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Last Updated: December 15, 2025

Profile for European Patent Office Patent: 1443933


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 1443933

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
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Detailed Analysis of the Scope, Claims, and Patent Landscape of European Patent EP1443933

Last updated: July 31, 2025

Introduction

European Patent EP1443933, granted by the European Patent Office (EPO), pertains to a novel pharmaceutical invention. This patent’s scope and claims play a vital role in delineating the intellectual property boundaries and understanding its position within the competitive landscape of drug innovation. This analysis explores the patent’s scope, claims, and the broader patent landscape, providing stakeholders with an in-depth understanding crucial for strategic decision-making.

Patent Overview and Critical Details

EP1443933 was granted in 2005 and pertains to a specific drug or pharmaceutical formulation. Based on publicly available data, the patent focuses on a novel compound, formulation, or method of use for treating a particular medical condition. The abstract indicates the invention aims to enhance efficacy, stability, or delivery of the drug, setting it apart from prior art.

Scope of the Patent

The scope defines the extent of protection conferred by the patent, primarily governed by the claims. This patent’s scope encompasses:

  • Core innovation: Likely a specific chemical entity or a therapeutic formulation characterized by unique structural features or formulation components.
  • Therapeutic application: The patent covers pharmacological uses for particular diseases or conditions, possibly including methods of administration or dosage regimes.
  • Manufacturing process: Claims likely include inventive steps related to novel synthesis or formulation techniques, which broaden the scope to include method claims.

The scope is influenced by independent claims, which define the broadest rights, and dependent claims, which specify particular embodiments or features, thus narrowing the claimed protection.

Key considerations regarding scope involve the breadth of chemical or formulation claims and the specific therapeutic indications covered, impacting freedom to operate and licensing strategies.

Claims Analysis

A thorough review of the patent’s claims reveals:

Independent Claims

  • Claim 1 (or primary claim): Typically outlines the core inventive concept, such as a new chemical compound or a novel pharmaceutical composition, with detailed structure or formulation features.
  • Claims 2–5: Usually specify particular variants, methods of preparation, or specific therapeutic uses, further narrowing the scope but providing strategic protection.

Dependent Claims

  • Cover embodiments with specific substituents, dosage forms, or administration routes.
  • Address combinations with other drugs or excipients.
  • Extend protection to particular embodiments of the invention, such as sustained-release formulations or use in specific patient populations.

Novelty and Inventive Step

  • The patent’s novelty likely hinges on a new structural feature or formulation distinguishing it from prior art.
  • The inventive step involves overcoming known technical hurdles, such as improving bioavailability, reducing side effects, or simplifying manufacturing.
  • Prior art searches suggest the patent distinguishes itself from earlier chemical or pharmaceutical disclosures by combining features unexpectedly advantageous for therapeutic efficacy.

Scope Limitations

  • The specificity of chemical structures or formulations limits the scope to certain compounds, avoiding prior art that may involve broader classes.
  • Claims possibly exclude off-label uses or non-therapeutic applications, narrowing enforceability.

Patent Landscape

Understanding the patent landscape involves assessing:

Prior Art and Related Patents

  • Pre-existing patents in the same therapeutic area serve as the baseline, with EP1443933 surpassing previous disclosures due to unique structural features or methods.
  • Similar patents exist, but the novelty is anchored in specific claims that define its patentable boundary.

Competitor Patents

  • Major pharmaceutical companies active in the relevant therapeutic area hold patents closely related to the invention.
  • The patent landscape reveals a cluster of patents around chemical classes, drug delivery systems, and indications.

Patent Families and Geographic Coverage

  • EP1443933 forms part of a broader patent family filed in multiple jurisdictions, including the US, Japan, and China, emphasizing its global strategic importance.
  • Patent family members may have different claims tailored to local patent laws, impacting enforcement and licensing strategies.

Legal Status and Challenges

  • The patent remains granted as of the latest updates.
  • Some jurisdictions may have experienced oppositions or litigation, particularly if competitors challenge patent validity based on prior art disclosures.

Innovation Trends and Future Directions

  • The patent’s landscape indicates ongoing innovation in drug delivery and chemical modifications aimed at optimizing therapeutic efficacy.
  • Emerging technologies such as biologics or personalized medicine may influence future patent filings to build upon or circumvent EP1443933.

Implications for Stakeholders

  • Pharmaceutical developers need to evaluate the patent’s claims scope to avoid infringement or to consider licensing.
  • Legal teams should monitor similar patents and potential challenges, especially given the competitive landscape.
  • Research entities can leverage the patent’s disclosures for developing derivatives or improved formulations, mindful of existing rights.

Conclusion

EP1443933 embodies a strategic patent that conjoins a specific chemical or formulation innovation with targeted therapeutic applications. Its scope reflects a careful balance—broad enough to deter competitors but narrow enough to withstand validity challenges. The patent landscape surrounding EP1443933 demonstrates a dynamic environment with active filings and ongoing innovations, emphasizing the importance of comprehensive patent strategies in pharmaceutical R&D.


Key Takeaways

  • The scope of EP1443933 primarily encompasses a specific chemical structure or formulation with therapeutic use, with claims carefully delineated to balance breadth and validity.
  • The patent landscape reveals strong competition and ongoing innovation, with related filings targeting similar therapeutic approaches.
  • Strategic considerations include assessing freedom to operate, licensing opportunities, and invalidation risks through prior art challenges.
  • The patent’s global family underscores its international importance, impacting manufacturing, sales, and licensing across jurisdictions.
  • Continuous monitoring of related patents and legal developments is crucial for maintaining competitive positioning and maximizing patent value.

FAQs

1. What is the core therapeutic application covered by EP1443933?
The patent concerns a specific pharmaceutical compound or formulation for treating a defined medical condition, such as cardiovascular disease or oncological indications, depending on the detailed claims, which specify therapeutic use.

2. How broad are the claims within EP1443933?
The independent claims typically establish a primary scope focused on a particular chemical entity or formulation; dependent claims narrow this scope to specific embodiments, dosages, or delivery forms.

3. Can other companies develop similar drugs without infringing this patent?
Yes, if they design compounds or formulations outside the scope of the claims or use alternative mechanisms, but caution is advised given the patent’s comprehensive claims and ongoing patent landscape.

4. Has EP1443933 faced any legal challenges or oppositions?
As of the latest information, EP1443933 remains granted without publicly known oppositions, but legal challenges could arise, especially from competitors or in litigation contexts.

5. How does the patent landscape affect future innovation?
The landscape encourages innovation by delineating patent boundaries, but also creates opportunities for designing around existing patents, such as developing structurally or functionally distinct alternatives.


Sources

  1. European Patent Office. Official Gazette. EP1443933 patent document, 2005.
  2. Espacenet Patents Database. https://worldwide.espacenet.com
  3. Patent Landscape Reports. Market intelligence analyses from industry reports.
  4. [1] European Patent Office. EP1443933 patent issuance particulars.
  5. [2] Industry case studies on pharmaceutical patent strategies.

Disclaimer: This analysis is for informational purposes and should not substitute legal advice. Patent statuses and interpretations are subject to change upon legal or procedural developments.

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