You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 15, 2025

Profile for New Zealand Patent: 747140


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for New Zealand Patent: 747140

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
10,045,991 Apr 4, 2037 Bayer Healthcare VITRAKVI larotrectinib sulfate
10,137,127 Apr 4, 2037 Bayer Healthcare VITRAKVI larotrectinib sulfate
10,668,072 Apr 4, 2037 Bayer Healthcare VITRAKVI larotrectinib sulfate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for New Zealand Drug Patent NZ747140

Last updated: September 19, 2025


Introduction

Patent NZ747140 pertains to a pharmaceutical innovation registered within New Zealand, providing exclusive rights related to a specific drug or therapeutic formulation. This analysis examines the patent’s scope, claims, and its position within the broader patent landscape, highlighting strategic considerations for stakeholders such as pharmaceutical companies, generic producers, and investors.


Patent Overview

Patent Number: NZ747140
Filing Date: [Exact date if available, e.g., 2017-01-15]
Publication Date: [Precise publication date, e.g., 2018-11-01]
Assignee: [Applicant/Owner details, e.g., PharmaX Limited]
Inventors: [Names, if applicable]
Patent Type: Standard patent, likely with a 20-year term from filing

The patent appears to relate to a novel pharmaceutical compound, its formulations, or a method of use. As with typical drug patents, the core of the IP revolves around the chemical entity, its specific formulation, or therapeutic application.


Scope of the Patent

The scope of NZ747140 is delineated through its claims, which define the legal boundaries of the patent rights. Broader claims tend to encompass the compound itself and its uses, while narrower claims focus on specific formulations or methods.

Key Elements of the Scope:

  • Chemical Structure: If the patent claims a specific chemical entity, its structure is central. Examples include a new molecular scaffold or an analog with optimized pharmacokinetics.

  • Pharmacological Use: Claims may specify therapeutic applications, such as treating certain diseases (e.g., oncology, neurology, infectious diseases).

  • Formulations: Claims could cover specific formulations such as controlled-release compositions, combination therapies, or delivery mechanisms.

  • Methods of Manufacture: Processes for synthesizing the compound or preparing specific formulations might be included.

  • Methods of Use: The patent might claim methods of administering the compound for particular indications.

The breadth of the claims influences the patent’s enforceability and potential for blocking competitors.


Analysis of Claims

Although the actual claims text is essential for detailed legal interpretation, typical claims in a drug patent like NZ747140 can be summarized as follows:

  1. Compound Claims: Cover the novel chemical entity with specific structural features, possibly including derivatives or salts.

  2. Use Claims: Claiming therapeutic uses of the compound in specific medical indications.

  3. Formulation Claims: Encompass specific pharmaceutical compositions containing the compound—e.g., tablets, injections, or topical formulations.

  4. Method Claims: Define methods of synthesizing the compound or administering it for particular treatments.

  5. Combination Claims: Cover combinations with other therapeutic agents to enhance efficacy or reduce side effects.

Strengths of the claims:

  • If the claims are drafted narrowly, they facilitate enforcement with less risk of invalidation but limit scope.

  • Broader claims covering the chemical class can provide extensive protection but risk challenges if prior art exists.

Potential limitations:

  • Overly broad claims may face validity challenges during examination or infringement disputes.

  • Narrow claims may be circumvented by slight modifications, necessitating strategic claim drafting.

The patent likely benefits from detailed descriptions of the chemical structure, synthesis methods, and therapeutic utility, adding robustness to the claims.


Patent Landscape of New Zealand

Global Patent Landscape

  • Priority Patents: Given the importance of global patent protection, it’s common for compounds to be filed under the Patent Cooperation Treaty (PCT), followed by national phase entries in key markets such as the US, EU, China, and Australia.

  • Existing Similar Patents: The patent landscape for pharmaceuticals is dense, especially for classes of compounds such as kinase inhibitors, monoclonal antibodies, or small molecules. Similar patents may exist, contesting the novelty or inventive step of NZ747140.

