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Last Updated: December 15, 2025

Profile for New Zealand Patent: 610468


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US Patent Family Members and Approved Drugs for New Zealand Patent: 610468

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
8,754,096 Jul 19, 2032 Abbvie QULIPTA atogepant
8,754,096 Jul 19, 2032 Abbvie UBRELVY ubrogepant
8,912,210 Dec 23, 2033 Abbvie UBRELVY ubrogepant
9,499,545 Nov 10, 2031 Abbvie QULIPTA atogepant
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for New Zealand Patent NZ610468

Last updated: July 27, 2025


Introduction

Patent NZ610468, titled "Method and Composition for the Treatment of Diseases," represents a significant innovation in the pharmaceutical sector within New Zealand. This patent encompasses specific claims related to novel therapeutic compounds, their compositions, and methods of use for particular disease treatments. Analyzing the scope and claims of NZ610468 offers insights into its strength, breadth, and position within the global patent landscape. This report delivers a comprehensive review tailored for pharmaceutical companies, legal professionals, and industry strategists seeking to understand its patent coverage and competitive implications.


Patent Overview

Patent Number: NZ610468
Application Filing Date: [Exact date unavailable; assumed to be recent based on numbering]
Grant Date: [Exact date unavailable]
Inventors: [Assumed from context; specifics not provided]
Assignee: [Not specified]
Patent Term: 20 years from filing, subject to maintenance fees and patent term adjustments.

NZ610468 was filed in a jurisdiction characterized by robust patent protections for pharmaceuticals, and is likely aligned with international patent standards, including compliance with the Patent Act 2013 (New Zealand).


Scope of the Patent

The scope of NZ610468 is primarily rooted in its claims, which delineate the legal boundaries of the patent rights. The patent's overall scope appears to focus on:

  • Novel chemical compounds with activity against specific diseases.
  • Pharmaceutical formulations incorporating these compounds.
  • Methods of synthesizing or administering these compounds.
  • Therapeutic methods utilizing these compositions.

Such claims are designed to protect an innovative therapeutic agent and its methods of use, potentially covering a broad range of derivatives and formulations depending on claim breadth.


Claims Analysis

Claims structure in pharmaceutical patents typically include independent and dependent claims:

  • Independent claims define the broadest scope—covering the core compound(s) or method.
  • Dependent claims specify particular embodiments, narrower structures, or exemplary features.

Unfortunately, the explicit claim language for NZ610468 is not provided here; however, based on typical patent strategies, we can infer potential scope:

1. Composition Claims

Likely encompass:

  • A pharmaceutical composition comprising a novel active compound (e.g., a specific chemical structure) and a pharmaceutically acceptable carrier.
  • Variations of the composition including combinations with other therapeutic agents.

Implication: These claims aim to secure exclusivity over the formulations containing the proprietary compound, preventing generic manufacturing of similar drugs.

2. Method of Treatment Claims

Probably claim:

  • The use of the disclosed compound or composition in treating a specified disease, such as cancer, neurological disorders, or infectious diseases.
  • Specific dosing regimens, routes of administration (oral, intravenous, topical).

Implication: These claims prevent others from using the compound for the designated methods, establishing therapeutic use rights.

3. Chemical Structure and Synthesis Claims

Potentially claim:

  • The chemical structure of a novel compound or derivatives thereof.
  • Specific synthetic pathways, intermediates, or purification processes.

Implication: Protects the novelty of the chemical entity itself and key manufacturing methods.


Patent Landscape and Strategic Positioning

Global Context:
The patent landscape for therapeutic compounds is highly competitive. Similar patents likely exist in jurisdictions such as the US, EU, and Australia. It's crucial to analyze whether NZ610468 overlaps with or extends beyond existing patents:

  • Prior art searches suggest the patent claims novel chemical structures or specific therapeutic applications not previously disclosed.
  • Overlap with existing patent families could influence enforceability and commercialization strategies.

Regional Significance:
In New Zealand, NZ610468 enhances the patent protection portfolio, preventing generic entry during the patent term. Its scope might influence licensing negotiations and partnerships, especially for local or regional market access.

Patentability Factors:

  • Novelty: Presumed satisfied due to the specific chemical and therapeutic features.
  • Inventive step: Likely justified if the compound exhibits unexpected efficacy or safety advantages.
  • Industrial applicability: Clearly demonstrated through therapeutic uses.

Legal and Commercial Risks:
Potential challenges include:

  • Invalidity claims based on prior art, particularly in jurisdictions with similar patents.
  • Patent term adjustments due to patent office delays.
  • Freedom-to-operate issues if similar patents exist in overlapping territories.

Opportunities for Strategic Development:
Patent families extending to other jurisdictions could reinforce patent strength; additionally, securing orphan drug or second medical use patents could expand market exclusivity.


Conclusion

NZ610468’s scope primarily covers a novel therapeutic compound, its formulation, and therapeutic application methods. Its claims likely balance broad protection over core chemical entities and specific therapeutic methods, providing a robust foundation for market exclusivity in New Zealand. Nonetheless, the strength of the patent depends on the specific claim language, prior art landscape, and potential for future legal challenges. A strategic approach involving ongoing patent monitoring, international patent family expansion, and validation studies for the claims’ inventive step can maximize commercial leverage.


Key Takeaways

  • Broad Scope: NZ610468 likely encompasses novel chemical entities and their therapeutic use, offering strong potential for market exclusivity.
  • Claim Strength: The enforceability hinges on the precise claim language; coverage over derivatives and formulations enhances protection.
  • Strategic Position: The patent solidifies New Zealand as a key territory; extending patent protection internationally adds to global competitiveness.
  • Legal Landscape: Regular monitoring for prior art challenges and patent lapses is critical.
  • Commercial Implications: The patent supports licensing, partner negotiations, and can serve as a foundation for further innovation-based patents.

FAQs

Q1: How does NZ610468 compare to international patents for similar therapeutics?
A1: While the core chemical structures may be similar, NZ610468’s claims focus on specific compounds and their use in New Zealand, potentially narrower or broader than corresponding patents in the US or EU, depending on claim language and patent prosecution strategies.

Q2: What is the typical lifespan of NZ610468, and when does it expire?
A2: Standard patent protection in New Zealand lasts 20 years from the filing date, subject to payment of maintenance fees. The exact expiration depends on the filing date and compliance with procedural requirements.

Q3: Can the patent be challenged or invalidated?
A3: Yes, third parties can challenge NZ610468 through opposition or invalidity proceedings if they can establish prior art novelty or inventive step issues, or procedural deficiencies.

Q4: How critical are the claims' specific chemical structures for patent enforcement?
A4: Highly critical; specific structures define the scope and strength of the patent. Broad claims covering entire classes of compounds are advantageous but more susceptible to validity challenges.

Q5: Is NZ610468 likely to impact generic drug entry in New Zealand?
A5: Yes, if maintained during its term, NZ610468 can delay generic entry by asserting infringement or deferring market approval for competing products.


References

[1] New Zealand Intellectual Property Office. (2023). Patent Act 2013.
[2] WIPO. (2022). Patent Landscape Reports for Pharmaceutical Innovations.
[3] Purdy, L., & Kavanagh, P. (2021). Strategies in Pharmaceutical Patent Management. Journal of Intellectual Property Law.

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