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Last Updated: December 19, 2025

Profile for New Zealand Patent: 733104


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US Patent Family Members and Approved Drugs for New Zealand Patent: 733104

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
⤷  Get Started Free Jun 12, 2027 Incyte Corp OPZELURA ruxolitinib phosphate
⤷  Get Started Free Jun 24, 2028 Incyte Corp OPZELURA ruxolitinib phosphate
⤷  Get Started Free Jun 24, 2028 Incyte Corp JAKAFI ruxolitinib phosphate
⤷  Get Started Free Jun 24, 2028 Incyte Corp OPZELURA ruxolitinib phosphate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of New Zealand Patent NZ733104

Last updated: July 27, 2025


Introduction

Patent NZ733104 pertains to a specific pharmaceutical invention granted in New Zealand, and its detailed analysis offers insights into the scope of intellectual property rights it confers, the breadth of its claims, and its position within the patent landscape. This assessment aims to inform stakeholders—including pharmaceutical companies, patent attorneys, and research organizations—about its strategic relevance.


Overview of Patent NZ733104

Patent NZ733104 was granted to protect a novel chemical compound or pharmaceutical formulation. Its application path, priority date, and publication details—though not provided here—are typical components influencing its enforceability and landscape position. The patent's key focus is to safeguard inventive aspects of a molecule or composition with potential therapeutic utility.


Scope of Patent NZ733104

The scope of a patent defines the extent of legal rights conferred and directly impacts its commercial utility and freedom-to-operate considerations. It encompasses:

  • Claims: A series of legal statements that delineate the invention’s boundaries.
  • Description: Detailed disclosure supporting the claims, including chemical structures, synthesis methods, and potential therapeutic uses.
  • Drawings and Examples: Visual and practical embodiments illustrating the invention.

In this case, NZ733104 appears to cover:

  • A specific chemical entity—likely a novel small molecule or biologic.
  • Pharmaceutical compositions incorporating the compound.
  • Method of use or treatment claims targeting particular diseases or conditions.
  • Manufacturing processes related to the compound or formulation.

The patent emphasizes the compound’s therapeutic application—potentially as an anti-inflammatory, anticancer, or neuroprotective agent—commonly seen in pharmaceutical patent filings.


Claims Analysis

The claims form the core enforceable component and critically influence the patent's breadth:

  • Independent Claims: Usually define the broadest concept, such as the chemical structure or class of compounds, with minimal structural limitations. These may encompass a genus of compounds with structural variations.
  • Dependent Claims: Add specific limitations, such as particular substituents, pharmaceutical formulations, or methods of administration, thereby narrowing the scope but strengthening the patent’s defensibility.

In NZ733104, the claims likely include:

  • Chemical structure claims — likely a core scaffold with specified substituents.
  • Pharmaceutical formulations — comprising the compound with excipients, delivery systems.
  • Method claims — treatment methods utilizing the compound.
  • Synthesis claims — method of manufacturing the compound.

Potential scope implications:

  • Broad claims covering a chemical class could prevent competitors from developing similar compounds within the same class.
  • Narrow claims might limit the patent to specific compounds, enabling freedom of operation around closely related molecules.

Claim drafting quality influences enforceability and validity. Precise, enablement-focused claims prevent easy design-arounds while ensuring patent robustness.


Patent Landscape Context

Understanding NZ733104’s landscape involves analyzing:

1. Prior Art and Novelty

The patent’s novelty hinges on the uniqueness of the chemical entity and its synthesis compared to prior art. For pharmaceutical patents, prior art databases—such as PubMed, patent databases (WIPO, EPO), and chemical repositories—must be scrutinized to confirm the compound’s non-obviousness and originality.

2. Anticipation and Obviousness

The patent’s claims must overcome challenges of anticipation (prior art disclosing the invention fully) and obviousness (a skilled person would find it evident). Its robustness depends on demonstrating inventive step, supported by comparative data or unexpected results.

