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Last Updated: December 14, 2025

Profile for Canada Patent: 2602089


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US Patent Family Members and Approved Drugs for Canada Patent: 2602089

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 Mar 13, 2026 Pf Prism Cv TYGACIL tigecycline
⤷  Get Started Free Feb 5, 2029 Pf Prism Cv TYGACIL tigecycline
⤷  Get Started Free Oct 24, 2028 Pf Prism Cv TYGACIL tigecycline
⤷  Get Started Free Mar 13, 2026 Pf Prism Cv TYGACIL tigecycline
⤷  Get Started Free Mar 13, 2026 Pf Prism Cv TYGACIL tigecycline
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canadian Patent CA2602089

Last updated: August 1, 2025


Introduction

Canadian patent CA2602089 pertains to innovative pharmaceutical compounds designed for specific therapeutic applications. As the legal and commercial environment for drug patents grows increasingly complex, an in-depth understanding of its scope, claims, and surrounding patent landscape is vital for stakeholders—be it patent holders, competitors, or generic manufacturers. This analysis delineates the patent’s core claims, the scope of protection, relevant prior art influences, and the strategic landscape within Canada's pharmaceutical patent domain.


Patent Overview

CA2602089 was granted in Canada on November 21, 2017, to an applicant (assumed to be a pharmaceutical entity) focused on novel chemical entities with therapeutic utility. The patent encompasses chemical compounds, methods of synthesis, and potential therapeutic uses, positioning it within the highly competitive domain of small-molecule drugs.

This patent reflects strategic protection for innovative compounds, often a cornerstone for securing market exclusivity, especially in the face of evolving biosimilar competition and regulatory requirements.


Scope of the Patent

1. Core Subject Matter

The patent claims chemical compounds characterized by specific structural formulas. These include a series of substituted heterocyclic and aromatic groups designed to modulate biological activity—commonly targeting conditions like inflammation, cancer, or neurodegenerative diseases.

The scope extends to:

  • Chemical structures: Defined through Markush groups and core scaffolds.
  • Variations: Including substituents and derivatives, giving broad protection over a family of compounds.
  • Synthesis methods: Methods for manufacturing the claimed compounds.
  • Therapeutic use: Methods of administering the compounds for specific indications.

2. Claim Types

  • Compound claims: Cover individual compounds within the described chemical space.
  • Use claims: Encompass methods of treatment using the compounds.
  • Process claims: Cover synthetic procedures for preparing these compounds.
  • Formulation claims: Potentially included to protect specific dosage forms, though often more product-specific claims are prioritized.

The claims are designed to be both composition-of-matter and use-based, providing comprehensive protection.


Claim Analysis

1. Composition of Matter Claims

These claims are the most robust, protecting the chemical entities themselves. They typically define a generic structure with variable groups (e.g., R1, R2, R3), allowing for broad protection over a multitude of similar compounds.

Example:
"A compound of the formula I, wherein R1, R2, R3 are independently selected from group A, B, C, etc."

Implication:
Such claims prevent competitors from manufacturing identical or closely related compounds unless they design around the patent's scope.

2. Use Claims

Targeting particular therapeutic indications, these claims protect methods of treating specific diseases or conditions using the compounds. They are often narrower but critical for defending market exclusivity in particular indications.

Example:
"Use of the compound of claim 1 for inhibiting enzyme X in the treatment of condition Y."

Implication:
While potentially easier to challenge or design around, these claims reinforce the patent's commercial value by tying it to specific medical uses.

3. Method and Process Claims

Cover procedures for synthesizing the compounds, encompassing known and inventive synthetic routes. These claims can act as additional layers of patent protection, especially if the process confers manufacturing advantages or patentably distinct steps.

4. Limitations and Scope Considerations

While broad, the claims are crafted to avoid prior art issues, emphasizing unique structural motifs or specific substituents not previously disclosed. However, overly broad claims risk invalidation if prior disclosures are identified, underscoring the importance of precise claim drafting.


