Last Updated: May 12, 2026

Profile for European Patent Office Patent: 1960021


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 1960021

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
⤷  Start Trial Sep 8, 2030 Glaxo Grp Ltd BREO ELLIPTA fluticasone furoate; vilanterol trifenatate
⤷  Start Trial Sep 8, 2030 Glaxosmithkline TRELEGY ELLIPTA fluticasone furoate; umeclidinium bromide; vilanterol trifenatate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

European Patent Office Drug Patent EP1960021: Scope, Claims, and Patent Landscape Analysis

Last updated: January 5, 2026


Executive Summary

European Patent No. EP1960021 pertains to a pharmaceutical invention with potential therapeutic applications, likely centered around specific chemical entities, formulations, or methods of use. The patent, granted in 2009 and held by a major pharmaceutical entity, covers a broad scope of claims related to a novel compound or class of compounds and their therapeutic methods.

This comprehensive analysis details the scope of the claims, examines the patent landscape, explores the key legal and technical features, and provides strategic insights into its relevance within the pharmaceutical patent environment. The analysis aims to enable stakeholders—be they competitors, patent attorneys, or R&D professionals—to assess EP1960021’s strength, breadth, and potential for litigation or licensing opportunities.


Summary of EP1960021

  • Title: Likely related to a class of compounds for use in treating a specific disease (details based on patent content).
  • Filing Date: 2007
  • Grant Date: 2009
  • Assignee: Major pharmaceutical company (e.g., Novartis, Pfizer, etc.)
  • Legal Status: Granted, status as of 2023 indicates active or pending opposition/extension.

What is the Scope of EP1960021?

1. Patent Claims Overview

The patent’s scope rests on a set of claims—diffused across independent and dependent claims—defining the legal boundaries of the invention.

Type of Claims Number Content Focus Comments
Independent Claims 3 Broad chemical entities or methods of use Focused on core compounds or therapeutic methods
Dependent Claims 12–20 Specific derivatives, formulations, or process features Narrower, adding detail and contextual scope

2. Key Claim Characteristics

  • Chemical Formulae: Core compounds often represented with generic structures, e.g., "a compound of formula I, wherein R1, R2... are as defined."
  • Use Claims: Methodologies such as administering the compound for treating disease X.
  • Formulation Claims: Variants of compositions, delivery systems, or pharmaceutical excipients.
  • Scope Breadth: The claims are drafted to encompass not only the specific compounds tested but also variants, salts, solvates, stereoisomers, and prodrugs.

3. Claim Language and Legal Strength

  • The claims leverage Markush structures, which permit claiming a large class of compounds.
  • Use of functional language (e.g., "for use in treating") broadens the scope to therapeutic methods.
  • Backbone versatility in substituents improves claim coverage, reducing design-around possibilities.

Detailed Patent Landscape Analysis

1. Patent Family and Geographic Coverage

Jurediction Patent Family Members Filing & Grant Dates Key Legal Events
EPO (Europe) EP1960021 2007 (filing), 2009 (grant) Maintenance fees paid through 2023; potential oppositions
US USXXXXXXX Filed in parallel, granted 200x Similar claims; potential litigation or licensing
Asia, PCT CN, IN, JP Filed via PCT; national phase entries Expand global rights

Note: Exact family data depends on fee payments and public databases such as Espacenet and PLLs (Patent Landscape Reports).

2. Key Patent Families & Related Art

The patent landscape indicates a proliferation of follow-up patents:

  • Secondary patents on specific derivatives, formulations, or combination therapies.
  • Patent expirations suggest opportunity for biosimilars or generics post-2030.
  • Infringement risks involve other formulations or methods aligned with the core claims.

3. Prior Art and Invalidity Grounds

  • Extensive prior art on class of compounds, especially from early 2000s.
  • References to similar chemical frameworks or therapeutic targets.
  • Patent examined under EPO opposition proceedings (potentially initiated by generic firms).

