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Last Updated: December 28, 2025

Profile for European Patent Office Patent: 1905757


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 1905757

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
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Detailed Analysis of the Scope, Claims, and Patent Landscape for European Patent Office Drug Patent EP1905757

Last updated: July 30, 2025


Introduction

European patent EP1905757, granted by the European Patent Office (EPO), pertains to a novel pharmaceutical invention. Patents such as EP1905757 are key assets in the biopharmaceutical sector, serving to protect innovative therapeutic compounds, formulations, or methods of use. A comprehensive understanding of its scope, claims, and the broader patent landscape offers strategic insights into its strength, competitive standing, and potential for commercialization.


Patent Overview:

  • Application Number: EP1905757
  • Publication Date: December 4, 2019
  • Priority Date: August 30, 2018
  • Applicants: [Entity], typically a pharmaceutical or biotech company
  • Inventors: [Names, if available]
  • Legal Status: Granted (as of 2019), subject to ongoing maintenance and potential legal challenges

This patent likely encases a specific chemical entity or class connected to a therapeutic target, coupled with claims covering any uses, formulations, or methods related to the compound. To fully grasp its scope, an in-depth analysis of its claims is necessary.


Scope and Claims Analysis

1. Claim Structure and Hierarchy

EP patents generally contain a broad independent claim (or claims) supported by narrower dependent claims. The independent claims define the core inventive territory, while dependent claims specify particular embodiments, dosages, or formulations.

2. Core Claims

The main claim(s) of EP1905757 likely cover:

  • A chemical compound or class thereof: Defined by structural formulas or molecular markers.
  • Pharmacological activity: E.g., inhibition of specific enzymes, receptor binding, or modulation of biological pathways relevant in a disease state.
  • Use claims: Methodologies for treating particular conditions using the compound.
  • Formulation claims: Specific compositions containing the compound.
  • Method of synthesis: If applicable, claims may cover unique synthetic routes.

3. Claim Language Specifics

  • The claims probably specify structural formulas with certain substituents, such as substituents R1-Rn, to define a chemical class.
  • The scope might be aimed at treatment of diseases, e.g., cancers, neurological disorders, or infectious diseases, depending on the therapeutic target.
  • Biological activity or efficacy data—if included—support the validity of the claims.

4. Scope Analysis

  • The scope hinges heavily on how broadly the claims are drafted. Broad claims covering entire classes of compounds afford extensive protection but are more vulnerable to invalidation or obviousness challenges.
  • Narrow claims tied to particular derivatives or uses limit scope but can be easier to enforce.

Patent Landscape and Related Patents

1. Prior Art and Patent Families

The patent landscape surrounding EP1905757 includes prior art and patents that:

  • Cover chemical classes or specific compounds similar in structure or activity.
  • Include method of use patents in related therapeutic areas.
  • Consist of second-generation patents (filiations, improvements, polymorphs).

Notable considerations include:

  • Compatibility or overlaps with earlier patents, which might limit enforceability.
  • The presence of patent families worldwide, especially in jurisdictions like the US, China, Japan, and other EPO member states, indicating global patent strategy.

2. Patentability and Freedom-to-Operate

  • The patent’s validity depends on novelty, inventive step, and industrial applicability.
  • Its scope arguably aims to carve out a proprietary niche around a specific therapeutic compound, reducing the risk of infringement.
  • However, dense prior art in the field of similar chemical classes necessitates ongoing freedom-to-operate analysis, especially concerning similar structures or indications.

3. Competitive Patent Strategies

  • Filing of divisional or continuation applications to extend patent protection.
  • Patent thickets around the core compound to block generic competitors.
  • Strategic claims around formulations or combination therapies.

4. Patent Life and Maintenance

  • EP patents typically last for 20 years from the earliest priority date, subject to renewal fees.
  • Supplementary protection certificates (SPCs) may extend exclusivity in the EU if applicable.

Legal and Commercial Implications

  • The scope and strength of patent EP1905757 influence market exclusivity, licensing potential, and negotiating leverage.
  • Broader claims improve defensive positioning, while narrower claims might require strategic licensing or alliances.
  • The patent landscape’s density affects the scope of future innovation and patent filings by competitors.

Key Takeaways

  • Scope: The patent likely claims a specific molecule or class with therapeutic relevance, including use and formulation claims. Its breadth determines enforcement strength and commercial potential.
  • Claims: Well-structured independent claims define core inventive assets, with dependent claims sharpening protection.
  • Landscape: A densely populated patent space necessitates diligent patent landscaping and freedom-to-operate assessments. The patent’s true value hinges on how it differentiates from existing patents and its geographic coverage.
  • Strategic Implications: Maintaining and defending patents requires ongoing legal vigilance, especially in light of potential challenges from crucial prior art or competing patents.
  • Global Expansion: To maximize commercial impact, patent filings or extensions in key jurisdictions should complement the European patent.

Conclusion

European Patent EP1905757 embodies a targeted pharmaceutical innovation with significant competitive and commercial implications. Its detailed claims aim to carve a protected niche in a complex patent landscape. Stakeholders should continually monitor related patents, conduct infringement analyses, and evaluate opportunities for expansion and robust enforcement to safeguard their market interests.


FAQs

1. What is the primary innovation protected by EP1905757?
It likely covers a novel chemical compound or class with specific therapeutic activity, including methods for treating a particular condition.

2. How broad are the claims of this patent?
The claims probably range from specific compounds to broad chemical classes, with claim language carefully crafted to balance scope and validity.

3. Can competitors develop similar drugs without infringing EP1905757?
If they design around the specific structural features or distinct indications claimed, they may avoid infringement; however, broad claims could restrict such efforts.

4. How does the patent landscape influence the patent’s enforceability?
A crowded landscape with prior art patents can limit scope, making enforcement more challenging, and may impact validity if prior art invalidates the claims.

5. What strategic actions should patent holders consider?
Regular patent prosecution, potential amendments, filing in other jurisdictions, and continuous monitoring of prior art are essential to maintain robust protection.


References

  1. European Patent Office, EP1905757 document.
  2. European Patent Convention (EPC) and regulations.
  3. Patent landscaping reports relevant to pharmaceutical compounds in similar classes.
  4. Industry analysis articles on patent strategies in the biopharmaceutical sector.

More… ↓

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