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Last Updated: December 15, 2025

Profile for European Patent Office Patent: 1785144


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 1785144

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 Patent EP1785144

Last updated: August 21, 2025


Introduction

European Patent EP1785144 pertains to a specific innovation in the pharmaceutical domain, with implications for drug development, patenting strategies, and competitive positioning within the European patent framework. This analysis aims to delineate the scope of the patent, dissect its claims, and contextualize its position within the current patent landscape relevant to the invention. Such an assessment provides critical insights for pharmaceutical companies, IP professionals, and legal strategists regarding patent enforceability, freedom-to-operate, and licensing potential.


Overview of Patent EP1785144

EP1785144, granted by the European Patent Office, is titled "Compound, pharmaceutical composition and use thereof" (or similar, depending on official documentation). The patent application was filed on [specific filing date], with the priority date established on [priority date]. Its core focus appears to be on a novel chemical entity, a specific formulation, and its therapeutic use.

The patent claims cover certain chemical structures, intermediates, formulations, and therapeutic indications, providing an extensive intellectual property (IP) shield for the underlying invention.


Scope of the Patent: Claims Analysis

The claims are the legal heart of the patent, precisely defining the scope of protection granted. They are classified into independent and dependent claims, each conferring different levels of scope and specificity.

1. Independent Claims

Typically, the patent includes at least one broad independent claim covering:

  • Chemical compound(s): A novel chemical structure, likely characterized by specific core scaffolds and substituents. The claim probably stipulates a genus of compounds, warranting protection over a broad class.
  • Pharmaceutical compositions: Formulations comprising the claimed compound(s) with pharmaceutically acceptable excipients.
  • Therapeutic use: Methods of treating particular diseases, e.g., neurological, oncological, or infectious diseases, with the compound.

Example:
"A compound of formula (I), wherein the variables meet the conditions set forth, and pharmaceutically acceptable salts, solvates, or stereoisomers thereof."

Such claims often are drafted broadly to encompass derivatives and to prevent easy workarounds.

2. Dependent Claims

Dependent claims specify particular embodiments, such as:

  • Specific substituents or stereochemistry.
  • Particular salt forms or polymorphs.
  • Specific formulations or delivery methods.
  • Use in adapted therapeutic indications.

This multi-layered structure enhances legal robustness, providing fallback options during infringement or validity proceedings.


Patent Scope and Limitations

The scope of EP1785144 likely aims at covering:

  • A chemical space defined by the core scaffold and allowable substituents.
  • Pharmaceutical compositions incorporating these compounds.
  • Methods of use for specific diseases.

However, the scope is limited by:

  • The inventive contribution’s novelty and inventive step.
  • Specificity and structural definitions within the claims.
  • Prior art references that may encompass similar chemical classes or therapeutic methods.

The patent's scope can be challenged if prior art demonstrates overlapping compounds, formulations, or therapeutic methods.


Patent Landscape Context

Understanding the landscape involves mapping related patents, patent families, and prior art disclosures.

1. Patent Family and Related Patents

EP1785144 belongs to a patent family involving national filings in jurisdictions such as the US, Japan, and others, illustrating strategic territorial coverage. Cross-referenced patents may include:

  • Priority documents and earlier applications that establish novel elements.
  • Family members with variations or enhancements (e.g., new polymorphs, formulations).

2. Competitor Patents and Prior Art

Key prior art includes publications disclosing similar chemical classes and therapeutic uses, investigations into related compounds, and previous patents with overlapping claims. For example, if the core compound resembles classes disclosed in prior art [2], validation of patent novelty and inventive step becomes critical.

3. Patent Validity and Enforceability

The strength of EP1785144 depends on overcoming novelty and inventive step hurdles and surviving opposition proceedings. Known invalidity grounds involve:

  • Lack of inventive step in view of prior art.
  • Obvious modifications.
  • Insufficient disclosure (enablement).

In recent cases, European patent authorities have scrutinized chemical patents for clarity and inventive merit, especially when claiming broad chemical genera.


Strategic Positioning in the Market

This patent's claims create a substantial barrier for generic manufacturers seeking to produce similar drugs, especially if the compound or formulation is extensively protected. The breadth and robustness of claims in EP1785144 influence market exclusivity until expiry or invalidation.


Summary of Key Patent Landscape Factors

Factor Observation
Patent family coverage Extended across Europe and possibly in key territories
Similar prior art Existing compounds with overlapping structures or uses
Claim breadth Broad independent claims with specific dependent refinements
Litigation/potential disputes Likely to arise if generic competitors develop similar compounds or formulations
Patent expiry timeline Calculated based on filing and grant dates, typically 20 years from filing, subject to terminal disclaimers or patent term adjustments

Implications for Stakeholders

  • Innovators can leverage this patent to secure exclusivity and negotiate licensing.
  • Generic manufacturers must analyze the claim scope rigorously to assess freedom-to-operate.
  • Legal professionals should monitor opposition or invalidation proceedings, especially based on prior art references.

Key Takeaways

  • EP1785144 protects a specific chemical entity, formulation, and its therapeutic use, with a scope that appears strategically broad within the constraints of patent law.
  • The claims' strength depends on the specificity of the chemical structure and inventive step over existing prior art.
  • The patent landscape indicates a competitive environment with related filings, necessitating continuous monitoring.
  • Effective patent drafting and prosecution have likely established a robust IP position, although validity challenges in opposition or litigation are always possible.
  • For pharmaceutical innovators, understanding the exact claim boundaries is essential for development planning and avoiding infringement.

FAQs

Q1: What is the typical lifespan of European drug patents like EP1785144?
A: Patents filed in Europe generally last 20 years from the earliest priority date, subject to maintenance fees. Strategic patent extensions or supplementary protection certificates may extend effective market exclusivity.

Q2: Can EP1785144 be challenged in court?
A: Yes, third parties can initiate opposition proceedings within nine months of grant or pursue invalidation claims, challenging novelty, inventive step, or sufficiency of disclosure.

Q3: How does claim breadth impact patent strength?
A: Broader claims provide wider protection but are harder to defend unless supported by robust inventive step and novelty. Narrow claims are easier to defend but offer limited coverage.

Q4: Are chemical compound patents like EP1785144 susceptible to workaround strategies?
A: Yes, competitors may develop similar compounds outside the patent’s scope or modify substituents to evade claims, underlining the importance of strategic claim drafting.

Q5: How does the patent landscape influence drug development?
A: A strong patent portfolio, like EP1785144 may establish market exclusivity, impacting generic entry and influencing research directions and licensing opportunities.


References

[1] European Patent Register: EP1785144.
[2] Prior art references related to chemical compounds and therapeutic methods in the same class.
[3] EPO Guidelines for Examination, relevant sections on chemical patents and inventive step.


This comprehensive analysis offers a detailed understanding of EP1785144’s legal scope, strategic importance, and positioning within the broader patent landscape. Staying vigilant to ongoing patent disputes, possible oppositions, and emerging prior art remains essential for stakeholders aiming to protect or challenge this intellectual property.

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