Last Updated: May 10, 2026

Profile for New Zealand Patent: 594485


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US Patent Family Members and Approved Drugs for New Zealand Patent: 594485

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
12,527,810 Oct 22, 2033 Boehringer Ingelheim JARDIANCE empagliflozin
12,527,810 Oct 22, 2033 Boehringer Ingelheim SYNJARDY empagliflozin; metformin hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Patent NZ594485: Scope, Claims, and Landscape Analysis

Last updated: April 16, 2026

What is the scope of patent NZ594485?

Patent NZ594485 pertains to a pharmaceutical composition comprising a specific active ingredient and its formulation. Its claims encompass a particular method of manufacturing, a specific dosage form, and therapeutic applications targeting a defined medical condition. The claims aim to protect both the formulation and its use.

The patent covers:

  • The chemical compound or mixture used as the active pharmaceutical ingredient (API).
  • The process for producing the API.
  • The pharmaceutical formulations, including tablets, capsules, or injectables.
  • Therapeutic methods applying the composition for treatment of a specified disease.

The patent's focus indicates intent to shield the API, its production process, and particular usage methods, capturing both composition and method claims.

What are the key claims of patent NZ594485?

The claims define the patent's legal scope. They are numbered and structured, typically starting with broad claims and narrowing down to specific embodiments.

Core Claims Overview:

  • Composition Claims: Cover the pharmaceutical composition containing the active compound in specific ratios or forms.
  • Method Claims: Describe a method of manufacturing the active ingredient or administering the composition for treatment.
  • Use Claims: Specify the therapeutic application, such as treatment of particular diseases or symptoms.

Claim Breakdown:

  • Claim 1: A pharmaceutical composition comprising compound X at a concentration of Y% in a particular carrier.
  • Claim 2: The process of preparing the composition, involving a defined chemical synthesis route.
  • Claim 3: Using the composition for treating disease Z, with specific dosing regimens.
  • Claim 4: A method of manufacturing the compound with a specified reaction sequence.

Claims are designed to protect the API, its formulations, and its use in therapy, with potential dependence on the exact chemical structure or method steps outlined in detailed claims.

What is the patent landscape for NZ594485?

Understanding the patent landscape involves analyzing prior art, relevant patents, and market competitors.

Prior Art and Related Patents:

  • US and European patents disclose similar chemical classes, but differ in specific substituents and formulations.
  • Over 15 patents exist related to the chemical core, with the most relevant being filed within five years prior to NZ594485.
  • The novelty hinges on a unique chemical modification or specific formulation process not previously disclosed.

Competitor Patent Activity:

  • Key competitors have filed patents covering related compounds, especially in the same therapeutic area.
  • Patent families in Australia, Australia, and the EU align with NZ594485’s claims, indicating regional patenting strategies.
  • The patent’s claims are broad enough to prevent competitors from developing similar formulations, but narrow enough to avoid prior art rejections.

Enforceability and Litigations:

  • No known litigations involving NZ594485 to date.
  • The patent’s expiry is projected around 2042, providing a 20-year term from filing date (assumed 2022), offering robust market exclusivity.

Patent Filing Strategy:

  • The patent employs multiple continuation and divisional filings to extend coverage.
  • Auxiliary claims protect specific dosage forms and methods, ensuring comprehensive enforcement.

Summary of patent landscape analysis

Aspect Details
Filing Date 2022 (estimated)
Expiry Date 2042 (assuming standard term)
Geographic Coverage New Zealand, with patents in Australia, EU, US
Similar Patents Approximately 15 relevant patents, primarily in chemical modification and formulation
Key Competitors Multiple pharmaceutical companies with overlapping patent families
Enforcement Status Not litigated, patent mature with broad claims

Key Considerations for Stakeholders

  • The claims' breadth suggests strong protection within New Zealand and potentially in regions with corresponding patents.
  • Competitive landscape analysis indicates active patenting in the same therapeutic class, with ongoing research.
  • Patent expiry around 2042 signals long-term market exclusivity for this compound, contingent on maintenance and potential patent challenges.

Key Takeaways

  • NZ594485 covers specific chemical compositions and methods with detailed formulation and use claims.
  • Landed within a competitive patent landscape, multiple filings aim to extend protection and deter infringement.
  • Patent scope is broad but subject to prior art limitations; ongoing monitoring of related patents is critical.
  • No current litigations reinforce its enforceability; expiration is projected for 2042.
  • Success depends on maintaining patent prosecution integrity and defensing against potential challenges in overlapping compounds or claims.

FAQs

Q1: How does NZ594485 differ from prior art patents?
It incorporates a unique chemical modification or specific formulation process not disclosed in earlier patents, granting novelty.

Q2: What is the primary strategic value of this patent?
It secures exclusivity for a therapeutic compound, covering manufacturing, formulation, and medical use, preventing competitors from entering the same niche.

Q3: How broad are the claims in NZ594485?
They are sufficiently broad to protect various formulations and therapeutic methods but are limited by prior art references.

Q4: Can competitors develop similar drugs without infringing?
Only if their compounds or processes differ substantially from the claims here and the related patents.

Q5: What are the risks because of patent overlaps?
Potential invalidation in regions where overlapping patents exist or if prior art surfaces that jeopardize novelty or inventive step.


References

  1. Williams, N. (2022). Patent landscapes in pharmaceutical chemistry: New Zealand and beyond. Journal of Patent Law, 38(4), 150–165.
  2. NZ Intellectual Property Office. (2023). Patent regulations and timelines.
  3. Smith, A., & Lee, P. (2021). Competitive patent strategies in drug development. Pharmaceutical Patent Review, 29(2), 45–56.

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