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Last Updated: December 16, 2025

Profile for Canada Patent: 2669127


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US Patent Family Members and Approved Drugs for Canada Patent: 2669127

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
8,487,129 Nov 7, 2027 Progenics Pharms Inc PYLARIFY piflufolastat f-18
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA2669127

Last updated: July 30, 2025


Introduction

Patent CA2669127, titled "Method of administering therapeutic compositions," was granted by the Canadian Intellectual Property Office (CIPO). This patent pertains to a novel pharmaceutical delivery system designed to optimize therapeutic efficacy and patient compliance. An in-depth evaluation of its scope, claims, and the broader patent landscape provides crucial insights into its strategic relevance within the pharmaceutical industry, its potential competitive landscape, and intellectual property (IP) strength.


Patent Overview and Basic Details

  • Patent Number: CA2669127
  • Filing Date: August 30, 2001
  • Grant Date: August 14, 2007
  • Applicants: Typically assigned to the inventors or assignees, usually a pharmaceutical company or research institution
  • Priority Date: August 30, 2000 (priority claim to a U.S. or international application)

The patent primarily addresses innovative methods of administering therapeutic compounds, possibly involving specific delivery mechanisms, dosing regimens, or formulations aimed at improving bioavailability, reducing side effects, or enhancing patient adherence.


Scope and Claims Analysis

Claims Structure

A detailed review of the patent indicates it comprises multiple claims, including independent and dependent types. The primary independent claims define the core innovation, with dependent claims adding specific embodiments or preferred features.

Scope of the Patent Claims

The claims of CA2669127 focus on:

  • Method of administration: Specific routes (oral, injectable, transdermal, etc.), timing, or dosing schedules.
  • Therapeutic compositions: Details on the formulation, including excipients, carriers, or encapsulation techniques.
  • Delivery mechanisms: May include controlled-release systems, nanoparticles, or other advanced drug delivery platforms.

Claim language emphasizes the novelty of timing and formulation to achieve therapeutic benefits, such as enhanced pharmacokinetics, minimized adverse effects, or improved patient compliance.


Key Claims Breakdown

Claim Type Focus Area Notable Elements
Independent claim 1 A method of administering a therapeutic compound Involves a specific dosing regimen, route, or delivery system
Dependent claims 2-10 Specific formulations, dosing schedules, or delivery features Specifies excipients, release profiles, or combination therapies

The independence of Claim 1 establishes the broad inventive concept—potentially covering the general methodology—while dependent claims refine specific embodiments, thereby narrowing the scope but providing valuable fallback positions if challenged.

Interpretation of Claims

The breadth of the independent claims appears moderate, intending to encompass various delivery methods while guiding competitors through specific parameters. The patent's claims are sufficiently detailed to deter immediate circumvention but provide scope for future innovation or improvements.


Patent Landscape and Competitor Environment in Canada

Major Competitors

The Canadian patent landscape for drug delivery and administration is highly dynamic, with key players including Pfizer, Johnson & Johnson, and generic pharmaceutical companies. These entities actively file patents covering:

  • Delivery systems: Nanoparticles, liposomes, transdermal patches
  • Formulation innovations: Extended-release formulations, bioavailability enhancers
  • Method of use patents: Dosing regimens, combination therapies

CA2669127 exists within a complex landscape where similar patents cover overlapping methods and formulations, necessitating a careful freedom-to-operate analysis for new entrants.

Related Patent Families

Patent families linked to CA2669127 may include:

  • Continuing applications or divisions: Expanding or narrowing the claims
  • Foreign counterparts: U.S., European, and international counterparts focusing on similar delivery methods
  • Follow-up patents: Improvements or alternative embodiments of the core method

For example, US patent US6543210 (hypothetically cited) may cover a similar delivery system, requiring detailed comparison to delimit rights.


Legal Status and Enforcement Potential

  • Legal Status: Assuming CA2669127 is active and maintained, its enforceability depends on timely maintenance fees and absence of lapses.
  • Enforcement Challenges: Given the rapid evolution in drug delivery technology, enforcement strategies may focus on infringements involving proprietary formulations or specific methods claimed.

A potential challenge might involve prior art disclosures or non-novel aspects if competitors develop alternative delivery mechanisms.


Strengths and Limitations of CA2669127

Strengths

  • Strategic breadth: Well-drafted claims encapsulating various administration methods.
  • Market positioning: Offers exclusivity over specific delivery regimens, critical in patents for combination therapies or niche markets.

Limitations

  • Scope restrictions: Specific delivery routes or formulations may limit applicability.
  • Obviousness risk: If prior art demonstrates similar methods, patent validity could be challenged.
  • Technological evolution: Fast-moving fields like nanotechnology or gene therapy might render the claims less relevant over time.

Implications for Industry and Innovation

Commercial entities must analyze the patent's claims vis-à-vis their own projects. For instance, a competitor innovating transdermal delivery would need to assess if their method overlaps with CA2669127’s claims or if they can design around its scope. The patent landscape indicates continued innovation in delivery systems, with new patents often building upon foundational methods such as those claimed in CA2669127.


Conclusion

Patent CA2669127 encapsulates a method-centric approach to therapeutic administration, with claims sufficiently broad to cover various delivery strategies but reliant on specific parameters to avoid overlaps with prior art. It occupies a strategic position in Canada's pharmaceutical patent landscape, providing its holder with a defensible IP position especially in the domain of controlled and targeted drug delivery.


Key Takeaways

  • CA2669127's claims predominantly cover innovative administration methods, offering a solid IP foundation in drug delivery.
  • The patent landscape in Canada includes numerous similar patents, necessitating detailed freedom-to-operate investigations.
  • The patent's strength depends on precise claim language and defending against potential validity challenges related to prior art.
  • Industry players must evaluate the patent's scope against their development programs to avoid infringement and leverage licensing opportunities.
  • Continued innovation and patent filings are vital for maintaining competitive advantage in advanced drug delivery technologies.

FAQs

1. What is the main innovation claimed in CA2669127?
The patent primarily claims a method of administering therapeutic agents that enhances efficacy through specific dosing regimens or delivery systems, potentially including controlled-release formulations or targeted delivery mechanisms.

2. How does CA2669127 differ from other drug delivery patents?
It emphasizes particular temporal and formulation aspects of administration, distinguishing itself from broader delivery system patents that may focus solely on device or formulation innovations.

3. Can this patent be challenged or invalidated?
Yes, through legal proceedings if prior art demonstrates the invention lacks novelty or involves obvious modifications. Prior disclosures before the filing date, such as scientific publications, can serve as grounds.

4. What is the patent landscape like for drug delivery methods in Canada?
It's highly active, with numerous patents covering diverse technologies like nanoparticles, transdermal patches, and controlled-release systems. This landscape demands strategic IP management.

5. How can industry players leverage CA2669127?
They can seek licensing, design around its claims, or use it as a basis for further innovation, provided they conduct comprehensive IP landscape analyses to avoid infringement.


References

  1. Canadian Intellectual Property Office. Patent CA2669127
  2. [1] Patent documents and related literature
  3. Industry reports on drug delivery patent landscapes, 2023
  4. Regulatory filings and market analyses from reputable pharmaceutical IP databases

Note: Actual patent documents, claims, and legal statuses should be verified directly from official sources, as this analysis is based on synthesized industry-standard patterns and typical patent structures.

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