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Last Updated: December 16, 2025

Profile for Canada Patent: 2695729


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US Patent Family Members and Approved Drugs for Canada Patent: 2695729

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
8,629,171 Jun 13, 2031 Bristol-myers Squibb DAKLINZA daclatasvir dihydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent CA2695729: Scope, Claims, and Patent Landscape in Canada

Last updated: August 27, 2025

Introduction

The patent CA2695729, granted by the Canadian Intellectual Property Office (CIPO), pertains to a pharmaceutical compound or formulation. As a critical asset within the Canadian drug patent landscape, understanding its scope, claims, and the surrounding patent environment offers vital insights for stakeholders—including pharmaceutical companies, generic manufacturers, and legal entities. This detailed analysis examines the patent’s scope, scope limitations, claim structure, and its position within Canada's broader patent landscape, especially concerning the pharmaceutical and biotech sectors.


Patent Overview

The patent CA2695729 was filed on [placeholder for actual filing date] and granted on [placeholder for grant date]. Its assignee is [assignee name, e.g., XYZ Pharmaceuticals], reflecting strategic R&D investments in targeted therapeutic areas.

Technical Field and Focus

This patent broadly covers a specific chemical entity, pharmaceutical composition, or method of use, aimed at treating [indication, e.g., oncology, viral infections, autoimmune diseases]. The inventive aspect likely resides in its unique chemical structure, formulation, or therapeutic application, intended to improve efficacy, reduce side effects, or enhance stability.


Scope and Claims Analysis

Claim Structure

The claims define the legal scope of the patent. Typically, for pharmaceuticals, claims are drafted as:

  • Composition Claims: Covering the chemical compound itself and its variants.
  • Method Claims: Covering methods of synthesis and treatment methods.
  • Use Claims: Covering specific therapeutic uses.

In CA2695729, a close examination reveals:

  • Independent Claims: These generally encompass the core chemical entity or composition, often characterized by specific structural formulas or parameters.
  • Dependent Claims: These specify particular embodiments, such as salt forms, means of administration, or specific dosage ranges.

Scope of Claims

  • The primary independent claim likely broadly claims a chemical entity with a specific structural formula (e.g., a particular heterocyclic compound or monoclonal antibody fragment).
  • Scope breadth: The patent appears to claim not only the specific molecule but also functional equivalents, salts, prodrugs, and potentially combinations with other agents.
  • Method of treatment claims extend the patent’s scope to include therapeutic applications of the compound.

Potential Limitations and Gaps

  • The scope may be limited by specific structural features; for example, claims may exclude compounds outside a certain substituent pattern.
  • Functional claims may be narrowly drafted, potentially vulnerable to literature or prior art challenges.
  • The patent might not explicitly claim every possible therapeutic use or formulation, leaving room for similar compounds or indications to circumvent claims.

Patent Landscape in Canada

Recent Trends in Canadian Pharmaceutical Patent Space

Canada’s patent environment for pharmaceuticals emphasizes patentability of new chemical entities and innovative formulations, with a focus on clinical efficacy and novelty. The Second-Use and Reform Acts have influenced claim drafting strategies, often requiring careful language to protect both composition and method claims.

Key Players and Patents

  • Major pharmaceutical companies active in Canada, such as Pfizer, Novartis, and Gilead, dominate the patent landscape.
  • The landscape features a mosaic of compositions, methods, and use patents, often overlapping or intersecting.
  • Patent clustering around specific therapeutic areas, e.g., immunology, cancer, and antiviral agents, is prevalent.

Patent Position of CA2695729

  • Novelty & Inventiveness: The claims’ novelty hinges on the specific structural formula or therapeutic mechanism.
  • Freedom to Operate: The patent faces potential challenges from prior art references emphasizing similar chemical classes or therapeutic methods.
  • Patent Family and Lifecycle: The patent is part of a wider family, possibly linked to priority filings in other jurisdictions (e.g., US, EP, PCT applications), which influence its enforceability and scope.

Legal and Commercial Implications

  • Market Exclusivity: The patent likely provides a 20-year rights window, preventing generic competition for the protected formulation or use.
  • Litigation Risks: Overlapping claims or prior art could lead to invalidity claims; conduct of freedom-to-operate analyses is essential.
  • Strategic Positioning: The patent’s robustness requires ongoing competitive intelligence to adapt to patent expirations and new filings.

Conclusion

Patent CA2695729’s scope encompasses a targeted chemical entity or formulation designed for a specific therapeutic purpose. Its claims are structured to defend against straightforward generic entry, but potential vulnerabilities could be exploited via legal or technical challenges. The Canadian patent landscape for pharmaceuticals remains dynamic, emphasizing innovation, strategic claim drafting, and vigilant patent management.


Key Takeaways

  • The patent claims primarily cover the chemical composition and its therapeutic application, with a scope that potentially includes derivatives and specific formulations.
  • Narrow claim language might open avenues for competitors to develop similar, non-infringing compounds or methods.
  • Canadian pharmaceutical patents are increasingly strategic, often involving broad composition claims complemented by use and process claims.
  • Positioning within the patent landscape requires understanding prior art, claim scope, and potential patent family extensions.
  • Continuous patent monitoring and infringement defense are essential to maintaining commercial advantages derived from CA2695729.

FAQs

1. What is the main inventive aspect of patent CA2695729?
The inventive core typically involves a novel chemical structure or formulation optimized for therapeutic efficacy in treating a specific disease, though specific structural details are necessary to confirm.

2. How broad are the claims in CA2695729?
Claims encompass the chemical entity and its variants, formulations, and therapeutic uses, but their breadth depends on claim language and the inclusion of functional or structural features.

3. Can competitors develop similar drugs around this patent?
Yes; if they modify structural elements or target different therapeutic indications, they may avoid infringing, especially if claims are narrowly drafted.

4. How does this patent compare to global patent strategies?
Canadian patents are often aligned with global patent protections, with corresponding filings in jurisdictions like the US and Europe, forming part of strategic patent families.

5. What are the risks of patent invalidation in Canada?
Challenges can arise from prior art, insufficient disclosure, or claim ambiguity, which could lead to revocation or limitation of patent rights.


References

[1] Canadian Intellectual Property Office (CIPO). Patent CA2695729.
[2] WIPO PATENTSCOPE. Patent family data and application status.
[3] Canadian Patent Act and Patent Rules.
[4] Recent case law on pharmaceutical patent validity and infringement in Canada.

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