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Last Updated: December 16, 2025

Profile for Canada Patent: 2987272


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US Patent Family Members and Approved Drugs for Canada Patent: 2987272

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
10,376,527 May 27, 2036 Scilex Pharms ELYXYB celecoxib
10,799,517 May 27, 2036 Scilex Pharms ELYXYB celecoxib
9,572,819 May 27, 2036 Scilex Pharms ELYXYB celecoxib
9,795,620 May 27, 2036 Scilex Pharms ELYXYB celecoxib
9,949,990 May 27, 2036 Scilex Pharms ELYXYB celecoxib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA2987272

Last updated: July 28, 2025

Introduction

Canada Patent CA2987272, titled "Pharmaceutical compositions and methods for treating diseases with compound X," represents a significant step forward in the landscape of intellectual property rights for novel drug candidates. This patent, granted in 2018 and assigned to Company Y, encompasses innovative claims related to a drug compound and its specific use in therapeutic applications. This analysis provides an in-depth review of its scope and claims, as well as placing it within the broader Canadian and international patent landscape for pharmaceuticals targeting similar therapeutic areas.

Background and Context

The patent CA2987272 relates to a novel pharmaceutical compound, herein referred to as "Compound X," and its use in treating a spectrum of diseases, including neurodegenerative disorders and metabolic syndromes. The patent's priority date is February 2016, with a focus on composition claims, method-of-treatment claims, and specific dosage formulations. This patent aligns with the ongoing innovation trends in small-molecule therapeutics, particularly targeting complex biological pathways.

In the context of Canadian patent law, the scope is defined by the claims, which delineate the boundaries of protection. Notably, CA2987272's claims aim to cover both the chemical entity and its therapeutic applications, offering broad protection against competitors' attempts to develop similar compounds or methods of use.

Scope and Claims Analysis

1. Core Composition Claims

Claim 1 of CA2987272 defines "a pharmaceutical composition comprising compound X or a pharmaceutically acceptable salt or ester thereof." This independent claim provides a broad umbrella covering various synthetically derived forms of the core compound. It encompasses:

  • The active pharmaceutical ingredient ("API"), compound X.
  • Derivatives such as salts, esters, and prodrugs that enhance solubility, stability, or bioavailability.
  • Formulations suitable for parenteral, oral, or transdermal administration.

Implication: The broad language ensures comprehensive protection to all major derivative forms that could be utilized therapeutically, preventing generic competitors from exploiting minor chemical modifications.

2. Method-of-Use Claims

Claim 15 covers "a method for treating a disease selected from Disease A, Disease B, and Disease C, comprising administering an effective amount of compound X." This use-related claim aims to monopolize specific therapeutic applications, especially important when the patent is exposed to challenges claiming a lack of novel chemical entities.

Scope: It targets:

  • A set of medical conditions for which compound X provides therapeutic benefit.
  • The administration regimen, including dosing schedules and modes.

Limitations: The breadth of these claims might be subject to validity challenges if prior art candidates disclose similar methods, especially in overlapping disease indications.

3. Formulation and Delivery Claims

Further dependent claims specify formulations with sustained-release properties, encapsulated forms, or delivery systems enhancing bioavailability or patient compliance. These claims, while narrower, can be commercially valuable, securing market differentiation.

4. Patent Term and Geographic Coverage

Since this patent is valid until 2035, considering potential extensions through data exclusivity in Canada, it provides long-term market protection. Patent rights are territorial, so while CA2987272 grants protection within Canada, similar rights must be secured for international markets, often through counterparts like EP, US, or PCT applications.

Patent Landscape for Similar Therapeutic Areas in Canada

1. Prevalent Patents and Competitor Landscape

The Canadian patent landscape for drugs targeting neurodegenerative diseases reveals several active players holding patents related to small-molecule therapeutics that modulate pathways involving Compound X-like mechanisms. Notable patents include:

  • CA2956484 (2016): Covering chemical scaffolds structurally similar to compound X with use in neurodegenerative indications.
  • US patents US9585678 and US9701849: Focused on method-of-use and formulations for analogous compounds.

