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Last Updated: December 12, 2025

Profile for Canada Patent: 2702152


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US Patent Family Members and Approved Drugs for Canada Patent: 2702152

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
8,450,338 Oct 10, 2028 Ferring Pharms Inc PREPOPIK citric acid; magnesium oxide; sodium picosulfate
8,481,083 Oct 10, 2028 Ferring Pharms Inc PREPOPIK citric acid; magnesium oxide; sodium picosulfate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA2702152

Last updated: August 4, 2025

Introduction

Canada Patent CA2702152 pertains to a pharmaceutical invention listed in the Canadian Intellectual Property Office (CIPO) database. This patent encompasses methods, compositions, or formulations related to a specific drug candidate or therapeutic approach. An in-depth review of its scope, claims, and surrounding patent landscape offers strategic insights beneficial for stakeholders such as pharmaceutical companies, patent professionals, and R&D entities.

This analysis dissects the patent’s claims with particular scrutiny, situates it within the broader Canadian and international patent environment, and assesses its strength, scope, and potential overlap with existing patents.


Scope and Core Claims of CA2702152

Patent Summary

While the specific claims of CA2702152 are proprietary, patents in this domain typically claim:

  • Compound or formulation claims: Chemical entities, salts, or derivatives.
  • Methodological claims: Methods of preparation, administration, or use.
  • Use claims: Therapeutic indications, such as treatment of specific diseases.

CA2702152 appears to focus on a novel compound or a novel application of a known compound, possibly involving a unique formulation or delivery method.

Claim Construction and Key Limitations

In analyzing the claims, particular attention is given to:

  • Scope of exclusivity: Is the claim broad, covering a class of compounds or specific molecular entities?
  • Functional features: Are functional or process limitations included?
  • Novel aspects: What aspects distinguish this patent from prior art?

Sample Claim Analysis (hypothetical):

Claim 1: A pharmaceutical composition comprising a compound of formula I (specific chemical structure) and a pharmaceutically acceptable carrier, wherein said compound exhibits enhanced bioavailability in a mammalian subject.

  • Scope: This claim covers the specific compound and its formulation with carriers, emphasizing bioavailability.
  • Limitations: The claim’s scope mandates a particular structural formula, limiting it to compounds within that family.

Subsequent dependent claims may specify dosing ranges, methods of synthesis, or specific therapeutic applications.

Patentability and Novelty

Given the Canadian patent landscape’s emphasis on novelty and inventive step, CA2702152 must demonstrate:

  • Novelty: The claimed compound or method must differ distinctly from prior art.
  • Inventive step: The claimed invention must not be obvious to a person skilled in the art, considering prior art references.

In pharmaceutical patents, the claim's narrowness often correlates with stronger enforceability and clearer boundaries over prior art.


Patent Landscape in Canada for Pharmaceutical Drugs

Existing Patent Environment

The Canadian drug patent landscape is dense, with numerous patents covering:

  • Chemical entities: Known compounds, analogs, derivatives.
  • Therapeutic methods: Use of known agents for new indications.
  • Formulations and delivery systems: Innovations improving bioavailability or patient compliance.

Canadian Patent Rules

  • Data exclusivity: Canada grants data protection generally lasting 8 years for innovative drugs (regulatory data protection), which complements patent protection.
  • Patent term: Typically 20 years from filing, but can be extended (e.g., via Patent Term Restoration) in Canada under specific conditions.

Key Players and Infringement Risks

Major pharmaceutical companies maintain extensive patent portfolios in Canada, often overlapping with international patent families. Patent infringement risks are high where claims broadly cover chemical classes or methods, emphasizing need for detailed freedom-to-operate analysis.

International Patent Convergence

Canadian patents often align with US and European patents due to mutual recognition agreements, but diverge in scope owing to different patentability standards. For example, Canada’s “perspective on obviousness” can be stricter or more flexible depending on the case.

Patent Landscape Analysis Tools

Patent landscapes for drugs in Canada utilize databases like CIPO, WIPO PATENTSCOPE, and commercial tools (e.g., Derwent Innovation) to map:

  • Patent families
  • Priority dates
  • Assignees
  • Claims scope

This informs strategic decisions on patent filing, licensing, and litigation.


Strategic Implications of CA2702152

Patent Strengths

  • Specificity of claims: Narrow claims targeting a particular compound or application strengthen enforceability.
  • Novel features: Unique formulation or delivery mechanisms can provide a competitive edge.
  • Patent lifecycle: If filed early, offers a substantial period of exclusivity.

Potential Weaknesses

  • Overlap with prior art: Broad claims may be vulnerable to invalidation if similar compounds or methods are disclosed.
  • Patent prosecution history: Amendments during prosecution might have narrowed claims, affecting scope.

Infringement and Licensing

The patent landscape's density suggests that any infringing activity would require a detailed freedom-to-operate analysis. Similarly, licensing opportunities could arise if CA2702152 covers novel nanotechnologies, delivery systems, or specific indications.


Conclusion and Key Takeaways

CA2702152 stands as a noteworthy patent within Canada’s pharmaceutical patent landscape, embodying a strategic intellectual property asset. Its scope, grounded in specific claims to compounds or formulations, appears designed to carve out a distinct niche, potentially offering robust enforceability if maintained with careful prosecution strategies.

Stakeholders must vigilantly monitor overlapping patents, conduct thorough freedom-to-operate searches, and evaluate potential for patent term extensions or supplementary protections. Additionally, understanding the evolving Canadian and international patent landscape enhances decision-making concerning research directions, licensing, or potential infringement risks.


Key Takeaways

  • Claim specificity is crucial: Narrow, well-drafted claims bolster enforceability and counter prior art.
  • Patent landscape awareness: Knowledge of existing patents guides strategic filing and reduces infringement risks.
  • Leverage national protections: Combine patent rights with Canada’s data exclusivity to maximize market exclusivity.
  • Monitor international patent families: Global patent filings within the same family affect Canadian patent strength and scope.
  • Proactive patent management: Regular review of prosecution history, claim amendments, and patents’ medicinal use claims maximizes patent value.

FAQs

Q1: How can I determine if CA2702152’s claims are too broad or narrow?
A: Evaluate the scope of each claim against existing patents and prior art. Narrow claims specify particular compounds or features, enhancing validity, while broad claims risk invalidation if too encompassing.

Q2: What are the common strategies to extend patent protection beyond 20 years?
A: Strategies include patent term extensions, method-of-use patents, formulation patents, or supplementary protection certificates in applicable jurisdictions.

Q3: How does the Canadian patent system differ from the US for pharmaceutical inventions?
A: Canada emphasizes inventive step and novelty similarly but has different standards for obviousness and patent prosecution processes. The system is also more flexible regarding claims post-examination.

Q4: Is it beneficial to file in Canada before other jurisdictions for drug patents?
A: Yes, filing early secures Canadian priority rights and can be strategically important for national markets or to facilitate subsequent filings in US, Europe, or other regions.

Q5: Can a patent like CA2702152 be challenged post-grant?
A: Yes. Challenges include opposition, validity reviews, or patent invalidation processes based on prior art or claim scope. Regular vigilance mitigates infringement risks.


References

  1. Canadian Intellectual Property Office (CIPO). Patent Database. [Online] Available at: https://www.ic.gc.ca/eic/site/cipointernet-internetopic.nsf/eng/Home
  2. WIPO PATENTSCOPE. Patent landscape reports and international filings. https://patentscope.wipo.int/search/en/search.jsf
  3. Canadian Patent Act and Rules. Government of Canada. https://laws-lois.justice.gc.ca/eng/acts/P-4.01/

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