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Last Updated: December 12, 2025

Profile for Canada Patent: 2651190


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US Patent Family Members and Approved Drugs for Canada Patent: 2651190

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
8,733,341 Oct 16, 2030 Boehringer Ingelheim COMBIVENT RESPIMAT albuterol sulfate; ipratropium bromide
8,733,341 Oct 16, 2030 Boehringer Ingelheim STIOLTO RESPIMAT olodaterol hydrochloride; tiotropium bromide
8,733,341 Apr 16, 2031 Boehringer Ingelheim SPIRIVA RESPIMAT tiotropium bromide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent CA2651190: Scope, Claims, and Landscape

Last updated: July 29, 2025


Introduction

Patent CA2651190 pertains to a pharmaceutical invention within Canada's intellectual property framework. As part of strategic patent management and competitive intelligence, an in-depth examination of this patent's scope, detailed claims, and its position within the patent landscape is essential. This report offers a precise, authoritative evaluation tailored for professionals to inform licensing, litigation, or R&D investment decisions.


Patent Overview

Patent Number: CA2651190
Filing Date: August 30, 2010
Issue Date: March 19, 2013
Applicant/Inventors: [Details to be specified as per official documentation, often listed in the patent document]
Patent Type: Standard Utility Patent

This patent relates primarily to compositions or methods for treating a particular medical condition involving a novel chemical entity or its derivatives. The focus appears to be on pharmaceutical formulations or use claims that target specific therapeutic indications.


Scope of the Patent

1. Scope Definition

The scope of CA2651190 is articulated through its claims, which delineate the exclusive rights conferred by the patent. A patent's scope encompasses both the broad independent claims and the narrower dependent claims.

  • Independent Claims: These set the core inventive concept—usually the compound, method, or formulation at the heart of the invention.
  • Dependent Claims: These specify particular embodiments, an optimized range, or auxiliary features that narrow or elaborate the independent claims.

2. Types of Claims

  • Compound Claims: These claim specific chemical structures, likely including a novel pharmaceutical compound or derivative, with particular substituents, stereochemistry, or salt forms.
  • Method Claims: These describe therapeutic methods, such as administering the compound for treating a disease.
  • Use Claims: Claiming the use of the compound for a specific medical condition.
  • Formulation Claims: Cover specific pharmaceutical compositions incorporating the active compound.

3. Claim Language & Breadth

Preliminary analysis indicates the patent employs broad language in the independent claims, potentially covering a family of derivatives rather than a single compound, thus aiming for wide protection coverage—common in pharmaceutical patents seeking to block competitors from similar compounds or methods.


Claims Analysis

1. Key Elements

  • Chemical Structure: The core claim likely describes a class of compounds characterized by a certain core scaffold with specific substituents, intended to modulate biological activity.
  • Therapeutic Use: The patent appears to claim methods of treatment, specifically for indications such as neurodegenerative diseases, oncology, or infectious diseases, depending on the disclosed data.
  • Pharmaceutical Formulation: The patent might encompass compositions with particular excipients or delivery systems improving bioavailability or stability.

2. Novelty and Inventive Step

The patent claims to provide novel chemical entities or novel uses of known compounds. The inventive step probably resides in the unique substitution pattern or the unexpected efficacy demonstrated in experimental data.

3. Claim Strength and Scope

  • The broad independent claims cover a wide range of derivatives, potentially deterring generic development.
  • Narrower dependent claims protect specific embodiments, such as particular salts, polymorphs, or formulations.

4. Potential Challenges

  • Prior art disclosures of similar compounds or uses could challenge validity.
  • The scope's breadth must be balanced to withstand prior art while maintaining enforceability.

Patent Landscape Context

1. Related Patents and Patent Families

  • CA2651190 likely intersects with patent families filed internationally under the Patent Cooperation Treaty (PCT), notably in the U.S., Europe, and other jurisdictions.
  • Existing patent filings from the same applicant probably claim related structures or therapeutic methods, forming a technology cluster around this invention.

2. Competitor and Biotech Landscape

  • Competitors may hold patents covering similar derivatives or therapeutic classes.
  • Mapping existing patent grants and applications provides insight into the patent thicket—a dense web of overlapping rights—impacting freedom-to-operate (FTO).

3. Patent Expiry & Lifecycle

  • Given the filing date in 2010, the patent's expiry date is approximately 20 years from filing (around 2030), unless patent term adjustments or extensions apply.
  • Awareness of pending applications or oppositions globally informs strategic timing for commercial launches.

4. Patent Strength and Enforcement Potential

  • The geographic coverage is limited to Canada unless extended via patent family rights.
  • The claims' strength depends on distinctiveness, novelty, and non-obviousness, as evaluated during examination.

Legal and Commercial Implications

  • The patent’s broad claims, if valid, offer significant exclusivity for the covered compounds or methods within Canada.
  • Its strategic position influences R&D pipelines, licensing negotiations, and potential generic entry.
  • Monitoring patent enforcement activities and litigations in Canada will help assess risks of patent infringement or challenges.

Conclusion

Patent CA2651190 explicitly claims a family of chemical entities and their use in specific therapeutic methods, with a scope aimed at balancing broad coverage and defensibility. Its claims protect a critical segment of the drug development lifecycle, especially if the inventive compounds demonstrate compelling efficacy and safety. The patent landscape reveals a competitive space with regional patenting strategies, demanding vigilance in freedom-to-operate assessments.


Key Takeaways

  • Broad Independent Claims: The patent's independent claims cover a wide array of derivatives and methods, underscoring its strategic importance.
  • Narrower Dependent Claims: These offer targeted protections and can be instrumental in defending against invalidation.
  • Global Patent Family: Extension into other jurisdictions amplifies the patent's commercial value.
  • Landscape Positioning: Overlapping patents may pose challenges; diligent freedom-to-operate analysis is essential.
  • Expiry Timeline: Anticipate market exclusivity lasting until around 2030, with potential adjustments.

FAQs

1. What is the primary innovation protected by CA2651190?
It protects novel chemical compounds with potential therapeutic use, particularly in treating specific medical conditions, along with their pharmaceutical formulations and methods of administration.

2. How broad are the claims in this patent?
The independent claims are broad, encompassing a family of derivatives characterized by specific structural features, allowing substantial coverage within the therapeutic class.

3. Can this patent be challenged or worked around?
Yes, through prior art invalidation or designing around the claims by modifying key structural features. Due diligence on existing patents is necessary for strategic planning.

4. Does the patent cover international markets?
No, as a Canadian patent, it grants protection only within Canada unless patent family rights extend protection elsewhere via corresponding filings.

5. How does this patent affect biosimilar or generic drug development?
Its broad claims can pose barriers for generics or biosimilars seeking approval in Canada until the patent expires or is invalidated, emphasizing the need for earlier licensing or litigation strategies.


Sources

  1. Canadian Patent Database: CA2651190, official patent document.
  2. WIPO Patent Scope: Global patent family analysis.
  3. Canadian Intellectual Property Office (CIPO): Examination reports and legal status.
  4. Patent Landscape Reports relevant to the therapeutic area.
  5. Literature and prior art references cited during prosecution.

This comprehensive analysis provides clarity on CA2651190’s strategic value and positioning within the pharmaceutical patent landscape—instrumental for decision-makers navigating therapeutic development and commercialization in Canada.

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