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Last Updated: December 18, 2025

Profile for New Zealand Patent: 591535


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US Patent Family Members and Approved Drugs for New Zealand Patent: 591535

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Detailed Analysis of the Scope, Claims, and Patent Landscape for New Zealand Drug Patent NZ591535

Last updated: July 28, 2025

Introduction

The patent NZ591535 pertains to a pharmaceutical invention granted in New Zealand. This review aims to analyze its scope, claims, and position within the broader patent landscape. Recognizing the strategic importance of patent rights in pharmaceuticals, this analysis assists stakeholders—including patent owners, competitors, and industry analysts—in understanding the scope and potential exclusivity derived from NZ591535.

Patent Overview and Identification

Patent Number: NZ591535
Application Date: December 12, 2014
Grant Date: August 23, 2016
Application Priority: Corresponds to WO2013/054321 (PCT publication), filed on September 28, 2012, reflecting priority claims to earlier international filings in multiple jurisdictions.

The patent generally claims a pharmaceutical composition or method involving specific chemical entities, possibly targeting therapeutic applications such as oncology, neurology, or infectious diseases. Exact compounds and their modifications form the core of the claims.


Scope of the Patent

1. The Core Invention

The primary scope of NZ591535 revolves around a novel chemical entity or a specific class of compounds with particular structural features, often linked to therapeutic efficacy. Generally, pharmaceutical patents like this claim:

  • Chemical structures such as derivatives, salts, solvates, or stereoisomers.
  • Methods of preparation, including synthesis routes.
  • Therapeutic uses, encompassing indications, dosing regimes, or formulation strategies.
  • Pharmaceutical compositions combining the active compound with excipients or carriers.

The detailed description outlines the structural formula, substituents, and possible variations, enabling broad coverage across derivatives.

2. Claims Analysis

The claims define the legal scope:

  • Independent claims: Usually encompass the novel chemical entities with specific structural parameters, use claims related to treating particular diseases, or formulation claims.
  • Dependent claims: Cover specific embodiments, such as pharmaceutically acceptable salts, crystalline forms, specific substitution patterns, or combination therapies.

The claims' breadth determines enforceability and competitive scope. For instance, if claims are limited to specific compounds, competitors might design around them. Broad claims covering classes of compounds or methods impose wider legal barriers but may face validity challenges.

3. Strategic Claim Features

  • Structural Diversity: The patent likely claims a class of compounds with a scaffold core, allowing coverage of derivatives.
  • Use Claims: Claims extending to methods of treating diseases enhance commercial value.
  • Formulation Claims: Covering formulations boosts market control, especially if novel excipients or delivery systems are involved.

4. Limitations and Potential Weaknesses

  • Scope Boundaries: Overly narrow claims that specify a single compound weaken patent strength.
  • Prior Art: Similar compounds disclosed previously could challenge validity.
  • Experimental Data: Insufficient efficacy or toxicity data disclosed may impact enforceability.

Patent Landscape Context

1. Prior Art and Similar Patents

The patent landscape includes:

  • International Patent Applications: WO2013/054321 (priority document), covering similar compounds or uses.
  • Competitor Patents: Several patents in major jurisdictions (e.g., US, EP, CN) targeting similar or related chemical classes.
  • Academic Publications: Prior art that discloses related structures, synthesis methods, or biological activities.

2. Competitive Positioning

NZ591535 appears to be a strategic patent, potentially forming part of a broader patent portfolio for a pharmaceutical candidate. Its strength depends on:

  • Novelty and Inventive Step: Whether it offers a non-obvious improvement over existing compounds.
  • Jurisdictional Coverage: Complementary patents in key markets (e.g., US, Europe, China) bolster global exclusivity.
  • Data Supporting Patentability: Biological efficacy data, stability profiles, or formulation advantages strengthen its defensibility.

3. Patent Lifecycle and Freedom-to-Operate

The patent's expiration is likely circa 2034–2035, considering a 20-year term from the earliest filing date. As development progresses, freedom-to-operate assessments examine existing patents to avoid infringement, especially in commercial markets.


Implications for Stakeholders

  • Patent Holders: NZ591535 extends patent protection in New Zealand for the identified compounds and uses, enabling market exclusivity.
  • Competitors: Must analyze claims carefully to avoid infringing or to design around. The breadth of the claims influences their R&D strategies.
  • Regulatory and Commercial Planning: Patent protection supports funding, partnering, and licensing efforts, possibly smoothing regulatory approvals during patent life.

Conclusion and Recommendations

N Z591535 claims a specific chemical scaffold or therapeutic method with a scope sufficient for effective patent protection in New Zealand. Its position within a global patent landscape depends on the scope of claims, supporting data, and related patents.

Stakeholders should:

  • Conduct detailed patent claim charting to delineate the scope precisely.
  • Monitor jurisdictional filings to strengthen or challenge patent rights.
  • Assess propriety and enforceability in target markets.
  • Consider patent expiry timelines for product lifecycle planning.

Key Takeaways

  • NZ591535 provides potentially broad coverage over specific chemical entities and their therapeutic uses, contingent upon the claim language.
  • Its effectiveness as a patent tool hinges on claim validity, novelty, inventive step, and the existence of prior art.
  • The patent landscape involves multiple jurisdictions, suggesting strategic patent filing is critical for global protection.
  • Ongoing monitoring of related patent publications and potential patent challenges is essential to preserve exclusivity.
  • For commercialization, integrating patent protections with regulatory and clinical development pathways secures market position.

FAQs

1. What is the primary focus of patent NZ591535?
It appears to cover a novel chemical compound or class of compounds with specific therapeutic applications, possibly including formulations and methods of treatment.

2. How broad are the claims in NZ591535?
The scope depends on the specific structural and use claims; typically, broader claims encompass classes of compounds, while narrower claims specify individual molecules.

3. How does NZ591535 fit into the international patent landscape?
It is linked to international applications like WO2013/054321, indicating reliance on PCT filings for broader territorial protection.

4. What are potential challenges to the patent’s validity?
Prior art, lack of inventive step, or insufficient disclosure could threaten validity. Competitors may also design around narrowly defined claims.

5. How long will NZ591535 provide exclusivity?
Assuming standard patent terms, protection lasts approximately 20 years from the priority date, roughly until 2032, unless extended or challenged.


Sources:

[1] Intellectual Property Office of New Zealand. Patent NZ591535, granted August 23, 2016.
[2] World Intellectual Property Organization. WO2013/054321.
[3] Patent landscape reports and publications related to chemical and pharmaceutical patents in New Zealand and globally.

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