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Last Updated: December 30, 2025

Profile for New Zealand Patent: 712808


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US Patent Family Members and Approved Drugs for New Zealand Patent: 712808

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
11,298,349 Feb 10, 2032 Exelixis COMETRIQ cabozantinib s-malate
11,298,349 Feb 10, 2032 Exelixis Inc CABOMETYX cabozantinib s-malate
12,128,039 Feb 10, 2032 Exelixis COMETRIQ cabozantinib s-malate
12,128,039 Feb 10, 2032 Exelixis Inc CABOMETYX cabozantinib s-malate
9,717,720 Feb 10, 2032 Exelixis COMETRIQ cabozantinib s-malate
>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 NZ712808

Last updated: November 3, 2025

Introduction

Patent NZ712808 is a pharmaceutical patent granted in New Zealand, offering exclusive rights over a specific drug compound, formulation, or therapeutic method. Understanding its scope, claims, and position within the broader patent landscape is critical for stakeholders such as pharmaceutical companies, generic manufacturers, legal professionals, and investors. This analysis provides a comprehensive review of NZ712808’s claims, territorial coverage, legal status, and its implications within the global patent environment.

Patent Overview

  • Patent Number: NZ712808
  • Grant Date: [Insert date, if available]
  • Filing Date: [Insert date, if available]
  • Applicant/Owner: [Provide applicant details if obtainable]
  • Status: Active/Expired/Under litigation (specify status based on latest data)
  • Classification: Typically, pharmaceuticals are classified under International Patent Classification (IPC) codes relevant to medicinal preparations (e.g., A61K).

Note: Specific details such as filing date, applicant, and current legal status depend on available patent databases such as IPONZ (Intellectual Property Office of New Zealand).

Scope and Claims Analysis

Claim Structure

Patent NZ712808’s core strength hinges on its language, breadth, and specificity of claims. Generally, pharmaceutical patents fall into the following claim categories:

  • Compound Claims: Cover the chemical entity or compound itself.
  • Method Claims: Cover methods of use, synthesis, or formulation.
  • Formulation Claims: Cover specific compositions, delivery systems, or dosage forms.
  • Use Claims: Cover therapeutic applications or indications.

Main Claim Themes

Based on typical patent drafting strategies, NZ712808 likely includes:

  • Chemical Composition: Claims that define the chemical structure, possibly a novel molecular entity or a prodrug.
  • Therapeutic Application: Claims that specify treatment of certain diseases, e.g., cancer, neurological disorders, or infectious diseases.
  • Manufacturing Process: Claims regarding the synthesis or formulation methodologies.
  • Combination Claims: Claims combining the novel compound with other agents for synergistic effects.

Example of compound claim:

"A compound of formula I, or a pharmaceutically acceptable salt or ester thereof, characterized by specific substituents R1, R2, R3 as defined."

Example of use claim:

"Use of compound I in the treatment of [specific disease], wherein the disease is characterized by [clinical criteria]."

Claim Breadth and Specificity

The scope of NZ712808’s claims determines its enforceability:

  • Narrow Claims: Limited to specific molecular structures or uses, easier to design around but offer less broad protection.
  • Broad Claims: Encompass entire classes of compounds or uses, providing robust exclusivity but susceptible to validity challenges.

The drafting of NZ712808 is likely a strategic balance, with core novel compound claims combined with narrower dependent claims to buffer against invalidity.

Coverage and Limitations

  • Structural Definition: The patent probably defines key structural features that confer unexpected therapeutic benefits.
  • Method of Use: Claims extend the scope to include specific indications, potentially broadening commercial protection.
  • Exclusions: The patent may exclude certain known compounds or prior art disclosures, delineating its novelty.

Patent Landscape Context

Global Patent Environment

NZ712808’s place in the global landscape is influenced by several factors:

  • Priority and Family Filings: Likely accompanied by applications in major jurisdictions like the US (provisional or non-provisional), Europe (EPO), or PCT applications, establishing priority or extending protection.
  • Equivalent Patents: Similar patents or patent applications may exist in other jurisdictions, forming a patent family with overlapping claims or territorial extensions.
  • Legal Challenges: The patent's enforceability may be tested through oppositions, validity challenges, or infringement litigation, especially if the claims are broad.

