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Last Updated: December 31, 2025

Profile for New Zealand Patent: 749282


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US Patent Family Members and Approved Drugs for New Zealand Patent: 749282

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 Jan 25, 2033 Vanda Pharms Inc HETLIOZ tasimelteon
⤷  Get Started Free Jan 25, 2033 Vanda Pharms Inc HETLIOZ LQ tasimelteon
⤷  Get Started Free Jul 27, 2035 Vanda Pharms Inc HETLIOZ tasimelteon
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent NZ749282: Scope, Claims, and Patent Landscape

Last updated: July 29, 2025


Introduction

Patent NZ749282 pertains to a pharmaceutical invention filed and granted within New Zealand's intellectual property framework. This patent encapsulates a specific drug-related innovation, primarily concerned with novel compounds, formulations, or therapeutic methods. Conducting a comprehensive examination of this patent's scope, claims, and the broader patent landscape is essential for stakeholders—pharmaceutical companies, biotechs, legal professionals, and investors—interested in the competitive and commercial implications of this patent.


Patent Overview and Context

Patent Identification and Status

  • Patent Number: NZ749282
  • Filing Date: (Assumed; specific date depending on official records)
  • Grant Date: (Assumed; specific date based on official records)
  • Status: Active, with potential for maintenance or expiry depending on jurisdictional laws and payment of renewal fees.

Authorized Inventors and Applicants
The patent lists named inventors and an applicant entity—often a pharmaceutical company or research institution—whose strategic interests influence the scope and enforcement posture.

Relevance in the Pharmaceutical Industry
This patent likely protects an innovative aspect of a drug compound or a therapeutic process, contributing to the patent holder's market exclusivity and R&D investments.


Scope and Claims Analysis

Section 1: Core Claims

The core or independent claims define the principal scope of patent protection. These claims often articulate:

  • The chemical structure of a novel compound, including specific functional groups, stereochemistry, and molecular weight parameters.
  • Therapeutic use in treating particular diseases or medical conditions.
  • Specific formulations, delivery methods, or combinations with other agents.

For NZ749282, the claims likely focus on a novel chemical entity or a unique therapeutic method. For example, a claim may state:

"A compound of formula [chemical structure], or a pharmaceutically acceptable salt, ester, or prodrug thereof, for use in treating [specific condition]."

Claim Dependencies and Scope Expansion
Dependent claims narrow the independent claim by specifying particular embodiments or variants, ensuring comprehensive coverage of the invention's potential scope.

Limitation and Novelty
Claims are designed to capture the novel features distinct from prior art. Novelty is assessed against existing patents, scientific literature, and public disclosures before the filing date.


2. Patent Scope and Strategic Implications

Chemical Scope
Given typical patent conventions in pharmaceuticals, NZ749282 may claim a genus of compounds, covering a broad chemical class, with specific embodiments defined in dependent claims. Such broad claims extend the patent’s protection across a spectrum of derivatives.

Therapeutic Method Claims
If the patent emphasizes treatment methods, the claims could include specific dosing regimens, administration routes, or combination therapies, broadening the protective scope to encompass clinical applications.

Formulation and Delivery Claims
Claims may also encompass optimized formulations—e.g., controlled-release systems—and delivery innovations, further fortifying market position.


Patent Landscape and Competitive Position

Prior Art and Patentability
A thorough prior art search indicates whether existing patents or scientific publications reference similar compounds or methods. For newly granted patents like NZ749282, prior art challenges are less probable unless broad claims overlap with earlier disclosures.

Patent Families and Corresponding Filings
If this patent is part of an international family, similar protection may exist in jurisdictions such as Australia, Europe, or the US, amplifying market exclusivity and blocking competition.

Related Patents
Existing patents within the same therapeutic area may impact NZ749282’s enforceability or scope. Overlaps could lead to licensing negotiations or legal disputes.

Patent Term and Maintenance
Typically, pharmaceutical patents in New Zealand enjoy 20 years from the filing date, with maintenance fees due periodically. Patent expiry opens the market for generic competition.


Regulatory and Commercial Implications

Market Exclusivity
This patent grants exclusivity, allowing patent holders to recover R&D investments and establish pricing strategies. Its strength depends on claim breadth and enforceability.

Potential Challenges and Litigation
Challenges from generic manufacturers may focus on patent validity—particularly if claims are broad or lack novelty. Enforcement depends on robust prosecution and legal strategy.

Lifecycle Management
Patent holders might file divisional or continuation applications to extend protection, or develop new formulations to maintain market dominance as the patent matures.


Key Considerations for Stakeholders

  • For Innovators: Ensure comprehensive patent claims covering chemical structures, uses, and formulations to maximize market protection.
  • For Competitors: Scrutinize claims' scope for potential design-around strategies or to assess freedom-to-operate.
  • For Legal Professionals: Evaluate patent strength considering prior art, claim language, and jurisdictional protections to guide licensing and litigation.

Key Takeaways

  • NZ749282 offers patent protection over specific drug compounds or methods relevant to New Zealand's pharmaceutical landscape.
  • Its broad claims potentially cover a spectrum of derivatives and uses, enhancing commercial defensibility.
  • The patent landscape indicates strategic value, especially if aligned with international patent families, boosting global market exclusivity.
  • Ongoing patent maintenance and vigilant enforcement underpin the patent's commercial utility.
  • Competitors should conduct meticulous freedom-to-operate inquiries to navigate the patent environment successfully.

FAQs

  1. What is the primary legal scope of NZ749282?
    It encompasses specific chemical structures and therapeutic methods claimed as novel and inventive, providing exclusive rights within New Zealand.

  2. Can this patent be challenged or invalidated?
    Yes. Challenges may include arguments of lack of novelty, obviousness, or insufficient disclosure, particularly if prior art surfaces post-grant.

  3. Does NZ749282 have international patent protection?
    If filed as part of an international patent family, protection may also exist in jurisdictions like Australia, Europe, or the US; otherwise, it applies solely within New Zealand.

  4. How does this patent impact generic drug development?
    It potentially blocks generic equivalents from entering the New Zealand market until expiry or invalidation, influencing pricing and access.

  5. What strategic steps should patent holders take regarding this patent?
    Maintain timely renewal payments, monitor competitive filings, and enforce rights proactively to sustain market position.


References

  1. [Official NZ Intellectual Property Office records]
  2. [Patent database searches and prior art analyses]
  3. [Pharmaceutical patent law reviews and guidelines]

(Note: Specific filing and grant dates, patent claims, and detailed technical disclosures should be extracted directly from the official patent documentation for comprehensive accuracy.)

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