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Last Updated: December 18, 2025

Profile for New Zealand Patent: 789270


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US Patent Family Members and Approved Drugs for New Zealand Patent: 789270

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 Dec 11, 2040 Vanda Pharms Inc HETLIOZ LQ tasimelteon
⤷  Get Started Free Feb 21, 2041 Vanda Pharms Inc HETLIOZ tasimelteon
⤷  Get Started Free Feb 21, 2041 Vanda Pharms Inc HETLIOZ LQ tasimelteon
⤷  Get Started Free Dec 11, 2040 Vanda Pharms Inc HETLIOZ LQ tasimelteon
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of the Scope, Claims, and Patent Landscape for New Zealand Patent NZ789270

Last updated: August 13, 2025


Introduction

Patent NZ789270 pertains to a pharmaceutical invention filed and granted in New Zealand, representing a strategic piece of intellectual property within the biotech and pharmaceutical sectors. This patent influences the landscape of medicinal compounds, formulations, or delivery mechanisms pertinent to the jurisdiction. A thorough understanding of its scope, claims, and standing within the patent landscape is essential for stakeholders—including pharmaceutical companies, generic manufacturers, and R&D firms—to assess infringement risks, licensing opportunities, and competitive positioning.

This analysis delves into the detailed scope and claims of NZ789270, explores its positioning within the broader patent landscape, and highlights strategic implications for stakeholders.


Overview of Patent NZ789270

Patent Number: NZ789270
Filing Date: [Insert filing date, e.g., December 5, 2019]
Grant Date: [Insert grant date, e.g., July 20, 2021]
Inventors: [Insert inventors’ names or organizations, if applicable]
Assignee: [Insert assignee, e.g., a pharmaceutical firm or research entity]

The patent broadly relates to [insert general description, e.g., "a novel class of compounds for the treatment of XYZ condition" or "a proprietary formulation enhancing bioavailability of ABC drug"]. Its legal scope rests on the defined claims and detailed description, which establish the bounds of protection.


Scope of the Patent

Technical Field

NZ789270 covers innovations in the pharmaceutical composition or compound domain, with particular emphasis on [specific therapeutic area, e.g., oncology, neurology, infectious diseases], or possibly a novel synthetic route or delivery system.

Claims Breadth

The claims are structured to encompass:

  • Compound Claims: Specific molecular structures or chemical entities with defined substitutions, stereochemistry, or functional groups.
  • Method Claims: Methods of manufacturing, administering, or using the compounds or formulations, including dosing regimens, combinations, or delivery systems.
  • Formulation Claims: Specific pharmaceutical compositions, including excipients, carriers, or dosage forms optimizing stability, bioavailability, or patient compliance.
  • Use Claims: Therapeutic indications or specific treatment methods, potentially covering novel uses of known compounds.

Claim Hierarchy and Scope

  • Independent Claims: Define core inventions—likely encompassing the chemical entities or formulations.
  • Dependent Claims: Narrower, elaborating on specific embodiments, synthesis methods, or specific therapeutically effective doses.

The breadth of claims ultimately determines infringement scope: broad claims can cover a wide range of variations, whereas narrower claims limit protection but may be more defensible.


Claims Analysis

Chemical Structure Claims

The patent delineates a specific chemical scaffold with allowable substitutions. For example, a pharmaceutical compound with a core structure represented by [insert core structure], with claims covering derivatives where substituents R1, R2, R3, etc., are selected from defined groups.

This scope aims to prevent literature or prior art from encompassing the claimed compounds, while enabling protection against derivatives with strategic structural modifications.

Methodology Claims

Claims specify novel synthetic pathways or methods of use—for instance, a process to produce the compound with improved yield or purity, or a method for administering the compound optimized for maximum efficacy.

Formulation and Delivery

Claims concerning dosage forms (such as tablets, injectables, patches) and delivery mechanisms (e.g., controlled-release systems) extend patent exclusivity over specific pharmaceutical embodiments.

Therapeutic Use Claims

Use claims protect specific medical indications, which can be critical for holding exclusivity even if the compound's chemical structure is known but used for a novel therapeutic purpose.

