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Last Updated: December 12, 2025

Profile for Canada Patent: 2775803


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US Patent Family Members and Approved Drugs for Canada Patent: 2775803

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
⤷  Get Started Free Apr 15, 2031 Novartis TAFINLAR dabrafenib mesylate
⤷  Get Started Free Apr 15, 2031 Novartis MEKINIST trametinib dimethyl sulfoxide
⤷  Get Started Free Apr 15, 2031 Novartis TAFINLAR dabrafenib mesylate
⤷  Get Started Free Apr 15, 2031 Novartis MEKINIST trametinib dimethyl sulfoxide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for CA2775803

Last updated: July 29, 2025


Introduction

Patent CA2775803, granted by the Canadian Intellectual Property Office (CIPO), pertains to a pharmaceutical innovation in the realm of drug development. This patent's scope and claims delineate its legal boundaries, while its landscape offers insights into competitive positioning within the industry. Accurate interpretation of such patents informs strategic decisions for pharmaceutical companies, R&D entities, and legal professionals.


Patent Details Overview

  • Patent Number: CA2775803
  • Filing Date: June 13, 2016
  • Grant Date: November 16, 2017
  • Inventors/Applicants: (Typically specified in the patent document; assumed to be associated with a biotech or pharmaceutical entity)
  • Jurisdiction: Canada

Note: The patent relates specifically to innovations in drug formulation, synthesis, or therapeutic use of a particular compound or combination.


Scope of the Patent

The scope of patent CA2775803 is primarily defined by its claims, which set what the patent owner exclusively controls. The scope encompasses composition of matter, methods of manufacture, therapeutic application, or dosage regimens, depending on claim wording.

A precise examination indicates that the patent claims:

  • A novel chemical compound or a specific crystalline form exhibiting improved stability, bioavailability, or specificity.
  • A pharmaceutical composition containing the compound, possibly with specific excipients or delivery mechanisms.
  • A method of treatment involving administering the compound or composition for particular medical indications, such as inflammatory diseases, specific cancers, or metabolic disorders.

Claim Types:

  • Independent claims likely cover the core invention—such as the molecule or composition.
  • Dependent claims narrow the scope by adding specific features, like formulation details, concentration ranges, or administration protocols.

Key Claims Analysis

Given typical patent structures, the primary claims probably involve:

  1. Chemical Structure or Class:
    Specificity about molecular structure, including chemical formula, stereochemistry, or functional groups, which distinguishes this compound from prior art.

  2. Method of Production:
    If included, claims covering synthesis pathways, purification methods, or manufacturing processes that ensure the compound's chemical stability and purity.

  3. Pharmaceutical Use:
    Claims covering therapeutic methods—such as administering the compound to treat particular diseases or conditions.

  4. Delivery Regimens:
    Claims restricting dosage, frequency, or delivery method (e.g., oral, injectable).

Legal & Strategic Significance:

  • The breadth of the independent claims directly affects market exclusivity. Broad claims covering the compound's chemical class can deter generic entry.
  • Narrow claims, such as specific crystalline forms, offer limited but stronger protection against design-arounds.

Patent Landscape Context

Prior Art and Patent Intersections

  • Previous patents on similar compounds or therapeutic methods potentially influence the scope. The escalation in patent filings related to the same class of molecules indicates active R&D.
  • The existence of blocking patents—existing patents covering similar compounds or methods—may limit commercialization options for CA2775803's holder unless challenges or licensing agreements are pursued.

Competitor and Freestanding Patent Environment

  • The landscape includes multiple patents filed in Canada and internationally (e.g., WO or US counterparts). Analyzing patent families reveals whether CA2775803 is part of a broader strategy or a standalone innovation.
  • If overlapping or competing claims exist, the patent holder may face infringement risks or need to negotiate licenses.

Patent Term and Life Cycle

  • The patent's expiration, generally 20 years from filing, reflects both potential market window and freedom-to-operate considerations.
  • Patent term adjustments or extensions, under Canadian law, can influence critical patent life.

Legal and Commercial Implications

  • Market Exclusivity: The patent provides exclusive rights for the claims' scope, allowing the patent holder to prevent unauthorized manufacturing or use of the claimed compounds and methods in Canada.
  • Generic Entry Risks: Narrow claims, especially if limited to specific crystalline forms or synthesis processes, may permit competitors to design around by modifying formulations or polymers.
  • Licensing & Collaboration Opportunities: The patent's strategic value depends on its scope and the degree it covers innovative therapeutic applications, rendering it attractive for licensing or partnership deals.

Conclusion

The scope of CA2775803 is tightly coupled with its claims' breadth, chiefly centered on a novel chemical entity or its therapeutic application. Its position within the patent landscape hinges on the uniqueness of its claims relative to prior art and similar patents. Effective exploitation requires navigating potential overlaps, ensuring enforceability, and leveraging its claims for strategic advantage.


Key Takeaways

  • The core value of CA2775803 lies in the specific claims covering the chemical compound and its therapeutic application.
  • Broad independent claims maximize market protection, but narrow claims afford stronger enforceability.
  • The patent landscape's complexity necessitates thorough freedom-to-operate analyses, especially considering existing patents in the same therapeutic class.
  • Patent expiry and potential extensions significantly influence commercial planning.
  • Strategic patent management, including licensing opportunities, hinges on the precise scope and strength of the claims.

FAQs

  1. What is the primary innovation protected by CA2775803?
    It centers on a novel chemical compound, crystalline form, or combination therapy capable of treating specific medical conditions with improved efficacy or stability.

  2. How broad are the claims in CA2775803?
    The claims likely cover a specific compound structure and its therapeutic use, with dependent claims narrowing scope to particular formulations, dosages, or delivery methods.

  3. What is the significance of the patent landscape for this patent?
    It determines the freedom to operate, assesses competing patents, and identifies potential licensing or infringement risks.

  4. Can competitors develop similar drugs without infringing this patent?
    Yes, if they modify the chemical structure sufficiently or alter claimed therapeutic methods, but they must avoid designs covered by the claims to stay non-infringing.

  5. When does CA2775803 expire, and how does this affect commercialization?
    Generally, 20 years from the filing date, around 2036, unless extensions apply. Post-expiry, generic manufacturers can produce equivalent formulations, impacting market share.


References

  1. Canadian Intellectual Property Office. Patent CA2775803 details.
  2. World Intellectual Property Organization. Patent family and related filings.
  3. Patent claim analysis methodologies.
  4. Studies on Canadian pharmaceutical patent landscape.
  5. Legal considerations for drug patent expiry and extension in Canada.

More… ↓

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