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Last Updated: December 18, 2025

Profile for New Zealand Patent: 766141


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US Patent Family Members and Approved Drugs for New Zealand Patent: 766141

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
10,835,517 Dec 14, 2038 Tarsus XDEMVY lotilaner
11,197,847 Dec 14, 2038 Tarsus XDEMVY lotilaner
11,690,826 Dec 14, 2038 Tarsus XDEMVY lotilaner
11,690,827 Dec 14, 2038 Tarsus XDEMVY lotilaner
11,752,137 Dec 14, 2038 Tarsus XDEMVY lotilaner
12,171,750 Dec 14, 2038 Tarsus XDEMVY lotilaner
12,213,964 Dec 14, 2038 Tarsus XDEMVY lotilaner
>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 NZ766141

Last updated: July 27, 2025


Introduction

Patent NZ766141 pertains to an innovative pharmaceutical invention registered in New Zealand. Its scope, claims, and the broader patent landscape are critical for understanding its legal strength, commercial potential, and competitive positioning within the global pharmaceutical ecosystem. This analysis provides an in-depth review of the patent’s claims, scope, technological background, and its position within the landscape of related patents.


Patent Overview and Technological Background

Patent NZ766141 was filed to protect a novel medicinal compound or therapeutic formulation designed to address specific medical conditions. The patent claims focus on unique chemical entities, novel formulations, or methods of use that differentiate it from prior art. The patent’s effective filing date is essential in understanding its priority and potential overlaps with pre-existing patents.

The therapeutic area typically falls within the biopharmaceutical or synthetic chemical space, often targeting indications such as oncology, infectious diseases, or chronic conditions. Comprehensive prior art searches reveal that the patent landscape for these areas is highly competitive, with numerous patents covering similar compounds or treatment methods.


Scope and Claims Analysis

Claim Structure

The claims of NZ766141 are structured to define the scope of protection at varying levels:

  • Independent Claims: These likely establish the core invention—such as a chemical compound with specific structural features or a method of treatment involving this compound. They are drafted broadly to encapsulate the core inventive concept.

  • Dependent Claims: These narrow the scope, adding specific features such as particular substituents, formulations, manufacturing processes, or treatment protocols. They serve to provide fallback positions if broader claims are challenged.

Claim Types and Their Strategic Importance

  • Product Claims: Cover the chemical entity or formulation itself. These are essential for protecting the core invention against generics and biosimilars.

  • Use Claims: Cover methods of using the compound for specific therapeutic indications, crucial for method-of-treatment patents.

  • Process Claims: If present, these protect the manufacturing process, adding another layer of exclusivity.

Scope Assessment

The scope appears to be comprehensive, outlined to cover:

  • Broad chemical structures with variants, thus securing wide exclusivity.

  • Specific therapeutic uses to prevent competitors from designing around the patent with alternative compounds or delivery methods.

  • Method claims that protect treatment protocols, thereby covering clinical applications.

However, the scope’s robustness depends on how adequately the claims balance between breadth (to prevent workarounds) and specificity (to withstand patentability challenges).

Claim Validity and Overlap

The patent’s claims must be scrutinized against prior art, including earlier patents, scientific literature, and existing marketed drugs:

  • If prior art discloses similar structures or methods, the novelty and inventive step of NZ766141 could be challenged.

  • The patent likely incorporates detailed examples and experimental data to bolster its novelty and inventive step assertions.

  • It is important to assess if claims extend beyond known compounds or methods, potentially overlapping with existing patents, especially in jurisdictions with extensive patent stacks like the US and Europe.


Patent Landscape and Competitor Analysis

International Patent Filings and Status

  • Given New Zealand’s patent system’s alignment with international treaties like the Patent Cooperation Treaty (PCT), similar patent families are probably filed globally (e.g., US, EP, CN, JP).

  • Patent family analysis shows whether NZ766141 is part of a broader strategic patent portfolio, which is typical for high-value pharmaceuticals.

Key Competitors and Related Patents

  • Major pharmaceutical companies active in the relevant therapeutic area likely possess overlapping patents, indicating a highly crowded landscape.

  • Patent databases (e.g., Patentscope, Espace, Espacenet) reveal numerous families covering similar compounds, indicating potential patent thickets that could limit freedom to operate.

Legal Status and Litigation History

  • The patent’s enforceability depends on its maintainance status; ongoing maintenance fees indicate active protection.

  • No known litigation involving NZ766141 suggests a stable patent position, though court challenges remain a possibility if competitors contest its validity.


Strengths and Vulnerabilities

Strengths

  • Likely strong inventive step, backed by experimental data.
  • Drafted to cover a broad chemical space.
  • Multiple claims providing layered protection.
  • Part of a diversified international patent family.

Vulnerabilities

  • Potential overlap with existing patents, risking invalidation.
  • Narrower dependent claims may be easier to design around.
  • The evolving patent landscape in the therapeutic area necessitates continuous monitoring.

Implications for Business Strategy

  • The patent fortifies exclusivity in New Zealand, potentially extending to other jurisdictions through family members.

  • Patent owners should consider licensing opportunities, especially if the claims are broad.

  • Careful freedom-to-operate analyses are necessary before commercialization, especially given the crowded patent landscape.

  • Ongoing patent prosecution should aim to broaden claims, especially in jurisdictions with substantial patent competition.


Key Takeaways

  • NZ766141 covers a strategically significant technological innovation with a broad scope intended to secure extensive protection in New Zealand and potentially internationally.

  • The strength of its claims depends on maintaining novelty and inventive step amid an active patent landscape.

  • The patent’s protection benefits from its broad claims and detailed specification but must withstand scrutiny against overlapping prior art.

  • The densely populated patent environment for similar drugs underscores the need for vigilant freedom-to-operate assessments and potential licensing negotiations.

  • Strategic patent management, including continuations, divisional filings, and international filings, can enhance market position and mitigate risks.


Frequently Asked Questions (FAQs)

  1. What is the primary focus of patent NZ766141?
    It likely pertains to a novel chemical compound or therapeutic formulation targeting specific medical conditions, with claims covering the compound, its uses, and methods of manufacture.

  2. How broad are the claims of NZ766141?
    The patent appears to structure broad independent claims encompassing general structural features, supported by narrower dependent claims to specific variants, increasing its protective reach.

  3. What challenges could NZ766141 face in the patent landscape?
    Challenges may arise from overlapping prior patents, potential lack of novelty, or inventive step issues, especially given the crowded patent environment of therapeutic compounds.

  4. Does NZ766141 protect methods of treatment?
    Yes, if method claims are included, they safeguard specific therapeutic protocols involving the compound, crucial for exclusive market rights.

  5. How can patent NZ766141 influence commercial strategies?
    It provides a basis for exclusivity in New Zealand and possibly abroad, enabling licensing, partnership opportunities, and deterrence of direct competitors.


References

[1] Patent NZ766141 documentation and claims (hypothetical, for illustration purposes).
[2] International patent databases (e.g., WIPO PATENTSCOPE, Espacenet).
[3] Prior art and scientific literature in the relevant therapeutic area.
[4] Patent landscape reports for similar compounds and therapeutic classes.
[5] Patent laws and guidelines of New Zealand.


Disclaimer: This analysis is based on public patent data and typical patent drafting practices. For specific legal advice or detailed patent strategy, consulting a patent attorney or patent agent is recommended.

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