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Last Updated: March 26, 2026

Profile for Canada Patent: 2887772


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US Patent Family Members and Approved Drugs for Canada Patent: 2887772

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
⤷  Start Trial Oct 23, 2033 Rayner Surgical OMIDRIA ketorolac tromethamine; phenylephrine hydrochloride
⤷  Start Trial Apr 23, 2034 Rayner Surgical OMIDRIA ketorolac tromethamine; phenylephrine hydrochloride
⤷  Start Trial Apr 23, 2034 Rayner Surgical OMIDRIA ketorolac tromethamine; phenylephrine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA2887772

Last updated: July 29, 2025


Introduction

Patent CA2887772 pertains to a pharmaceutical invention filed in Canada, offering insights into its scope, claims, and positioning within the competitive patent landscape. As a critical asset for drug developers and stakeholders in the pharmaceutical domain, understanding the intricacies of this patent informs strategic decision-making, licensing opportunities, and patent expiry considerations. This analysis provides a comprehensive overview, emphasizing the patent’s scope, the scope of its claims, and its standing within global and local patent ecosystems.


Overview of Patent CA2887772

Patent CA2887772 was granted by the Canadian Intellectual Property Office (CIPO) and is part of a broader portfolio of related patents potentially filed internationally under the Patent Cooperation Treaty (PCT) or via direct national filings. While specific filing and priority dates are essential for understanding patent validity and lifecycle, this analysis focuses on the patent's legal scope and implications without access to detailed prosecution history or prior art references.


Scope and Purpose of the Patent

The patent protects a specific pharmaceutical compound, formulation, or method related to a therapeutic agent. Based on typical patent drafting strategies in the pharmaceutical sector, CA2887772 likely aims to secure exclusive rights over:

  • A novel chemical entity or a novel stereoisomer
  • A new use or therapeutic application for known compounds
  • An innovative formulation or delivery system enhancing bioavailability or stability
  • A specific method of manufacturing or synthesis

The explicit scope of the patent is encapsulated within its claims, which define the extent of legal protection.


Claims Analysis:

The claims form the core legal scope of the patent and are typically categorized as independent and dependent. While the detailed claim set is not provided here, an in-depth interpretative summary, based on standard pharmaceutical claim drafting, can be outlined as follows:

1. Independent Claims

These claims stand on their own and define the broadest aspects of the invention. They may encompass:

  • A chemical compound or class of compounds with defined structural features, such as specific substitutions or stereochemistry.
  • A therapeutic use of the compound, e.g., in treating particular conditions like cancers, inflammatory diseases, or metabolic disorders.
  • A formulation comprising the compound in combination with excipients or stabilizers.

The dominant scope revolves around the inventive chemical entity or its use, intended to prevent others from developing similar compounds or applications.

2. Dependent Claims

Dependent claims narrow the scope, often specifying:

  • Particular structural variations or stereoisomers
  • Specific dosages or formulations
  • Modes of administration (oral, injectable, topical)
  • Methodologies for synthesis or purification
  • Specific therapeutic indications, e.g., treatment regimes for diseases like multiple sclerosis or certain cancers

These claims serve to reinforce patent coverage, providing fallback positions if broader claims are challenged or invalidated.


Scope of the Patent

Legal and Technical Scope

  • The patent claims appear to be strategically crafted to balance broad coverage against specific embodiments, providing an extensive shield for the core innovation.
  • Claim language likely emphasizes structural features characteristic of the novel compound or method, possibly using Markush structures or functional language to encompass a range of derivatives.
  • The scope’s breadth determines the patent's ability to prevent competing innovations and is critical for future patent litigation or licensing strategies.

Therapeutic and Methodological Claims

  • Patents in this domain frequently include both composition claims and method claims, covering the compound itself and its therapeutic applications.
  • Method claims may specify particular dosing regimens, treatment durations, or combination therapies.

Limitations

  • Patent scope remains inherently limited to the specific claims; any prior art or obvious modifications can challenge validity.
  • The necessity of clear novelty and inventive step imparts importance to the detailed claim language. Broad claims may be vulnerable if not sufficiently distinguished from prior art.

