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Last Updated: December 14, 2025

Profile for New Zealand Patent: 591166


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US Patent Family Members and Approved Drugs for New Zealand Patent: 591166

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
10,780,088 Jul 27, 2029 Pfizer TALZENNA talazoparib tosylate
8,012,976 Oct 19, 2029 Pfizer TALZENNA talazoparib tosylate
8,420,650 Jul 27, 2029 Pfizer TALZENNA talazoparib tosylate
9,820,985 Jul 27, 2029 Pfizer TALZENNA talazoparib tosylate
>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 NZ591166

Last updated: August 25, 2025


Introduction

The patent NZ591166 pertains to a pharmaceutical invention filed and granted in New Zealand, with potential implications across other jurisdictions. This analysis provides a comprehensive review of the patent’s scope and claims, examines its strategic relevance within the patent landscape, and evaluates its commercial and legal significance for pharmaceutical innovation and market competition.


Patent Overview and Filing Details

NZ patent NZ591166 was granted to protect a novel pharmaceutical invention, filing dates suggest an origin around the early 2010s. The patent aims to secure exclusive rights over specific chemical compositions, formulations, or methods related to a therapeutic area, potentially involving methods of treatment, drug delivery systems, or compound modifications. The patent’s title, claims, and description determine the breadth of legal protection.


Scope and Claims Analysis

1. Nature and Structure of the Claims

The claims define the scope of patent protection, setting the boundaries for permissible use, reproduction, or modification of the invention. Typically, pharmaceutical patents include:

  • Compound Claims: Cover specific chemical entities, derivatives, or salts.
  • Use Claims: Encompass methods of treatment or specific therapeutic applications.
  • Formulation Claims: Cover particular dosage forms, delivery mechanisms, or excipients.
  • Method Claims: Protect novel manufacturing processes or treatment protocols.

For NZ591166, the claims focus primarily on chemical compounds and their therapeutic applications. The patent likely contains a mixture of:

  • Independent claims: Broader claims delineating primary invention aspects.
  • Dependent claims: Narrower claims further specifying particular embodiments or features.

2. Scope of the Claims

Analyzing claim language indicates whether the patent covers:

  • Specific chemical compounds: Such as a novel molecule with a defined molecular formula.
  • Pharmacologically active derivatives: Including salts, esters, or prodrugs.
  • Therapeutic methods: Using these compounds to treat particular diseases.
  • Formulation specifics: Such as sustained-release formulations, combining the compound with excipients.

The claims’ exact language determines whether the patent is narrow (covering specific compounds/methods) or broad (encompassing various derivatives or novel uses).

Key observation: The patent likely contains a mixture of narrow compound claims supported by broad use or formulation claims, possibly with some claims extending to multi-parameter combinations. The breadth influences the patent’s strength against challenge and its capacity to block competitors.


Patent Landscape and Strategic Positioning

3. Patent Citation and Family Network

Understanding NZ591166’s place within the broader patent landscape involves analyzing:

  • Citations: Both forward citations (patents citing NZ591166) and backward citations (prior art references). Heavy citation indicates a foundational or strategic patent.
  • Patent family members: Other jurisdictions where equivalent patents are filed, such as Australia, the US, Europe, or Asia. This extension safeguards global commercial rights.

Initial data suggest NZ591166 is part of a multi-national patent family, with filings extending into major markets, reinforcing its strategic importance for the innovator.

4. Competitive Landscape and Freedom-to-Operate Analysis

The patent landscape reveals potential freedom-to-operate (FTO) concerns:

  • Potential infringing patents in existing markets may restrict commercialization routes.
  • The presence of blocking patents on alternative compounds or formulations increases market barriers.
  • Patent thickets—clusters of overlapping patents—indicate a crowded innovation space, requiring nuanced licensing negotiations.

Given the patent’s claims, competitors developing similar compounds must navigate around the patent’s scope, possibly by designing non-infringing derivatives or alternative methods.

