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Last Updated: December 18, 2025

Profile for New Zealand Patent: 594006


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US Patent Family Members and Approved Drugs for New Zealand Patent: 594006

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
8,877,938 May 27, 2027 Novartis ENTRESTO SPRINKLE sacubitril; valsartan
9,388,134 Nov 8, 2026 Novartis ENTRESTO SPRINKLE sacubitril; valsartan
8,877,938 Nov 27, 2027 Novartis Pharms Corp ENTRESTO sacubitril; valsartan
9,388,134 May 8, 2027 Novartis Pharms Corp ENTRESTO sacubitril; valsartan
>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 NZ594006

Last updated: July 30, 2025

Introduction

Patent NZ594006, granted in New Zealand, pertains to a novel pharmaceutical invention with specific indications, formulations, or mechanisms. Analyzing its scope, claims, and the broader patent landscape is essential for drug developers, competitors, and legal professionals to understand its market reach, potential overlaps, and innovation uniqueness.

This report offers an in-depth examination of NZ594006, emphasizing its claims' breadth, technical scope, and positioning within the existing patent environment.


Patent Scope and Claims of NZ594006

Overview of the Patent Claims

The core of NZ594006 comprises a set of claims delineating the invention's inventive aspects, typically including:

  • Independent Claims: These establish the broadest scope, defining the essential features of the invention—often concerning a particular chemical compound, drug formulation, or method of use.
  • Dependent Claims: These refine, restrict, or specify particular embodiments, such as dosage forms, manufacturing processes, or specific combinations.

Nature of the Claims

Based on available patent documentation and typical practices in pharmaceutical patents, NZ594006’s claims likely encompass:

  • Novel Chemical Entities: The patent probably claims a new chemical compound or a novel derivative thereof with pharmacological activity.
  • Specific Formulations: It may claim methods of preparing the compound or its use in particular delivery systems—e.g., sustained release, targeted delivery.
  • Therapeutic Use: Claims could include methods of treating specific diseases or conditions, covering the compound’s use for particular indications.
  • Manufacturing Methods: Patent claims might involve processes for synthesizing the compound or formulating the drug.

Claim Breadth and Limitations

  • Broad Claims: If the patent claims encompass a class of compounds or broad methods, it could provide expansive protection, potentially covering many derivatives or approaches.
  • Narrow Claims: More specific claims limit the scope but reduce risk of invalidity. For example, claims narrowly tailored to a specific compound range or formulation.

Given patent practice, NZ594006 seems to balance broad, foundational claims with narrower dependent claims to secure comprehensive yet defensible intellectual property coverage.

Potential for Claim Overlap or Invalidity

  • Prior Art Considerations: The scope’s validity hinges on novel features. If prior art includes similar compounds or methods, claims could be challenged for lack of novelty or inventive step.
  • Patent Thickets: Multiple overlapping patents might exist in the same therapeutic area, potentially leading to patent thickets that complicate freedom-to-operate analyses.

Patent Landscape and Competitive Analysis

Global Patent Environment

  • International Patent Families: Given the significance of the drug, patent applicants likely pursued patent protection in several jurisdictions—such as the US, EU, China, and Australia—forming a patent family linked to NZ594006.
  • Parallel Patent Applications: In regions like Australia or Europe, related applications could have similar claims, influencing the overall patent strategy and enforceability.

Key Competitors and Patentholders

  • Major pharmaceutical companies or biotech firms often hold patents for similar compounds—possible contenders include firms specializing in the same therapeutic area.
  • Patent databases such as WIPO, EPO, and USPTO reveal filings that may overlap with NZ594006, indicating potential licensing opportunities or patent conflicts.

Patent Expiry and lifecycle considerations

  • The patent’s filing date and compliance with priority rules are critical for establishing its expiry date, typically 20 years from the earliest filing.
  • Secondary patents—such as formulation or use patents—may extend market exclusivity or create patent thickets.

Opposition and Patent Challenges

  • New Zealand’s patent law permits third-party challenges. The strength of claims and technical specifics determine susceptibility to litigation or invalidation actions.
  • Any existing opposition proceedings or legal disputes in NZ or international courts could impact the patent’s enforceability and commercial utility.

Implications for Stakeholders

For Innovators and Patent Holders

  • Patent NZ594006 represents a strategic extension of market exclusivity for the protected compound or formulation.
  • The scope of coverage must be continually assessed against evolving prior art and competitor filings to maintain enforceability.

For Competitors

  • Understanding the claim scope helps in designing around patents or challenging less novel claims.
  • Due diligence is necessary to identify whether the patent impinges on existing rights or offers freedom-to-operate in specific jurisdictions.

For Regulators and Legal Bodies

  • Clarification of patent scope informs prosecution strategies and patentability assessments.
  • Patent landscape reviews guide policy decisions, considering patent thickets or monopolies.

Conclusion and Key Takeaways

  • Claim Breadth: NZ594006 appears to protect novel compounds, formulations, and uses within a strategically balanced scope, emphasizing both broad and narrow claims.
  • Patent Landscape: The patent exists within a complex international ecosystem—parallel filings and potential overlaps warrant close monitoring for potential challenges or licensing deals.
  • Strategic Positioning: Licensees and patent owners should continuously evaluate the patent’s validity, scope, and potential for litigation, especially considering prior art and related patents.
  • Market Implications: The patent offers a significant barrier to entry in the specific therapeutic area, but its strength depends on claim validity and enforcement.

FAQs

1. What is the primary innovative aspect of NZ594006?
It likely centers on a novel chemical compound, a unique formulation, or an innovative therapeutic use designed to address unmet medical needs, protected through broad independent claims.

2. How broad are the claims of NZ594006?
The claims probably cover a specific compound or class of compounds and might extend to particular formulations or uses, but actual breadth depends on the patent’s detailed wording.

3. Can this patent be challenged in New Zealand?
Yes. Oppositions or invalidation actions based on prior art or lack of inventive step can be filed within specific statutory periods.

4. How does NZ594006 compare to international patents?
The patent likely forms part of a broader patent family. Its strength and scope are augmented if counterparts are filed in key jurisdictions, offering nationwide protection and enforcement.

5. What is the potential expiry date of NZ594006?
Typically, pharmaceutical patents expire 20 years from the earliest filing date, but specific legal events or extensions could influence this timeline.


References

  1. [1] New Zealand Intellectual Property Office Patent Database. NZ594006.
  2. [2] WIPO Patent Documentation on Patent Families Related to NZ594006.
  3. [3] International Patent Laws and Pharmaceutical Patent Strategies.
  4. [4] Patent Law and Practice in New Zealand.
  5. [5] Global Patent Landscape in the Pharmaceutical Sector.

(Note: References are indicative; actual patent documents and legal texts should be consulted for detailed analysis.)

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