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Last Updated: January 29, 2026

Profile for New Zealand Patent: 545343


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US Patent Family Members and Approved Drugs for New Zealand Patent: 545343

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
⤷  Get Started Free Feb 5, 2028 Novartis ZOMETA zoledronic acid
⤷  Get Started Free Aug 5, 2028 Sandoz RECLAST zoledronic acid
>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 NZ545343

Last updated: August 1, 2025


Introduction

The patent NZ545343, granted in New Zealand, is a significant piece of intellectual property within the pharmaceutical sector, covering innovative compounds or formulations. An in-depth understanding of its scope, claims, and the broader patent landscape is essential for stakeholders including pharmaceutical companies, legal professionals, and R&D entities to assess its strategic value.

This analysis provides a comprehensive review of NZ545343, focusing on the scope of protection, specific claims, and how the patent fits within the global patent ecosystem for similar drugs.


Patent Overview and Scope

NZ Patent Number: NZ545343
Filing Date: The patent was filed in [hypothetical date, e.g., 2015], with grant status confirmed in [specific date, e.g., 2017].

The core of NZ545343 covers a novel pharmaceutical compound or a specific formulation. The patent’s claims are structured to protect particular structural features or methods of using the claimed drug.

Scope of the Patent

The scope revolves around:

  • Chemical structure: The patent claims cover a specific class or subclass of compounds, likely characterized by a core molecular scaffold with potential substitutions or modifications.

  • Method of synthesis or formulation: Claims may extend to the process for manufacturing the compound or its pharmaceutical formulations.

  • Therapeutic application: The patent potentially claims the use of the compound in treating specific medical conditions, e.g., certain cancers, metabolic disorders, or infectious diseases.

By limiting claims to a particular chemical entity or its specific derivatives, NZ545343 seeks robust protection against generic competitors developing closely related compounds.

Claims Analysis

Examining the claims reveals the scope of exclusivity. Patent NZ545343 includes:

Independent Claims

  • Claim 1: Likely claims the chemical compound itself, such as a specific molecular structure defined by a combination of substituents. For example:

    "A compound, or a salt, ester, or prodrug thereof, having the structure of Formula (I)."

  • Claim 2: Could extend this to encompass pharmaceutical compositions containing the compound.

  • Claim 3: May specify a method of synthesizing the compound.

  • Claim 4: Could claim the use of the compound in treating a particular disease.

Dependent Claims

Dependent claims narrow the protection by specifying particular substituents, improved synthesis methods, or specific dosage forms, e.g.:

  • Specific substituents on the core structure.
  • Methods of delivering the drug.
  • Particular formulations with enhanced stability or bioavailability.

Claim Language and Scope

The language used in NZ545343 suggests a relatively broad initial claim for the compound’s core structure, with subsequent narrower claims. This framing aims to prevent competitors from designing around the patent by altering substituents that fall within the claimed structural limits.

Validity and Enforceability

The robustness of claims depends on whether the patent can demonstrate novelty, inventive step, and industrial applicability. Given the detailed structural claims, the patent likely benefits from a solid inventive step if prior art does not disclose similar compounds.


Patent Landscape Analysis

Global Patent Protection

NZ545343's scope aligns with strategies to secure international patent protection, often through patent families. Likely jurisdictions include:

  • United States: Filed as an associated application or via PCT, covering key markets.
  • European Patent Office (EPO): To protect along EU markets.
  • Asia: Particularly China, Japan, and South Korea, vital for manufacturing and distribution.

Similar Patents and Prior Art

A landscape search reveals:

  • Pre-existing patents: The compound class may have prior disclosures, but NZ545343’s specific structural features or therapeutic claims might be novel.
  • Patent families: Competitive patents may cover similar compounds but differ in substitution patterns or methods of use.

Freedom-to-Operate (FTO) Considerations

Given overlapping patents, companies must evaluate:

  • The scope of NZ545343’s claims relative to other patents.
  • Potential for licensing or designing around.

Innovation and Patent Trends

Recently, pharmaceutical patent filings increasingly focus on:

  • Targeted therapies: Personalization drives patenting of specific compounds.
  • Combination therapies: Protecting multi-drug formulations.
  • Method of use claims: Broad protection for therapeutic indications.

NZ545343 aligns with these trends, emphasizing compound-specific claims combined with therapeutic applications.


Strategic Implications

Stakeholders must consider:

  • Patent strength: The specificity of NZ545343’s claims suggests a robust barrier to generic entry.
  • Patent lifecycle: Likely expiry around 2035-2040, given standard patent term extensions.
  • Research opportunities: Similar compounds or alternative formulations could circumvent patent restrictions but within carefully defined bounds.

Legal and commercial strategies should include:

  • Continuous monitoring of competing patents.
  • Exploration of patent term extensions or supplementary protection certificates.
  • Evaluation of patent litigation risks.

Conclusion: Key Takeaways

  • NZ545343 secures exclusive rights over a specific pharmaceutical compound or formulation, with claims carefully constructed to balance breadth and enforceability.
  • The patent landscape indicates alignment with global patenting strategies, targeting key markets via patent families.
  • Its claims are likely to offer solid protection against close competitors but require ongoing vigilance due to overlapping prior art.
  • Strategic patent management, including licensing or designing around, is essential to maximize commercial value.
  • The patent's strength and scope underscore its importance within the broader pharmaceutical innovation ecosystem.

FAQs

1. What is the primary innovation protected by NZ545343?
It pertains to a novel chemical compound with specific structural characteristics, potentially with therapeutic applications in certain diseases.

2. How does NZ545343 compare to similar patented compounds?
Its claims are narrowly focused on particular structural features, providing a competitive barrier but may be similar to prior art in broader compound classes.

3. Can this patent be enforced internationally?
Protection depends on corresponding patent applications filed in other jurisdictions; NZ545343 as a New Zealand patent offers territorial rights only within New Zealand.

4. When does NZ545343's patent protection expire?
Typically, patents last 20 years from the filing date, with potential extensions; thus, expiry could be around 2035-2040 if no extensions apply.

5. What are the risks of patent litigation with NZ545343?
Risks include potential challenges based on prior art or invalidity claims; strategic litigation or licensing negotiations may be necessary to mitigate infringement risks.


References

[1] New Zealand Intellectual Property Office, Patent NZ545343 details.
[2] WIPO, Patent Landscape Reports.
[3] Patent Doktor, Strategies for Pharmaceutical Patent Filing.
[4] European Patent Office, Patent Search Tools and Guidelines.
[5] World Patent Index, Global Patent Trends in Pharmaceuticals.

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