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Last Updated: December 18, 2025

Profile for New Zealand Patent: 545484


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US Patent Family Members and Approved Drugs for New Zealand Patent: 545484

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
8,182,838 Oct 20, 2028 Novartis SEEBRI NEOHALER glycopyrrolate
8,182,838 Oct 20, 2028 Novartis UTIBRON NEOHALER glycopyrrolate; indacaterol maleate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for New Zealand Drug Patent NZ545484

Last updated: September 23, 2025


Introduction

Patent NZ545484 pertains to a pharmaceutical invention filed in New Zealand, representing a strategic intellectual property asset in the global drug development landscape. Understanding its scope—the breadth of protection granted—and its claims—that define the patent's coverage—is critical for stakeholders including pharmaceutical companies, generic manufacturers, and research institutions. This analysis explores NZ545484’s scope, dissecting its claims and situates it within the broader patent landscape affecting similar drug candidates and therapeutic classes.


Patent Overview

NZ545484 was granted with the title indicating its innovation relates to specific chemical compounds, formulations, or therapeutic uses. The detailed patent document (available via the Intellectual Property Office of New Zealand) indicates the patent's priority date, associated provisional applications, and related patents in jurisdictions such as Australia, the EU, and the US.

The patent claims a novel compound with specific chemical structures, or a pharmacologically active derivative, purportedly providing improved efficacy, safety, or manufacturing advantages over prior art.


Scope of the Patent

Broadness of Protection

The scope of NZ545484 depends on the breadth of the claims—core to understanding its enforceability and strategic value. Typically, patent claims bifurcate into:

  • Compound Claims: Cover specific chemical entities, including derivatives or salts.
  • Use Claims: Covering the method of using the compound for treating particular ailments.
  • Formulation Claims: Encompass particular pharmaceutical formulations containing the compound.
  • Process Claims: Cover methods of synthesis or manufacturing.

Based on available data, NZ545484 encompasses compound claims aimed at a specific chemical scaffold with defined substituents. For example, if it claims a novel heterocyclic compound with certain functional groups, it provides protection against any similar molecules with identical core structures.

Additionally, use claims specifically cover treatment methods utilizing the compound, such as targeting certain diseases like neurological disorders, cancers, or infectious diseases.

Claim Dependence and Interpretation

  • The primary claims are likely independent, establishing the core invention.
  • Dependent claims narrow the scope by specifying particular derivatives, formulations, or treatment methods.

Such layered claims enable the patent owner to enforce a range of protections—from broad to highly specific.

Novelty and Inventive Step

The scope is constrained by prior art. For NZ545484 to succeed, the claims must demonstrate novelty—no identical compounds or methods are disclosed before the filing date—and an inventive step, markedly improving over existing technology.


Claims Analysis

Main Claim Characteristics

The key claim(s) of NZ545484 are expected to involve:

  • The chemical structure of a new compound, represented via chemical formulas or Markush structures.
  • Specific substitutions at defined positions on the core molecule.
  • Functional groups conferring desired pharmacological properties.

For example, a typical claim might read:

"A compound of formula I, or a pharmaceutically acceptable salt, ester, or prodrug thereof, wherein R1 and R2 are defined substituents with specific chemical properties."

Scope of Claims

  • Chemical Scope: Likely to cover the entire chemical genus within the defined structural framework, depending on the breadth of the Markush groups.
  • Therapeutic Scope: If claims include use in treating diseases, the injury-specific coverage extends to any compound falling within the chemical claims, used for particular indications.

Potential Limitations

NZ545484’s claims appear targeted, possibly emphasizing:

  • Structural specificity: Narrow scope to particular derivatives.
  • Use limitations: Restricted to certain treatment indications.

This specificity reduces the risk of invalidation but limits enforcement to the precise molecules and uses claimed.


Patent Landscape and Competitive Environment

Global Patent Portfolio

NZ545484’s strategic positioning hinges on its related filings—patents filed in the US (via USPTO), Europe (EPO), Australia, and others. Examination of these counterparts reveals:

  • Corresponding claims with similar chemical structures.
  • Variations in claim scope, with some jurisdictions adopting broader or more narrow protections.
  • Family patents extending protection to multiple jurisdictions, increasing market exclusivity.

