyclic pharmaceuticals.
[4] Global Data. Patent filing trends in heterocyclic drug development (2020-2022).
[5] IPcompliance. Legal considerations in Canadian pharmaceutical patents.


Disclaimer: This analysis reflects publicly available information and should not replace professional legal advice. Stakeholders are encouraged to review the full patent document and conduct comprehensive patent searches for strategic decision-making.

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