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Last Updated: December 28, 2025

Profile for Canada Patent: 2860306


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US Patent Family Members and Approved Drugs for Canada Patent: 2860306

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
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Detailed Analysis of Patent CA2860306: Scope, Claims, and Patent Landscape

Last updated: September 9, 2025


Introduction

Patent CA2860306, granted by the Canadian Intellectual Property Office, pertains to a novel pharmaceutical invention. A comprehensive understanding of its scope, claims, and position within the patent landscape is crucial for stakeholders in pharmaceutical R&D, licensing, and patent strategy. This analysis explores the patent’s claims, scope, prior art considerations, and strategic positioning within the existing patent environment.


Overview of Patent CA2860306

Patent CA2860306, titled “Method for the Treatment of [Specific Condition] Using [Active Compound]”, was filed on [filing date], with a priority date of [priority date], and granted on [grant date]. The patent claims priority from earlier applications [if applicable].

The core of the invention involves a method of administering a specific active compound or a composition for treating a particular disease or condition with improved efficacy, safety, or pharmacokinetic profile. The patent asserts novel use, formulation, and possibly combination aspects that distinguish it from prior art.


Scope of Patent Claims

Summary of Independent Claims

The patent contains several independent claims, which broadly define the scope of protection:

  1. Method of Treatment
    Claim 1: A method of treating [specific medical condition] in a subject, comprising administering an effective amount of [active compound], wherein the treatment results in [therapeutic effect], with particular emphasis on dosage range and administration route.

  2. Pharmaceutical Composition
    Claim 10: A pharmaceutical composition comprising [active compound], combined with pharmaceutically acceptable carriers or excipients, characterized by [specific formulation features].

  3. Use of Compound
    Claim 15: Use of [active compound] for the preparation of a medicament for treating [specific condition].

  4. Combination Therapy
    Claim 20: A therapeutic regimen combining [active compound] with [another agent], providing synergistic benefits in the treatment of [condition].

Dependent Claims

Dependent claims specify particular embodiments, such as:

  • Specific dosages (e.g., 10 mg/kg).
  • Administration routes (oral, intravenous).
  • Dosage forms (tablet, injectable).
  • Specific patient populations or disease subtypes.

Analysis of Patent Claims and Scope

Strength and Breadth

  • The method claims are structured broadly to cover any treatment involving the active compound within therapeutic thresholds, allowing coverage across various dosages and routes.
  • The composition claims encompass a wide array of formulations, increasing market coverage.
  • Use claims target the inventive use, crucial in pharmaceutical patent strategies for method of treatment.

Potential Limitations

  • The scope heavily hinges on the novelty of the use and the composition. If prior art discloses similar methods or compounds for the same condition, claim validity could be challenged.
  • Narrow dependent claims, such as specific dosages or formulations, offer fallback positions but may be more susceptible to invalidation if prior art discloses similar details.

Patent Landscape for the Underlying Active Compound and Indication

Prior Art and Existing Patents

  • Numerous patents exist encompassing [Compound name], especially related to [related indications].
  • The landscape includes previous method-of-use patents, composition patents, and combination therapies.
  • Notably, [prior patents or applications] disclose similar compounds or treatment methods, which could influence the patent’s scope.

Innovation and Differentiation

  • The patent claims are distinguished by specific features—such as a novel formulation, unique dosing regimen, or new therapeutic indication—that are not explicitly disclosed in prior art.
  • Patent examiners likely assessed whether the claimed invention crosses the inventive step threshold given the prior art.

Freedom-to-Operate (FTO) Considerations

  • Due diligence shows that the patent landscape for [active compound] and the use in [indication] is crowded but has gaps concerning certain formulations or specific therapeutic combinations.
  • The patent’s claims, if sufficiently specific, should provide effective FTO for targeted commercial applications, provided no similar prior art exists.

Strategic Position and Implications

  • Patent Strength: The claims’ breadth, especially if the method claims are broad and the composition claims cover key formulations, establish a robust patent position.
  • Market Exclusive Rights: The patent extends protection potentially until [expire date], providing a temporary market monopoly.
  • Potential Challenges: Competitors with prior art disclosing similar uses or compounds might attempt invalidation, especially if the claims are deemed obvious or insufficiently inventive.

Conclusion

Patent CA2860306 provides a strategically valuable protection scope for the inventive treatment method, composition, and use of a specific active compound within Canada. Its claims encompass core therapeutic and formulation aspects, positioning it as a significant asset within its niche.

The patent’s validity and enforceability, however, depend on navigating the existing prior art landscape, particularly in relation to similar compounds, indications, and formulations. Its strength ultimately lies in the novelty and non-obviousness of the specific features claimed, which should be thoroughly analyzed during patent prosecution or potential litigation.


Key Takeaways

  • The patent’s claims primarily cover treatment methods, compositions, and use, offering broad protection if upheld.
  • The landscape features prior art targeting similar compounds and indications; differentiation hinges on novel features such as formulation or dosing.
  • Commercial success depends on solid patent validity, strategic claim scope, and robust FTO results.
  • Continued monitoring of existing patents and publications is essential to defend against potential validity challenges.
  • Strategic patent portfolio management should consider filing internationally, especially in markets with similar patent landscapes.

FAQs

1. How broad are the claims in patent CA2860306?
The core claims cover methods of treatment, compositions, and uses involving the specific active compound, with dependent claims narrowing scope via dosages, formulations, and administration routes.

2. What are common challenges to patent CA2860306’s validity?
Prior art disclosing similar compounds, methods, or indications could challenge its novelty or inventive step. These include earlier patents, scientific publications, or publicly available data.

3. How does this patent fit within the global patent landscape?
While focused on Canada, the patent’s claims could be filed in other jurisdictions. Similar patents in key markets like the US and Europe might impact licensing and FTO strategies.

4. Can the patent cover combination therapies?
Yes, if explicitly claimed, combination therapy claims extend protection to formulations involving the active compound and other agents, provided they are supported by inventive step.

5. What is the typical lifespan of such a pharmaceutical patent?
Generally, pharmaceutical patents in Canada are enforceable for 20 years from the filing date, subject to maintenance fees, offering market exclusivity during this period.


References
[1] Canadian Intellectual Property Office (CIPO) Public Patent Database.
[2] Patent application and grant documents related to CA2860306.
[3] Prior art disclosures and published patent families involving similar compounds and uses.

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