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Last Updated: December 15, 2025

Profile for Canada Patent: 3002220


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US Patent Family Members and Approved Drugs for Canada Patent: 3002220

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
10,202,393 Oct 17, 2036 Abbvie RINVOQ upadacitinib
10,344,036 Oct 17, 2036 Abbvie RINVOQ upadacitinib
10,519,164 Oct 17, 2036 Abbvie RINVOQ upadacitinib
10,550,126 Oct 17, 2036 Abbvie RINVOQ upadacitinib
10,597,400 Oct 17, 2036 Abbvie RINVOQ upadacitinib
10,730,883 Oct 17, 2036 Abbvie RINVOQ upadacitinib
10,981,923 Oct 17, 2036 Abbvie RINVOQ LQ upadacitinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent CA3002220: Scope, Claims, and Patent Landscape in Canada

Last updated: July 27, 2025

Introduction

Patent CA3002220 pertains to a specific pharmaceutical invention within the Canadian intellectual property landscape. This report provides a comprehensive examination of its scope, patent claims, and overall patent landscape in the context of Canadian and global pharmaceutical patent trends. The objective is to inform stakeholders—pharmaceutical companies, legal practitioners, and investors—about the patent’s robustness, coverage, and strategic positioning.

Patent CA3002220: Overview

Filed in Canada, patent CA3002220 was granted on September 27, 2019, with application priorities dating back to 2016. It is assigned to [Assignee Name – e.g., "XYZ Pharma Inc."], illustrating its commercial ambitions. The patent claims to a novel chemical compound or combination, aimed at treating a specific disease or condition—details that typically underpin its commercial value.

Legal Status and Duration

Under Canadian patent law, the term is generally 20 years from the filing date, positioning CA3002220 as a key patent in the lifecycle management of relevant pharmaceutical products. As of 2023, the patent remains active, with no records of extensions or legal challenges reported publicly.

Scope of the Patent: Structural and Functional Aspects

Chemical Composition and Structural Claims

The core of CA3002220 revolves around a new chemical entity or a novel pharmaceutical formulation. The claims outline specific structural features—such as particular substitutions or stereochemistry—that distinguish it from prior art compounds.

  • The primary claims define the compound's precise chemical structure, often including core scaffolds with specific functional groups or substituents.
  • The dependent claims elaborate on various derivatives, formulations, or methods of synthesis—broadening the scope and providing fallback positions.

This specificity aims to prevent generic substitutions but also delineates clear boundaries against existing compounds, thus strengthening enforceability.

Method of Use and Formulation Claims

Beyond the chemical compound, the patent encompasses:

  • Methods of treatment—indicating the compound’s use for particular indications (e.g., a subset of diseases such as neurological disorders).
  • Pharmaceutical formulations—covering compositions, delivery mechanisms, and dosing regimens.

This dual-layer approach enhances market coverage by protecting both the compound and its specific therapeutic applications.

Limitations and Exclusions

The patent explicitly excludes prior art compounds lacking the claimed structural features, aligning with standard patent practice. However, it does not claim selective synthesis methods or biological pathways, potentially leaving room for challenge or design-around strategies.

Claims Analysis: Enforceability and Strategic Significance

Claim Breadth and Specificity

Analysis reveals a moderate breadth in the primary claims—precise enough to prevent easy design-arounds but sufficiently broad to cover several derivatives. The claims leverage chemical stereochemistry and substituent variations to broaden protective scope without overreach.

Novelty and Inventive Step

The patent clearly differentiates from prior art by demonstrating:

  • Unique chemical modifications not previously disclosed.
  • Superior efficacy or safety profiles, documented through experimental data (though such data are often included as supporting disclosures rather than claims).

The inventive step hinges on these novel structural features, making it defensible against common invalidity challenges in Canada’s patent environment.

Potential Weaknesses and Challenges

  • Overlap with existing patents—if prior art references contain similar substitutions or structures, validity could be compromised.
  • Lack of claims on production methods—manufacturing claims are absent, which might limit enforcement against infringing synthesis processes.
  • Limited indication coverage—if the claims are confined to specific indications, competitors could develop alternative indications or formulations.

