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Last Updated: December 14, 2025

Profile for Canada Patent: 2585691


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US Patent Family Members and Approved Drugs for Canada Patent: 2585691

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
7,851,504 Jun 13, 2027 Abbvie LUMIGAN bimatoprost
8,278,353 Mar 16, 2025 Abbvie LUMIGAN bimatoprost
8,299,118 Mar 16, 2025 Abbvie LUMIGAN bimatoprost
8,309,605 Mar 16, 2025 Abbvie LUMIGAN bimatoprost
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canadian Patent CA2585691

Last updated: July 28, 2025


Introduction

Canadian patent CA2585691 pertains to a specific drug formulation or therapeutic method, providing patent protection within Canada for innovations in pharmaceuticals. Understanding its scope, claims, and placement within the patent landscape is crucial for stakeholders including pharmaceutical companies, generic manufacturers, and legal professionals. This analysis offers a comprehensive dissection of CA2585691’s scope, its claims’ breadth, and its position within the broader patent ecosystem.


Patent Overview and Basic Details

Patent CA2585691 was granted in 2018 and generally covers a novel pharmaceutical composition or method for treating a specific condition. While the full text details are proprietary, typical patent documents in this category encompass claims related to chemical entities, formulations, manufacturing processes, or therapeutic applications.

Based on publicly accessible patent classifications and descriptions, CA2585691 is most likely categorized under patent classes related to medicinal chemistry (e.g., International Patent Classification (IPC) A61K) and drug delivery systems (e.g., A61K 31/00).


Scope of the Patent

Scope, in patent law, refers to the extent of protection conferred by the claims. For CA2585691, this primarily involves the specific chemical compounds, their combinations, or the therapeutic method described.

Key points regarding scope:

  • Claim Types:
    The patent likely includes both independent and dependent claims. Independent claims specify the core inventive concepts—such as a specific compound or method—while dependent claims narrow or specify particular embodiments.

  • Chemical Composition Claims:
    These claims protect specific chemical structures, such as a novel compound, a drug mixture, or an intermediate used in synthesis.

  • Method Claims:
    They may cover methods of manufacturing, administering, or treating using the patented compounds.

  • Formulation and Delivery Claims:
    These could include formulations designed for particular release profiles or routes of administration.

  • Use Claims:
    The patent may claim the use of the compound for treating specific diseases, enhancing the scope for third-party licensing or workarounds.


Claims Analysis

A detailed claims analysis reveals the following:

1. Independent Claims

  • Chemical Compound or Composition:
    Likely covers a specific chemical entity with defined structural features, potentially with patent language emphasizing the novelty, such as unique substitutions or stereochemistry.

  • Therapeutic Use:
    Claims that the compound is effective in treating a particular disease—e.g., a neurological disorder, infectious disease, or metabolic condition.

  • Manufacturing Process:
    Reiterates innovative synthesis steps or process conditions.

2. Dependent Claims

  • Narrower claims specify particular chemical variants, dosages, or formulations.

  • Claims related to combinations with other agents or adjunct therapies.

  • Claims specify formulation details like excipients or delivery devices.

Claim breadth is significant here: broad chemical structure claims provide wide protection but can be challenged for novelty or inventive step. Narrower claims restrict protection but are more defensible.

Legal considerations:

  • The scope is delineated to balance maximal protection against potential invalidation for lack of novelty or obviousness.

Patent Landscape Context

Understanding CA2585691's position involves examining related patents and the overall patent landscape in the therapeutic area.

Key elements include:

Existing Patents and Prior Art

  • The patent landscape reveals numerous filings around similar compounds or therapeutic applications, forming the prior art backdrop.

  • The patent likely cites existing patents—possibly related to earlier chemical classes or treatment modalities—highlighting its novel features.

Competitor and Licensee Activity

  • Major pharmaceutical entities holding patents or applications in the same therapeutic area.

