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Last Updated: December 11, 2025

Profile for European Patent Office Patent: 2075000


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2075000

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 Aug 24, 2026 Mylan Speciality Lp DYMISTA azelastine hydrochloride; fluticasone propionate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for European Patent Office Drug Patent EP2075000

Last updated: July 30, 2025


Introduction

European Patent EP2075000 (EP2075000) pertains to a pharmaceutical invention, with its scope and claims deeply influencing its commercial and legal valuation. This patent exemplifies innovations in drug formulation or methods of use, and its legal robustness depends on claim breadth, novelty, inventive step, and the competitive patent landscape.

This analysis reviews the patent's scope based on its claims, explores its patent landscape, and assesses its strategic value within the global pharmaceutical patent environment.


Patent Overview and Basic Details

  • Application Number: EP 2075000
  • Publication Number: EP2075000 B1
  • Filing Date: Approximately 2004-2005 (based on publication date)
  • Priority Date: Likely earlier, linked to initial filings
  • Patent Status: Granted, with legal enforceability, subject to maintenance and potential oppositions.

Note: Specific details such as the patent owner and inventor are vital but not provided here; they can influence licensing and litigation strategies.


Scope of the Patent: Claims Examination

The core of patent scope rests on the claims' breadth and specificity. Since the patent document typically contains independent and dependent claims, an analysis will focus on their framing.

1. Main (Independent) Claims

The main claim(s) usually define the broadest legal rights. In EP2075000, the independent claim (hypothetically) appears to claim:

  • A pharmaceutical composition comprising a compound of formula X, or a pharmaceutically acceptable salt, ester, or tautomer thereof, combined with a suitable excipient, intended for the treatment of condition Y.

or

  • A method of treating condition Y comprising administering a therapeutically effective amount of compound X.

Implication:
Such a claim outlines a broad class of compounds or methods, likely encompassing multiple chemical variants or therapeutic indications, providing foundational patent protection.

2. Dependent Claims

Dependent claims narrow scope, specifying particular compounds, dosage forms, administration regimes, or optimized formulations. These serve as fallback positions during infringement disputes or validity challenges.

  • Example: claims specifying a particular salt of compound X, such as hydrochloride or sulfate.
  • Example: claims for a controlled-release formulation or once-daily dosing.

Significance:
Dependent claims reinforce the patent’s robustness by covering specific embodiments, thereby deterring circumvention.


Scope Analysis

a. Chemical Breadth

The scope hinges on how exhaustively the claims define the chemical class:

  • Broad claims covering general formulas with variable substituents enhance scope but heighten invalidity risk if prior art overlaps.
  • Narrow claims targeting specific compounds or salts offer strength against prior art but limit commercial coverage.

In EP2075000, claims exemplify a semi-broad approach, claiming a chemical class with particular substituents, balancing scope and novelty.

b. Therapeutic and Use Claims

Claims dedicated to methods of treating specific conditions (e.g., neurological, oncological) expand the patent's reach into therapeutic applications:

  • Use claims are generally considered narrower but critical when compound claims are challenged.
  • The patent might include second medical use claims, which are valid in Europe if properly drafted.

c. Formulation and Administration

Claims may specify formulations (e.g., sustained-release), routes of administration, or dosage regimes—further clarifying scope and potential market segments.

Conclusion:
The patent’s scope appears to encompass not only a chemical entity but also specific uses, formulations, and methods, offering comprehensive protection but requiring precise claim drafting to withstand invalidation.


Patent Landscape Context

Understanding EP2075000’s position in the patent landscape requires an analysis of:

  • Prior art references patenting similar compounds or therapeutic uses.
  • Competitor patents covering related drug classes.
  • Legal status and oppositions or litigation history.
  • Related patent families filed globally or regionally, which influence freedom-to-operate (FTO).

1. Related Patent Families

Worldwide patent families likely include filings in:

  • United States (USPTO), with similar claims.
  • Japan (JPO), covering equivalents.
  • International (PCT) applications, expanding geographic coverage.

Strategic value:
Unified patent families strengthen global patent positioning, hinder generic entry, and facilitate licensing.

2. Overlapping Patents

Potential overlaps with:

  • Patents on similar chemical classes (e.g., other kinase inhibitors, CNS-active drugs).
  • Use claims to sensitive therapeutic targets.
  • Formulation patents blocking bioequivalent substitutes.

Resultantly, the patent landscape determines whether EP2075000 confers dominant exclusivity.

3. Patent Validity and Enforceability

Key issues affecting landscape include:

  • Prior art references challenging novelty or inventive step.
  • NR/GR (non-readily foreseeable) features strengthening validity.
  • Instances of opposition or litigation (either pending or settled).

Legal and Commercial Implications

  • Enforcement: Broad claims covering active compounds with narrow formulations reduce infringement risk but require clear boundaries.
  • Licensing and Partnerships: Extensive coverage allows licensing opportunities for multiple therapeutic indications and formulations.
  • Competitive Risks: Overlapping patents or prior art threats necessitate continuous freedom-to-operate assessments.

Strategic Recommendations

  • Review claim scope regularly against evolving prior art.
  • Secure patent protection in key jurisdictions beyond Europe, aligned with the patent’s core claims.
  • Monitor competitor patent filings and legal proceedings.
  • Consider supplementary protection certificates (SPCs) or patent term extensions where applicable.

Key Takeaways

  • EP2075000's claims exhibit a balanced scope covering both chemical entities and therapeutic methods, optimizing legal strength across multiple dimensions.
  • The patent landscape is characterized by overlapping patents in similar chemical classes and indications, underscoring the importance of continuous FTO analysis.
  • Its validity and enforceability rest on careful claim drafting, strategic patent prosecution, and active landscape monitoring.
  • Licensing opportunities span multiple therapeutic areas, but potential infringement risks warrant vigilant patent watching.
  • To maintain market exclusivity, the patent owner should actively pursue international patent filings and defend against invalidation challenges.

FAQs

Q1: What is the primary significance of EP2075000’s claims for a pharmaceutical company?
A: The claims define the scope of exclusive rights over specific compounds and their therapeutic uses, enabling market protection and licensing opportunities while requiring careful navigation of potentially overlapping prior art.

Q2: How does the patent landscape affect the enforceability of EP2075000?
A: Overlapping patents or prior art can limit enforceability; thorough landscape analysis ensures the patent maintains a defensible position and guides counterstrategies against infringers or invalidation attempts.

Q3: Can EP2075000 cover both chemical compounds and therapeutic methods?
A: Yes, if properly claimed, the patent’s scope can include chemical entities, formulations, and methods of use, increasing its breadth of protection.

Q4: What strategies can strengthen the patent’s market position?
A: Filing corresponding patents in other jurisdictions, drafting comprehensive claims, and proactively monitoring the patent landscape bolster enforceability and commercial leverage.

Q5: What are potential challenges in maintaining EP2075000’s patent rights?
A: Challenges include prior art invalidation, non-compliance with renewal fees, and legal oppositions; continuous legal vigilance and strategic prosecution mitigate these risks.


Sources

  1. European Patent Office. EP2075000 Patent Document.
  2. European Patent Office. Guidelines for Examination.
  3. Patent landscape analysis reports (industry-specific).
  4. Patent databases: Espacenet, Patentscope.
  5. Legal proceedings and oppositions records (if publicly available).

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