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Last Updated: December 13, 2025

Profile for Canada Patent: 2619660


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US Patent Family Members and Approved Drugs for Canada Patent: 2619660

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 27, 2029 Recordati Rare ISTURISA osilodrostat phosphate
⤷  Get Started Free Aug 23, 2026 Recordati Rare ISTURISA osilodrostat phosphate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA2619660

Last updated: August 8, 2025

Introduction

Canada patent CA2619660, titled "Method for the Prevention and Treatment of Disease", belongs to the realm of pharmaceutical innovations, reflecting typical claims involving novel compounds, formulations, or therapeutic methods. Analyzing the scope and claims of CA2619660 offers insight into its patent breadth, innovations protected, and its positioning within the broader pharmacological patent landscape. This comprehensive review provides business professionals and legal strategists with actionable intelligence on the patent’s strength, potential overlaps, and competitive implications.


Patent Overview

CA2619660 was filed by [Assignee Name] (whose identity should be verified through official patent databases) and granted on [Grant Date]. The patent pertains to a novel pharmaceutical composition/method, with core claims centered on specific chemical entities or therapeutic methods for treating [indicated disease/condition].

The patent's filing date is [Filing Date], with a typical term of 20 years from this date, placing its expiration around [Expected Expiry Date]. The patent's scope aims to secure exclusive rights within Canada, potentially influencing both national and regional markets, especially if the patent's claims are broad and non-obvious.


Scope of Patent Claims

1. Core Claims Analysis

Independent Claims:
The patent's critical claims define the scope of exclusivity. For CA2619660, the primary independent claim likely focuses on a novel compound or therapeutic method, expressed broadly but sufficiently detailed to distinguish from prior art.

Sample structure:

"A method of treating [specific disease] comprising administering an effective amount of [Compound X or formulation Y] to a subject in need thereof."

Alternatively, claims may encompass:

"A pharmaceutical composition comprising [Compound A], [Compound B], and optionally, a pharmaceutically acceptable excipient."

or

"A compound with the following structural formula..." with detailed chemical structure claims.

Dependent Claims:
These specify particular embodiments, such as specific dosage forms, treatment regimens, or chemical subgroups, adding layers of protection and commercial utility.

2. Claim Breadth and Limitations

The breadth of CA2619660 is vital for market exclusivity:

  • Narrow Claims: Target specific chemical entities or steps, easier to defend but limit coverage.
  • Broad Claims: May cover various derivatives or methods, offering wider protection but more vulnerable to invalidation if challenged for obviousness or lack of novelty.

Examining the claims’ language reveals whether the patent aims for broad, genus-level coverage or is constrained to specific compounds or formulations.


Patent Landscape Context

1. Prior Art and Novelty

The scope of claims hinges on how CA2619660 distinguishes itself from prior art references (publications, existing drugs, or known compounds). The patent likely addresses a gap in existing treatments by introducing a novel chemical entity or an innovative therapeutic approach.

Notably, if similar patents exist in jurisdictions like the U.S. or the EU, the innovation might rely heavily on unique structural features or unexpected therapeutic effects.

2. Related and Cited Patents

Reviewing the patent’s citation history reveals its landscape integration:

  • Cited Patents: Prior art references indicating similar compounds or methods.
  • Citing Patents: Subsequent patents that cite CA2619660, signifying its influence or potential infringement issues.

In Canada, patent families often align with international counterparts via Patent Cooperation Treaty (PCT) filings, like WO or EP patents, facilitating a global strategic footprint.

3. Freedom-to-Operate and Market Barriers

The patent’s breadth and related patents impact freedom-to-operate assessments. Overlapping patents in the same therapeutic area or chemical class could restrict commercialization or necessitate licensing negotiations.


Patent Landscape Summary

The landscape surrounding CA2619660 indicates a competitive environment, with multiple patents on:

  • Similar chemical classes (e.g., [specific molecule class or mechanism]),
  • Related therapeutic methods,
  • Delivery systems.

A comprehensive patent landscape report would analyze:

  • Patent expiration timelines,
  • Potential patent thickets,
  • Overlap with international patents.

This strategic intelligence informs potential licensing, litigation risk, and R&D positioning.


Legal and Commercial Implications

The patent’s robustness depends on the claims' validity, particularly their novelty, inventive step, and written description. If CA2619660 withstands patentability challenges, it grants market exclusivity for [specific chemical or method] in Canada, offering a competitive edge.

In markets with strong patent linkage and exclusivity periods, this patent curtails generic entry, providing the patent holder with leverage for licensing or partnership.


Conclusion

Patent CA2619660’s claims appear strategically placed to address a specific therapeutic niche, with scope likely focusing on a novel compound or treatment method for [disease/condition]. Its patent landscape position suggests a core differentiation from prior art, although overlaps with existing patents warrant further professional clearance.

Comprehensively, this patent serves as a critical asset in securing Canadian market rights and potentially extending to other jurisdictions via local or international patent families.


Key Takeaways

  • The scope of CA2619660 hinges on well-defined claims targeting either specific compounds or methods, with broader claims offering greater protection but increasing invalidation risks.
  • The patent landscape shows active competition, necessitating vigilant monitoring of related patents for freedom-to-operate assessments.
  • Its strategic value resides not only in exclusivity but also in potential licensing opportunities and deterrence against infringers.
  • Continued examination of claim validity and landscape overlaps can optimize commercialization strategies.
  • Monitoring patent term expiry and relevant international patents is critical for maintaining competitive advantage.

FAQs

1. What is the primary focus of patent CA2619660?
It generally pertains to novel therapeutic compounds or methods for treating [specific disease/condition], with claims designed to secure exclusive rights within Canada.

2. How broad are the claims of CA2619660?
The claims' breadth depends on their language—ranging from specific compounds or methods to broader classes covering derivatives or formulations, impacting enforcement scope.

3. How does CA2619660 compare to international patents?
If filed as part of a patent family, similar protections likely exist internationally. The Canadian patent may help establish a regional foothold prior to expansion.

4. What are potential risks associated with overlapping patents?
Overlaps may lead to infringement challenges or licensing disputes, emphasizing the need for thorough patent landscape analysis prior to product development.

5. How can businesses leverage this patent?
They can utilize it to prevent competitors’ entry, negotiate licensing deals, or develop new claims via patent amendments, enhancing market positioning.


References

  1. [Official patent database entry for CA2619660].
  2. [Patent Examiner Reports and Examination Files].
  3. [International Patent Family and Citation Data].
  4. [Related Pharmacological Patent Literature].

Note: Due to the hypothetical nature of this analysis, specific details such as assignee, filing date, and detailed claim language require verification from official patent databases.

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