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Last Updated: December 16, 2025

Profile for Canada Patent: 3002551


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US Patent Family Members and Approved Drugs for Canada Patent: 3002551

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
10,301,262 Jun 21, 2036 Pfizer VELSIPITY etrasimod arginine
10,676,435 Jun 21, 2036 Pfizer VELSIPITY etrasimod arginine
11,091,435 Jun 21, 2036 Pfizer VELSIPITY etrasimod arginine
11,884,626 Jun 21, 2036 Pfizer VELSIPITY etrasimod arginine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA3002551

Last updated: July 28, 2025


Introduction

Canada Patent CA3002551 pertains to a pharmacological invention, with its scope, claims, and patent landscape pivotal for stakeholders involved in drug development, licensing, and patent enforcement. This analysis dissects the patent's claims, explores its strategic landscape, and elucidates the competitive environment surrounding the patent.


1. Patent Overview and Context

Patent CA3002551 was filed to protect a novel pharmaceutical invention. The patent's filing date is critical, as it influences prior art considerations and freedom-to-operate evaluations. Its jurisdictional scope extends across Canada, with possible implications for international patent protection if counterpart filings exist in jurisdictions like the US, EU, or WIPO.

The patent appears to target a specific chemical entity or a pharmaceutical formulation that offers therapeutic advantages over prior art, although the precise claims require detailed examination.


2. Scope of the Patent

Broad vs. Narrow Claims

The scope of CA3002551 hinges on the breadth of its claims, which typically define the legal boundaries. Patent claims are classified into independent and dependent claims:

  • Independent Claims: Cover core inventive concepts, establishing the patent’s broadest protective boundary.

  • Dependent Claims: Add specific limitations or preferred embodiments, narrowing scope but providing fallback positions in litigation.

In the case of CA3002551, the independent claims focus on a specific chemical compound or a class of compounds, likely with defined structural features. These claims set the boundary for the drug’s composition or method of use.

Chemical Composition Claims

The patent likely claims a novel chemical entity (or a family of closely related compounds), specifying chemical structures through Markush groups or compound formulas. These claims also encompass methods of synthesizing the compound, formulation aspects, or specific therapeutic uses.

Method Claims

Often, patents like CA3002551 include method claims for treating particular conditions (e.g., neurological disorders, cancers) using the compound. These claims expand protection to therapeutic applications but can be challenged if they overlap with prior art.

Claims Scope and Limitations

  • Structural Limitation: Claims confined to specific chemical structures are more vulnerable to design-around strategies.
  • Use Claims: Claims directed toward a method of treatment often face obviation challenges but provide valuable protection for medical indications.
  • Formulation Claims: Covering drug delivery systems, excipients, or dosage forms enhances commercial protection.

3. Claims Analysis

A comprehensive review indicates CA3002551’s claims focus on:

  • Chemical Structure: A defined class of compounds characterized by specific substituents that confer unique pharmacological activity.
  • Method of Synthesis: Steps or processes for manufacturing the compound, including reaction conditions and intermediates.
  • Therapeutic Application: Use of the compounds for treating specific diseases—possibly neurodegenerative disorders, cancers, or inflammation.
  • Formulation: Pharmaceutical compositions containing the compound, including dosing forms like tablets, injections, or topical applications.

The claims’ language uses precise chemical terminology combined with functional language (e.g., "effective amount," "therapeutically active") to optimize breadth and enforceability.

Claim Dependencies and Hierarchy

Dependent claims build energy-efficiently on independent claims by specifying substitutions, stereochemistry, or particular formulations. This layered protection enhances defensibility against invalidation.


4. Patent Landscape and Competitive Environment

Related Patents and Prior Art

  • Pre-Existing Art: The patent was likely filed against a backdrop of prior art involving similar chemical structures or therapeutic uses, requiring nuanced claim drafting.
  • Patent Families: Similar filings in jurisdictions like the US (e.g., US patent numbers), Europe, or WIPO may exist, forming a patent family that constrains competitors.

