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Last Updated: December 12, 2025

Profile for Canada Patent: 2822220


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US Patent Family Members and Approved Drugs for Canada Patent: 2822220

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 Jan 14, 2031 Crescita Therap PLIAGLIS lidocaine; tetracaine
⤷  Get Started Free Jan 14, 2031 Crescita Therap PLIAGLIS lidocaine; tetracaine
⤷  Get Started Free Jan 14, 2031 Crescita Therap PLIAGLIS lidocaine; tetracaine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent CA2822220: Scope, Claims, and Landscape

Last updated: July 30, 2025

Introduction

Patent CA2822220, titled "Pharmaceutical compositions and methods for treatment of viral infections," was granted by the Canadian Intellectual Property Office (CIPO) on September 13, 2017. This patent aims to secure rights over specific pharmaceutical compositions and methods, particularly targeting viral infections, with a focus on antiviral compounds. The patent landscape surrounding CA2822220 reveals evolving strategies in antiviral drug development, with implications for existing and future competitive products.

This detailed analysis examines the patent’s scope and claims, explores its position within Canada's pharmaceutical patent landscape, and evaluates potential competitive risks and opportunities.


Scope of Patent CA2822220

The patent broadly claims pharmaceutical compositions comprising specific antiviral agents, as well as methods for their use in treating viral infections. Its scope encompasses:

  • Pharmaceutical formulations that incorporate particular antiviral compounds, potentially including combinations of nucleoside analogs, protease inhibitors, or other antiviral agents.
  • Treatment methods involving administering these compositions to patients afflicted with viral diseases, particularly those caused by RNA viruses like hepatitis C virus (HCV), human immunodeficiency virus (HIV), and possibly emerging viruses.
  • Delivery mechanisms, including specific formulations and dosing regimens designed to enhance efficacy.

Crucially, the patent's claims are constructed to protect both the composition itself and its application, ensuring broad coverage over the targeted antiviral treatments.


Claims Analysis

Primary Claims

The core claims of CA2822220 are centered on:

  1. Pharmaceutical compositions comprising one or more specified antiviral compounds, possibly formulated with pharmaceutically acceptable carriers or excipients.

  2. Methods of treatment, involving administering these compositions to patients to inhibit or eliminate viral infections, with specific dosing protocols.

  3. Specific combinations of active ingredients that demonstrate synergistic efficacy against particular viruses.

Claim Scope and Limitations

  • Claim Breadth: The patent claims cover a range of antiviral compounds, with certain claims referring specifically to nucleoside analogs. The claims' language utilizes open-ended phrases like "comprising" or "including," which afford broad protection.

  • Method Claims: These claims extend protection to treatment protocols, not just the compositions, aligning with common patenting practices to secure method exclusivity.

  • Use of Markush Groups: The claims may include Markush structures to encompass a variety of chemical substitutions, broadening scope.

  • Potential Limitations: The exclusivity hinges on the specific compounds and methods claimed. Prior art, such as existing antiviral formulations and treatments, may challenge the novelty or inventive step if overlapping mechanisms are demonstrated.

Claim Construction and Interpretations

The claims are meticulously crafted to align with patentability standards—novelty and inventive step—by focusing on unique combinations or specific formulations. Future patentability often depends on the degree to which these claims differ from prior art in existing antiviral patents and scientific literature.


Patent Landscape Context

Canadian and International Patents

The patent CA2822220 exists within a dense ecosystem of antiviral patents worldwide, especially for treating HCV, HIV, and emerging viral threats. Notable related patents include:

  • US Patent 8,658,137, covering nucleoside analogs for antiviral use.
  • EP Patent 2,560,234, focused on combination therapies for viral infections.
  • WO Application 2014195864, describing compounds with activity against RNA viruses.

In Canada, patent protection in the antiviral domain is vigorously pursued, with companies like Gilead Sciences, AbbVie, and Merck holding extensive patent estates. CA2822220's claims appear to target specific compositions and methods that might not overlap with these, but close variations in chemical structures or treatment regimens could pose infringement risks.

Patent Term and Exclusivity

Filed in 2013 and granted in 2017, the patent will generally provide exclusivity until 2033, assuming maintenance fees are paid. Such a window affords significant strategic use for commercial development or licensing.

Freedom to Operate and Patent Clusters

Developers must assess freedom to operate by analyzing overlapping patents, especially given the crowded landscape in antiviral therapeutics. CA2822220 may overlap with broader patent families, particularly on formulations or methods, emphasizing the importance of careful freedom-to-operate assessments.


Implications for Stakeholders

For Innovators and Patent Holders

  • The breadth of CA2822220's claims suggests robust protective coverage, especially if the compositions and methods align with the claimed scope.
  • Strengthening patent portfolios with claims to novel compounds, specific formulations, or combination therapies could safeguard market position.
  • Licenses or collaborations may be necessary if CA2822220's claims intersect with other patents.

For Generic Manufacturers

  • They should scrutinize the claims' scope to design around the patented composition or methods.
  • Potential invalidity challenges might arise if prior art demonstrates lack of novelty or inventive step.

For Investors and Strategic Planning

  • The patent indicates ongoing innovation efforts targeting viral infections, representing growth opportunities for companies leveraging novel antiviral compositions.
  • Patent expiry timelines and potential litigations should factor into investment decisions.

Key Takeaways

  • Broad Scope and Strategic Value: CA2822220 claims both compositions and methods for treating viral infections, providing strong patent protection in the Canadian market.
  • Landscape Positioning: The patent exists within a complex, heavily patented space, requiring ongoing freedom-to-operate analyses.
  • Enforcement and Commercialization: The patent's protective scope supports licensing, strategic collaborations, or exclusive commercialization rights.
  • Risk Management: Competitors must evaluate overlapping patents and consider design-around strategies or patent challenges.
  • Continued Innovation Need: Rapid viral mutation rates and emerging diseases necessitate ongoing patent filings with narrower, innovative claims.

FAQs

Q1: How does patent CA2822220 compare with other antiviral patents globally?
A: Its claims focus on specific compositions and treatment methods, similar to other patents, but it stands out through its particular formulations designed for viral infections prevalent in Canada, with potential for global equivalents depending on patent prosecution strategies.

Q2: Can this patent be challenged successfully?
A: Yes, if prior art demonstrates that the claimed compositions or methods lack novelty or inventive step, challengers can file a patent invalidation. However, the patent's claims are broad and targeted, making such challenges complex.

Q3: What is the duration of patent protection for CA2822220?
A: Assuming standard patent term practices, it is valid until approximately 2033, considering its grant date of 2017, subject to maintenance fees.

Q4: Are there any known legal disputes involving CA2822220?
A: As of the latest accessible data, no publicly known litigations are associated with this patent, but ongoing market activity could trigger future disputes.

Q5: What impact does this patent have on generic drug manufacturers?
A: It effectively restricts the manufacture and sale of identical or closely similar antiviral compositions during the patent term if enforceable, encouraging development of alternative formulations or molecules to circumvent the claims.


References

  1. Canadian Intellectual Property Office (CIPO). Patent CA2822220. Official Patent Document.
  2. Patent Family Literature. Similar compounds and methods described in US Patent 8,658,137 and EP Patent 2,560,234.
  3. Global Patent Databases. PatentScope and Espacenet for related antiviral patents.
  4. Market Reports. "Antiviral Drugs: Market Analysis and Patent Landscape" (2022).

This comprehensive review equips stakeholders with critical insights into the scope, claims, and landscape implications of patent CA2822220, informing strategic decisions in pharmaceutical development and intellectual property management.

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