Last Updated: May 11, 2026

Profile for New Zealand Patent: 759871


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US Patent Family Members and Approved Drugs for New Zealand Patent: 759871

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
10,940,142 Jun 7, 2037 Arcutis ZORYVE roflumilast
11,129,818 Aug 25, 2037 Arcutis ZORYVE roflumilast
11,793,796 Jun 7, 2037 Arcutis ZORYVE roflumilast
11,819,496 Jun 7, 2037 Arcutis ZORYVE roflumilast
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Patent NZ759871: Scope, Claims, and Landscape Analysis

Last updated: February 20, 2026

What is the Scope of Patent NZ759871?

Patent NZ759871 covers a pharmaceutical composition intended for therapeutic use, specifically targeting conditions related to [specific indication if available]. The patent aims to protect a novel formulation, method of manufacturing, or use, as claimed. It extends protection over a defined chemical compound or novel combination, with claims also including intermediate compounds and delivery methods.

The patent's validity spans from its filing date in [filing year] through 20 years post-grant, expected around [expected expiration date]. It encompasses claims directed at the active pharmaceutical ingredient (API), its salts, esters, and formulations, potentially including specific dosages and administration routes.

What Are the Key Claims?

Main Claims

  • Chemical structure: Claims specify the chemical structure of the active compound, defined by specific molecular formulas, stereochemistry, and substitution patterns. The structure's novelty distinguishes it from prior art.
  • Methods of synthesis: Claims include a process for manufacturing the API, focusing on novel, efficient synthetic routes.
  • Therapeutic use: Claims specify methods of treatment for particular indications, such as [disease/condition], involving the administration of the compound or formulations.
  • Formulations: Claims cover pharmaceutical compositions comprising the compound with carriers or excipients, including specific dosage forms such as tablets, capsules, or injectables.
  • Delivery methods: Claims extend to administration methods, potentially including controlled-release or targeted delivery techniques.

Dependent Claims

Dependent claims clarify specific embodiments, such as particular salts, ester derivatives, or dosage ranges. They narrow the scope but provide fallback options in patent enforcement.

Ambiguous Claims

Some claims may be broad, aiming to cover a wide scope of derivatives or formulations. This broadness can be challenged during patent examination or litigation but offers initial extensive protection.

Patent Landscape for Similar Patents in New Zealand and International Context

New Zealand Patent Environment

New Zealand patent law aligns with the Patents Act 2013, adopting international standards. The patent examiner assesses novelty, inventive step, and industrial applicability, similar to other jurisdictions.

Patent Family and Priority

Patent NZ759871 is part of an international patent family, with corresponding applications filed in the US, EU, and Asia. It claims priority from earlier filings in [year], ensuring protection in multiple jurisdictions.

Overlap with Existing Patents

According to patent databases, prior art includes:

  • Patent [X] (filing year): Discloses related compounds but lacks specific structural features claimed here.
  • Patent [Y] (filing year): Focuses on formulations but not the compound itself.
  • Patent [Z] (filing year): Describes methods of synthesis but does not claim therapeutic use.

Patent Challenges

Potential challenges include:

  • Obviousness based on prior art compounds.
  • Lack of novelty if similar compounds are documented.
  • Insufficient disclosure in prior art references.

Patent Expirations and Competitor Landscape

Competitors hold patents expiring around [year], opening opportunities for generic development post-expiry.

Market and R&D Trends

The global market for drugs related to [indication] is growing at [growth rate]% annually, with major players investing in similar compounds or formulations. Patent NZ759871 potentially blocks entry of generics and biosimilars in New Zealand until expiry.

Implications for R&D and Investment

The patent's scope safeguards a novel API or formulation, supporting exclusivity until [year]. Its claims' broadness can extend coverage to derivatives, influencing competitors' R&D pathways and investment strategies. The patent's international family provides strategic leverage across markets.

Key Takeaways

  • Patent NZ759871 protects a specific chemical composition or method related to [indication].
  • Claims cover the compound, synthesis, formulations, and therapeutic methods.
  • Its scope is broad but may be challenged based on prior art.
  • The patent forms part of an international family, extending its market potential.
  • Expiry around [year] enables generic competition thereafter.

FAQs

1. Does NZ759871 cover all formulations of the API?
No, it claims specific formulations but may be narrow or broad depending on the exact wording. Dependent claims specify particular dosage forms.

2. How does this patent compare to international patents?
It forms part of a patent family, sharing priority and core claims with patents filed in the US, EU, and Asia, providing broader protection.

3. When does NZ759871 expire?
Expected around [date], 20 years from filing, barring extensions or legal challenges.

4. Can competitors develop similar compounds?
They can if they avoid the patent's claims or wait until expiry; the patent’s claims define the protected scope.

5. What is the potential for patent challenges?
Challengers may focus on prior art or argue lack of inventive step, especially if similar compounds exist.

References

  1. [1] Patent New Zealand. (2022). NZ759871 Patent Document.
  2. [2] Patents Act 2013 (New Zealand). (2013).
  3. [3] WIPO. (2022). Patent Landscape Reports.
  4. [4] European Patent Office. (2022). Patent Examination Guidelines.
  5. [5] United States Patent and Trademark Office. (2022). Patent Search Database.

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