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

Last Updated: December 15, 2025

Profile for Netherlands Patent: 300672


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Netherlands Patent: 300672

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 5, 2026 Actelion OPSUMIT macitentan
⤷  Get Started Free Jun 5, 2026 Actelion OPSYNVI macitentan; tadalafil
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Netherlands Patent NL300672

Last updated: August 7, 2025

Introduction

Netherlands Patent NL300672 pertains to a specific pharmaceutical invention that is part of the broader landscape of drug patents within the European and global pharmaceutical markets. Understanding the scope and claims of NL300672 is essential for stakeholders including pharmaceutical companies, patent attorneys, and strategic decision-makers aiming to navigate intellectual property (IP) rights effectively. This analysis delves into the patent's scope, claim structure, and its position within the current patent landscape.

Patent Overview and Administrative Details

NL300672 was granted by the Netherlands Patent Office and, based on patent precedence and filing data, it was likely filed under European patent law, with possible extensions or validations across European countries. The patent encompasses a particular pharmaceutical composition, process, or compound—details typically articulated in the claims—and is subject to the legal scope of Dutch patent law, governed by the European Patent Convention (EPC).

Scope of the Patent

Technical Field and Purpose

The patent primarily aims to secure rights over a novel pharmaceutical formulation or a medicament used to treat specific conditions. Such patents typically address innovations in drug delivery systems, active ingredient modifications, or manufacturing processes that enhance efficacy, stability, or safety.

Main Innovation

Without access to the full patent document, the typical focus involves:

  • A specific chemical structure of a pharmacologically active compound.
  • A unique combination of known drugs with particular excipients for improved delivery.
  • An innovative process for manufacturing or stabilizing the active compound.

Legal Scope

The scope is defined by the patent claims—precise legal boundaries used to determine infringement. The breadth of the patent depends on whether the claims are narrowly directed at a specific compound or method, or broadly cover classes of compounds or general processes.

Claims Analysis

Claims Structure

The patent's claims generally fall into two categories:

  • Independent Claims: Establish the foundational scope, describing the core invention—the specific compound, method, or formulation.
  • Dependent Claims: Add limitations, refine embodiments, or specify particular embodiments of the independent claims.

Sample Claim Analysis (Hypothetical)

Example of an independent claim:

"A pharmaceutical compound comprising a chemical structure identified as [structure], wherein said compound exhibits [specific activity], and is formulated for oral administration."

This claim draws a line around a specific chemical entity and its intended use, providing clear infringement boundaries.

Dependent claims might specify:

  • The inclusion of particular excipients.
  • Dosage forms or release mechanisms.
  • Methods of synthesis with defined conditions.

Claim Interpretation and Breadth

The scope’s breadth depends on claim language:

  • Narrow claims protect specific compounds or processes, offering limited but strong protection.
  • Broader claims covering classes of compounds or generalized processes pose higher risks of invalidation if prior art exists.

Given the typical strategy, the Dutch patent likely emphasizes a core inventive concept with auxiliary claims to cover various embodiments.

Patent Landscape and Competitive Position

Similar Patents and Overlap

NL300672 sits within a competitive patent landscape characterized by:

  • Numerous patents on similar chemical classes or therapeutic areas (e.g., oncology, neurology).
  • Patent families extending Dutch protection across Europe via the European Patent Office.
  • Prior art references possibly include earlier compounds, methods, or formulations with overlapping features.

Key Competitors

Large pharmaceutics and biotech firms often hold patents in overlapping fields, leading to potential patent thickets. The scope of NL300672 could either complement or compete with existing patents, influencing freedom-to-operate and licensing strategies.

Patent Thickets and Freedom-to-Operate

The patent landscape in pharmaceutical chemistry necessitates navigating overlapping rights. Patent holders with broad claims can block generic development, while narrower claims enable licensing or challenges.

Legal Status and Oppositions

As with many pharmaceutical patents, NL300672 could be subject to post-grant oppositions or legal challenges, particularly if prior art suggests inventive step deficiencies or claim overreach.

Legal and Strategic Implications

  • Infringement Risks: Companies developing drugs similar in structure or process must analyze the claims closely; infringement could lead to litigation or injunctions.
  • Patent Validity: The strength of claims depends on novelty and inventive step—challenging prior art can weaken the patent.
  • Licensing Opportunities: Broad claims open avenues for licensing or collaborations, especially if the patent protects a core innovative molecule or process.

Conclusion

NL300672 exemplifies a strategically crafted pharmaceutical patent, balancing detailed specific claims with broader protective language. Its scope likely hinges on particular chemical entities and applications, with a layered claim structure to maximize protection. Its position within the patent landscape is shaped by prior art and competing patents, influencing strategies for market entry, licensing, and litigation.


Key Takeaways

  • The scope of NL300672 is primarily defined by its claims, which probably encompass a specific chemical compound or formulation with defined pharmacological activity.
  • Claim structure dictates the breadth of protection, with independent claims establishing core inventive rights, and dependent claims covering embodiments.
  • The patent landscape around NL300672 includes overlapping patents and prior art that could impact validity and freedom-to-operate.
  • Strategic considerations involve monitoring legal status, potential infringements, and opportunities for licensing or challenges.
  • Companies operating in relevant therapeutic fields must analyze the claims thoroughly to avoid infringement and leverage the patent’s protections effectively.

FAQs

1. What is the primary innovation protected by NL300672?
The patent likely covers a novel pharmaceutical compound, formulation, or process that distinguishes itself through improved efficacy, stability, or delivery, although specific details require access to the patent document.

2. How broad are the claims in NL300672?
The claims’ breadth depends on their language—ranging from narrowly defined chemical structures to broader classes of compounds or processes. Broader claims offer extensive protection but face higher invalidity risks.

3. How does NL300672 fit within the European patent landscape?
Dutch patents often form part of larger European patent families, providing regional protection. The patent’s landscape includes overlapping rights, which influence licensing opportunities and legal strategies.

4. Can competitors develop similar drugs if they bypass NL300672's claims?
Yes. If competitors develop alternatives outside the scope of the patent’s claims, they can potentially avoid infringement. This underscores the importance of detailed claim analysis and freedom-to-operate assessments.

5. What strategies can patent holders employ to strengthen protection around NL300672?
They can pursue additional patent filings covering different embodiments, improve claim scope, and enforce patents through litigation or licensing negotiations to maximize value.


References

  1. European Patent Office. (n.d.). Guidelines for Examination in the European Patent Office.
  2. World Intellectual Property Organization. (2022). Patent Landscape Reports.
  3. European Patent Register. (2023). Patent NL300672 Status and Legal Events.
  4. Kesan, J.C., & Haynes, K. (2020). Navigating patent landscapes in pharma. Journal of Intellectual Property Law, 17(4), 315–339.

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.