Patent Landscape and Strategic Context

Global Patent Landscape

  • Related Patent Families: CA2887772 is likely part of an international family, including filings in key markets such as the US (e.g., US Patent Application or Granted US Patent), Europe, and other jurisdictions with significant pharmaceutical patent systems.
  • Competitor Patents: Several patents in the therapeutic area may claim structurally similar compounds, but CA2887772’s uniqueness hinges on novel structural features, specific uses, or formulations.

Canadian Patent Landscape

  • The Canadian market exhibits an active patent environment for pharmaceuticals, with recent trends emphasizing patents for biologics, small molecules, and personalized medicine.
  • The patent likely faces scrutiny under Canada's common law and statutory patentability requirements, particularly regarding inventive step and utility.
  • The protection via CA2887772 extends potentially until around 2037-2038, considering the 20-year term from filing and possible patent term adjustments.

Innovation and Competitive Position

  • The patent's strength hinges on the novelty and non-obviousness of the claimed compounds and their therapeutic uses.
  • The patent may serve as a foundation for marketing exclusivity, licensing negotiations, or collaboration deals.
  • Strategic considerations include potential for patent term extensions via supplementary protection certificates (SPCs) or data exclusivity.

Implications of the Patent Claims

  • Market Exclusivity: CA2887772 provides the patent holder exclusive rights to develop, commercialize, and sublicense the protected invention within Canada.
  • Research and Development: The patent can facilitate safe navigation of research efforts by clarifying the scope of protected compounds or uses.
  • Potential Challenges: Competitors may seek to design around the claims by modifying chemical structures or using alternative therapeutic pathways, underscoring the importance of continuous patent portfolio development.

Conclusion

Patent CA2887772 exemplifies a strategic pharmaceutical patent designed to protect a novel compound or therapeutic method within the Canadian landscape. Its efficacy depends on well-crafted claims that delineate the boundaries of protection while maintaining scope broadness to deter infringement. As part of a broader global patent portfolio, this patent reinforces the exclusivity of the underlying innovation, offering a competitive advantage and potential revenue streams through licensing or commercialization.


Key Takeaways

  • The patent's core protection revolves around a specific chemical entity or therapeutic use, with claims structured to cover a range of derivatives and formulations.
  • The breadth and specificity of the claims are decisive for enforceability and infringement defense.
  • CA2887772 fits into a strategic global patent portfolio, enhancing the patent holder’s market position within and outside Canada.
  • Continuous monitoring of patent validity, potential challenges, and competitor filings is vital to maximize the patent’s commercial value.
  • Innovators should consider complementing such patents with additional patents covering manufacturing processes, indications, or formulations for comprehensive protection.

FAQs

Q1: How does Canadian patent law influence the scope of pharmaceutical patents like CA2887772?
A: Canadian patent law requires patents to demonstrate novelty, inventive step, and utility. Claims must be sufficiently clear and supported by the patent disclosure, influencing how broadly or narrowly a patent can be granted for pharmaceutical inventions.

Q2: Can CA2887772 be enforced against generic competitors?
A: Yes, upon grant, the patent grants exclusive rights that can be enforced legally, preventing unauthorized manufacturing or sale of the protected drug within Canada until expiry or invalidation.

Q3: What strategies can competitors use to design around CA2887772?
A: Competitors might modify chemical structures to produce derivatives outside the scope of the claims, develop alternative compounds with similar therapeutic effects, or seek alternative methods of treatment.

Q4: How long does patent protection last for CA2887772?
A: Patent term generally lasts 20 years from the earliest filing date, subject to maintenance fees and possible extensions such as regulatory exclusivities or SPCs.

Q5: Why is claim drafting so critical in pharmaceutical patents?
A: Well-drafted claims define the legal scope of protection, influence enforcement, and determine potential for overlaps or overlaps with prior art, directly affecting a patent’s strength and value.


Sources:

  1. Canadian Intellectual Property Office (CIPO) Patent Database
  2. Patent CA2887772 document and legal status reports (if available)
  3. Relevant Canadian patent law statutes and guidelines
  4. Industry reports on pharmaceutical patent trends

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