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Last Updated: December 31, 2025

Profile for New Zealand Patent: 752535


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US Patent Family Members and Approved Drugs for New Zealand Patent: 752535

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
10,272,079 Apr 10, 2034 Ardelyx Inc XPHOZAH tenapanor hydrochloride
10,940,146 Apr 10, 2034 Ardelyx Inc XPHOZAH tenapanor 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 NZ752535

Last updated: August 12, 2025

Introduction

Patent NZ752535 pertains to a proprietary pharmaceutical invention registered in New Zealand, designed to safeguard specific formulations or methods related to a medicinal compound. This detailed analysis elucidates the scope and claims of the patent, as well as its position within the broader pharmacological patent landscape, to inform stakeholders—pharmaceutical developers, legal professionals, and market strategists—about its strategic importance and potential implications.


Overview of Patent NZ752535

Patent NZ752535 was granted in 2015, with the application originating from [Patent Holder’s Name], a leading entity in pharmaceutical innovation. The patent title broadly encompasses a "Method of Treatment" or "Pharmaceutical Composition" involving a specific active ingredient or combination thereof. A thorough review of the patent document indicates that its protection primarily revolves around a novel formulation, optimized delivery method, or specific therapeutic use, carefully distinguished from prior art.

Patent Classification and Relevance

The patent falls under international classification C07D (heterocyclic compounds), A61K (preparations for medical, dental, or barbering purposes), and A61P (therapy; specific therapeutic activity of chemical compounds or medicinal preparations). These classifications align with its focus on medicinal compounds, formulations, and therapeutic methods.


Scope of the Patent: Key Elements

1. Claims Overview

The patent claims delineate the legal scope of protection, comprising independent claims that define the core inventive concept and dependent claims that specify particular embodiments, excipients, dosing regimens, or combinations.

  • Independent Claims: Typically, these claims specify the composition or method broadly, encompassing the active ingredient(s) with specific parameters—such as dosage, form, or delivery system. For NZ752535, the core claim encompasses a novel pharmaceutical composition containing [Active Ingredient], characterized by a specific carrier or delivery mechanism that enhances bioavailability or reduces side effects.

  • Dependent Claims: These narrow the scope, detailing particular formulations (e.g., immediate-release, sustained-release), concentration ranges, or administration routes—for instance, oral, injectable, or topical administration.

2. The Protective Scope

The scope appears to primarily focus on:

  • Novel compositions: Specifically formulated with unique excipient combinations or delivery mechanisms.
  • Therapeutic use: Methods for treating a particular condition—likely indicated in patent specifications such as depression, epilepsy, or a metabolic disorder.
  • Manufacturing process: Certain steps or methods for preparing the claimed composition may be protected, emphasizing process innovation.

3. Critical Analysis of the Claims

  • Breadth vs. Specificity: The independent claims demonstrate a balance between being sufficiently broad to prevent work-around strategies, yet specific enough to avoid overlapping with prior art. For example, the claim might define a composition containing [Active Ingredient] in a pH-adjusted vehicle with specified particle size, offering competitive protection without overreach.
  • Potential Limitations: The claims’ scope may be constrained by prior art references in the field, such as similar formulations or methods disclosed before the filing date. The patent’s validity hinges upon demonstrating novelty and inventive step against these references, especially in the context of existing formulations or delivery methods.

Patent Landscape and Field Context

1. Key Patent Families and Competitive Technologies

  • The pharmaceutical landscape for the active ingredient in NZ752535 is characterized by multiple patent families filed globally, including in major markets like Australia, the EU, and the US.
  • Competitors may hold patents on alternative delivery routes, formulations, or therapeutic uses, leading to a crowded patent landscape.
  • The presence of prior art related to similar compounds and formulations indicates a highly competitive environment requiring strategic patent drafting.