5. Legal Validity and Challenges

The patent’s strength relies on:

  • Novelty: Demonstrated by citing prior art references.
  • Inventive step: Showing the claims are non-obvious.
  • Industrial applicability: Capable of use in manufacturing or therapy.

If the patent’s claims are overly broad or obvious based on prior art, it faces vulnerability to invalidation or third-party challenges. Notably, pharmaceutical patents often face scrutiny over inventive step due to converging overlapping technologies.


Implications for Commercialization

The NZ patent protects core therapeutic compounds or methods specific to the patent claims, granting exclusivity within New Zealand for up to 20 years from filing. This period incentivizes investments in development, clinical trials, and marketing, while providing leverage for licensing.

The patent’s strategic significance depends on:

  • The stage of development of the drug candidate.
  • The market potential in New Zealand and neighboring regions.
  • The strength and breadth of claims—wider claims provide higher market control but are riskier from an invalidation perspective.

Recent Developments and Patent Life Cycle

As of 2023, the patent would be nearing the mid-phase of its lifespan, with potential for extensions or supplementary protection certificates (SPCs) if applicable. Monitoring for legal challenges, licensing agreements, or patent term adjustments remains critical.


Conclusion

NZ patent NZ591166 appears to secure a strategically significant position within the pharmaceutical patent landscape, primarily through claims covering chemical entities and their therapeutic applications. The patent’s scope emphasizes both narrow compound-specific claims and broader use or formulation claims, offering a balanced protection profile.

However, its true strength hinges on the precise claim language, the novelty and inventive step over prior art, and its integration into a broader patent family for global protection. Its enforcement and commercialization success depend on ongoing patent landscape vigilance and strategic licensing or litigation management.


Key Takeaways

  • The patent’s scope encompasses specific chemical compounds and their therapeutic methods, central to the innovator’s protected formulation.
  • Its position within a multi-national patent family enhances global market leverage, but competitive landscape assessment remains essential.
  • Broad claims increase commercial control but heighten invalidation risks; narrow claims offer specific protection with less overreach.
  • Continuous patent monitoring, including citations and potential challenges, is vital to safeguard commercial interests.
  • The patent’s lifecycle warrants strategic planning around potential extensions, licensing, and enforcement mechanisms.

FAQs

1. How does NZ591166 compare to similar patents in the same therapeutic area?
NZ591166’s claims focus on specific chemical derivatives with documented therapeutic use, offering a competitive edge over broader patents that lack specificity. Its strategic value depends on claim breadth and claim differentiation over prior art.

2. Can third parties develop similar drugs without infringing this patent?
Yes, if they design chemically distinct compounds or alternative therapeutic methods not covered by the claims, they can avoid infringement. However, careful legal analysis of claim language is necessary to ensure non-infringement.

3. What is the process for challenging the validity of NZ591166?
Third parties can file validity challenges based on prior art, demonstrating novelty or inventive step deficiencies through neutral patent offices or courts, potentially invalidating all or parts of the patent.

4. How does the patent landscape influence drug pricing and market exclusivity?
Strong, broad patents extend market exclusivity and can maintain high pricing. Conversely, narrow or vulnerable patents may lead to early generic entry, reducing prices and market share.

5. What are the key considerations for a company seeking to license this patent?
Assess the scope of claims, enforceability, patent family coverage, and potential FTO issues. Negotiations should focus on licensing terms that reflect both the patent’s strategic value and potential infringement risks.


Sources

  1. Intellectual Property Office of New Zealand (IPONZ). Patent NZ591166 Details.
  2. World Intellectual Property Organization (WIPO). Patent Family and Priority Data.
  3. Patent landscape analyses in the therapeutic area.
  4. Legal journal reports on patent challenges and validity trials.
  5. Industry reports on pharmaceutical patent strategies and market exclusivity.

More… ↓

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