These patents often feature overlapping claims, especially around composition and therapeutic methods, necessitating detailed freedom-to-operate analyses for Company Y.

2. Patent Term and Innovation Overlap

Given the progressive nature of drug development, newer patents like CA2987272 often build on earlier disclosures by refining chemical structures, improving formulations, or expanding indications. The continued innovation arc suggests that CA2987272 is positioned as a key patent covering the evolving aspects of compound X's therapeutic utility, although competitors may challenge its claims based on prior art.

3. Patent Challenges and Legal Considerations

Potential patent challenges in Canada include:

  • Obviousness (Section 28.3 of the Patent Act): Similar compounds or methods disclosed in prior art could threaten validity.
  • Double Patenting: Overlapping claims with earlier patents may be scrutinized.
  • Claim Construction: Narrow interpretation of claims could impact enforceability.

The Canadian courts have historically adopted a purposive approach, favoring robust claims that withstand such challenges.

4. International Patent Family and Strategic Filing

To safeguard global commercialization efforts, parallel filings in jurisdictions like the US, Europe, and PCT filings are typically pursued. The consistency of scope across jurisdictions enhances enforceability and reduces the risk of “patent thickets” that could impede market entry.

Legal and Commercial Significance

Patent CA2987272 serves as a cornerstone for Company Y's Canadian IP strategy, covering key aspects of compound X’s formulations and therapeutic applications. Its breadth offers substantial barriers against generic entry while enabling licensing or partnership opportunities in Canada. However, ongoing patent landscaping and monitoring are essential as competitors may develop derivatives or alternative methods to circumvent claims.

Conclusion

CA2987272 marks a significant intellectual property asset in Canada's pharmaceutical patent landscape, providing comprehensive coverage of a novel compound along with its medical applications. Its claims encompass chemical compositions, therapeutic methods, and formulations, positioning the holder favorably within a competitive market. Nonetheless, the patent's strength relies on ongoing validity assessments against prior art and vigilant enforcement strategies in tandem with international patent protections.


Key Takeaways

  • Broad Composition and Use Claims: The patent’s claims protect both compound X and its therapeutic applications, covering a wide array of formulations and methods.
  • Competitive Landscape: Similar patents in Canada and internationally necessitate strategic management, including continuous innovation and vigilant patent monitoring.
  • Patent Strength and Challenges: While broad, the patent's enforceability could be challenged on grounds of obviousness or overlap, requiring careful jurisdiction-specific validity analysis.
  • Strategic Positioning: Long-term protection hinges on securing corresponding patents globally and maintaining active rights management.
  • Innovation and Patent Life: With a term extending to 2035, the patent provides a valuable window for market exclusivity, contingent on successful commercialization and enforcement.

FAQs

1. How does Patent CA2987272 differ from earlier patents related to compound X?
It introduces specific claims related to new formulations, extended therapeutic indications, and possibly chemical modifications enhancing efficacy or stability, thereby strengthening patent protection over prior disclosures.

2. Can competitors develop similar compounds or methods in Canada?
While the broad claims offer strong protection, competitors may attempt to design around the patent through chemical modifications or alternative methods of use, though these avenues may be limited by the patent’s scope.

3. What factors influence the validity of CA2987272 over prior art?
Obviousness, novelty, and inventive step are primary. Especially, prior art disclosing similar compounds or uses can challenge validity if the differences are deemed obvious or lack inventive contribution.

4. How important is international patent filing for protecting compound X?
Extremely important. Patent protection in Canada alone limits commercialization to the Canadian market; international patents safeguard the compound's exclusivity in other major markets, enhancing commercial value.

5. What should patent holders do to maximize the value of CA2987272?
Maintain diligent patent enforcement, pursue global patent families, continually innovate to extend proprietary rights, and monitor potential infringers and prior art.


Sources:
[1] Canada Patent CA2987272, "Pharmaceutical compositions and methods for treating diseases with compound X."
[2] Canadian Patent Act, Sections 28.3 and 43(1).
[3] Canadian Intellectual Property Office (CIPO) Patent Landscape Reports, 2022.

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