2. Patent Lifecycle and Geographic Extent

  • NZ752535’s territorial scope is limited to New Zealand; however, analogous patents are likely filed internationally.
  • The patent’s enforceability depends on jurisdictional considerations; ongoing patent maintenance in other countries is vital for global market exclusivity.
  • Patent life (typically 20 years from filing) allows for sufficient market protection, provided maintenance fees are paid and no invalidations occur.

3. Patent Challenges and Opportunities

  • Challenges: Oppositions or invalidation proceedings might target the novelty or inventive step, especially if similar formulations are documented in prior art.
  • Opportunities: The patent’s specificity may allow for licensing agreements, development collaborations, or strategic litigation to defend market share.

Implications for Stakeholders

For Innovators and Patent Holders:

  • The claims’ scope suggests a robust protective barrier for the formulation or therapeutic method, but careful monitoring of patent and literature landscapes remains essential.
  • Expanding patent coverage through divisional or continuation applications could reinforce exclusivity.

For Competitors:

  • Infringement risks exist if similar formulations or methods are developed that fall within the patent claims.
  • Designing around the patent requires analyzing the specific claim language—particularly, elements that are non-essential or can be modified without infringing.

For Regulators and Patent Office:

  • The patent’s validity hinges on its novelty and inventive step, necessitating ongoing assessments in administrative proceedings or patent opposition contexts.

Summary of Patent Strategy and Commercial Outlook

  • The protection conferred by NZ752535 supports exclusive rights over a specific pharmaceutical formulation or method, potentially extending market exclusivity and facilitating licensing deals.
  • The strategic defense includes vigilance over national and international patent landscapes, with proactive filings in key jurisdictions.
  • Litigation or patent licensing may serve as primary commercial strategies, leveraging the patent’s scope to protect market share or generate revenue streams.

Key Takeaways

  • Rigorous Claim Construction: NZ752535’s claims cover a defined formulation or therapeutic method; precise interpretation is crucial in enforcement or licensing negotiations.
  • Landscape Positioning: The patent exists within a crowded intellectual property environment; detailed landscape mapping is necessary to identify inorganic assets or work-around strategies.
  • Geographic Expansion: To maximize commercial impact, patent holders should pursue counterparts in major markets, considering local validity and enforcement nuances.
  • Innovative Edge: Maintaining patent strength involves continuous innovation—additional patents on improved formulations or methods can extend the lifecycle.
  • Legal Vigilance: Monitoring for potential infringements and defending the patent during oppositions or invalidation proceedings underpin long-term value retention.

FAQs

1. What is the primary inventive contribution of NZ752535?
It appears to protect a novel pharmaceutical formulation or method involving a specific active ingredient and delivery mechanism that improves therapeutic efficacy or reduces side effects.

2. How broad are the claims in NZ752535?
The independent claims are sufficiently broad to cover various formulations sharing core features but are supported by narrower dependent claims detailing specific embodiments.

3. How does this patent fit into the global landscape?
Similar patents are filed internationally, especially in markets like the US, EU, and Australia, forming a complex patent ecosystem with opportunities and challenges—such as potential infringement and patent opposition.

4. Can competitors develop similar drugs without infringing?
Yes, by designing around the claims—altering formulations or delivery methods that fall outside the patent’s scope—though this requires meticulous legal and technical analysis.

5. What strategic actions should patent holders consider?
They should maintain vigilant patent monitoring, seek to expand coverage with additional filings, enforce rights proactively, and explore licensing opportunities to maximize value.


References

[1] New Zealand Intellectual Property Office (NZIPO) Patent Database. Details on patent NZ752535.
[2] WIPO Patentscope. International patent families related to similar compounds/formulations.
[3] Patent analysis reports and literature reviews on similar pharmaceutical compositions.
[4] Cases of patent validity and litigation in comparable pharmaceutical patents.
[5] Regulatory guidelines concerning patentability and innovation in pharmaceuticals.

(Note: Specific document references, including the detailed patent claims and specifications, should be reviewed directly from the NZIPO database for comprehensive legal analysis.)

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