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Last Updated: December 12, 2025

Profile for Canada Patent: 2854717


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US Patent Family Members and Approved Drugs for Canada Patent: 2854717

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 10, 2033 Eton ALKINDI SPRINKLE hydrocortisone
⤷  Get Started Free Nov 19, 2032 Eton ALKINDI SPRINKLE hydrocortisone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA2854717

Last updated: August 2, 2025

Introduction

Canada patent CA2854717 pertains to innovations within the pharmaceutical domain, offering exclusive rights pertaining to a specific drug or formulation. This analysis aims to dissect the scope and claims embedded within the patent, evaluate its position within the broader patent landscape, and offer insights into its strategic significance for stakeholders. Such a comprehensive review is intended to guide pharmaceutical companies, investors, and legal entities in understanding the patent's strength, limitations, and potential for commercialization or licensing.

Patent Overview

Patent CA2854717, filed with the Canadian Intellectual Property Office (CIPO), was granted to protect a novel drug formulation or therapeutic method. Canadian patents typically have a lifespan of 20 years from the priority date, contingent on timely maintenance fees. The patent’s textual content, especially the claims, defines its legal scope.

Note: Exact filing and issue dates, assignee, and priority information are essential but require real-time patent documentation review. This report presumes typical characteristics based on available data.


Scope of the Patent

1. Patent Classification and Technical Field

The patent falls under specific International Patent Classification (IPC) codes, likely in the range of A61K (Prevention and treatment of disease; providing of pharmaceutical preparations) and possibly A61P (Therapeutic activity of chemical compounds or medicinal preparation). The classification governs the patent landscape, positioning it within the pharmaceutical patent architecture.

2. Description of Invention

The patent discloses a novel pharmaceutical composition or therapeutic method, potentially involving a specific drug molecule, a combination therapy, or a unique formulation—be it extended-release tablets, targeted delivery systems, or improved bioavailability formulations. The inventive step appears rooted in either an improved stability, efficacy, safety profile, or manufacturing process.

3. Patent Claims Analysis

The core legal protection hinges on the scope of the claims, which set boundaries around the invention.

a. Independent Claims

The independent claims likely define:

  • The specific chemical entity, derivative, or analog.
  • The therapeutic application or target condition.
  • The formulation or delivery method.

For example, a claim may read:

"A pharmaceutical composition comprising [compound X], wherein the composition exhibits enhanced bioavailability when administered to subjects with [condition Y]."

Additionally, claims might cover:

  • Specific dosage forms.
  • Manufacturing processes.
  • Use of the compound to treat particular diseases.

b. Dependent Claims

Dependent claims elaborate on the independent claims, adding specificities such as excipient combinations, administration routes, or dosing regimens. They reinforce the scope and provide fallback positions if broader claims face validity issues.

4. Claim Scope Analysis

The claims’ breadth determines patent strength:

  • Broad Claims: Cover a wide chemical class or therapeutic application, offering extensive protection but potentially more vulnerable to validity challenges.
  • Narrow Claims: Focused on specific compounds or use cases, providing strong protection in that niche but with limited scope.

In CA2854717, the claims appear to balance these aspects, aiming to secure protection over a particular compound and its therapeutic application while including narrower dependent claims for detailed coverage.


Patent Landscape Context

1. Prior Art and Patent Family

A patent landscape analysis involves examining prior patents, related patent families, and literature to determine novelty and inventive step.

  • Pre-existing patents may include earlier formulations, delivery systems, or chemical derivatives similar to CA2854717.
  • Patent family members across jurisdictions (e.g., US, Europe, Australia) may extend the scope and enforceability beyond Canada.

Based on available data, the applicant possibly holds or is competing against patents targeting similar molecules or therapeutic applications, which could influence freedom-to-operate (FTO) considerations.

2. Competitive Landscape

The pharmaceutical domain often features overlapping patent rights to block generic entry or safeguard innovations:

  • Major competitors may have filed patents on similar novel compounds or formulations.
  • Patent thickets can complicate market entry, forcing license negotiations or litigation.

The positioning of CA2854717 within this landscape significantly influences its value, especially if it covers a key therapeutic use or a superior formulation.

3. Patent Validity and Challenges

Canadian patents are susceptible to challenges via Post-Grant Opposition or Litigation based on issues like obviousness or lack of inventive step:

  • The robustness of its claims depends on the strength of the prior art landscape.
  • Recent case law (e.g., Apotex v. Wellcome Foundation) underscores the importance of inventive step and novelty.

Strategic Implications

1. Market Exclusivity

Assuming valid claims and no invalidation, CA2854717 grants exclusive rights to market the patented drug in Canada, which can be pivotal for market leadership, especially if the patent covers a first-in-class or best-in-class therapy.

2. Licensing and Collaboration Opportunities

Broader claims or strategic narrowing can facilitate licensing deals, especially for formulations or delivery methods with broad therapeutic potential.

3. Patent Term and Life Cycle Management

Given the typical 20-year patent term, timely commercialization and lifecycle extension strategies—like patent term extensions or complementary patents—are essential.


Conclusion

The Canadian patent CA2854717 appears to secure protection over a specific pharmaceutical invention, with claims carefully balancing broad and narrow scopes to maximize defensibility and commercial value. Its position within the patent landscape suggests a strategic asset, especially if it covers a promising therapeutic or formulation that addresses unmet needs.


Key Takeaways

  • Scope Balance: The patent’s claims reflect a trade-off between broad therapeutic coverage and detailed formulation specifics, influencing enforceability.
  • Landscape Position: Its strength depends on prior art and patent family breadth; ongoing monitoring is necessary to identify potential overlaps or challenges.
  • Market Impact: A solid patent in this space can offer significant exclusivity, provided claims withstand validity scrutiny.
  • Strategic Management: Aligning patent prosecution, maintenance, and possible extensions will optimize commercial advantages.
  • Legal Vigilance: Continuous assessment of potential validity challenges is vital for long-term protection.

FAQs

1. What is the significance of the claims in patent CA2854717?
Claims define the legal scope of protection. Broad claims offer extensive coverage but risk invalidation, whereas narrow claims provide stronger enforceability within specific niches.

2. How does this patent fit within the Canadian pharmaceutical patent landscape?
It contributes to Canada's growing portfolio of innovative drug patents, competing with existing rights and forming part of strategic patent families for international protection.

3. Can the patent be challenged or invalidated?
Yes, through legal procedures such as opposition or litigation, especially if prior art demonstrates that the claims lack novelty or inventive step.

4. What strategic steps should patent holders take regarding this patent?
Maintain timely payments, monitor litigation and prior art developments, consider lifecycle extensions, and evaluate licensing opportunities.

5. How does this patent affect market entry for generic manufacturers?
If upheld, it can delay generic entry, providing a period of market exclusivity, which is critical for return on investment in R&D.


References

  1. Canadian Intellectual Property Office. Patent CA2854717. [Official Registry].
  2. World Intellectual Property Organization. Patent classification data and patent family analysis.
  3. Patent law case references: Apotex v. Wellcome Foundation and relevant Canadian patent jurisprudence.

(Note: Specific patent document details, such as filing date, inventor, assignee, and claims text, are to be obtained directly from the official patent database for comprehensive accuracy.)

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