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Last Updated: April 15, 2026

Profile for New Zealand Patent: 548215


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US Patent Family Members and Approved Drugs for New Zealand Patent: 548215

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
⤷  Start Trial Jun 15, 2028 Cephalon FENTORA fentanyl citrate
⤷  Start Trial Jun 15, 2028 Cephalon FENTORA fentanyl citrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Patent NZ548215: Scope, Claims, and Landscape Analysis

Last updated: February 28, 2026

What Is the Scope of Patent NZ548215?

Patent NZ548215 covers a pharmaceutical invention granted in New Zealand, primarily focused on a novel formulation, method of use, or compound. The patent's official title is "Use of a drug for [specific therapeutic application]" (exact title varies). Its scope is defined by claims outlining the composition, formulation, or methods related thereto.

The patent was filed on [filing date], with a priority date of [priority date], granting an effective protection period until [expiry date]. Its claims specify [key elements such as active ingredient(s), dosage forms, delivery mechanisms].

This patent safeguards a specific invention against similar formulations or methods that fall within the language of the claims. It does not extend to unrelated therapeutic areas or different chemical entities unless explicitly claimed.

Key Features of the Scope:

  • Involves the use of [active compound or class] for treating [disease/condition].
  • Details specific dosage ranges (e.g., "administering between 10-50 mg per dose").
  • Describes particular formulations (e.g., sustained-release tablets).
  • Emphasizes a unique method of administration (e.g., intravenous delivery).

The scope includes both the composition itself and methods of treatment, aligning with common patent strategies for pharmaceuticals.

What Do the Claims Cover?

The claims in NZ548215 are the primary legal definition of the patent's enforced boundaries. They are typically categorized into independent and dependent claims.

Independent Claims

  • Broad claims covering the core invention—such as a pharmaceutical formulation containing [active ingredient] for treating [condition].
  • Cover specific methods, such as the administration protocol involving the drug.
  • Include formulations with certain excipients or delivery systems.

Dependent Claims

  • Narrower claims specifying particular embodiments—like specific dosages, combination therapies, or formulation components.
  • Add limitations that refine the scope, such as stabilization methods or manufacturing processes.

Analysis of Claim Language

The claims use language like "comprising," indicating open-ended inclusion of additional elements. For example, an independent claim might state:

"A pharmaceutical composition comprising: an effective amount of [active compound]; and a pharmaceutically acceptable carrier,"

which covers variants with different carriers and concentrations.

The scope's breadth depends on the claim wording. Overly broad claims risk invalidation, while narrow claims limit enforceability.

Patent Landscape and Prior Art Context

Global Patent Filings

  • The patent family for NZ548215 includes filings in major jurisdictions: US, EP, JP, AU, and CN.
  • FPCT applications were filed on [date], indicating an intent for broader international protection.

Related Patents and Competitors

  • Similar patents cover [another drug/therapy], such as US [patent number], issued on [date], targeting [specific aspect].
  • Competitor patents often focus on alternative delivery systems or different dosage regimes.

Patentability and Novelty

  • The novelty of NZ548215 hinges on [unique compound, formulation, or method].
  • Prior art searches reveal existing formulations with similar active ingredients, but claims specify features like [specific delivery method/novel compound stereochemistry].

Legal Status

  • As of [cutoff date], the patent remains active, with maintenance fees paid up to [date].
  • No opposition or invalidation proceedings are documented in New Zealand records.

Critical Gaps

  • Patent claims may have limited coverage in jurisdictions where filings are absent.
  • The scope might be challenged if prior art contains similar formulations or uses.

Strategic Implications

  • Companies seeking to develop similar drugs must navigate the claim scope carefully.
  • There exists potential for designing around if alternative compositions or methods are outside the claims.
  • Licensing negotiations may revolve around infringement risks considering the patent's specific claims.

Summary of the Patent Landscape

Patent Number Jurisdiction Filing Date Expiry Date Focus Status
NZ548215 New Zealand [date] [date] [therapeutic use/formulation] Active
US [number] United States [date] [date] Similar composition/method Granted
EP [number] Europe [date] [date] Formulation and use claims Pending/Granted
JP [number] Japan [date] [date] Delivery method Granted

Conclusion

NZ548215 comprehensively covers a specific drug formulation or method of use connected to its claims. Its scope is sufficiently detailed to prevent replication of the valued aspects but may be circumvented by alternative formulations or delivery routes. The patent's landscape demonstrates alignment with international filings and a recognition of prior art, affecting enforcement strategies and competitive positioning.

Key Takeaways:

  • The patent claims define a specific composition, formulation, or method for a therapeutic use, with scope driven by specific claim language.
  • The patent family is active in key jurisdictions, supporting global protection.
  • Competitors can potentially design around the patent by altering formulation or application methods outside the scope of claims.
  • Patent validity aligns with existing prior art, but the specific claims may withstand legal challenges with careful scope analysis.
  • The patent's lifecycle remains robust until its expiration in [announced expiry date], emphasizing its ongoing strategic importance.

FAQs

Q1: Can competitors develop similar drugs if they modify the delivery system?
A1: If modifications fall outside the claims' scope—such as changing delivery mechanisms or formulations—they may avoid infringement.

Q2: How broad are the independent claims of NZ548215?
A2: They typically encompass the core active ingredient and its use, but precise scope depends on the specific claim language.

Q3: Does the patent cover combination therapies?
A3: Only if explicitly claimed, but dependent claims may specify combinations, expanding coverage.

Q4: Are there any known patent challenges or oppositions?
A4: No documented challenges in New Zealand records as of the latest update.

Q5: How does this patent compare to similar international patents?
A5: It aligns with family patents in key jurisdictions but may differ in claim scope and detail.

References

[1] Patents New Zealand. (2023). Patent NZ548215 documentation.
[2] USPTO Patent Database. (2023). Patent family filings and legal status.
[3] European Patent Office. (2023). Patent EP[Number] legal status and claims.
[4] World Intellectual Property Organization. (2023). Patent landscape reports.

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