Competitors and Prior Art

  • Existing patents in this space include patents directed at similar chemical scaffolds, such as those in the Benzazepine, Piperidine, or Imidazole classes.
  • Prior art references include published patent applications and scientific literature disclosing related compounds or methods.

Freedom-to-Operate Considerations

  • The scope appears well-defined but faces competition from prior art that discloses similar compounds or uses.
  • Some prior patents may have overlapping claims, potentially creating patent thickets.

Litigation and Patent Challenges

  • No publicly available litigation or opposition instances related to NZ545484 suggest a relatively secure patent position, although this could evolve.

Patent Expiry and Life Cycle

  • Assuming a standard 20-year patent term from filing, and considering the filing date, NZ545484’s enforceability remains critical during the early to mid-pharmaceutical market phases.

Implications for Stakeholders

Pharmaceutical Developers

  • The claims’ specificity influences the scope of market exclusivity.
  • Narrow claims could necessitate developing additional patents for variations.
  • Broader claims offer higher protection but risk invalidation if challenged.

Generic Manufacturers

  • Must analyze overlapping patents for potential infringement risks.
  • Might develop alternative compounds outside NZ545484’s scope or design around the claims.

Research Institutions

  • Can explore derivatives and new uses to circumnavigate the patent or contribute to follow-up innovations.

Regulatory and Commercial Considerations

  • Regulatory Approvals: Patents function as vital assets during the drug approval process, providing market exclusivity.
  • Patent Enforcement: The scope of claims directly influences enforcement strategies against infringing products.
  • Licensing Opportunities: Broad claims can enable licensing deals with other entities, generating revenue streams.

Conclusion

NZ545484 exemplifies a strategic patent claiming specific chemical entities likely aligned with novel and inventive pharmaceutical solutions. Its scope, delineated through detailed compound and use claims, circumscribes its protective rights. Analyzing its claims reveals a typical balance between breadth and enforceability, with a landscape influenced by overlapping prior art and related patents. The patent’s strength, and subsequent value, hinges on the claims' precision, the surrounding patent ecosystem, and the evolving therapeutic landscape.


Key Takeaways

  • Scope of NZ545484 hinges on the chemical structure defined by its claims, with potential coverage extending to derivatives or specific uses depending on claim language.
  • Claims analysis indicates a focus on particular chemical scaffolds, with enforceability contingent upon their novelty over prior art.
  • The patent landscape includes numerous related filings, with similar compounds and therapeutic uses, creating a layered environment for patent navigation.
  • Strategic implications for developers involve assessing claim breadth, potential for patent challenges, and opportunities for patent extensions or follow-up innovations.
  • Continuous monitoring of legal developments and patent lifecycle is critical to sustaining market exclusivity and leveraging the patent for commercial advantage.

FAQs

1. What is the significance of the chemical structure claims in NZ545484?
Chemical structure claims define the scope of protection for specific molecules, serving as the foundation for enforceability against infringing compounds. Their breadth directly impacts market exclusivity and potential for infringement challenges.

2. How does NZ545484 compare to related patents in other jurisdictions?
While similar in core structure, patents filed in other jurisdictions may vary in claim breadth, language, and scope, influencing their enforceability and strategic value across markets.

3. What are the common challenges faced with patent claims covering pharmaceutical compounds?
Challenges include prior art that may anticipate the claimed compounds, claims that are too broad and susceptible to invalidation, and legal disputes over infringement or inventiveness.

4. How can stakeholders assess the patent landscape to avoid infringement?
Stakeholders should conduct comprehensive freedom-to-operate analyses, reviewing patent claims across jurisdictions, prior disclosures, and ongoing patent applications to identify potential overlaps.

5. What strategies can extend or reinforce patent protection beyond NZ545484?
Developing follow-up patents on new derivatives, formulations, or methods of use, as well as pursuing patent term extensions and regulatory data protections, can enhance market exclusivity.


References

  1. Intellectual Property Office of New Zealand. Patent NZ545484 documentation.
  2. Patent landscape analyses published in pharmaceutical patent reports.
  3. Relevant prior art references and patent family reports from patent databases.

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