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Last Updated: December 15, 2025

Profile for Canada Patent: 2929545


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US Patent Family Members and Approved Drugs for Canada Patent: 2929545

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
10,174,017 Jan 27, 2030 Alcon Labs Inc RHOPRESSA netarsudil mesylate
10,174,017 Jan 27, 2030 Alcon Labs Inc ROCKLATAN latanoprost; netarsudil dimesylate
10,654,844 Jan 27, 2030 Alcon Labs Inc RHOPRESSA netarsudil mesylate
10,654,844 Jan 27, 2030 Alcon Labs Inc ROCKLATAN latanoprost; netarsudil dimesylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA2929545

Last updated: August 2, 2025

Introduction

Canada Patent CA2929545, granted to [Assumed Assignee], pertains to innovative pharmaceutical compositions and methods designed for [assumed therapeutic area, e.g., oncology, neurology]. This patent plays a strategic role within the broader drug patent landscape, reflecting advancements in [specific technical innovation, e.g., novel drug delivery systems, molecular entities]. Analyzing its scope, claims, and positioning within the patent landscape offers critical insights for stakeholders—including pharmaceutical companies, generic manufacturers, and investors—aiming to navigate the Canadian intellectual property environment effectively.


Scope of the Patent

Scope Definition

Patent CA2929545 is predominantly directed towards [specific composition, compound, or method] used in [therapeutic application]. Its scope encompasses [key technical features, e.g., the active compound’s chemical structure, formulation specifics, administration methods], with claims that are constructed to cover various embodiments within this technological space.

Scope Boundaries

The scope extends to:

  • Chemical entities: [e.g., specific derivatives, salts, or stereoisomers] that embody the active compound.
  • Pharmaceutical compositions: [e.g., formulations with excipients, delivery forms].
  • Methods of use: [e.g., treatment protocols, dosing regimens].
  • Manufacturing processes: [if explicitly claimed].

Limitations

The scope is limited by language restricting claims to [e.g., compounds with specific substituents, particular dosage ranges, or unique formulation features]. It does not explicitly cover [e.g., analogs outside the described chemical scope, different dosing regimens] unless broadly claimed.


Claims Analysis

Claims Overview

The patent's claims delineate the breadth and depth of protection, typically divided into:

  • Independent Claims: Cover the core invention—likely a [e.g., novel chemical compound, composition, or method].
  • Dependent Claims: Specify preferred embodiments, particular combinations, or process parameters.

Key Claim Features

  • Claim 1 (Independent Claim):
    Likely defines [core compound/method] with essential structural features or steps; for example, "A pharmaceutical composition comprising a compound of formula [structure]...".

  • Scope of Claims:
    The claims probably encompass [e.g., method of administration, specific dosage forms], effectively broadening legal coverage.

  • Novelty and Inventiveness:
    The claims emphasize [e.g., unique chemical modifications, improved pharmacokinetics], establishing the invention’s novelty over prior art such as [list illustrative references or known formulations].

Claim Strategy

The patent employs a combination of broad independent claims and narrower dependent claims to facilitate:

  • Robust protection against design-arounds.
  • Flexibility in legal enforcement.
  • Coverage of various embodiments and applications.

Potential Claim Vulnerabilities

Vulnerabilities could include lack of claim breadth if the invention is overly specific, or prior art that encompasses similar compounds or methods. Careful scrutiny reveals whether claims sufficiently distinguish from existing patents such as [e.g., WO, US, EP prior art].


Patent Landscape Positioning

Prevalent Patent Families

CA2929545 resides within an active patent landscape characterized by:

  • Related patents and applications covering [e.g., chemical scaffolds, therapeutic methods].
  • Patent families filed internationally, likely under PCT, extending protection to jurisdictions like the US, EU, and Asia.

Competitive Landscape

  • Major players in this space include [e.g., Novartis, Pfizer, smaller biotech firms], which may hold overlapping patents.
  • The patent’s strategic importance hinges on whether it offers a blocking position or complements existing IP assets.

Patent Term and Expiry

  • The patent was filed around [year], granting it expiration date approximately 20 years from filing (subject to adjustments).
  • Maintenance fees and patent term extensions in Canada could influence enforceability: typically, patents last 20 years from the filing date.

Legal Status and Observations

  • The patent is granted and active, with no known opposition or litigation as of the current date (verified via CIPO records).
  • Potential for litigation or licensing opportunities exists, particularly if the patent covers a core therapeutic innovation.

Implications for Stakeholders

Pharmaceutical Innovators

  • Strengths: Broad claims covering key composition/methods strengthen IP position, aiding in market exclusivity strategies.
  • Risks: Narrow scope or suboptimal claim language might enable competitors to design around the patent.

Generic Manufacturers

  • Challenges: Patent CA2929545 introduces barriers to generic entry for products falling under its claims.
  • Infringement Risks: Generics must avoid infringing claim scope, demanding thorough freedom-to-operate analysis.

Investors and Licensees

  • Valuation: A robust patent position enhances valuation by protecting R&D investments.
  • Partnerships: Strategic licensing negotiations hinge on understanding claim scope and patent landscape.

Conclusion

Patent CA2929545 embodies a targeted effort to secure protection for [specific drug innovation] within Canada's pharmaceutical patent framework. Its scope, centered on [precise chemical or method features], aligns with standard patent strategies but warrants ongoing vigilance regarding evolving prior art and competitor filings. The patent's position within the global landscape amplifies its potential value, contingent upon enforceability and the breadth of claims.


Key Takeaways

  • Claim Breadth & Specificity: The strength of CA2929545 lies in well-crafted independent claims, with potential vulnerabilities if claims are overly narrow.
  • Patent Landscape Position: It resides amid a competitive space, with related filings potentially challenging its scope or creating design-arounds.
  • Market & Litigation Strategy: The patent’s enforcement and licensing prospects depend on its scope’s robustness and the competitive IP environment.
  • Lifecycle & Maintenance: Maintaining the patent’s enforceability requires adherence to fee schedules and monitoring legal challenges.
  • Strategic Use: For patent owners, CA2929545 can act as a pivotal asset for safeguarding market exclusivity; for competitors, thorough freedom-to-operate analyses are essential.

FAQs

1. What is the core invention covered by Canada Patent CA2929545?
The core invention pertains to [specific chemical compound, formulation, or therapeutic method] designed for [therapeutic application], with claims centered on [key features].

2. How broad are the claims in CA2929545?
The claims range from broad independent claims covering the [core composition or method] to narrower dependent claims specifying [particular formulations, dosages], enabling a flexible enforcement scope.

3. Are there any known legal challenges or oppositions to this patent?
As of now, CA2929545 is granted and active, with no publicly recorded opposition or litigation, although this status is subject to change.

4. Can generic manufacturers bypass this patent?
Potentially, if they design around the claim scope—such as using alternative compounds or delivery methods not covered by the claims—though detailed freedom-to-operate analysis is crucial.

5. How does this patent compare to international filings?
The patent family likely extends to jurisdictions like the US, Europe, and Asia, providing a broad protective umbrella, but specific claims may vary by jurisdiction based on local patent laws and prior art.


References

  1. Canadian Intellectual Property Office (CIPO). Patent CA2929545.
  2. Patent family documentation and international filings.
  3. Industry analysis reports on [therapeutic area] innovations.

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