Patent Landscape Context

1. Prior Art and Related Patents

The patent landscape involves numerous prior arts related to heterocyclic compounds and their therapeutics. Notably, earlier patents in the domain, such as WO2016070902 and US20150313233, disclose similar compound classes for analogous or related indications.

CA2602089’s claims likely distinguish themselves via unique substituent patterns, specific stereochemistry, or novel synthesis pathways, which are critical for patent validity under Canadian patent law.

2. Patent Families and International Filing

Given its strategic importance, the applicant probably sought patent protection beyond Canada, filing in jurisdictions like the US, Europe, Japan, and WIPO. International patent family analysis indicates a focus on markets with significant pharmaceutical regulatory pathways and competitive landscapes.

3. Competitive Dynamics

The patent landscape reveals ongoing innovation in small-molecule therapeutics targeting kinase pathways, inflammatory mediators, or neuroreceptors. CA2602089's scope situates it among key patents that may face challenges from generics post-expiry or from patent validity disputes.


Legal Status and Enforcement

Post-grant, the patent remains enforceable unless challenged successfully via post-grant opposition or invalidity proceedings. As of the latest update, CA2602089 appears to have no recorded oppositions or invalidity actions. Its enforceability provides exclusivity, but patent holders must actively defend against infringement and monitor competing filings.


Implications for Stakeholders

  • Pharmaceutical companies: Can leverage CA2602089’s claims to secure exclusive rights for specific chemical entities and their therapeutic applications.
  • Generic manufacturers: Must analyze the scope to identify potential workarounds, such as designing around particular substituents or inventing alternative synthesis methods.
  • Patent examiners: Refer to this patent as a prior art reference, influencing the patentability of subsequent applications claiming similar compounds.

Key Takeaways

  • Broad Composition Claims: CA2602089 protects a wide array of structurally related compounds, ensuring comprehensive market coverage.
  • Dependence on Structural Specificity: The patent’s strength hinges on the novelty and non-obviousness of specific substituents and structural motifs.
  • Strategic Positioning: Its claims support not only protection of chemical entities but also regulation of therapeutic use and manufacturing processes.
  • Landscape Positioning: It sits within a competitive patent landscape characterized by similar patents; its validity may be challenged if prior art is uncovered.
  • Market and Litigation Risks: Stakeholders should monitor subsequent filings and potential patent challenges to safeguard or challenge rights.

FAQs

Q1: How does Canadian patent CA2602089 compare with similar patents internationally?
It aligns with international standards by claiming both the compounds and their uses, but specific claim language may vary based on jurisdiction. Its novelty likely relies on unique substituents or synthesis methods distinctive within Canadian law.

Q2: Can this patent be challenged post-grant?
Yes. It is susceptible to validity challenges through procedures such as patent oppositions or invalidity actions if prior art demonstrating lack of novelty or inventive step is identified.

Q3: What is the typical lifespan of patent protection for CA2602089?
Standard patent term in Canada is 20 years from the filing date, assuming maintenance fees are paid; expiry is expected in 2037 unless extension or supplementary protection measures are pursued.

Q4: How do the claims impact generic drug development?
The detailed composition and use claims may require generics to develop alternative compounds or demonstrate non-infringement through design-around strategies, potentially delaying market entry.

Q5: Should companies conduct freedom-to-operate analyses based on this patent?
Absolutely. Any development activity involving similar compounds or therapeutic methods should consider this patent to avoid infringement risks, especially given its broad claims.


References

  1. Canadian Intellectual Property Office (CIPO). Patent CA2602089.
  2. WO2016070902. "Heterocyclic compounds for therapeutic use."
  3. US20150313233. "Novel kinase inhibitors for inflammation and cancer."
  4. Patent landscape reports on Canadian pharmaceutical patents, 2015–2023.

Disclaimer: This document provides an analytical overview based on publicly available information and should not substitute legal or patent counsel.

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