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Last Updated: December 16, 2025

Profile for Canada Patent: 2832342


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US Patent Family Members and Approved Drugs for Canada Patent: 2832342

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
9,629,842 Apr 30, 2032 Chimerix MODEYSO dordaviprone hydrochloride
RE46290 Apr 30, 2032 Chimerix MODEYSO dordaviprone hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canadian Patent CA2832342

Last updated: October 7, 2025

Introduction

Canadian patent CA2832342 pertains to a novel pharmaceutical invention, with specific claims aimed at protecting a unique formulation or method. This analysis offers an in-depth review of its scope, claims, and the broader patent landscape, enabling professionals to understand its strategic position within the pharmaceutical patent ecosystem.

Patent Overview

CA2832342 was granted to secure intellectual property rights over a specific drug composition or method of use. While detailed specifics of the patent’s claims are essential, generally, such patents relate to formulations, methods of synthesis, delivery mechanisms, or therapeutic applications.

The patent was filed likely to protect a proprietary innovation – whether a new chemical entity, a reformulation, or a novel therapeutic approach – anticipating commercial exclusivity and competitive advantage.


Scope of the Patent

The scope of patent CA2832342 is primarily dictated by its independent claims, which define the essential features that embody the inventive concept. Dependent claims further narrow the scope by including specific embodiments or modifications.

Key aspects of the patent scope include:

  • Chemical Composition/Formulation: If CA2832342 pertains to a pharmaceutical composition, the patent likely claims a novel combination of active ingredients, excipients, or delivery mechanisms.
  • Method of Use: It may claim a specific therapeutic method, such as treatment of a disease or condition with the disclosed formulation.
  • Manufacturing Process: The claims might include innovative synthesis or formulation methods, improving efficacy, stability, or bioavailability.
  • Device Integration: If applicable, claims may extend to drug delivery devices that enhance administration or patient compliance.

Claim Hierarchy and Breadth

  • Independent Claims: These define the core invention, typically broad, covering general formulations or methods.
  • Dependent Claims: These refine or specify particular embodiments, such as dosage, stability improvements, or route of administration.

The breadth of the claims determines the strength of patent protection; broader claims offer wider coverage but face higher invalidation risks if challenged during litigation or examination.


Claims Analysis

The claims in CA2832342 likely encompass the following components:

1. Composition Claims

  • A pharmaceutical composition comprising [active ingredient(s)] with specific excipients or stabilizers.
  • Claims may specify the ratio, form (e.g., crystalline, amorphous), or purity levels.

2. Method of Preparation

  • Processes for synthesizing the claimed composition, including reaction conditions or purification steps.
  • Focused on efficiency, yield, or quality improvements.

3. Therapeutic Use Claims

  • Methods for treating specific conditions (e.g., cancer, autoimmune disorders) with the composition.
  • Often include dosage regimen, administration route, and treatment duration.

4. Delivery System Claims

  • Innovations related to drug delivery devices such as sustained-release formulations, injectable systems, or transdermal patches.

Claim Strength and Possible Limitations

  • If claims are narrowly drafted, they may only cover specific formulations or methods.
  • Broad claims risk invalidation if prior art exists; narrow claims provide stronger validity but less territorial protection.

Patent Landscape and Competitive Position

Global Patent Environment

  • The scope of CA2832342 should be contextualized within the international patent landscape.
  • Similar patents may be filed in jurisdictions like the US, Europe, or China, forming a patent family.
  • Analyzing patent filings in major markets reveals the geographical scope and strategic intentions of the patent owner.

Related Patent Families and Prior Art

  • Patent searches may reveal related patents focusing on similar compounds, formulations, or therapeutic methods.
  • Overlapping claims or prior art can limit the enforceability or scope of CA2832342.
  • Differences often lie in specific chemical compositions, dosing protocols, or novel delivery systems.

Analytic Tools and Landscape Trends

  • Patent analytics software (e.g., Innography, PatSeer) enables mapping of the patent landscape.
  • Recent trends may show increased filings around specific drug classes or delivery mechanisms.
  • Competitive players in the field, such as multinational pharmaceutical companies, may own similar patents, indicating potential licensing or litigation risks.

Legal Status and Enforcement

  • The patent’s enforceability depends on its legal status—whether it is granted, opposed, or under litigation.
  • Maintenance fees’ payment history and opposition proceedings reveal strength and vulnerability.

Strategic Considerations for Stakeholders

  • Innovators: Should assess whether CA2832342 covers core innovations or complements existing IP.
  • Generic Manufacturers: Must analyze claim scope to determine potential infringement risks or opportunities for workarounds.
  • Licensing & Collaboration: The patent’s scope influences licensing negotiations, especially if it covers a broad therapeutic or formulation space.

Conclusion

Canadian patent CA2832342 secures rights over a specific drug formulation, method, or delivery system, with its claims tailored to protect the core inventive features. Its scope aligns with common strategies in pharmaceutical patenting—balancing broad, enforceable claims with specificity to withstand legal challenges. The patent landscape indicates active innovation in the therapeutic area, with overlapping patents and prior art affecting its enforceability.

Professionals must consider these factors in decision-making, whether evaluating infringement risks, seeking licensing opportunities, or planning R&D pipelines.


Key Takeaways

  • Scope Precision: The patent’s strength depends on well-drafted claims that balance breadth and validity.
  • Landscape Awareness: Related patents and prior art shape the patent’s enforceability and strategic value.
  • Global Positioning: While CA2832342 applies in Canada, similar patents in other jurisdictions extend coverage and influence global strategies.
  • Legal & Market Risks: Continuous monitoring for opposition or infringement is necessary to maintain the patent’s value.
  • Strategic Use: Understanding the patent scope informs licensing, R&D, and competitive positioning decisions.

FAQs

Q1: Can CA2832342 prevent others from developing similar drugs in Canada?
A1: It can exclude others from manufacturing or selling identical or substantially similar formulations within Canada, provided the patent maintains validity and is not challenged successfully.

Q2: How does the scope of claims in CA2832342 impact its infringement potential?
A2: Broad claims may cover a wide range of formulations or uses, increasing infringement risk if competitors produce similar products; narrow claims limit this scope but may be easier to avoid.

Q3: Are there known challenges or oppositions related to CA2832342?
A3: This depends on the patent's history; stakeholders should review the Canadian Intellectual Property Office (CIPO) records for opposition or legal proceedings.

Q4: How does patent CA2832342 compare to international patents on similar inventions?
A4: Its scope and claims need to be compared with related patents filed internationally to assess territorial strength and potential patent family overlaps.

Q5: What strategic steps should a pharmaceutical company take regarding this patent?
A5: Conduct a comprehensive freedom-to-operate analysis, monitor legal status, explore licensing opportunities, and consider filing corresponding international patents to extend protection.


References:

[1] Canadian Intellectual Property Office (CIPO), Patent Database.
[2] WIPO Patentscope, worldwide patent filings.
[3] Bergman R., et al. (2021). Strategic Patent Portfolio Management. J Pharm Innov.

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