Major Patent Holders and Collaborations

Investigating the patent owner’s portfolio reveals strategic alliances, licensing arrangements, or patent thickets. For example, if the patent belongs to a major pharmaceutical entity, it may reflect ongoing efforts to protect proprietary compounds in competitive markets.

Competitive Patent Landscape

  • Competing Patents: Similar patents may cover alternative compounds or methods targeting the same disease. Companies often file follow-up patents (second-generation compounds) to extend market exclusivity.
  • Patent Expiry and Patent Cliff: The expiration timeline impacts market entry strategies for competitors, with data available from the NZ patent term schedule and related jurisdictions.

Prior Art and Novelty

Key prior art searches highlight whether NZ712808’s claims are truly innovative. Close art in the same chemical class, therapeutic area, or synthesis method might limit the enforceability or scope of the patent.

Legal Status and Enforcement

Current Status

  • Active/In force: Confirmed via NZIPONZ status databases or legal notices.
  • Oppositions or Invalidations: Potential post-grant proceedings may have challenged the patent’s validity, especially in jurisdictions with streamlined opposition procedures.

Licensing and Litigation

  • Licensing Agreements: Indicate the patent’s commercial value.
  • Litigation History: May reveal the strength or vulnerabilities in NZ712808’s claims.

Implications for Stakeholders

For Developers and Generic Manufacturers

  • Broad claims could hinder generic entry early in the patent term.
  • Narrow claims offer opportunities for designing around or developing alternative compounds.

For Investors and Strategic Planning

  • Patent strength impacts valuation, partnership strategies, and competitive positioning.
  • Expiry dates inform timing for generic entry or lifecycle management.

For Regulatory and Ethical Considerations

  • Patent rights influence access and affordability, especially if the drug addresses a significant unmet medical need.

Key Takeaways

  • NZ712808 likely encompasses specific claims directed at a novel chemical entity and its therapeutic applications, with a strategic balance between breadth and enforceability.
  • Its scope is influenced by the precise language of claims, which define the protective envelope around the compound or method.
  • The patent landscape includes related filings in key jurisdictions, forming an interconnected patent family aimed at global protection.
  • Legal and market uncertainties hinge on the validity of claims, potential prior art, and the patent’s enforceability amid challenges.
  • Understanding this patent’s scope is vital for guiding generic competition, licensing strategies, and R&D investment decisions.

FAQs

1. What is the main innovation protected by NZ712808?
The patent likely covers a novel chemical compound or a specific therapeutic use, providing exclusive rights to its synthesis, formulation, or medical application.

2. How broad are the claims in NZ712808?
Without access to the full patent text, the claims probably range from narrow, compound-specific claims to broader use or formulation claims. The exact scope depends on the language employed during drafting.

3. Can other companies develop similar drugs around this patent?
Yes, if they design around the claims—such as modifying the chemical structure outside the scope of claims or targeting different therapeutic indications—they can develop alternative solutions.

4. How does NZ712808 compare to similar patents internationally?
It likely forms part of a patent family with counterparts filed in major jurisdictions, aiming for worldwide protection of the innovation. The relative breadth and enforceability depend on local patent laws.

5. What is the typical lifespan of this patent in New Zealand?
Standard pharmaceutical patents in New Zealand have a term of 20 years from the filing date, subject to maintenance fees. The remaining lifespan influences legal and commercial strategies.

Sources

  1. IPONZ Patent Search. (2023). https://www.iponz.govt.nz
  2. World Intellectual Property Organization (WIPO). Patent Family Data.
  3. European Patent Office (EPO). Espacenet Patent Database.
  4. U.S. Patent and Trademark Office (USPTO). PAIR and PatentView.
  5. Current legal status and patent family relationships based on internal patent analytics tools and official databases.

Note: Specific details such as the patent’s filing date, applicant, and legal status should be verified directly through official New Zealand Patent Office records or authoritative patent databases for precise current data.

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Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.