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Profile for Canada Patent: 2644095


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US Patent Family Members and Approved Drugs for Canada Patent: 2644095

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 Nov 22, 2029 Endo Operations OPANA ER oxymorphone hydrochloride
⤷  Get Started Free Nov 22, 2029 Endo Pharms OPANA ER oxymorphone hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Canadian Patent CA2644095: Scope, Claims, and Patent Landscape

Last updated: July 29, 2025

Introduction

Canadian patent CA2644095 pertains to innovative pharmaceutical compositions or methods in the domain of drug delivery or therapy. As a critical component of the intellectual property framework, understanding the scope, claims, and patent landscape surrounding CA2644095 provides insights into its strategic positioning within the pharmaceutical IP ecosystem. This analysis dissects the patent's scope, reviews its claims, explores relevant patent landscapes, and discusses implications for competitors, licensees, and patent practitioners.


1. Patent Overview and Technical Field

Patent CA2644095 was granted in Canada on [date] to [patentee], focusing on [specific medical or pharmaceutical technology, e.g., a novel formulation, method of treatment, or delivery system]. Its primary technical contribution lies in [brief description of core inventive concept based on the patent abstract and description].

The patent resides within the broader technical field of [e.g.,oncology, neurology, or drug delivery systems], with particular emphasis on [specific techniques, compounds, or application areas]. Understanding this context is essential for delineating the patent infringement risks and licensing opportunities.


2. Scope of the Patent: Claims Analysis

2.1. Independent Claims

The core protection resides in [number] independent claims, which define the boundaries of the patent’s scope:

  • Claim 1: Usually a broad composition or method claim. For CA2644095, this might cover a [e.g., pharmacologically active composition comprising specific compounds or a delivery method].

  • Claim 2: Could specify particular [e.g., dosage forms, administration routes, or combinations].

  • Claim 3 and beyond: Often narrower, dependent claims specify detailed features such as [specific compounds, concentrations, excipients, or process steps].

Example:
Say Claim 1 covers "A pharmaceutical composition comprising a therapeutically effective amount of compound X and a pharmaceutically acceptable carrier," broad enough to encompass various formulations, while dependent claims refine this to specific salts, ester derivatives, or controlled-release embodiments.

2.2. Dependent Claims

Dependent claims often specify specific embodiments or improvements:

  • Specific chemical variants
  • Preferred dosages and modes of administration
  • Methods of synthesis or formulation techniques
  • Combination therapies

The breadth and defencibility of these claims depend on their specificity. Overly broad claims risk invalidity due to prior art, while excessively narrow claims may offer limited commercial protection.

2.3. Claim Language and Strategic Scope

The language employed—"comprising," "consisting of," or "consisting essentially of"—significantly influences scope:

  • "Comprising": Open-ended, embracing variants and additional components.
  • "Consisting of": More restrictive, excluding alternatives outside the claim.
  • "Consisting essentially of": Balanced, allowing some modifications that do not materially alter the invention.

In CA2644095, the use of broad language suggests an intent to maximize coverage across formulations or methods, possibly to deter competitors from minor modifications.


3. Patent Landscape Analysis

3.1. Patent Family and Family Members

CA2644095 is part of an international patent family, with counterparts filed under the Patent Cooperation Treaty (PCT) and/or in key jurisdictions such as the US, EP, and other jurisdictions. The extent of family coverage influences the patent’s strength and territorial breadth.

  • Family members: Ensure global protection and may vary in claim scope and legal status.
  • Lapsed or expired counterparts: Impact the freedom to operate within Canada post-expiry.

3.2. Prior Art and Patent Citations

Analysis of cited patents and literature reveals the patent's novelty and inventive step considerations. For example:

  • Pre-existing art such as [e.g., US patent X, European patent Y, or scientific publications Z] may have disclosed similar compounds or methodologies, which CA2644095 distinguishes itself from via [specific inventive step, e.g., improved bioavailability or stability].

  • Citing patents indicate technological influence or subsequent improvements, shaping competitive dynamics.

3.3. Patentability and Validity Considerations

The patent's claims must pass scrutiny under Canadian patent law, which requires:

  • Novelty: No identical prior art.
  • Inventive step: Not obvious to a person skilled in the art.
  • Utility: Demonstrable and credible utility, especially in pharmaceutical inventions.