3. Patent Family and Global Coverage

While NZ patent rights are territorial, the applicant may pursue family patents in jurisdictions like Australia, Europe, US, and Asia. This strategic positioning forms a comprehensive patent portfolio, mitigating risks from infringement and enabling global commercialization.

4. Competitive Landscape

  • Existing patents: Similar compounds or formulations existing in patent literature could pose overlapping rights.

  • Patent expirations: The remaining enforceable life influences R&D timing and licensing negotiations.

  • Patent expiry dates: Typically, pharmaceutical patents last 20 years from filing, but adjustments for patent term extensions or pediatric exclusivities may apply.

  • Major players: If the patent was filed or assigned by a large pharmaceutical company, it signals strategic interest; if by smaller entities, it may signify niche targeting or early-stage development.

5. Potential Patent Challenges

Challenges include:

  • Invalidity assertions based on prior art.
  • Claims narrowing or reissue proceedings if prior art surfaces post-grant.
  • Generic and biosimilar threats once patent expires.

Strategic Implications

The scope of NZ733104’s patent claims directly influences its commercial potential:

  • Broad claims can secure market exclusivity but risk invalidity if overly ambitious.
  • Narrow claims provide stronger validity but may limit market coverage.
  • Effective patent landscape navigation ensures maximal territorial coverage and freedom to operate.

Pharmaceutical innovators should monitor subsequent patent filings and freedom-to-operate analyses grounded in NZ733104’s claims, considering evolving patent strategies globally.


Conclusion

Patent NZ733104 exemplifies a typical pharmaceutical patent with claims likely encompassing novel chemical entities and their therapeutic uses. Its scope, tailored through carefully drafted claims, aims to maximize protection while navigating prior art. The strategic landscape depends on potential overlaps with existing patents, jurisdictional filings, and the patent's enforceability. Stakeholders should continually evaluate the patent’s position relative to ongoing research, competitors’ portfolios, and global patent trends.


Key Takeaways

  • Claim Breadth: Broad, well-drafted claims serve as a strong foundation but must balance validity risks.
  • Patent Strategy: Coupling NZ patent rights with international filings enhances global commercial potential.
  • Landscape Vigilance: Continuous monitoring of prior art and competing patents safeguards against infringement and invalidity challenges.
  • Lifecycle Management: Early planning for patent term extensions and reissuance prolongs market exclusivity.
  • R&D Alignment: Patent claims should align with ongoing research to prevent infringement and optimize commercial delivery.

FAQs

1. How does the scope of claims impact the enforceability of NZ733104?
The scope determines the extent of legal rights; broader claims provide wider protection but may be more vulnerable to invalidity challenges, whereas narrower claims are easier to defend but limit market exclusivity.

2. Can NZ733104 be challenged post-grant?
Yes, through invalidity procedures based on prior art or obviousness, typically initiated by competitors or interested third parties.

3. What is the importance of patent family coverage for NZ733104?
Patent family coverage ensures international protection, vital for global commercialization and preventing infringement across multiple jurisdictions.

4. How do claims related to synthesis methods influence patent strength?
Claims on synthesis methods can prevent competitors from copying manufacturing processes, ensuring a comprehensive protective scope around the compound.

5. What should stakeholders consider regarding the patent landscape?
Stakeholders should analyze overlapping patents, impending expirations, and their own freedom-to-operate to formulate effective business and R&D strategies.


References

  1. [1] Patent NZ733104 - Official documentation (if accessible).
  2. [2] WIPO Patent Scope Database.
  3. [3] European Patent Office (EPO) Patent Database.
  4. [4] PubMed and chemical patent repositories.
  5. [5] Relevant patent transformations and legal analyses from major patent law firms.

Note: Specific details about NZ733104’s chemical compound or claims are hypothetical in this analysis due to limited data provided. For precise legal advice or patent drafting, consult the official patent documents and professional patent attorneys.

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