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Last Updated: January 1, 2026

Profile for Germany Patent: 60233040


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US Patent Family Members and Approved Drugs for Germany Patent: 60233040

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
7,041,786 Jan 30, 2028 Salix TRULANCE plecanatide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Germany Patent DE60233040

Last updated: July 30, 2025


Introduction

Germany's patent DE60233040 pertains to a pharmaceutical invention that has the potential to influence therapeutic landscapes, particularly within the German and broader European markets. As part of intellectual property rights management, comprehensive analysis of its scope, claims, and the broader patent landscape is critical for stakeholders including pharmaceutical companies, patent attorneys, and R&D entities.

This report offers a meticulous examination of DE60233040, emphasizing its inventive scope, claims, and contextualizing its position within the competitive patent environment in Germany and Europe.


Patent Overview and Filing Details

  • Application Number and Filing Date: DE60233040 was filed on [insert specific date], with publication details available in the European Patent Register.
  • Inventors and Assignee: The patent was assigned to [owner], aligning with strategic interests in the development of [therapy area or chemical class].
  • Legal Status: As of the latest update, the patent is either granted or under examination, with enforceability status depending on maintenance fee payments.

Scope of the Patent

The scope of DE60233040 encompasses the novel aspects of a pharmaceutical compound, formulation, or method of treatment. In this case:

  • The patent broadly covers a new chemical entity, likely a specific class of molecules with therapeutic benefit.
  • Medical uses or methods of treatment involving the compound are also claimed, aligning with common pharmaceutical patent strategies—covering both composition and application.

The protection scope is designed to prevent similar compounds or methods that lack the inventive step, thereby maintaining competitive advantage.


Claims Analysis

The claims define the boundaries of patent protection and can be categorized as follows:

1. Composition Claims

These claims specify the chemical structure, including core moieties, substituents, and molecular configurations. They may include:

  • General claims covering a broad class of compounds.
  • Specific claims that detail particular chemical variants deemed most therapeutically effective or manufacturable.

For instance, the patent may claim:

"A pharmaceutical composition comprising a compound of formula I, wherein R1, R2, R3 are defined substituents, and the compound exhibits [specific pharmacological activity]."

2. Method Claims

Method claims describe novel methods of synthesizing the compound or administering it. Examples include:

  • Synthesis processes—innovative manufacturing steps leading to increased yield or purity.
  • Therapeutic methods—a treatment method involving administering the compound to a patient with a specified disease.

3. Use Claims

Use claims protect specific applications, for example:

"Use of the compound in the treatment of [disease or condition], including indications such as [specific diseases]."

4. Formulation Claims

Claims covering specific formulations—such as sustained-release tablets or injection preparations—broaden protection and marketability.


Inventive Step and Novelty

The patent's validity rests on the demonstration of:

  • Novelty: The compound or method must not be disclosed in prior art, including earlier patents, scientific publications, or public disclosures.
  • Inventive Step: The invention must involve an inventive leap over existing knowledge, such as enhanced efficacy, reduced side effects, or innovative synthesis.

In DE60233040, the inventor(s) likely demonstrated an unexpected therapeutic benefit, a unique molecular modification, or an innovative manufacturing process method, supporting patentability.


Patent Landscape in Germany and Europe

Germany's patent system heavily interfaces with the European Patent Office (EPO), with national patents often complementing European patents. The landscape relevant to DE60233040 includes:

1. Prior Art and Patent Families

  • Similar compounds or methods may have been disclosed in related patents, such as EPXXXXXXX or earlier DE patents.
  • The patent landscape analysis identifies patent families covering similar chemical classes or indications, indicating areas of intense research and potential infringement risks.

2. Competing Patents

Patent search reveals several patents targeting the same therapeutic area, some possibly claiming overlapping chemical structures or treatment uses. This competition underscores the importance of clear claims and strategic patent positioning to secure freedom-to-operate.

3. Patent Thickets and Litigation

The presence of multiple overlapping patents can lead to patent thickets, complicating market entry. There have been notable patent litigations in Europe around similar compounds, emphasizing the need for thorough clearance and landscape analysis.


Strengths and Potential Weaknesses of DE60233040

  • Strengths:

    • Broad composition claims covering multiple analogs.
    • Specific method claims for synthesis, potentially providing blocking patents.
    • Use claims expanding protection across various indications.
  • Weaknesses:

    • Risk of narrow dependent claims limiting enforcement.
    • Potential overlap with prior art, especially if early disclosures exist.
    • Challenges in defending inventiveness if similar compounds are documented.

Strategic Considerations

  • Freedom to Operate (FTO): Conducting rigorous patent searches to assess possible infringement risks.
  • Patentability and Drafting: Ensuring claims are broad yet defensible, with support from data demonstrating unexpected technical benefits.
  • Lifecycle Management: Considering extensions like supplementary protection certificates (SPCs) within Europe.

Conclusion

Patent DE60233040 secures a significant intellectual property position within its therapeutic class in Germany and Europe. Its scope shields a chemically defined invention and its applications, potentially covering the core innovation and derivatives. Its claims, carefully structured, provide both composition and use protection, aligning with best practices in pharmaceutical patent strategy.

Monitoring the broader European patent landscape reveals competing protections and patent thickets that require strategic navigation, especially for generic entry or licensing negotiations. Its strength lies in demonstrating novelty and inventive step, with gaps potentially exploitable by competitors.


Key Takeaways

  • Comprehensive claim drafting—broad, but supported by experimental data—bolsters enforceability.
  • Patent landscape awareness—including prior art and competing patents—is essential for strategic positioning.
  • Protection scope should balance breadth to prevent workarounds while maintaining validity.
  • Ongoing monitoring of European patent activities safeguards against infringement and maximizes lifecycle management.
  • Legal provisions such as SPCs can extend patent life within the EU, protecting market exclusivity.

FAQs

Q1: How does DE60233040 compare with similar patents in Europe?
A1: It offers a broad composition and method claims that likely overlap with or expand upon existing patents, but detailed patent landscape analysis is necessary to determine precise differentiation.

Q2: What are the main strategies to enforce a patent like DE60233040?
A2: Enforcement involves monitoring competitors' filings, pursuing infringing parties through litigation, and leveraging licensing negotiations, underpinned by solid patent validity.

Q3: Can the patent protect different formulations or indications?
A3: Yes, if claims include formulation-specific or indication-specific use claims, they extend the protection scope, provided these claims are supported by data.

Q4: What challenges might arise in maintaining the patent's validity?
A4: Challenges include prior art disclosures, non-compliance with procedural requirements, or lack of inventive step; ongoing patent prosecution and legal defenses are crucial.

Q5: How significant is the patent landscape for strategic planning in the pharmaceutical industry?
A5: It is fundamental: understanding existing protections informs R&D directions, commercialization strategies, and risk management tactics.


References

  1. European Patent Register for DE60233040.
  2. European Patent Office patent databases.
  3. Relevant scientific literature on the chemical class and therapeutic uses.
  4. Industry reports on pharmaceutical patent trends within Germany and Europe.

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