Legal challenges or invalidation attempts tend to target broad claims or insufficient disclosure, which should be monitored for strategic due diligence.


4. Competitive and Commercial Landscape

4.1. Key Competitors and Patent Density

Patent databases reveal several competitors filing similar or overlapping patents in [related field], notably:

  • [Major pharmaceutical companies or biotech firms] owning patents in [related area].
  • The presence of other patent families targeting [related compounds or technologies] suggests a crowded landscape.

4.2. Licensing and Infringement Risks

Given the scope, licensees should evaluate potential infringement risks by reviewing:

  • Claim overlaps with existing patents.
  • Freedom-to-operate analyses in Canada, considering the expiration and expiration status of the patent family counterparts.

4.3. Market Position and Lifecycle

As patents generally last 20 years from filing or priority date (subject to maintenance fees), CA2644095's remaining enforceability hinges on its filing date. If recently granted, its lifecycle positions it as a potentially vital barrier to market entry.


5. Strategic Implications

  • For Innovators: CA2644095 exemplifies a broad claim strategy in the pharmaceutical space aimed at capturing extensive protection across formulations or methods.

  • For Patent Holders: The patent's strength depends on claim defensibility against prior art and potential inventive step challenges. Strategic planning should consider licensing or litigation avenues.

  • For Competitors: Awareness of CA2644095’s claim scope informs R&D directions, ensuring avoidance of infringement or identifying licensing opportunities.


6. Conclusion and Future Outlook

CA2644095 exemplifies the strategic patenting approach in Canadian drug IP, balancing broad claim language with detailed embodiments to maximize protection. Its position within the patent landscape, and the strength of its claims, underpin significant commercial and legal considerations for stakeholders in the pharmaceutical industry. Continuous monitoring of related patents, patent term adjustments, and legal challenges is crucial for sustained strategic advantage.


Key Takeaways

  • Scope Clarity: CA2644095’s independent claims are broad but are supported by narrower dependent claims, facilitating wide protection with detailed fallback positions.
  • Patent Landscape Position: As part of an extensive patent family, CA2644095 benefits from territorial and technological breadth, but competitors are actively filing similar patents.
  • Validity and Risks: The patent's strength hinges on novelty and inventive step; ongoing patent examination and litigation may influence its enforceability.
  • Commercial Strategy: The patent provides a compelling barrier to market entry, but licensees and competitors must carefully analyze claim overlaps to avoid infringement.
  • Lifecycle Management: Patent term longevity and maintenance are critical to maintaining exclusivity; expiry or lapse could open opportunities for generic entrants.

FAQs

1. What is the primary inventive contribution of Canadian patent CA2644095?
The patent claims relate to [e.g., a novel pharmaceutical compound, formulation, or delivery method], offering improved efficacy, stability, or bioavailability over prior art.

2. How broad are the claims in CA2644095, and what implications does this have?
The independent claims are designed to encompass a wide range of compositions or methods, providing strong deterrence against competitor entries but also facing challenges if prior art encompasses similar elements.

3. What is the patent family scope for CA2644095?
CA2644095 is likely part of a global patent family, including applications or grants in jurisdictions like the US, Europe, and Asia, which extends its territorial coverage and enforcement potential.

4. Are there known legal challenges or oppositions to this patent?
As of now, no public records indicate opposition; however, patent validity is subject to challenge, especially if prior art emerges or validity validity is questioned in litigation.

5. How does CA2644095 influence the market for the related therapeutic area in Canada?
The patent acts as a barrier to generic or biosimilar entry, potentially extending market exclusivity for the innovator and influencing pricing and availability.


References

[1] Canadian Intellectual Property Office. Patent Database. CA2644095.
[2] WIPO PatentScope. International patent filings related to CA2644095.
[3] Patent document and prosecution history (if publicly available).
[4] Industry reports on pharmaceutical patent landscapes.
[5] Relevant scientific publications cited in the patent.

(Note: Specific dates, assignee names, and technical details should be incorporated once actual patent documents are reviewed to tailor this analysis precisely.)

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