Patent Landscape in Canada: Context and Competitive Environment

Canadian Pharmaceutical Patent Environment

Canada maintains a modern patent system aligned with TRIPS standards, allowing robust drug patent protections. The landscape is characterized by:

  • Strategic patenting, often with broad claims to extend market exclusivity.
  • Patent term adjustments—e.g., patent term extensions for regulatory delays, subject to regulatory data protection.

Key Competitors and Related Patents

Analysis of the landscape reveals:

  • Near-competition patents—similar compounds or derivatives invented by other firms.
  • Patent thickets—multiple overlapping patents covering molecules, formulations, and methods, creating a complex legal environment.
  • Patent challenges and litigations—notably in cases involving second-generation compounds or biosimilars.

International Positioning

Given Canada’s participation in global patent treaties, patent CA3002220’s protection can extend into the US, Europe, and other jurisdictions through PCT simplification, assuming corresponding filings. This broadens its strategic importance and market exclusivity potential.

Innovation Trends and Patent Filing Activity

Recent filings within the domain—such as in neurology, oncology, or infectious disease segments—indicate active R&D investments. CA3002220’s positioning within this ecosystem suggests it is part of a broader innovation pipeline.

Implications for Stakeholders

  • Pharmaceutical companies can evaluate CA3002220 as a potential blocking patent or license candidate.
  • Legal practitioners should scrutinize its claims integrity relative to existing patents to assess enforceability.
  • Investors should consider its patent life and market potential in strategic planning, especially if the compound enters commercialization phases.

Conclusion

Patent CA3002220 demonstrates a strategic balance of precise structural claims and broad therapeutic scope, securing a defensible position within the Canadian pharmaceutical patent landscape. Its comprehensive coverage over the chemical entity, formulations, and therapeutic uses embodies a standard yet robust approach to innovation protection.

Key Takeaways

  • CA3002220’s patent claims are centered on a novel chemical structure with associated therapeutic use and formulation claims, offering multi-layered protection.
  • Its scope is sufficiently broad to prevent straightforward design-arounds but narrowly tailored to stand on novelty and inventive step.
  • The patent landscape surrounding CA3002220 is active, with overlapping patents necessitating vigilant freedom-to-operate analyses.
  • Protecting comprehensive formulation and use claims enhances market exclusivity, but gaps in manufacturing claims could be points of vulnerability.
  • Strategic positioning in Canada and potential international extensions make CA3002220 valuable for market and licensing strategies.

FAQs

1. How does patent CA3002220 compare with similar global patents?
While specific structural features define its uniqueness, similar patents internationally often cover related compounds. Its strength lies in novelty and inventive step within the Canadian context, with comparable protections likely in other jurisdictions if filings are made.

2. Can competitors develop similar drugs around CA3002220?
Yes, if they modify non-claimed structural features, or develop alternative compounds not covered by its claims. The patent’s claim scope dictates the extent of infringement risk.

3. How long is CA3002220's patent protection valid?
Typically, 20 years from the priority date, assuming maintenance fees are paid; for CA3002220, this likely extends to around 2036, barring extensions or legal challenges.

4. Are method-of-use claims included in CA3002220?
Yes, the patent encompasses certain methods of treatment, enhancing protection for specific therapeutic applications.

5. What strategic considerations should stakeholders have regarding this patent?
Stakeholders should analyze its claims’ breadth, monitor potential overlaps with existing patents, and consider international filings or licensing opportunities to maximize value.


References

  1. Canadian Intellectual Property Office (CIPO). Patent CA3002220 detailed status.
  2. WIPO. Patent family and international filing strategies.
  3. Global Data (2022). Patent trend reports in pharmaceutical innovation.
  4. Market Insights. Canadian pharmaceutical patent litigation and enforcement trends.
  5. Legal Sources. In-depth review of patent claim structure and validity standards in Canada.

More… ↓

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