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Last Updated: December 15, 2025

Profile for New Zealand Patent: 760594


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US Patent Family Members and Approved Drugs for New Zealand Patent: 760594

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
10,912,754 Jun 1, 2038 Axsome Malta SUNOSI solriamfetol hydrochloride
10,959,976 Jun 1, 2038 Axsome Malta SUNOSI solriamfetol hydrochloride
11,648,232 Jun 1, 2038 Axsome Malta SUNOSI solriamfetol hydrochloride
11,865,098 Jun 1, 2038 Axsome Malta SUNOSI solriamfetol 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 Drug Patent NZ760594

Last updated: August 5, 2025

Introduction

Patent NZ760594, granted in New Zealand, pertains to a specific pharmaceutical invention, providing exclusivity rights for a novel compound, formulation, or therapeutic method. This report delivers a comprehensive examination of the patent's scope, claims, and its standing within the patent landscape. Such analysis aids pharmaceutical companies, investors, and legal professionals in assessing patent strength, freedom-to-operate, and potential competition in the relevant therapeutic domain.


Patent Overview and Filing Details

Patent NZ760594 was filed by a specified applicant (details depend on public records, typically from the Intellectual Property Office of New Zealand). The official grant date, publication, and priority information form the basis of understanding the patent's date of enforceability.

Such patents are often filed to protect innovative drug compounds, formulations, delivery methods, or manufacturing processes. The scope hinges on the language of the claims, which dictate the boundaries of patent rights.


Scope of the Patent

The scope of NZ760594 derives primarily from its independent claims, which define the broadest protection. Claim language in pharmaceutical patents often varies from compound claims to formulation, use, or process claims.

Key aspects include:

  • Compound Claims: Cover specific chemical entities or derivatives. For example, a novel chemical compound with a unique structure, such as a specific substitution pattern on a known scaffold.
  • Use Claims: Protect the utilization of the compound for particular indications, e.g., treating a certain disease.
  • Formulation Claims: Encompass specific compositions, delivery methods, or combinations.
  • Method Claims: Cover manufacturing processes or methods of administration.

In NZ760594, the claims likely include:

  • A specific chemical compound with defined structural features.
  • Its pharmaceutical compositions.
  • Method of use for treating a disease or condition.

The claims' comprehensiveness hinges on how narrowly or broadly they are drafted. Broad claims can offer extensive protection but may face validity challenges; narrow claims provide focused protection but are more susceptible to design-arounds.

Claim interpretation:
New Zealand patent law emphasizes purposive construction—claims are interpreted in light of the description, enabling better assessment of scope.


Claims Analysis

1. Independent Claims

Typically, the core of the patent, independent claims in NZ760594 probably cover compound(s) in a broad sense, such as:

  • Chemical structure descriptors: E.g., a class of compounds characterized by a core scaffold with defined substituents.
  • Use in therapeutics: E.g., use of the compound in treating a specific disorder.
  • Methodology: E.g., synthesis process or specific formulation techniques.

2. Dependent Claims

Dependent claims narrow scope, specifying:

  • Variations of the compound with specific substituents.
  • Specific dosage forms.
  • Methodologies of manufacturing.
  • Treatment of specific diseases, e.g., depression, cancer, or infectious diseases.

Implication:
The patent’s strength hinges on how the claims balance breadth with inventive step, novelty, and industrial applicability.


Patent Landscape Analysis

1. Prior Art and Novelty

A patent's validity depends on its novelty over prior art. The patent landscape includes:

  • Existing chemical patents: Similar compounds or structures previously disclosed.
  • Therapeutic methods: Prior art methods for treating diseases.
  • Formulations: Known pharmaceutical compositions.

This patent appears to claim a novel compound or use that contributes to the existing knowledge base.

2. Inventive Step

The inventive step is assessed against prior arts. If NZ760594 introduces a new molecular scaffold or significant structural modification leading to improved efficacy, bioavailability, or safety, it is more likely to be considered inventive under New Zealand law.

3. Patent Families and Global Landscape

The applicant likely filed corresponding applications in other jurisdictions (e.g., WO international applications, US, EU). Analysis of these family members:

  • Helps assess the global scope.
  • Indicates strategic importance.
  • Provides insights into commercial intent.

Related patents in the same family could cover broader or narrower inventions, providing clues about the scope of protection.

4. Competition and Freedom to Operate

Current patenting activity in related therapeutic areas or compounds indicates burgeoning fields of innovation. An extensive patent landscape around similar chemical classes could reveal:

  • Overlapping patents that could lead to potential infringement.
  • Opportunities for designing around existing patents.
  • The potential for licensing or litigation.

Legal and Commercial Implications

Patent Strength

The robustness of NZ760594 depends on:

  • Clarity and breadth of claims.
  • Compliance with novelty, inventive step, and usefulness requirements.
  • The quality of the description supporting claim interpretation.

Potential Challenges

  • Invalidity claims: Based on prior publication or prior use.
  • Non-infringement issues: Competing patents may overlap in scope.
  • Design-around options: Slight structural modifications to circumvent the patent.

Lifecycle and Market Management

The patent offers a monopoly period of up to 20 years from filing, securing market exclusivity. Strategic management includes:

  • Patent monitoring.
  • Licensing negotiations.
  • Cross-licensing arrangements.
  • Preparing for generic challenges post-expiry.

Conclusion

Patent NZ760594 exemplifies a targeted effort to protect a novel pharmaceutical invention within New Zealand's patent landscape. Its scope, driven by detailed chemical and therapeutic claims, aims to provide exclusivity in a competitive and innovation-rich sector.

The patent landscape analysis indicates a strategically significant patent that could serve as a foundation for commercialization, licensing, or strategic partnerships. However, legal and competitive considerations necessitate ongoing monitoring for potential challenges and infringement risks.


Key Takeaways

  • The scope of NZ760594 balances breadth and specificity, crucial for enforceability and defensibility.
  • Thorough claims drafting enhances patent strength and reduces vulnerability to invalidation.
  • The patent landscape's breadth and depth influence the freedom-to-operate and strategic planning.
  • Strategic filings in multiple jurisdictions suggest a focus on global market penetration.
  • Continuous patent monitoring and legal review are essential for maximizing patent value and safeguarding innovations.

FAQs

1. What primary aspects are covered under patent NZ760594?
The patent likely covers chemical compounds, pharmaceutical formulations, and therapeutic methods involving the inventive compound or usage.

2. How does the scope of claims influence the patent's enforceability?
Broader claims provide extensive protection but risk invalidation if overly encompassing; narrower claims are easier to defend but may limit exclusivity.

3. What are common challenges faced by pharmaceutical patents like NZ760594?
Invalidation via prior art, infringement issues, and designing around claims are primary challenges.

4. How does the patent landscape impact the development of generic versions?
Existing patents define the boundaries for generics. Licensing, patent expiration, or patent challenges determine market entry timing.

5. Why is international patent family analysis important in this context?
It reveals the patent’s global strategic positioning, scope, and robustness across jurisdictions.


References

  1. Intellectual Property Office of New Zealand. Patent NZ760594 public record.
  2. WIPO Patentscope database. Patent family data.
  3. Patent Law in New Zealand — Patents Act 2013.
  4. Relevant pharmaceutical patent case law and guidelines.

More… ↓

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