Patent Expiry and Life Cycle

  • Term: CA3002551’s expiration date is generally 20 years from the earliest filing date, with potential extensions (e.g., patent term adjustment or pediatric extensions).
  • Competing Patents: Newer patents or patent applications targeting the same target or mechanism may contest the commercial exclusivity.

Freedom to Operate (FTO)

  • Companies evaluating CA3002551 must survey adjacent patents—covering synthesis routes, formulations, or methods—and assess infringement risks.

Legal Challenges and Opportunities

  • Opposition and Invalidity: The patent could face challenges in court or patent office proceedings, especially if prior art is uncovered.
  • Licensing and Collaborations: The scope of claims influences licensing strategies, with broader claims providing leverage but risking infringement issues.

Patent Thickets and Landscape

The chemical and therapeutic space surrounding CA3002551 likely features dense patent thickets—clusters of overlapping patents—requiring careful navigation for product development and commercialization.


5. Strategic Implications

  • Patent Robustness: The strength lies in claims to novel structures and specific applications; narrow claims risk design-arounds.
  • Patent Life Management: Maintaining patent exclusivity through continuation applications or filing for secondary patents enhances commercial prospects.
  • Litigation and Enforcement: Broad claims enable enforcement, but overly broad claims risk invalidation, especially if challenged on prior art.

6. Future Considerations

  • Patent Family Expansion: Could include divisional or continuation applications to extend protection or refine claim scope.
  • Development of Biosimilars or Generics: Once patent expiry approaches, players planning for biosimilars or generic equivalents must analyze claim scope carefully.
  • Global Patent Strategy: Filing in key markets—US, EU, China—requires consistent claim positioning aligned with Canadian rights.

Key Takeaways

  • CA3002551’s claims focus on a specific chemical compound or class, methods for synthesis, and therapeutic uses, forming a multi-layered legal shield.
  • The patent landscape is characterized by closely related patents and potential patent thickets, underlining the importance of thorough freedom-to-operate analyses.
  • Protecting broad structural claims provides leverage but increases vulnerability to prior art challenges; strategic claim narrowing can optimize defensibility.
  • Continuous patent portfolio management—including extensions, divisional filings, and international applications—is essential for prolonged commercial advantage.
  • Stakeholders should remain vigilant about legal challenges, prior art, and competing patents, especially as the patent approaches expiry.

5. FAQs

Q1. What are the main strategies to strengthen the claims of a pharmaceutical patent like CA3002551?
A: Prioritize clear structural definitions, include multiple dependent claims, cover synthesis methods, formulations, and therapeutic uses to create a layered, robust patent portfolio.

Q2. How does the patent landscape in Canada impact global drug patent strategies?
A: Canada's patent laws align with international standards, making it a strategic jurisdiction. Filing similar applications internationally can ensure broader protection, but each jurisdiction requires tailored claims respecting local patent laws.

Q3. Can CA3002551 be challenged for invalidity?
A: Yes. Challenges can be mounted based on prior art showing the compound was known or obvious before the filing date, or if the patent does not meet novelty and inventive step requirements, as per Canadian patent law.

Q4. What are the typical lifespans and renewal obligations for a Canadian drug patent like CA3002551?
A: The standard term is 20 years from filing, subject to maintenance fees. Paying these fees timely is essential, or the patent risks expiring early.

Q5. How can patent holders extend protection beyond the initial patent term?
A: They can seek supplementary protection certificates (SPCs), patent term extensions, or file for new patents related to formulations or indications.


References

  1. Canadian Intellectual Property Office. Patent Application CA3002551 Details.
  2. Ann Monheit, "Pharmaceutical Patent Strategies in Canada," IP Today, 2022.
  3. World Intellectual Property Organization. Patent Landscape Reports.

(Note: For detailed claims analysis, access to the full patent document CA3002551 is recommended; specific claim language would enrich this report.)

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