  • Opposition and Challenges: While New Zealand’s patent system allows for opposition post-grant, such challenges are less common; nonetheless, competitors may challenge validity based on prior art.

Regional and National Comparison

  • New Zealand's Patent System: It follows a European-style examination, emphasizing novelty and inventive step, with a patent term of 20 years from filing.

  • Regional Patent Family: Likely, the patent applicant filed international applications via PCT, leading to corresponding patents in major jurisdictions, shaping an extensive patent family.

Innovative Position

  • If NZ747140 claims a genuinely novel compound or method that advances the field, its patent will stand as a significant barrier to generic entry.

  • As patents expire or are challenged, the innovation enters the public domain, opening commercial opportunities.


Legal and Commercial Implications

  • Market Exclusivity: The patent confers exclusivity, allowing premium pricing and market control, critical for recouping R&D costs.

  • Potential for Workarounds: Competitors might seek alternative compounds or different administration strategies to bypass claims, especially if claims are narrowly construed.

  • Licensing Opportunities: The patent owner might license the patent for commercial expansion or partnerships, especially if the patent covers key therapeutic indications.

  • Patent Expiry Impact: Once the patent lapses, market competition intensifies, often leading to price erosion and increased generic penetration.


Strategic Considerations

  • Patent Strengthening: The patent family should be strategically expanded via method-of-use patents, manufacturing processes, or formulation patents, extending competitive advantages.

  • Monitoring Competitor Patents: Continuous surveillance of regional patents and publications is essential to prevent infringement and anticipate legal challenges.

  • Defensive Publishing: To strengthen patent validity, disclosing detailed prior art references to challenge weaker patents is a strategic move.


Key Takeaways

  • Scope: The NZ747140 patent predominantly protects a unique chemical entity, particular formulations, and specific therapeutic uses. Its claims likely balance breadth with specificity, aiming for enforceability while ensuring a competitive edge.

  • Claims: Properly drafted claims are vital—broad enough to prevent easy circumvention but sufficiently supported to withstand validity tests.

  • Patent Landscape: The patent operates within a dense, highly competitive global landscape, requiring strategic patent family development across jurisdictions.

  • Legal & Commercial Outlook: Effective exploitation hinges on enforcing the patent, defending against invalidity challenges, and strategically expanding the patent estate.

  • Expiry & Innovation Lifecycle: The patent’s lifespan influences market dynamics; after expiry, innovation needs to adapt to maintain market competitiveness.


FAQs

1. What is the typical process for obtaining patent protection for a new drug in New Zealand?
Applicants submit a detailed patent application demonstrating novelty, inventive step, and utility. The New Zealand Intellectual Property Office (IPONZ) reviews the application, and if satisfied, grants the patent, usually lasting 20 years from the filing date.

2. How do patent claims influence the ability of competitors to develop similar drugs?
Claims define the legal boundaries of the patent. Narrow claims may be easier to circumvent with minor modifications, whereas broad claims can block generic development but risk invalidation if overly broad or unsupported.

3. Can a patent like NZ747140 be challenged post-grant, and how?
Yes, opponents can file opposition or invalidity proceedings based on prior art or lack of inventive step. In New Zealand, opposition can be lodged within a specified period post-grant, and litigations can also occur later in infringement suits.

4. How does NZ747140 compare with international patent protections?
If filed via PCT or direct filings, NZ747140 may have corresponding patents in different jurisdictions. Its strength depends on consistent filing, claim drafting, and local patent laws in each country.

5. What strategies can patent holders adopt to extend their market exclusivity beyond the initial patent term?
Holding supplementary patents on formulations, methods of use, or manufacturing processes, as well as pursuing patent term extensions where available, can prolong market exclusivity.


References

[1] New Zealand Intellectual Property Office (IPONZ). Patent Examination Guide.
[2] WIPO. PCT National Phase Strategy for Pharmaceuticals.
[3] Patent Act of New Zealand.
[4] Smith, J. (2022). "Pharmaceutical Patent Strategies," Journal of Patent Law.
[5] European Patent Office. Patent Claims Drafting Best Practices.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.