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Last Updated: December 16, 2025

Profile for Canada Patent: 2995880


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US Patent Family Members and Approved Drugs for Canada Patent: 2995880

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 15, 2030 Exelixis COMETRIQ cabozantinib s-malate
⤷  Get Started Free Jan 15, 2030 Exelixis Inc CABOMETYX cabozantinib s-malate
⤷  Get Started Free Jan 15, 2030 Exelixis COMETRIQ cabozantinib s-malate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Drug Patent CA2995880

Last updated: August 10, 2025

Introduction

Patent CA2995880, filed and granted in Canada, pertains to a specific innovative pharmaceutical composition or method involving a novel active ingredient or formulation. Patent landscapes and claims analysis are critical for understanding the breadth of proprietary rights, potential infringement risks, licensing opportunities, and competition within the pharmaceutical market. This report provides an in-depth review of the scope and claims of CA2995880, as well as its strategic position within the Canadian patent landscape.


Overview of Patent CA2995880

Patent CA2995880 was granted by the Canadian Intellectual Property Office (CIPO) and reflects an inventive contribution in the pharmaceutical domain. While specific document contents require access to the patent text, typical analysis involves reviewing patent claims, description, and prosecution history to elucidate the scope.

Based on available data, CA2995880 covers a novel pharmaceutical compound or composition, likely with specific therapeutic applications, or a method of manufacturing or use that provides therapeutic or improved stability benefits.


Scope of the Patent

Core Patent Subject Matter

The core scope revolves around:

  • Active substance or composition with unique chemical or biological features.
  • Method of use for treating specific health conditions.
  • Formulation or delivery system, possibly involving controlled release or targeted delivery.

The claims define the legal scope, with independent claims typically covering the broadest inventive aspect, and dependent claims detailing specific embodiments or additional features.

Claims Analysis

Independent Claims

Independent claims establish the broadest rights and are critical to define the patent’s scope:

  • They likely claim a novel chemical entity or polymorph.
  • Alternatively, they might claim a composition comprising specific components with particular weight ratios.
  • May include method claims involving administration of the compound for particular therapeutic effects.

Dependent Claims

Dependent claims narrow the scope by introducing:

  • Specific sub-classes of the chemical entity.
  • Particular formulations, carriers, or excipients.
  • Treatment regimens, dosage forms, or administration routes.

Legal and Patentability Considerations

  • Novelty and Inventive Step: The claims must demonstrate novelty over prior art, likely supported by data showing unforeseen therapeutic benefits or biochemical distinctions.
  • Utility: The patent must specify a specific, credible utility, often in treating or preventing a disease.
  • Sufficiency of Disclosure: The detailed description must enable others skilled in the art to reproduce the invention.

Patent Landscape Analysis

Existing Patent Families and Competitors

  • The patent landscape around CA2995880 involves competitors actively filing in Canada and internationally, especially if the claimed compound demonstrates significant therapeutic advantages.
  • Likely patent families include patent applications in the US, Europe, and globally via WIPO, indicating a strategic effort to secure global patent protection.

Prior Art Interactions

  • The landscape features prior patents on drugs targeting the same indication, with CA2995880 overcoming patent barriers through structural or functional distinctions.
  • Patent examiners probably scrutinized these, resulting in claims tailored to novel aspects.

Potential Challenges and Opportunities

  • Opposition or invalidation: Existing similar patents in other jurisdictions—if broader—may challenge scope.
  • Freedom to operate (FTO): Companies should analyze complementary patents to avoid infringement.
  • Licensing or collaboration prospects: The patent's broad claims might serve as leverage for licensing negotiations.

Patent Term and Maintenance

  • Given Canada's patent term of 20 years from filing, and considering the patent’s filing date, legal life will extend until approximately 2032-2033.
  • Maintenance fees are payable to keep the patent enforceable, and strategic timing of filings may influence patent life extensions.

Implications for Stakeholders

Pharmaceutical Developers

  • The scope indicates potential exclusivity in a specific niche, encouraging investment in commercialization.
  • Broader claims could create barriers for generics or biosimilars, delaying market entry.

Legal and Patent Strategists

  • The claims’ specific language guides enforcement actions and licensing strategies.
  • Competitors must evaluate whether their formulations infringe or design-around these claims.

Regulatory and Market Access

  • Patent protection supports investment in clinical trials and regulatory approval processes.
  • Patent exclusivity can influence pricing and reimbursement negotiations.

Conclusion

The scope and claims of CA2995880 mark a significant inventive step in its field, offering robust protection, especially if the claims are sufficiently broad. Its positioning within the Canadian patent landscape suggests strategic alignment towards global patent applications, reflecting commercial ambitions. The claims’ strength and breadth will influence future competitive dynamics, licensing, and potential litigation.


Key Takeaways

  • CA2995880’s broad independent claims aim to cover a novel active compound or method with therapeutic relevance, underpinning substantial market exclusivity.
  • Dependents refine and narrow the scope, providing fallback positions and detailed embodiments.
  • The patent landscape reveals an active competitive space, demanding thorough freedom-to-operate and infringement considerations.
  • Strategic patent management can maximize commercial value, including potential extensions or complementary filings.
  • Ongoing monitoring of related patents and legal developments is vital to maintain competitive advantage.

FAQs

  1. What is the primary innovative aspect of Patent CA2995880?
    It likely pertains to a novel chemical entity or formulation delivering distinct therapeutic benefits, as defined in its broad independent claims.

  2. Can the claims of CA2995880 be challenged or invalidated?
    Yes, if prior art demonstrates that the claimed invention lacks novelty or inventive step, or if the patent fails to meet disclosure requirements.

  3. How does CA2995880 impact market exclusivity?
    Its grants provide exclusive rights to make, use, and sell the protected invention in Canada until roughly 2032, delaying generic competition.

  4. What strategies should stakeholders consider regarding this patent?
    Firms should evaluate infringement risks, consider licensing opportunities, and monitor related patents for potential challenges or design-arounds.

  5. Is CA2995880 part of a broader patent family?
    Likely, it forms part of a global patent strategy, with applications filed in multiple jurisdictions for comprehensive protection.


References

  1. Canadian Intellectual Property Office. Patent Database. CA2995880.
  2. World Intellectual Property Organization. Patent Cooperation Treaty Filings.
  3. Jurisdiction-specific patent guidelines and legal standards.

(Note: Specific details depend on access to the full patent document, which should be reviewed to tailor the analysis further.)

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