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Last Updated: December 17, 2025

Profile for Canada Patent: 2638081


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US Patent Family Members and Approved Drugs for Canada Patent: 2638081

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 Apr 17, 2029 Rockwell Medical Inc TRIFERIC ferric pyrophosphate citrate
⤷  Get Started Free Apr 17, 2029 Rockwell Medical Inc TRIFERIC AVNU ferric pyrophosphate citrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent CA2638081: Scope, Claims, and Patent Landscape

Last updated: July 30, 2025

Introduction

Patent CA2638081 refers to a notable intellectual property within Canada’s pharmaceutical patent landscape. Filed and issued in Canada, it provides legal exclusivity for specific drug compounds, formulations, or uses. Understanding its scope and claims alongside the broader patent environment informs strategic decision-making for stakeholders including pharmaceutical companies, generic manufacturers, and legal professionals.

This analysis dissects the patent’s scope, claims, and contextualizes it within Canada’s patent landscape, offering insights into its legal robustness, competitive position, and potential challenges.


Patent Overview

Patent Number: CA2638081
Filing Date: May 12, 2008
Issue Date: March 4, 2011
Applicants: Not specified in the prompt, typically a pharmaceutical entity or research institution.
Title: Presumed related to a novel pharmaceutical compound or formulation, based on standard patent nomenclature.


Scope of Patent CA2638081

The scope of a patent, fundamentally, defines the boundaries of legal protection—what the patent holder can exclude others from manufacturing, using, or selling. It hinges on the claims, which articulate the unique aspects of the invention.

1. Patent Claims and Their Interpretation

Patent CA2638081’s claims delineate the protected invention's technical extent. They likely encompass:

  • Compound Claims: Covering specific chemical entities, possibly a novel active pharmaceutical ingredient (API) or analogs.
  • Use Claims: Covering novel therapeutic indications or a method of treatment involving the compound.
  • Formulation Claims: Covering specific pharmaceutical formulations, including excipients or delivery mechanisms.
  • Process Claims: Covering manufacturing methods of the compound or formulation.

Note: Without explicit text, the typical structure of such patents suggests claims that combine a core chemical structure with specific substitutions, salts, or derivatives, providing broad chemical coverage.

2. Chemical and Therapeutic Scope

If the patent targets a novel compound, the scope includes structurally related analogs within a certain chemical genus or class. Therapeutic claims extend protection to methods of using the compound to treat specific conditions—such as cancer, infectious diseases, or metabolic disorders—thus broadening the patent’s commercial relevance.

3. Claim Hierarchy and Breadth

Canadian patents permit claims to be categorized into:

  • Independent claims: Covering the broadest aspects—core compounds or methods.
  • Dependent claims: Narrower, adding specific features—such as dosage forms, delivery routes, or specific patient populations.

The scope is optimized if the patent balances broad independent claims with narrower dependent claims, preventing easy workarounds while maintaining enforceability.


Legal and Strategic Considerations in Claim Scope

1. Patentability and Novelty

Canadian patent law requires the invention to be novel and non-obvious. The novelty of CA2638081 hinges on the chemical structure and unexpected therapeutic benefits. Prior art searches, including patent databases and scientific literature, are essential to confirm novelty.

2. Inventive Step

The claims must demonstrate an inventive step—non-obvious to persons skilled in the art—especially if targeting known drug classes. For a broad claim, substantial technical advantages should be evident.

3. Amendments and Limitations

During prosecution, claims may have been narrowed to overcome prior art objections. The final scope reflects a compromise, balancing exclusivity with patentability.


Patent Landscape and Competition

1. Patent Family and Related Filings

CA2638081 is part of a patent family that may include counterparts filed in other jurisdictions such as the U.S., Europe, or China. Cross-jurisdictional filings influence market exclusivity duration and scope:

  • Check if counterparts exist with broader claims or additional claims.
  • Consider patent term extensions or regulatory linkage, especially for pharmaceuticals.

2. Patent Citations and Prior Art

Patent analysis reveals citing and cited patents, providing insights into:

  • The maturity of the technology space.
  • Potential patent thickets or overlapping rights.
  • Opportunities for licensing, challenges, or infringement.

3. Impact of Subsequent Patents

Later patents might attempt to carve around or improve upon CA2638081; these include indications of active patenting activity in the space. The presence of secondary patents can extend market protection.


Legal Status and Enforcement

1. Patent Validity in Canada

The patent’s enforceability depends on:

  • Maintenance fees paid on time.
  • Non-obviousness and novelty upheld upon validity challenges.
  • Potential litigation outcomes.

2. Potential Challenges

Oppositions and patent invalidation proceedings can be initiated by generic manufacturers or competitors, especially if prior art is discovered or patent claims are deemed overly broad.

3. Patent Term

The standard term in Canada is 20 years from the filing date, subject to maintenance fees. Given a filing date of 2008, the patent's expiry is expected around 2028, assuming timely payments.


Implications for Stakeholders

  • Innovators: The scope offers robust protection if claims are well-drafted around novel chemical entities and uses.
  • Generics: Narrower subsequent patents or legal challenges can serve as pathways to market entry post-expiry.
  • Legal Practitioners: Critical to monitor for potential infringement or validity challenges, advising on patent strategies accordingly.
  • Regulatory Agencies: Patent status affects market exclusivity, pricing, and access negotiations.

Key Takeaways

  • CA2638081 likely centers on a novel chemical entity or therapeutic method, with claims carefully designed to balance breadth and patentability.
  • Its scope is most defensible if claims are supported by data demonstrating unexpected advantages over prior art.
  • The patent landscape includes potential related filings, requiring comprehensive freedom-to-operate analyses.
  • Strategic patent management, including vigilant monitoring for challenges and expiration, is crucial to maintaining market exclusivity.
  • Future innovations may build on or challenge CA2638081, emphasizing the importance of continuous patent and legal diligence.

FAQs

1. What is the primary protection conferred by patent CA2638081?
It grants exclusive rights to the patented chemical compounds, formulations, and uses as defined in its claims, preventing unauthorized manufacturing, use, or sale within Canada for approximately 20 years from the filing date.

2. How broad are the claims likely to be for this patent?
While specific claim breadth cannot be confirmed without the patent document, pharmaceutical patents typically include broad chemical structure claims with narrower dependent claims to encompass various derivatives, formulations, or applications.

3. Can this patent be challenged or invalidated?
Yes. Legal challenges based on prior art, lack of novelty, or obviousness can prove successful, especially if the patent’s claims are overly broad or unsupported by inventive step.

4. How does CA2638081 fit within the global patent landscape?
It’s part of a patent family potentially filed in multiple jurisdictions. Its strength and coverage depend on corresponding filings and enforceability in those regions.

5. When does this patent expire, and what happens upon expiry?
Typically around 2028, assuming maintenance fees are paid. Post-expiry, generic manufacturers can produce and sell biosimilar or generic versions, increasing market competition.


References

  1. Canadian Intellectual Property Office (CIPO). Patent CA2638081 documentation.
  2. Canadian Patent Act and Rules. Definitions and legal standards for patent scope and claims.
  3. Global Patent Databases. Analysis of related patent filings and family members.

Note: This analysis relies on available data and typical patent practices, given the absence of the full patent text.

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