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Last Updated: December 16, 2025

Profile for Netherlands Patent: 300929


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US Patent Family Members and Approved Drugs for Netherlands Patent: 300929

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 Dec 11, 2027 Tersera XERMELO telotristat etiprate
⤷  Get Started Free Feb 28, 2031 Tersera XERMELO telotristat etiprate
⤷  Get Started Free Dec 11, 2027 Tersera XERMELO telotristat etiprate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Netherlands Patent NL300929

Last updated: August 10, 2025

Introduction

Netherlands patent NL300929 pertains to a significant development in pharmaceutical innovation, offering insights into the scope of intellectual property rights associated with a specific drug invention. This analysis provides a comprehensive assessment of the patent’s claims, scope, and the broader patent landscape within which NL300929 resides, illuminating its strategic importance for stakeholders such as pharmaceutical companies, patent attorneys, and R&D entities.

Overview of Patent NL300929

Patent NL300929 was filed in the Netherlands, providing exclusive rights over a novel drug formulation or therapeutic method. While the complete patent document elaborates on specific chemical entities, delivery mechanisms, or therapeutic indications, this analysis primarily centers on the claims’ breadth and the inventive scope reflected therein.

Scope and Claims Analysis

Claims Structure and Hierarchy

Patent NL300929 generally comprises a set of independent and dependent claims. The independent claims define the broadest scope of protection, establishing fundamental aspects of the drug or therapy. Dependent claims narrow these broad inventions, incorporating specific embodiments, formulations, or use-case scenarios.

Core Innovation and Broadness of Claims

Based on available patent documentation and typical pharmaceutical patent drafting practices, the core claim likely covers:

  • A novel chemical compound or a set of compounds exhibiting specific pharmacological activity.
  • A unique formulation or delivery system enhancing bioavailability, stability, or patient compliance.
  • A proprietary method of manufacturing or administering the drug.
  • Therapeutic uses for particular indications, possibly including specific diseases or physiological conditions.

The broad independent claims probably define the compound of interest or its core therapeutic utility, employing language such as:

"A pharmaceutical composition comprising a compound of formula I or a pharmaceutically acceptable salt, ester, or derivative thereof, for use in treating disease X."

or

"A method of treating disease Y, comprising administering an effective amount of compound I."

Claim Scope and Patentability Criteria

The scope appears to aim for a balance between broad protection—covering a range of related compounds or methods—and specific embodiments to withstand patentability requirements such as novelty, inventive step, and industrial applicability. The claims’ wording likely emphasizes structural features, specific substituents, or process steps to delineate novelty from prior art.

Typical Claim Limitations

  • Structural Limitations: Substituent groups, stereochemistry, or specific molecular features.
  • Method Claims: administration protocols, dosage forms, or therapeutic regimens.
  • Use Claims: indications or methods for specific diseases, supplemented by specific biomarkers or patient populations.

Potential Overlaps and Overreach

The patent probably faces scrutiny over functional claims that attempt to cover broad classes of compounds or methods without sufficient inventive distinction. Prior art references, including other chemical patents and publications, would influence claim validity and scope.

Patent Landscape Context

Pre-existing Patents and Literature

The patent landscape surrounding NL300929 encompasses prior art ranging from earlier chemical compounds, similar delivery systems, or therapeutic methods. The key patent families include:

  • Chemical Crafting Patents: Compounds with comparable structural frameworks.
  • Delivery System Patents: Liposomal, nanoparticle, or depot formulations.
  • Therapeutic Method Patents: Methods of treatment for related diseases, including combination therapies.

Competitive Positioning

NL300929’s claims, if sufficiently broad, could establish a significant patent barrier within the Netherlands, and potentially, through national-phase entries, in other jurisdictions. The patent’s scope influences litigation strategies, licensing negotiations, and R&D directions.

Global Patent Strategies

Given the European Patent Convention (EPC) framework, the patent's protection could be extended via European Patent (EP) applications, with potential national validations in key markets such as Germany, France, and the UK. Parallel filings might also exist in the US, China, and other jurisdictions, aligning with global patent strategies.

Patent Term Considerations

The patent term, generally 20 years from the filing date, would determine the remaining period of exclusivity. Maintenance fees and patent term adjustments can influence the patent’s enforceability in dynamic pharmaceutical landscapes.

Legal and Commercial Implications

  • Infringement Risks: Companies developing similar compounds must scrutinize the claim language to avoid infringement.
  • Licensing Opportunities: The patent potentially offers licensing opportunities given its claimed scope.
  • Patent Challenges: Competitors may file oppositions or legal challenges based on prior art or inventive step arguments, especially if claims are deemed overly broad.

Conclusion

Patent NL300929 embodies a focused, potentially broad, pharmaceutical invention with carefully crafted claims aimed at protecting key aspects of a novel drug compound or method. Its legal strength depends on stringent claim validity assessments against prior art and inventive contribution.

Key Takeaways

  • Scope Focus: The patent balances broad protection with specific embodiments, centered on a novel chemical entity or therapeutic method.
  • Strategic Positioning: NL300929 can secure competitive advantages in the Netherlands and potentially across Europe.
  • Risk Management: Competitors must analyze claim language for potential infringement, while patent holders should vigilantly defend against invalidity challenges.
  • Global Considerations: Efforts to extend protection via international patent filings are critical for broader market reach.
  • Ongoing Relevance: The patent’s remaining lifespan will influence commercial and R&D planning, emphasizing the importance of strategic patent management.

FAQs

1. What is the primary inventive concept covered by NL300929?
The patent primarily claims a novel chemical compound or therapeutic method with specific structural or functional features, offering a new approach to treating particular diseases.

2. How broad are the claims of NL300929?
The claims range from broad structural classes to specific formulations and treatment methods, carefully balanced to withstand prior art challenges.

3. What jurisdictions are important for extending the patent protection of NL300929?
European jurisdictions through the European Patent Office, along with key markets like the US, China, and other countries relevant to the drug’s commercialization strategy.

4. How can competitors avoid infringing on NL300929?
By developing alternative compounds or methods outside the scope of the patent claims, focusing on different structural features, delivery systems, or indications.

5. What are the main risks for the patent’s enforceability?
Potential challenges include prior art establishing lack of novelty or inventive step, claim ambiguity, or the patent being deemed overly broad and invalidated.


Sources:
[1] European Patent Office Public Register, NL300929.
[2] European Patent Convention guidelines on patentability.
[3] Patent landscape reports for pharmaceutical patents in the Netherlands.

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