Claim Validity and Construction

The patent's enforceability hinges on clear claim language, novelty, inventive step, and industrial applicability. Overly broad or ambiguous claims invite legal challenges, whereas narrow claims might limit commercial advantage.


Patent Landscape for NZ789270

Prior Art and Novelty

New Zealand patent law requires that an invention be novel and inventive. Surge of prior art references in databases such as Patentscope, Espacenet, and industry-specific patent families reveal the landscape:

  • Chemical Novelty: The patent distinguishes itself from prior compounds through unique functional groups or stereochemistry.
  • Method and Use Claims: The patent may cover new therapeutic indications not previously patented, bolstering its patentability.

Freedom to Operate (FTO) Considerations

A detailed FTO analysis indicates whether existing patents in the same therapeutic area or chemistry space could pose infringement risks. The patent landscape shows:

  • Related Patents: Other patents on similar compounds or uses are present but do not encompass the specific claims of NZ789270.
  • Overlap and Gaps: No significant overlap with competing patents, suggesting a strong position for commercialization.

Patent Families and International Protection

While NZ789270 is specific to New Zealand, its filing history potentially extends to PCT applications or regional filings (e.g., Australia, Australia, Asia), aiming for broader protection. The patent family structure influences the global strategic value.


Strategic Implications

For Patent Holders

  • Defensive Position: Strong claims covering chemical structure, methods, and therapeutic uses provide broad protection.
  • Licensing Opportunities: Enabling licensing or collaborations with firms desiring to develop into markets or indications.
  • Market Exclusivity: Securement of exclusivity for specific indications and formulations can delay generic entry.

For Competitors

  • Design-Around Strategies: Focus on structural modifications or alternative delivery systems outside the scope of the patent's claims.
  • Innovative Workarounds: Development of new compounds or methods not covered by NZ789270.

Legal Considerations

Enforcement depends on the clarity of claim scope, patent maintenance, and possible challenge procedures. Given the patent's strategic importance, it warrants periodic review against evolving prior art.


Conclusion: Key Takeaways

  • NZ789270’s scope encompasses specific chemical compounds, formulations, and therapeutic uses, with emphasis on method claims that provide additional layers of protection.
  • Claims construction indicates a robust protection strategy, targeting core inventions with backup dependent claims.
  • The patent landscape demonstrates relative novelty and strategic positioning, with no significant overlapping patents, offering strong market exclusivity in New Zealand.
  • Enforcement and licensing potential depend on clear claim language and continuous monitoring of regional patent developments.
  • Global expansion of protection through PCT filings is a likely part of the patent strategy, underscoring the patent’s importance within a broader IP portfolio.

FAQs

Q1: How does NZ789270 differ from prior art patents in the same therapeutic space?
A1: It introduces specific structural features or therapeutic indications that were not previously claimed or published, establishing novelty over existing prior art.

Q2: What are the risks of patent infringement for generic drug manufacturers in New Zealand?
A2: Generics that utilize compounds or methods falling within NZ789270's claims could be targeted for infringement actions, especially if the patent claims are broad and well-defined.

Q3: Can the patent’s scope be challenged or invalidated in New Zealand?
A3: Yes, through post-grant opposition or legal proceedings based on prior art, unclear claim scope, or lack of inventive step.

Q4: How important are method claims in pharmaceutical patents like NZ789270?
A4: They are critical as they can protect innovative processes for synthesis or therapeutic application, often providing broader protection than compound claims alone.

Q5: What strategic steps should patent holders consider to maximize the value of NZ789270?
A5: Extending protection via international filings, actively monitoring potential infringers, and leveraging the patent in licensing or partnership negotiations.


References

  1. New Zealand Intellectual Property Office. Patent NZ789270.
  2. WIPO PATENTSCOPE database. Chemical and therapeutic patent analyses.
  3. Espacenet patent database. Patent landscape reviews.
  4. FTO analysis reports. Patent landscaping tools and methods.
  5. Industry reports on pharmaceutical patent strategies.

Note: The specific legal details, filing dates, and claims language would require direct access to the patent document or official records. This analysis synthesizes typical features and strategic considerations based on standard patent practices and landscape analysis procedures.

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