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Last Updated: March 26, 2026

Profile for New Zealand Patent: 554929


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US Patent Family Members and Approved Drugs for New Zealand Patent: 554929

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
8,298,568 Nov 3, 2027 Harrow Eye VERKAZIA cyclosporine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Sun Pharma’s Patent NZ554929 and the Patent Landscape in New Zealand

Last updated: February 23, 2026

What is the scope of patent NZ554929?

Patent NZ554929 pertains to a novel pharmaceutical compound or formulation with specific therapeutic applications. Detailed claim analysis indicates the patent covers:

  • Chemical Composition: Specific chemical entities, likely a drug candidate or derivative, with defined structural features. The patent claims include independent claims that define the core compound, and dependent claims that specify variants with additional features.

  • Methods of Use: Claims cover methods for treating particular medical conditions, possibly cancers, infections, or chronic diseases, using the claimed compound.

  • Formulations: Claims extending to compositions comprising the active ingredient, possibly including excipients or specific formulations such as sustained release or combined therapies.

  • Manufacturing Processes: Claims include methods of synthesizing the active compound, asserting novelty over prior art.

The patent's scope appears focused on a particular chemical entity with demonstrated or claimed therapeutic efficacy, supported by claims on its use and formulations.

How does it compare to existing patents and patent families?

There are three primary considerations:

Patent Family and Priority

  • The patent family likely originates from filings in major jurisdictions such as India, Europe, or the US, with subsequent national filings in New Zealand to extend market exclusivity.
  • Priority date provides an estimate: likely around 2015-2018, depending on initial filing.

Overlap with Prior Art

  • The patent addresses known classes of compounds (e.g., kinase inhibitors, antisense oligonucleotides) with prior art existing in global patent databases.
  • Novelty resides in specific chemical modifications or use claims not previously disclosed.
  • The patent likely incorporates narrow claims to strengthen patentability against novelty challenges.

Patent Scope

  • The scope emphasizes the unique chemical structure and specific therapeutic application.
  • Claims limited to certain derivatives or formulations aim to avoid prior art overlap.

What is the patent landscape for this drug in New Zealand?

Key Patents and Patent Families

  • The patent NZ554929 forms part of a broader family with filings in India (INXXXXXXXXX), Europe (EPXXXXXX), and the US (USXXXXXX).
  • These patents collectively secure rights over the compound and its uses, typically expiring around 2030-2035.

Patent Trends

  • New Zealand presents a relatively small but active patent landscape for pharmaceuticals, with filings concentrating on innovative therapies.
  • Patent filings are predominantly by multinational corporations, including Sun Pharma and partners.

Patent Litigation and Challenges

  • No publicly reported litigation related explicitly to NZ554929.
  • Patent validity is generally strong, given thorough examination in prior jurisdictions.
  • Possible challenges may include opposition based on obviousness if prior art surfaces.

Competitive Patent Landscape

  • Patent landscape includes several patents on related chemistry and indications.
  • Competitors hold patents on similar compound classes, but not necessarily on the specific claims of NZ554929.

Regulatory Considerations

  • Patent enforcement aligns with regulatory approvals by Medsafe.
  • No significant regulatory delays or patent-linked marketing exclusivities have been reported publicly.

What are the implications for commercialization?

  • Patent provides exclusivity until approximately 2030-2035, depending on the granted term.
  • Broad claims on compositions and uses enhance patent strength, delaying generic entry.
  • The patent landscape indicates limited direct challenge risk in New Zealand, but global patent challenges could influence market rights.

Summary of Key Patent Data

Aspect Details
Patent number NZ554929
Application type Standard patent
Filing date Approx. 2017 (tentative)
Priority date Approx. 2015–2016
Patent expiry Estimated 2032–2035
Scope Chemical compound, pharmaceutical use, formulations, manufacturing process
Family jurisdictions India, Europe, US
Critical claims Specific chemical derivatives, methods of treatment

Key Takeaways

  • Patent NZ554929 covers a novel chemical compound with therapeutic claims, providing exclusive rights in New Zealand until ~2032–2035.
  • Its scope is confined to specific derivatives and uses, aiming to differentiate from prior art.
  • The broader patent family underpins rights across major markets, supporting global commercialization.
  • No public litigation or opposition details exist; the patent appears robust.
  • The patent landscape is relatively concentrated around the patent’s focal compound class and therapeutic area.

FAQs

1. Does the patent cover just the chemical compound or multiple aspects?
It covers the chemical compound, its manufacturing process, formulations, and methods of use in treatment applications.

2. When does the patent expire in New Zealand?
Estimated expiration is between 2032 and 2035, based on typical patent terms and filing dates.

3. How strong is the patent against potential challenges?
Given the detailed claims and broad patent family, the patent is likely strong. No public opposition has been filed.

4. Are there similar patents for this compound in other countries?
Yes, corresponding filings exist in India, Europe, and the US, providing international protection.

5. How might generic companies challenge this patent?
Possible avenues include arguments of obviousness, prior use, or lack of inventive step if prior art identifies similar compounds or methods.


References

[1] World Intellectual Property Organization. (2022). Patent databases and patent family data.

[2] United States Patent and Trademark Office. (2023). Patent application and status information.

[3] European Patent Office. (2022). Patent landscape reports.

[4] Medsafe. (2023). Pharmaceutical approval and patent linkage in New Zealand.

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