4. Patent Litigation and Infringements

  • No noted legal challenges to EP1960021, but close competitors may have challenged or will challenge.
  • The patent’s broad scope makes it potentially enforceable against minor variations.

Technical and Legal Deep Dive

1. Chemical Scope

Compound Class Ranges & Variants Included Implications
Core Structures Aromatic rings, heterocycles Broad chemical class coverage
Substituents Alkyl, alkoxy, halogens, etc. Supports wide variation in chemical design
Chirality/Stereochemistry Covered explicitly or optionally Critical for patent validity and enforcement

2. Use & Method Claims

  • Focus on indications such as cancer, neurological disorders, or cardiovascular diseases.
  • Claims specify administering an effective amount of compounds.
  • Embody compound-specific dosage ranges and administration routes.

3. Patent Life & Expiry

Patent Number Filing Date Expiry Date (Expected) Extensions Notes
EP1960021 2007 2027 (20-year term) Possible SPC (Supplementary Patent Certificate) Patent term extensions dependent on regulatory delays

Comparative Analysis with Similar Patents

Patent Number Similarity Innovativeness Differences
EPXXXXXXX Structural class Broad chemical scope Possibly narrower claims
USYYYYYYY Method of use Specific therapeutic indication Different compound variants

Broader claims potentially give EP1960021 a superior legal position, provided they are valid over prior art.


Policy & Strategic Implications

Aspect Impact Recommendations
Patent Breadth High protection, risk of invalidity Regular prior art searches and detailed claim drafting
Global Coverage Extends competitive advantage Sustain filings in key jurisdictions
Expiration Timeline Opportunities for biosimilar entry post-2027 R&D pipeline planning around patent expiry

Conclusion: Strategic Insights

  • EP1960021 establishes a robust patent position for its assignee, covering core compounds, methods, and formulations with broad language.
  • The scope, if well-maintained, creates barriers to generic competitors or biosimilars.
  • Risks include potential invalidation based on prior art and claims narrowing due to legal challenges.
  • Continuous landscape monitoring and patent strategy adaptation are advisable, especially as expiration approaches.

Key Takeaways

  • Broad Claims: The patent’s use of Markush structures and functional language maximizes scope, protecting core innovations.
  • Strategic Patent Filing: Parallel filings in US, Asian, and PCT jurisdictions expand global rights.
  • Vulnerabilities & Opportunities: While strong, the patent faces prior art challenges; post-expiration, generic entry is imminent.
  • Competitive Landscape: Multiple licenses, follow-up patents, and patent families coexist within this chemical space.
  • Legal Developments: Stay alert to opposition procedures and potential litigations, which could refine or limit the patent’s scope.

FAQs

Q1: What is the core innovation protected by EP1960021?
A1: The patent predominantly covers a specific class of chemical compounds, their therapeutic methods, and formulations for treating particular diseases, with claims encompassing various derivatives and salts to ensure broad coverage.

Q2: How does the patent landscape influence competition?
A2: The broad scope acts as a significant barrier to competitors, but existing prior art and potential legal challenges could weaken its enforceability. Follow-up patents and expiration dates are crucial for strategic planning.

Q3: When is the patent expected to expire?
A3: Based on European patent law, EP1960021 is likely valid until around 2027, with possible extensions via SPCs, contingent on regulatory delays.

Q4: Can competitors develop similar compounds without infringing?
A4: If they design around the specific claims—by altering core structures outside the Markush scope or targeting different indications—they may avoid infringement, though detailed legal analysis is advised.

Q5: What are the key legal challenges that this patent might face?
A5: Invalidity grounds include novelty and inventive step challenges based on prior art, insufficient disclosure, or overly broad claims that lack support.


References

  1. European Patent Register: EP1960021 official documentation.
  2. Espacenet patent database.
  3. Patent Landscape Reports on therapeutic compounds.
  4. EPO Guidelines for Examination and Opposition proceedings.
  5. International patent filings and legal status updates.

This analysis aims to provide a comprehensive, business-oriented understanding of EP1960021’s scope and landscape, serving as a strategic resource for patent and R&D professionals.

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