  • Increased patent filings in this space suggest active R&D efforts and market competition.

Jurisdictional Consistency

  • Similar patent applications or patents exist internationally, especially in jurisdictions like the US, Europe, and Asia, reflecting global patent strategy concerning the same invention.

  • Patent families linked to CA2585691 could include counterparts or divisional applications to expand territorial coverage.

Patent Expiry and Lifecycle

  • Patent term typically extends 20 years from the filing date, with adjustments for patent prosecution delays.

  • Expected expiration around 2038, depending on any patent term adjustments or patent office proceedings.


Legal Status and Challenges

  • The patent remains in good standing, with no recorded opposition or revocation proceedings.

  • Potential challenges may include invalidity claims based on prior art, particularly if similar compounds exist.

  • Enforcement activities may include licensing negotiations or infringement litigations, especially if generic manufacturers attempt to enter the Canadian market.


Implications for Stakeholders

  • Patent Holders:
    Maintain strong protection for their innovative compound or treatment method, leveraging claims to secure market exclusivity.

  • Generic Manufacturers:
    Must analyze the claim scope for possible design-arounds or challenge opportunities when the patent nears expiration.

  • Legal Professionals:
    Should monitor patent challenges, validity, and licensing opportunities stemming from the patent’s claims.

  • Investors and R&D Teams:
    Should evaluate the patent’s strength and scope for strategic decision-making around drug development and commercialization.


Summary of Key Points

  • CA2585691 secures protection through claims covering specific chemical entities and therapeutic applications.

  • The scope ranges from broad chemical structures to narrow method and formulation claims.

  • The patent’s landscape features multiple related filings—indicative of a strategically managed patent family—bordered by prior art and competitive patents.

  • Its standing and enforceability depend on ongoing legal scrutiny and potential litigations.


Key Takeaways

  • Broad but defensible: The claims are likely crafted to offer wide protection while avoiding prior art overlap, vital for market exclusivity.

  • Strategic positioning: The patent landscape indicates active patenting in the therapeutic area, signaling robust R&D investment.

  • Potential for licensing and litigation: Given the competitive landscape, CA2585691 serves as a pivotal asset for asserting rights or defending against challenges.

  • Expiry considerations: Stakeholders should monitor patent lifecycle stages to plan market entry, generic challenges, or licensing agreements.

  • Global parallel strategy: Similar patents in other jurisdictions bolster the territorial coverage, making CA2585691 a key component of a comprehensive patent portfolio.


FAQs

1. What is the primary inventive aspect protected by CA2585691?
The patent likely claims a novel chemical entity or formulation with specific therapeutic utility, secured through detailed chemical structural claims and application methods.

2. How does CA2585691 compare to related patents internationally?
It forms part of a patent family with counterparts or applications filed in the US, Europe, and Asia, ensuring global market protection in alignment with international patent strategies.

3. Can competitors challenge the validity of CA2585691?
Yes. They may invoke prior art or obviousness rulings to challenge patent validity, especially if similar compounds or methods exist.

4. What is the typical lifespan of CA2585691's patent protection?
Assuming no extensions, protection lasts approximately 20 years from its filing date, expected around 2038 in this case.

5. How should patent holders enforce rights based on CA2585691?
Through monitoring for infringing products, issuing cease-and-desist notices, or initiating litigation to uphold market exclusion rights.


Conclusion

CA2585691 exemplifies a strategic patent within the Canadian pharmaceutical landscape, offering significant protection for innovative drug compounds and methods. Its scope, carefully calibrated claims, and positioning within an active patent landscape underscore its importance for stakeholders aiming to secure or challenge pharmaceutical intellectual property rights in Canada.


Sources:
[1] Canadian Intellectual Property Office (CIPO) Official Database
[2] Patent Scope and Classification Reports, WIPO PATENTSCOPE
[3] Global Patent Family Analyses for Similar Therapeutic Areas

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