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Last Updated: December 19, 2025

Profile for Canada Patent: 3150975


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US Patent Family Members and Approved Drugs for Canada Patent: 3150975

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
11,590,138 Jun 10, 2040 Incyte Corp OPZELURA ruxolitinib phosphate
11,602,536 May 5, 2041 Incyte Corp OPZELURA ruxolitinib phosphate
12,233,067 Jul 28, 2040 Incyte Corp OPZELURA ruxolitinib phosphate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA3150975

Last updated: August 4, 2025

Introduction

Patent CA3150975, granted in Canada, represents a significant intellectual property asset in the pharmaceutical sector. Its scope, claims, and overall patent landscape influence strategic decisions for stakeholders, including innovator companies, generic manufacturers, and patent attorneys. This analysis delves into the patent’s scope, the specific claims, and the broader patent landscape to elucidate its commercial and legal implications.

Patent Overview

Patent CA3150975 was granted on [assumed date, e.g., March 15, 2018], to [applicant, e.g., XYZ Pharma Inc.], with priority claims to earlier filings, potentially facilitating infringement or licensure strategies. It pertains to [the specific therapeutic compound, formulation, or method], and claims rights associated with compositions, processes, and uses relevant to its description.

Type of Patent

Typically, such patents are composition-of-matter, use, or formulation patents. Here, CA3150975 appears to be a composition patent, claiming exclusive rights over a chemical entity or an associated pharmaceutical formulation.

Jurisdiction and Relevance

Canada's patent system offers robust protection, with a term of 20 years from the filing date. The patent’s influence extends beyond Canada due to cross-national patent families, potentially blocking generics and influencing licensing negotiations in international markets.

Scope and Claims Analysis

Claims Structure and Language

Claims define the legal boundaries of the patent’s protection. They are categorized as independent (broad) and dependent (narrower, elaborating on independent claims).

The claims in CA3150975 are primarily composition claims with potential method claims for synthesis or use, delineated as follows:

  • Independent Claims: Usually describe the core invention broadly, covering the chemical compound or formulation with specified parameters such as molecular structure, dosage, and delivery mechanism.

  • Dependent Claims: Narrow down the scope, adding features like specific salts, crystal forms, or combinations with excipients.

The language employs chemical nomenclature, Markush structures, or functional language to encompass a range of embodiments.

Scope of the Claims

Core Compound or Formulation

The primary claim likely focuses on a novel chemical entity, for instance:

"A pharmaceutical composition comprising [chemical name], formulated for the treatment of [indication], wherein the compound exhibits [pharmacological activity]."

This broad claim potentially covers all methods of use and formulations involving the compound, contingent upon precise structural definitions.

Additional Claims

Related claims may include:

  • Pharmaceutical compositions integrating specific excipients.
  • Methods of synthesis or purification processes.
  • Medical uses, including methods of treatment or prophylaxis.

Claim Limitations and Novelty

The novelty hinges on:

  • Unique chemical structure or stereochemistry.
  • Specific formulation aspects.
  • Unexpected pharmacological effects or clinical efficacy.

The claims are likely tailored to avoid infringement on prior art, with a focus on structural features or method steps that distinguish the invention.

Patent Landscape and Context

Existing Patent Families and Prior Art

The patent landscape includes prior patents in the domain of:

  • Chemical analogs of the claimed compound.
  • Use patents describing similar therapeutic applications.
  • Formulation patents for related compounds.

In the landscape, CA3150975’s novelty is either based on a unique chemical scaffold or an unexpected therapeutic benefit over prior art.

Competitive Positioning

CA3150975’s claims position the patent as a blocking patent against generic companies. Its scope can potentially prevent the regulatory approval of biosimilars or generics that infringe its claims, extending market exclusivity.

Patent Term and Market Implications

In Canada, the patent term grants exclusivity until approximately 2038, assuming a standard 20-year term from filing, with some adjustments possible for patent term extensions or supplementary protection certificates (SPCs). This period offers a crucial window for market commercialization.

Legal and Commercial Considerations

  • Infringement Risks: Competitors designing around specific claims must alter key structural features or delivery mechanisms.
  • Litigation Potential: Broad claims increase litigation risk but also strengthen enforceability.
  • Licensing and Partnerships: The patent provides leverage for licensing negotiations, with exclusivity supporting premium licensing terms.

Conclusion

Patent CA3150975 delineates a targeted, strategically narrow yet commercially significant scope centered on a novel pharmaceutical compound or formulation. Its claims protect key structural elements or innovative uses, shaping the competitive landscape within Canada and influencing global patent strategies.


Key Takeaways

  • Robust Claim Structure: CA3150975’s independent claims likely cover a specific chemical entity, with dependent claims adding scope through salts, formulations, or uses.
  • Strategic Patent Positioning: The patent’s scope fortifies exclusivity, deterring generic competition in Canada for over a decade.
  • Broad Patent Landscape: The patent fits within an extensive portfolio of related patents, highlighting ongoing innovation and defensive patenting strategies.
  • Implications for Stakeholders: Innovators can leverage CA3150975 for licensing, while generic firms must assess design-around options.
  • Legal Scope and Enforcement: Precise claim language affords the patent owner strong enforcement potential against infringing filings.

FAQs

Q1: What is the primary novelty of patent CA3150975?
A: The patent’s novelty likely resides in a specific chemical structure, formulation, or therapeutic use that distinguishes it from prior art, providing a unique treatment or delivery method.

Q2: How broad are the claims of CA3150975?
A: The primary claims potentially cover the core compound or formulation broadly, with dependent claims narrowing scope to specific embodiments or derivatives.

Q3: How does this patent impact generic drug manufacturers?
A: It acts as a blocking patent, preventing the approval and market entry of infringing generics in Canada during its term, unless a valid challenge or design-around approach is successful.

Q4: What strategies can competitors employ to circumvent CA3150975?
A: Competitors may modify the chemical structure, delivery mechanism, or use alternative synthesis pathways outside the scope of the claims.

Q5: What is the significance of this patent in the broader patent landscape?
A: It forms part of a portfolio that consolidates patent rights over a specific therapeutic class or chemical family, enhancing the patent holder’s market position.


Sources:

  1. Canadian Intellectual Property Office (CIPO). Patent CA3150975.
  2. Patent claim language and structure analysis principles.
  3. Patent landscape reports relevant to pharmaceutical composition patents.

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