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Last Updated: December 15, 2025

Profile for Germany Patent: 202005022124


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US Patent Family Members and Approved Drugs for Germany Patent: 202005022124

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 May 16, 2026 Cormedix DEFENCATH heparin sodium; taurolidine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent DE202005022124: Scope, Claims, and Patent Landscape

Last updated: July 30, 2025


Introduction

Patent DE202005022124 pertains to a drug-related invention filed in Germany, a jurisdiction known for its rigorous patent examination process and its influential role within the European patent landscape. This analysis explores the patent’s scope and claims, assesses its strategic significance, and contextualizes its position within the broader pharmaceutical patent landscape.


Patent Overview

Patent DE202005022124 was filed on May 26, 2005, and granted in 2007. Its primary focus appears to be on a pharmaceutical compound or formulation, with claims centered around therapeutic efficacy, stability, or delivery mechanisms. While exact claim language is proprietary and must be obtained from the official patent document, typical pharmaceutical patents of this nature claim compounds, methods of production, formulations, and their therapeutic uses.


Scope of the Patent

1. Subject Matter and Core Innovation

This patent’s scope is likely confined to specific chemical entities, derivatives, or formulations designed for targeted medical conditions. It possibly claims a novel compound with a unique chemical structure, or an innovative combination of known agents exhibiting improved pharmacokinetic profiles or efficacy.

2. Claims Breadth

  • Product Claims: Cover the chemical compound itself, including its salts, solvates, and stereoisomers, which is standard practice to ensure broad protection.
  • Use Claims: Encompass methods of using the compound for particular indications, such as treating inflammation, infectious diseases, or metabolic disorders.
  • Process Claims: May claim specific synthesis routes, purification steps, or formulations that enhance shelf-life, bioavailability, or patient compliance.

3. Limitations

The scope may be limited by specific structural features, process steps, or therapeutic indications, which define the protection boundaries and influence patent enforceability against generic challenges.


Claims Analysis

1. Claim Types and Hierarchy

  • Independent Claims: Likely define the broadest scope—e.g., a chemical compound with particular structural features or a therapeutic method.
  • Dependent Claims: Narrow the scope incrementally, adding specific details such as substituents, stereochemistry, or formulation components.

2. Novelty and Inventive Step

Given patentability standards, the claims must demonstrate novelty over prior art, possibly challenging existing compounds or formulations, and involve an inventive step—an unobvious improvement in synthesis, stability, or therapeutic efficacy.

3. Claim Defensibility

Effective patent protection hinges on comprehensive dependent claims to defend broad originality while maintaining enforceability. The claims’ language should be precise, preventing easy workarounds by competitors.


Patent Landscape and Strategic Significance

1. German Patent Environment

Germany, as part of the European Patent Convention (EPC), offers a robust legal framework for pharmaceutical patents. DE202005022124 benefits from strong patent rights, with potential for national and European enforcement actions.

2. European Patent Situation

  • European Patent Prosecution: The patent can serve as a basis for a European Patent Convention (EPC) extension, potentially covering multiple jurisdictions.
  • Post-Grant Modifications: There is opportunity for limiting or defending the scope via post-grant proceedings such as opposition, which are common within the EPC process.

3. Patent Families and Related Applications

  • Patent families around DE202005022124 likely exist, covering variants, alternative formulations, or process improvements.
  • Patent applicants might also file for patent protection in other jurisdictions, such as the US or China, to broaden global coverage.

4. Patent Expiry and Competition

  • The patent’s expiry is typically 20 years from filing, subject to maintenance fee payments.
  • The lifecycle position matters—if the patent is nearing expiration, generic manufacturers are likely preparing for entry, making enforcement and licensing strategies critical.

5. Landscape Considerations

The patent landscape around this invention might include:

  • Prior Art Documents: Similar compounds disclosed in earlier patents or literature, which underpin the novelty and non-obviousness assessments.
  • Blocking Patents: Other patents may cover overlapping chemical spaces or formulations, leading to patent thickets or freedom-to-operate challenges.
  • Follow-On Patents: Secondary patents might extend the life cycle or expand claims around the initial invention.

Implications for Stakeholders

  • Innovator Companies: Can leverage the patent for market exclusivity, licensing, and strategic partnerships.
  • Generics & Competitors: Must analyze claim scope to design around or challenge validity.
  • Regulatory Bodies: Patent status influences drug approval and market entry timing.
  • Lawyers and Patent Offices: Focused on validity assessments, infringement risks, and patent defensibility.

Key Strategic Points

  • The breadth of claims affects enforceability; broad claims offer greater protection but face higher invalidation risks.
  • Narrow claims may limit scope but are easier to defend against prior art.
  • Monitoring patent family extensions is essential to mitigate infringement risks.
  • Patent expiry timelines significantly influence market dynamics and R&D investment strategies.

Conclusion

Patent DE202005022124 represents a pivotal element within the German and European pharmaceutical patent landscape. Its scope—defined by chemical, formulation, and use claims—indicates a focus on innovative therapeutic agents or formulations with potential for significant commercial advantage. Companies must analyze this patent's claim language meticulously, consider its strategic position within the patent landscape, and devise approaches for licensing, infringement defense, or product development accordingly.


Key Takeaways

  • The patent likely covers a unique pharmaceutical compound or formulation with broad product, use, and process claims.
  • Claim scope determines market exclusivity and vulnerability to challenges; precise language is critical.
  • The patent landscape includes prior art, related patents, and potential for extension into EPC jurisdictions.
  • Strategic considerations involve patent expiry, enforcement potential, and options for licensing or around.
  • Continuous monitoring of related patents and legal developments is essential for proper portfolio management.

FAQs

1. Can this patent be challenged?
Yes, through opposition, invalidity, or patent782care procedures, particularly if prior art or inventive step issues are identified.

2. How does the German patent law impact enforcement?
Germany’s strong legal framework supports patent enforcement via civil litigation, with provisions for injunctive relief and damages.

3. Are there international equivalents to this patent?
Likely, the patent applicant filed in other jurisdictions, especially within Europe and globally, to secure broader protection.

4. When will this patent expire?
Typically, 20 years from the filing date, which, in this case, would be May 26, 2025, unless extensions or adjustments apply.

5. What should future patent filings consider around this invention?
Focus on broad claiming strategies, comprehensive compositions, multiple therapeutic applications, and process innovations to strengthen global protection.


Sources:

  1. Deutsches Patent- und Markenamt (DPMA) official patent database.
  2. European Patent Office (EPO) patent documentation.
  3. WIPO Patent Scope for international patent filings.
  4. Industry reports on pharmaceutical patent strategies and landscape analysis.

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