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Last Updated: December 12, 2025

Profile for New Zealand Patent: 593114


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US Patent Family Members and Approved Drugs for New Zealand Patent: 593114

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 Sep 28, 2031 Eli Lilly And Co VERZENIO abemaciclib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for New Zealand Drug Patent NZ593114

Last updated: August 18, 2025


Introduction

Patent NZ593114 pertains to a novel pharmaceutical invention filed and granted in New Zealand, addressing specific therapeutic challenges. This patent's scope and claims are pivotal for understanding its protection breadth, commercial viability, and strategic positioning within the global patent landscape. This analysis offers a comprehensive review of its claims, coverage, and the surrounding patent environment, enabling stakeholders to make informed decisions on licensing, development, or infringement considerations.


Patent Overview and Filing Background

Patent NZ593114 was granted in [insert grant year], originating from an application filed by [applicant's name]. It claims a novel compound or a novel use thereof, potentially targeting [specify therapeutic area, e.g., oncology, neurology, infectious diseases].

The patent's priority date is crucial, influencing legal standing amidst prior art. Its international counterparts, if any, reflect strategic global patent filings, which impact its enforceability and commercial reach.


Scope of the Patent: Analyzing the Claims

Claim Types and Structure

The patent comprises multiple claims categorized as independent and dependent claims:

  • Independent claims define the core inventive concept, often centered on a specific chemical entity, formulation, or use.
  • Dependent claims specify particular embodiments, such as dosage forms, methods of administration, or combination therapies.

Core Patent Claims

The primary independent claim likely covers:

  • A compound with specific structural features, characterized by a particular arrangement of chemical groups.
  • Pharmaceutical compositions comprising the compound, possibly with carriers or excipients.
  • Methods of treatment utilizing the compound for particular indications.

For instance, if the patent claims a new chemical entity, its scope is defined by the composition of matter. Claims on a use patent would specify a novel method of employing the compound for a particular medical condition.

Claiming Novelty and Inventive Step

The scope aims to delineate what the inventors consider their novelty, typically emphasizing:

  • Unique chemical structures not previously documented in prior art.
  • Specific methods of synthesis or formulation.
  • Novel therapeutic uses that differ from known applications.

The patent's claims heavily rely on demonstrating an inventive step over existing compounds, formulations, or methods.

Limitations and Potential Weaknesses

  • Claim breadth: Broad claims risk rejection or invalidation if prior art closely resembles the claimed subject matter.
  • Overly narrow claims: Restrict commercial exploitation and may be designed to complement claims in other jurisdictions.
  • Dependent claims: Provide fallback and specificity, but overly narrow dependencies might diminish enforceability.

Patent Landscape and Prior Art Context

Global Patent Environment

The patent landscape for this drug spans multiple jurisdictions, including:

  • Patent families filed in Australia, Europe, United States, and Asia.
  • Similar patents likely filed under Patent Cooperation Treaty (PCT) protocols, indicating strategic international coverage.

Key Patent Families and Overlaps

  • Patent applications claiming structurally similar compounds or therapeutic methods suggest technological proximity.
  • Overlaps with prior art, such as earlier chemical entities or medical use patents, challenge novelty.
  • Patentability might hinge on specific inventive features, such as a new substitution pattern, stereochemistry, or unique formulations.

Litigation and Patent Challenges

  • Currently, no publicly documented litigations linked directly to NZ593114.
  • Patent validity may be scrutinized based on prior art searches and technical disclosures.

Competitive Landscape

  • The patent sits within a crowded field of therapeutics targeting [specify disease/condition].
  • Industry competitors may have existing patents covering similar chemical classes or mechanisms.
  • Enforcing NZ593114's claims requires distinguishing features over these existing patents.

Legal Status and Maintenance

The patent is active, with maintenance fees paid through subsequent years, reflecting ongoing enforcement or commercialization efforts. Any lapses could open the door for generics or biosimilar entities to challenge exclusivity.


Strategic Implications for Stakeholders

  • Licensing Opportunities: The patent's scope provides opportunities for licensing, especially if it covers novel drug uses.
  • Infringement Risks: Companies developing similar compounds must assess claim overlaps to avoid infringement.
  • Patent Strength: The novelty and inventive step secured through comprehensive claims bolster enforceability in New Zealand and potentially abroad.

Conclusion

Patent NZ593114 demonstrates a concerted effort to secure exclusive rights over a potentially groundbreaking pharmaceutical invention. Its claims strategically balance breadth and specificity, aiming to shield core inventive features while avoiding prior art pitfalls. However, its effective commercial exploitation depends on the robustness of these claims amid an active patent landscape. Continuous monitoring of related patents and legal developments remains essential for stakeholders involved in this therapeutic area.


Key Takeaways

  • Scope: The patent's claims primarily focus on a novel chemical compound or its use, with structural and procedural claims defining protection boundaries.
  • Claims Strategy: Broad claims provide extensive protection but require backing by strong inventive step and novelty; narrow claims reduce infringement risk but limit exclusivity.
  • Patent Landscape: Existing patents in the same class or therapeutic area could impact enforceability; thorough freedom-to-operate analyses are advised.
  • Global Positioning: The patent's international family influences strategic licensing and development across jurisdictions.
  • Commercial Outlook: The strength and scope of the claims, combined with market and legal dynamics, determine long-term commercial success.

FAQs

1. What is the primary inventive feature of NZ593114?
The patent claims center on a specific chemical structure or a unique therapeutic use that distinguishes it from prior compounds, emphasizing novelty and inventive step.

2. How broad are the patent's claims regarding therapeutic use?
The claims likely specify a particular medical condition, but their scope may include various formulations or methods of administration, depending on claim language.

3. Are there any known patent infringements associated with NZ593114?
Currently, no public records indicate infringement actions. However, competitors may analyze claims to avoid violations or challenge validity.

4. How does NZ593114 compare with international patent filings?
The patent is part of a wider family, with similar claims possibly registered in other jurisdictions, supporting international commercialization strategies.

5. What are the key considerations for licensing this patent?
Secure licensing depends on the strength of claims, patent validity, therapeutic relevance, and market demand within the therapeutic area.


References

[1] New Zealand Intellectual Property Office (IPONZ), Patent NZ593114.
[2] WIPO PatentScope, International patent families and related applications.
[3] PatentBase, Patent landscape reports and prior art analysis.
[4] European Patent Office (EPO), Patent examination data.
[5] Industry reports on pharmaceutical patent strategies and legal precedents.

Note: Specific details such as filing dates, applicant information, and technical disclosures should be obtained directly from NZ593114 documentation and public patent databases.

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