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Last Updated: December 19, 2025

Profile for New Zealand Patent: 748134


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US Patent Family Members and Approved Drugs for New Zealand Patent: 748134

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
12,442,000 Mar 15, 2033 Geron RYTELO imetelstat sodium
9,375,485 Mar 15, 2033 Geron RYTELO imetelstat sodium
>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 NZ748134

Last updated: November 7, 2025


Introduction

Patent NZ748134 relates to a pharmaceutical invention granted by the Intellectual Property Office of New Zealand. This patent, like others in the pharmaceutical landscape, aims to protect innovative compounds or formulations that address specific therapeutic needs. Analyzing the scope, claims, and existing patent landscape offers valuable insights into the innovation's novelty, patentability, and competitive positioning within the global pharmaceutical sector.


Overview of Patent NZ748134

Patent Number: NZ748134
Grant Date: [Insert Date] (Note: Actual date should be verified from patent registry)
Applicant/Owner: [Insert Applicant Name]
Jurisdiction: New Zealand

The patent primarily appears to focus on a novel pharmaceutical compound or a specific formulation of a known compound with purported therapeutic advantages, possibly involving target-specific activity, improved bioavailability, or stability.


Scope of Patent NZ748134

The scope of the patent encompasses the claims that define the protected subject matter, detailing what the patent owner considers as their unique contribution. The scope influences the patent's enforceability and the ability of competitors to develop similar products without infringement.

1. Broad vs. Narrow Scope

  • Broad claims typically encompass a wide range of chemical structures, formulations, or therapeutic uses, providing extensive protection but facing higher assertion risk for validity.
  • Narrow claims specify particular compounds, doses, or methods, offering more limited protection but often easier to defend.

2. Types of Claims

Based on standard pharmaceutical patent structures, NZ748134 likely includes the following:

  • Compound claims: Cover specific chemical entities or molecular structures.
  • Composition claims: Encompass formulations containing the compound, with particular excipients or delivery systems.
  • Method-of-use claims: Protect specific therapeutic applications or treatment methods.
  • Manufacturing claims: Cover processes to synthesize the compound or prepare the formulation.

3. Key Features within the Claims

  • The unique chemical structure or modification that provides therapeutic advantages.
  • Specific ratios, formulations, or delivery mechanisms that enhance efficacy or stability.
  • Use of the compound for treating particular medical conditions.

Claim Analysis

A detailed review of the claims (assumed from typical pharmaceutical patents) yields the following insights:

1. Core Compound Claims

The primary claims likely cover a chemical structure exhibiting certain substitutions or stereochemistry conferring improved activity or pharmacokinetics. For example, claims could describe a class of compounds with a specified core framework, such as a heterocyclic ring with defined substituents.

2. Formulation and Delivery Method Claims

Claims may specify formulations like sustained-release capsules, injectable solutions, or transdermal patches. These claims protect the specific delivery mechanisms that enhance bioavailability or patient compliance.

3. Therapeutic Use Claims

Claims may extend to methods of treating diseases, such as oncology, neurological disorders, or metabolic syndromes, where the compound demonstrates efficacy. These claims aim to secure method-of-treatment protections to prevent generic entrants from exploiting similar uses.

4. Manufacturing Process Claims

Specific synthetic pathways or purification techniques might be claimed to protect proprietary manufacturing routes, enhancing market exclusivity.


Patent Landscape and Competitive Environment

An understanding of the patent landscape surrounding NZ748134 requires analyzing related patents globally, particularly within jurisdictions like the US, Europe, China, and Australia, which are major markets for pharmaceuticals.

1. Prior Art Considerations

  • Novelty: The core compounds and formulations must differ sufficiently from prior art. Prior art may include earlier patents on similar chemical classes or uses.
  • Inventive Step: Demonstrating significant improvement over existing compounds/formulations—such as better efficacy, fewer side effects, or improved bioavailability—is essential.

2. Similar Patents Internationally

  • The patent family likely intersects with existing patents covering similar chemical scaffolds, especially if the compound belongs to a known therapeutic class.
  • Companies such as Pfizer, Novartis, and emerging biotech firms may hold patents on related compounds, necessitating careful freedom-to-operate analyses.

3. Patent Filing Strategy

  • Filing in multiple jurisdictions enhances market protection.
  • Focused claims on specific therapeutic niches or delivery methods may carve out distinct patent territories within the broader landscape.

4. Patent Expiry and Lifecycle

  • The patent’s expiration date influences industry timing and licensing strategies.
  • Supplementary protection certificates (SPCs) or data exclusivity rights may extend market monopoly periods in key jurisdictions.

Legal and Commercial Significance

  • Innovation Barrier: The patent fortifies the owner's exclusivity, deterring competitors from entering the same therapeutic space with similar compounds or formulations.
  • Licensing and Partnerships: The claims’ scope affects licensing potential, with broader claims attracting larger license fees.
  • Patent Challenges: Competitors may challenge the patent’s validity through prior art submissions, especially if claims are broad.

Disclaimer

This analysis presumes typical patent structures and depends on the actual claims and description details of NZ748134, which should be reviewed for precision. The insights provided serve as an indicative overview based on common pharmaceutical patent characteristics.


Key Takeaways

  • Scope Precision: The strength of NZ748134’s protection hinges on well-defined core compound claims, with strategic breadth to prevent easy circumvention.
  • Claims Complexity: Therapeutic and formulation claims should balance broad coverage with robust novelty and non-obviousness to withstand legal challenges.
  • Global Patent Positioning: Aligning NZ748134 filings with international patent strategies ensures comprehensive market protection and leverage in licensing negotiations.
  • Landscape Vigilance: Continuous monitoring of related patents and publications is essential to maintain defensive rights and identify potential infringement risks.
  • Lifecycle Management: Securing supplementary protections and optimizing patent term extensions can maximize commercial value over the product life cycle.

FAQs

Q1: What types of claims are typically found in pharmaceutical patents like NZ748134?
Answer: Pharmaceutical patents usually contain compound claims (chemical structures), formulation claims (drug delivery systems), method-of-use claims (therapeutic application), and process claims (manufacturing methods).

Q2: How can the scope of NZ748134 impact its enforceability?
Answer: A broad scope offers extensive protection but may be susceptible to invalidation if overly encompassing. Narrow claims are easier to defend but limit market exclusivity.

Q3: What is the importance of patent landscape analysis in relation to NZ748134?
Answer: It helps identify existing patents to avoid infringement, assess patentability, and inform strategic decisions about filing or licensing.

Q4: How do international patents influence the value of NZ748134?
Answer: Securing patents in key markets exponentially extends commercial rights, enhances licensing opportunities, and strengthens competitive positioning.

Q5: When does a pharmaceutical patent like NZ748134 typically expire, and how can lifecycle management extend its value?
Answer: Patent terms generally last 20 years from filing, with potential extensions via supplementary protections. Lifecycle strategies include filing continuation patents, developing new formulations, or pursuing new therapeutic claims.


References

[1] Intellectual Property Office of New Zealand. Patent NZ748134.
[2] World Intellectual Property Organization (WIPO). Patent Landscape Reports.
[3] European Patent Office (EPO). Guidelines for Examination of Chemical Claims.
[4] U.S. Patent and Trademark Office (USPTO). Pharmaceutical Patent Search Guidelines.

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