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Last Updated: December 18, 2025

Profile for New Zealand Patent: 602279


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US Patent Family Members and Approved Drugs for New Zealand Patent: 602279

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
10,525,033 Mar 10, 2031 Acacia BARHEMSYS amisulpride
12,194,022 Mar 10, 2031 Acacia BARHEMSYS amisulpride
9,084,765 Feb 26, 2034 Acacia BARHEMSYS amisulpride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for New Zealand Patent NZ602279

Last updated: July 29, 2025

Introduction

New Zealand Patent NZ602279 pertains to a pharmaceutical invention within the scope of drug patent protection in New Zealand. This detailed analysis examines the patent’s claims, scope, and the surrounding patent landscape, providing insights valuable for industry stakeholders, patent practitioners, and potential licensers or infringers. The goal is to elucidate the patent’s breadth, enforceability, and positioning relative to existing patent rights, ensuring strategic alignment with business objectives.

Patent Overview and Context

Patent NZ602279 was granted in New Zealand, a jurisdiction with a well-established patent regime aligned with international standards. The patent’s primary aim is to protect an innovative drug compound, formulation, or method, contributing to the portfolio of pharmaceutical IP rights in the region.

While specific details—such as filing dates, assignees, and patent specifications—are critical for precise analysis, the focus here is on the general strategic assessment based on typical drug patent characteristics. The patent likely involves claims related to a novel active pharmaceutical ingredient (API), a unique formulation, or a therapeutic method. Understanding the scope involves scrutinizing the claims' language for breadth and define the boundaries of exclusivity.

Claims Analysis

Types of Claims

Patent NZ602279's claims can be broadly categorized into:

  • Compound Claims: Covering a novel chemical entity, its enantiomers, salts, and derivatives.
  • Process Claims: Detailing the synthesis or manufacturing method of the compound.
  • Formulation Claims: Encompassing specific pharmaceutical compositions or delivery mechanisms.
  • Method of Use Claims: Protecting particular therapeutic applications or indications.

Claim Language and Breadth

The scope of protection hinges on the specificity of claim language.

  • Independent Claims: Typically define the core inventive concept—e.g., “A compound represented by…” or “A pharmaceutical composition comprising…”. If these claims are narrowly drafted, they may limit infringement to exact molecules or formulations. Conversely, broader language such as “a compound selected from the group comprising…” extends coverage to analogous compounds.
  • Dependent Claims: Specify particular embodiments, such as specific salt forms or dosage forms, narrowing the scope and reinforcing patent robustness.

Strategic Implication: Broader independent claims increase enforceability but may encounter prior art challenges. Narrower claims provide stronger defensibility but limit scope.

Novelty and Inventive Step

The efficacy of NZ602279’s claims depends on their novelty and inventive step over existing art:

  • If the compound or formulation details are markedly different from prior art, the claims maintain a strong scope.
  • The patent’s specification must demonstrate that the claimed invention provides an unexpected technical benefit, satisfying inventive step criteria.

Potential Limitations

  • Scope Restrictions: Claims that are overly broad might be vulnerable to invalidation, especially if prior art references disclose similar compounds or methods.
  • Exact Language: Use of ambiguous terms (e.g., “effective amount,” “comprising”) may allow for loopholes or limit enforceability.

Patent Landscape Analysis

Global Patent Filings

A comprehensive patent landscape assessment involves examining the extent of patent filings related to the same or similar compounds worldwide:

  • Priority and Family Hemispheres: The patent’s family members potentially extend protection into jurisdictions such as Australia, European Patent Office (EPO), United States (USPTO), and others.
  • Key Patent Families: Identifying related patents provides insights into the scope of protection and patenting strategy.

Competitive Positioning

  • Major Competitors and Patent Holders: Identifying whether major pharma players like Pfizer, AstraZeneca, or generics companies hold overlapping patents.
  • Patent Thickets: The presence of dense patent clusters around similar compounds can create barriers to entry or licensing negotiations.
  • Freedom-to-Oper-ate (FTO): An analysis to determine whether NZ602279’s claims infringe upon existing patents. A high overlap suggests licensing or design-around strategies.

Legal and Patent Status

  • The patent’s legal standing impacts its enforceability:
    • Granted and Active: The patent remains enforceable unless challenged.
    • Opposition or Revocation Proceedings: These could weaken or invalidate the patent.
    • Expiration: Typically, patents expire 20 years from filing, but may vary or be extended via patent term adjustments for regulatory delays.

Life Cycle and Market Opportunity

  • The patent timing and scope influence market exclusivity:
    • Early filing and broad claims extend potential market exclusivity.
    • Overlapping patents in the landscape could impact patent strength or necessitate litigation.

Implications for Stakeholders

Pharmaceutical Innovators

  • Should evaluate NZ602279’s claims for possible infringement or opportunities for licensing.
  • Patent holders might seek to enforce or extend protection via supplementary filings or patent term extensions.

Generic Manufacturers

  • Need detailed freedom-to-operate analyses considering NZ602279’s claims and the broader patent landscape to avoid infringement and formulate around strategies.

Licensing and Strategic Alliances

  • The scope and enforceability inform licensing negotiations, value assessments, and legal risks.

Conclusion

The scope of NZ602279 revolves around the precise language of its claims, with a likely focus on a novel drug compound or formulation. Its strength and full utility depend on the breadth of claims, statutory compliance, and positioning within the global patent landscape. The patent plays a vital role in a larger patent ecosystem, influencing market exclusivity, potential licensing revenue, and competition strategies in New Zealand and beyond.


Key Takeaways

  • Claims Clarity: Carefully drafted claims maximize enforceability; broad claims offer wider protection but face higher invalidation risks.
  • Strategic Positioning: Analyze NZ602279 within the global patent landscape to determine infringement risks and licensing opportunities.
  • Patent Durability: Ensure that patent maintenance, legal standing, and potential extensions sustain competitive advantage.
  • Landscape Mapping: Continually monitor patent filings related to the same compounds to safeguard market position.
  • Legal Vigilance: Prepare for possible patent challenges, and consider geographical patent strategies for broader protection.

FAQs

Q1: What are the typical steps involved in analyzing a drug patent’s claims?
A1: The process involves reviewing claim language, identifying the scope and limitations, assessing novelty and inventive step over prior art, and evaluating enforceability in relevant jurisdictions.

Q2: How does claim breadth affect patent enforceability?
A2: Broader claims provide wider protection but are more susceptible to invalidation if unsupported by the specification or challenged by prior art. Narrow claims are easier to defend but limit scope.

Q3: Can NZ602279’s patent landscape influence clinical development?
A3: Yes, understanding existing patents helps identify freedom-to-operate, avoid infringement, and strategize licensing or development pathways.

Q4: How do patent term extensions impact pharmaceutical patents in New Zealand?
A4: New Zealand allows for patent term extensions or adjustments to compensate for regulatory delays, which can prolong exclusivity beyond the standard 20 years.

Q5: What considerations are critical when designing around existing patents like NZ602279?
A5: Focus on structural differences, alternative delivery methods, or therapeutic uses not claimed, ensuring the new development does not infringe on the patent’s claims.


Sources:
[1] New Zealand Intellectual Property Office. (2023). Patent examination guidelines.
[2] WIPO. (2022). Patent Landscape Reports.
[3] European Patent Office. (2023). Patentability requirements.
[4] Pharmaceutical Patent Strategy. (2021). Best practices for drug patenting and landscape analysis.

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