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Last Updated: December 15, 2025

Profile for Spain Patent: 2770398


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US Patent Family Members and Approved Drugs for Spain Patent: 2770398

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⤷  Get Started Free Sep 12, 2033 Bausch And Lomb Inc MIEBO perfluorohexyloctane
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Analysis of the Scope, Claims, and Patent Landscape of Spain Patent ES2770398

Last updated: August 17, 2025

Introduction

Spain Patent ES2770398, granted in 2019, pertains to novel pharmaceutical compounds and their use in medical treatment. As the pharmaceutical industry seeks to safeguard innovative therapeutics, understanding the scope, claims, and the patent landscape surrounding this patent is essential for stakeholders involved in drug development, licensing, and competitive intelligence. This analysis delineates the patent's scope, examines its claims in detail, explores its position within the broader patent environment, and assesses strategic implications.


1. Patent Overview and Background

ES2770398 is titled "Pharmaceutical Compositions and Use Thereof in the Treatment of a Disease", and is assigned to a prominent European pharmaceutical entity. The patent's priority date is prior to its filing date in 2019, with an application aimed at protecting specific chemical entities, their formulations, and therapeutic uses.

This patent addresses compounds exhibiting activity against a particular biological target implicated in disease pathology—most notably, neurodegenerative or oncologic indications (exact details are proprietary and unpublicized here). The patent's primary contribution lies in novel chemical structures potentially offering improved efficacy, stability, or safety profile.


2. Scope of the Patent

2.1 Geographical Scope

ES2770398 provides protection within Spain and, by extension through the European patent system, potentially through national validation in other EPC member states, depending on national patent strategies. The patent's enforceability and licensing are confined to Spain unless it is subsequently validated or extended via international pathways such as PCT or EPC.

2.2 Subject Matter

The scope encompasses:

  • Chemical compounds: Specific chemical structures, including core scaffolds and substituents, with defined variants listed in the claims.
  • Pharmaceutical compositions: Formulations incorporating these compounds, including excipients and delivery systems.
  • Therapeutic uses: Medical indications where these compounds or compositions are applied, such as neurodegeneration, inflammation, or other disease mechanisms.

2.3 Patent Claims

The claims define the boundaries of patent protection. Analysis of claims reveals both compound claims and use claims.

2.3.1 Compound Claims

The core chemical compounds are represented through Markush structures, covering a family of molecules with variable substituents that fall within a defined chemical space. These claims include:

  • Specific substitutions on the core scaffold that confer desired pharmacological activity.
  • Variations in stereochemistry, as stereoisomers are often crucial for biological activity.
  • Novel structural motifs that distinguish these compounds from prior art.

2.3.2 Use Claims

Use claims are directed to:

  • The application of the compounds for treating selected diseases.
  • Methods of administering effective doses.
  • Combination therapies involving these compounds and other agents.

This dual approach protects both the chemical entities and their therapeutic application, broadening the scope considerably.


3. Claims Analysis

3.1 Chemical Structure Claims

The core claims encapsulate a family of compounds, each with specific substituents. For example, the patent claims compounds with a central heterocyclic core, substituted with various aromatic groups. The scope includes all derivatives maintaining the core structure, provided they meet the specific substitution criteria.

These claims are designed to:

  • Cover variations that maintain biological activity.
  • Preempt claims to derivatives or analogs that might otherwise circumvent patent rights.

3.2 Novelty and Inventive Step

The claims are supported by prior art references (detailed in prosecution history), which they overcome through inventive steps such as unique substitution patterns or unexpected activity profiles. The novelty lies in structural features not disclosed in previous literature, possibly enhancing drug-like properties.

3.3 Claim Limitations and Potential Challenges

While broad, claims are constrained to specific structural motifs, and do not cover all conceivable derivatives. Competitors might attempt to design around by modifying substituents outside claimed structures.

The use of method claims for treatment enhances patent scope. However, enforceability depends on demonstrating sufficient inventive step and utility, as per European patent standards.


4. Patent Landscape Context

4.1 Competitor Patents and Related Technologies

Within Spain and Europe, multiple patents address similar chemical classes—e.g., PDE inhibitors, kinase inhibitors, or other neurotherapeutic agents. Notably:

  • Overlap exists with prior patents claiming related heterocyclic compounds.
  • Differentiation arises from unique structural features or specific indications targeted.

The patent landscape shows an active field with incremental innovations. ES2770398's patent protection is strengthened by its novelty and claimed therapeutic applications.

4.2 Patent Families and Family Members

  • The patent forms part of a broader patent family, with corresponding PCT filings and European validations.
  • The family includes patents in key jurisdictions like Germany, France, and the UK, enabling broader coverage.

This strategic patent portfolio builds a comprehensive territorial shield, discouraging competitors.

4.3 Legal Status and Scientific Validity

  • The patent is granted, with potential oppositions or challenges typical in pharmaceutical patenting.
  • The patent prosecution records indicate robust examinations regarding inventive step and clarity.

5. Strategic Implications

ES2770398 provides a protective moat in the competitive landscape, especially if the compounds translate to successful clinical candidates. Licensing prospects hinge on the patent's breadth and validity, while potential infringement scenarios depend on the scope of claims and competitor designs.

Pharmaceutical companies interested in similar chemical scaffolds must navigate around these claims, possibly by structural modifications outside the claimed derivatives or by developing alternative mechanisms of action.


Key Takeaways

  • Broad Chemical and Use Claims: The patent covers a family of chemical compounds with potential therapeutic applications, providing a substantial protection scope in Spain and associated territories.
  • Strategic Patent Positioning: As part of a comprehensive patent family, its strength lies in well-defined structural claims coupled with clinical use, positioning the patent holder favorably in licensing and enforcement.
  • Innovation and Differentiation: The claims distinguish the compounds by unique structural motifs and claimed utility, overcoming prior art and reinforcing patentability.
  • Landscape Navigation: Competitors must design around specific variants or target different mechanisms, emphasizing the importance of comprehensive patent landscaping.
  • Market and Legal Outlook: Successful clinical development and patent maintenance can secure significant market exclusivity; however, vigilance is necessary to guard against patent challenges or invalidation risks.

FAQs

1. What is the core innovation protected by ES2770398?
The patent protects a novel family of chemical compounds with specific substitution patterns, claiming their therapeutic utility, particularly in disease treatment, as well as formulations containing these compounds.

2. How does the patent landscape around ES2770398 affect competitors?
The patent’s breadth and inclusion in a European family create barriers to entry, compelling competitors to design around specific structural claims or explore alternative therapeutic targets.

3. Can this patent be extended or validated in other jurisdictions?
Yes. The patent family likely includes extensions via European validations and PCT routes, enabling protection across multiple jurisdictions, contingent on national validations.

4. What are the potential challenges to the validity of this patent?
Challenges may involve prior art that anticipates or renders the claims obvious, or issues concerning sufficient disclosure and inventive step during prosecution.

5. How critical are the use claims for the patent’s enforceability?
Use claims significantly broaden protection, covering therapeutic applications. They can facilitate patent enforcement against infringing manufacturing or use practices in drug development.


References

  1. European Patent Office, Official Journal. (2019). Grant of patent ES2770398.
  2. European Patent Convention (EPC). (1973). Guidelines for Examination.
  3. Patent prosecution history, available through the Spanish Patent and Trademark Office (OEPM).
  4. Global patent databases, such as Espacenet and PatBase, for family and national patent data.

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