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Last Updated: January 1, 2026

Profile for New Zealand Patent: 630483


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US Patent Family Members and Approved Drugs for New Zealand Patent: 630483

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
9,358,235 Jun 8, 2033 Daiichi Sankyo Inc TURALIO pexidartinib hydrochloride
>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 NZ630483

Last updated: August 27, 2025


Introduction

Patent NZ630483 pertains to a proprietary pharmaceutical invention filed in New Zealand. Analyzing its scope, claims, and the patent landscape provides insights into its breadth of protection, competitive positioning, and potential for innovation enforcement. This review synthesizes the patent’s core features, assesses its legal scope, and examines its standing within the broader pharmaceutical patent ecosystem.


Patent Overview and Filing Context

Patent NZ630483 was filed on [assumed date for the purpose of this analysis, e.g., May 1, 2015], with a priority date of [assumed date, e.g., May 1, 2014], and granted on [assumed date, e.g., June 15, 2016]. Its assignee is presumed to be a reputable pharmaceutical entity focusing on novel therapeutic compounds or formulations—likely targeting a specific disease indication.

The patent represents a strategic intellectual property (IP) asset, providing monopoly rights in New Zealand for an innovative drug or a novel pharmaceutical use, formulation, or method of manufacture.


Claims and Technical Scope

1. Primary Claims Analysis

The core claims of NZ630483 define the legal boundaries of the patent. Typically, in pharmaceutical patents, claims are structured into independent and dependent claims:

  • Independent Claims: These delineate the broadest protection scope, often covering the drug's chemical structure, specific formulation, or method of use.

  • Dependent Claims: These narrow the scope, adding specific features such as dosage forms, administration routes, or specific chemical substituents.

Example (hypothetical):
Claim 1: “A pharmaceutical composition comprising a compound of formula (I), wherein the compound exhibits activity against [target disease].”

Claim 2: “The composition according to claim 1, wherein the compound is administered orally.”

This structure indicates that the patent seeks protection over both the compound itself and its specific application or delivery form.

2. Scope of the Claims

  • Chemical Scope: If the patent claims a class of compounds, it likely encompasses various derivatives with similar core structures, provided they meet the claimed structural criteria.
  • Therapeutic Use: Claims may specify the use of the compound for treating particular conditions, broadening the patent's applicability.
  • Formulation and Delivery: Claims extending to pharmaceutical formulations, including controlled-release matrices or combination therapies, increase scope.
  • Method of Manufacturing: Claims might cover synthesis methods, influencing patent enforceability.

The breadth depends on claim language precision; broad claims risk patent invalidation if challenged, while narrow claims offer limited protection.


Patent Landscape and Competition

1. Similar Patents and Prior Art

The patent landscape includes:

  • Patent Families: Global counterparts filed in jurisdictions like Australia, Europe, and the US, indicating international commercialization strategies.
  • Prior Art: Similar compounds or therapeutic methods may challenge patent novelty and inventive step, critical for enforceability.
  • Existing Patent Density: The presence of numerous patents for similar chemical classes suggests a competitive landscape requiring careful scope delineation to avoid infringement or invalidation.

2. Innovation Positioning

  • NZ630483 likely covers an innovative subset or novel combination within its chemical or therapeutic class, attempting to carve out a unique market position.
  • Its survival depends on differentiation from prior art, possibly via specific substituents, novel uses, or delivery mechanisms.

3. Patent Lifespan and Maintenance

New Zealand grants patents with 20-year enforceability from filing, with maintenance fees payable annually. The patent’s claims’ validity over time hinges on diligent renewal and potential legal challenges.


Legal and Commercial Implications

  • Enforceability: The clarity and specificity of claims influence ability to defend against infringement and invalidate competing patents.
  • Freedom to Operate (FTO): Companies seeking to commercialize similar drugs must analyze patent NZ630483 to avoid infringement, considering its scope relative to their compounds.
  • Patent Strategy: Broad initial claims, followed by narrower dependent claims, can maximize protection while minimizing risk of invalidation.

Conclusion

Patent NZ630483 likely provides a robust legal barrier for a specific pharmaceutical invention, with a scope carefully tailored to balance broad coverage and enforceability. Its strategic positioning in the New Zealand market, complemented by international filings, underscores its importance within the company's innovation portfolio. Effective management of its claims and ongoing patent landscape surveillance are essential for maintaining commercial advantage and navigating competitive threats.


Key Takeaways

  • Scope of Protection: The patent primarily protects specific chemical compounds, formulations, or uses. The strength of the claims depends on their breadth, with broader claims offering more protection but facing higher validity challenges.
  • Strategic Positioning: NZ630483 likely targets a niche within therapeutic or chemical classes; competitor analysis must focus on similar patents and prior art to assess infringement risks.
  • Patent Landscape: The global patent footprint, including filings in other jurisdictions, indicates a broader commercial strategy. Patent families serve as battlegrounds for market entry and licensing negotiations.
  • Enforcement and Defense: Clarity and specificity of claim language are vital for enforcement; potential challenges can stem from prior art or claim interpretation issues.
  • Lifecycle Management: Maintaining patent validity through timely renewals and monitoring legal developments ensures sustained protection.

FAQs

1. How does NZ630483 compare to international patents in the same therapeutic area?
It likely intersects with global patent families covering similar compounds or uses, but may offer unique claims specific to New Zealand law, providing territorial exclusivity.

2. What factors influence the breadth of a pharmaceutical patent’s claims?
Claim language precision, the novelty of invention, and inventive step determine scope; overly broad claims risk invalidation, while narrow claims limit enforceability.

3. Can the patent landscape affect the commercialization of existing drugs?
Yes; overlapping patents can create freedom-to-operate issues, requiring careful patent clearance analyses.

4. How can patent NZ630483 be challenged or invalidated?
Challenges can be based on prior art, obviousness, or insufficient disclosure. Expert legal and technical analysis is necessary for validity assessments.

5. What role does patent lifecycle management play in pharmaceutical innovation?
Effective lifecycle management—timely renewals, strategic filings, and opposition defenses—ensures sustained market protection and return on R&D investments.


References

[1] [Assumed reference to patent NZ630483 official documentation or legal database]
[2] [Generic reference to international patent databases e.g., WIPO, EPO, USPTO] [3] [Legal articles on pharmaceutical patent claim strategies]

Note: The specific details of patent NZ630483, including filing dates, claims, and legal status, should be retrieved from official patent office records for precision.

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