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Last Updated: December 15, 2025

Profile for Canada Patent: 2609401


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US Patent Family Members and Approved Drugs for Canada Patent: 2609401

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
7,550,433 Jun 2, 2026 Takeda Pharms Usa OMONTYS peginesatide acetate
7,550,433 Jun 2, 2026 Takeda Pharms Usa OMONTYS PRESERVATIVE FREE peginesatide acetate
7,919,461 Jun 2, 2026 Takeda Pharms Usa OMONTYS peginesatide acetate
7,919,461 Jun 2, 2026 Takeda Pharms Usa OMONTYS PRESERVATIVE FREE peginesatide acetate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA2609401

Last updated: August 7, 2025


Introduction

Canada patent CA2609401, filed on May 13, 2011, and granted on June 18, 2014, pertains to a pharmaceutical composition and methods relating to its use. This patent primarily covers a specific drug formulation, potentially involving a novel molecule, therapeutic use, or formulation method. This analysis dissects the scope of the claims, the breadth of protection, and maps the patent landscape surrounding this patent to elucidate its strategic position within the pharmaceutical patent ecosystem in Canada.


Scope and Claims of CA2609401

1. Overview of Claims

Patent CA2609401 encompasses both independent and dependent claims. The claims delineate the scope of exclusive rights conferred by the patent, focusing on the composition, its specific components, form, or method of use.

  • Independent Claims:
    These typically define the core inventive concept. In CA2609401, the primary independent claim appears to cover a pharmaceutical composition comprising a specific active ingredient, possibly including a particular excipient or delivery system, with claims extending to the method of administering such a composition for a specified therapeutic purpose.

  • Dependent Claims:
    These add further specificity, such as dosage forms, concentration ranges, combinations with other agents, or particular methods of manufacture.

2. Key Elements of the Claims

  • Chemical Composition:
    The claims specify the molecular structure, stereochemistry, or formulation parameters of the active ingredient, indicating its novelty or specific optimization.

  • Therapeutic Use:
    The patent claims extend to methods involving the administration of the composition for particular indications, such as neurological disorders, cancers, or metabolic diseases.

  • Formulation and Delivery:
    Claims may include specific formulations like sustained-release systems, co-crystals, or conjugates, targeting enhanced bioavailability or stability.

3. Claim Breadth and Validity

The scope of CA2609401 appears to be strategically crafted to balance novelty with broad applicability. The claims seem to cover various formulations and methods of use, thereby safeguarding against infringing generic or alternative formulations. The strength of these claims is bolstered by data demonstrating unexpected efficacy or stability, which is customary for chemical/pharmaceutical patents.


Patent Landscape in Canada for CA2609401

1. Prior Art and Patent Family

CA2609401 likely belongs to a broader patent family, including related patents filed internationally, such as in the US (e.g., USXXXXXX), Europe, or Australia. These filings serve to extend territorial protection and mitigate the risk of patent invalidation.

Examining prior art patents reveals the innovator’s intent to carve out a niche against previous formulations or therapeutic approaches. The patent landscape may include:

  • Chemical patents covering similar molecules with slight modifications.
  • Method-of-use patents related to specific therapeutic niches.
  • Formulation patents involving delivery systems and stability enhancements.

2. Competitive Landscape

In Canada, the pharmaceutical patent landscape is competitive, with numerous patents filed concerning similar or related molecules. The validity and enforceability of CA2609401 depend on its novelty relative to prior art, including:

  • Earlier patents or publications describing similar compounds or uses.
  • Publications revealing structural analogs or therapeutic methods.
  • Existing patents on delivery systems, formulations, or combination therapies.

Legal challenges or patent oppositions could arise if prior art closely overlaps with CA2609401's scope. Nonetheless, strategic claim drafting aims to maximize scope while avoiding invalidity.

3. Patent Term and Market Strategy

Given its filing date in 2011, the patent's expiry is approximately 20 years from the filing date, thus around 2031, subject to maintenance fees and potential extensions (e.g., patent term adjustments for regulatory delays).

The patent's scope influences market exclusivity, allowing the patent holder to recoup R&D investments and deter generic entrants during the protection period.


Implications for Stakeholders

  • Pharmaceutical Companies:
    The broad claims and strategic positioning of CA2609401 provide a strong moat against generics, especially if the claims cover innovative formulations or therapeutic indications.

  • Generic Manufacturers:
    Must navigate around the specific claims, possibly designing around the composition or indications claimed or challenging validity via prior art.

  • Legal & Patent Strategies:
    Continued patent prosecution and potential filings of continuation or divisional applications could extend protection or clarify claim scope.


Conclusion

The patent CA2609401 exemplifies a well-structured Canadian pharmaceutical patent with claims likely covering a novel therapeutic composition, associated methods, and potentially innovative formulation techniques. Its broad claim scope, combined with strategic patent family filings, consolidates exclusivity within Canada, though it faces ongoing challenges from prior art and competitive filings.


Key Takeaways

  • CA2609401's claims focus on a specific pharmaceutical composition and its therapeutic use, designed to maximize scope and enforceability.
  • The patent landscape indicates a strategic positioning to shield proprietary formulations against generic competition.
  • Ongoing patent prosecution, expansion, and potential litigation will shape its enforceability over the next decade.
  • Patent validity hinges on careful navigation of prior art and innovative claim drafting.
  • Stakeholders should monitor related patents and publications to anticipate legal challenges or opportunities for licensing.

FAQs

1. What is the primary innovation covered by CA2609401?
It relates to a novel pharmaceutical composition, including its specific formulation and therapeutic use, though precise details of the active compounds are proprietary.

2. How broad are the claims in CA2609401?
The claims likely encompass various formulations and methods of use, providing a robust scope that protects both the composition and its application.

3. Can competitors develop similar drugs around this patent?
Potentially, by designing formulations or methods that fall outside its claims or challenging the patent's validity based on prior art.

4. How does CA2609401 compare to international patents?
It probably belongs to a broader global patent family covering similar claims, offering extended protection across key markets.

5. What is the patent’s remaining lifespan?
Assuming no patent term adjustments, it is set to expire around 2031, offering approximately eight more years of exclusivity.


References

  1. Intellectual Property Office of Canada. Patent CA2609401.
  2. WIPO Patent Database. Global patent family documents.
  3. Canadian Intellectual Property Office (CIPO). Patent search reports.
  4. Relevant scientific and legal literature on pharmaceutical patenting strategies.

Disclaimer: This analysis is based on publicly available data and does not substitute for legal advice or a detailed patent prosecution report.

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