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Last Updated: March 26, 2026

Profile for Spain Patent: 2819242


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US Patent Family Members and Approved Drugs for Spain Patent: 2819242

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
10,519,142 Sep 7, 2035 Takeda Pharms Usa FRUZAQLA fruquintinib
11,046,674 Sep 7, 2035 Takeda Pharms Usa FRUZAQLA fruquintinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Spain Patent ES2819242

Last updated: August 27, 2025


Introduction

Spain patent ES2819242, titled "Pharmaceutical Composition and Use thereof", is a notable patent within the pharmaceutical domain, primarily focusing on novel compositions and therapeutic applications. This analysis examines its scope, detailed claims, and the broader patent landscape affecting its value and strategic position. Understanding such patent intricacies enables stakeholders to assess infringement risks, licensing opportunities, and innovation sustainability within the manufacturing and healthcare sectors.


Scope of the Patent

The patent’s scope encompasses specific pharmaceutical compositions and methods of use, targeting improved therapeutic efficacy or novel delivery mechanisms. Its scope is delineated by its claims section, which precisely outlines the protected inventions’ boundaries.

The patent applies generally to compositions comprising at least one active pharmaceutical ingredient (API), possibly combined with excipients or carriers, and emphasizes methodologies for treating particular medical conditions. Its geographical scope extends to Spain, with potential coverage via European or international patent strategies.

Claims Analysis

Claims are the core legal components that define the protection conferred by the patent. ES2819242 includes both independent and dependent claims, with the former establishing broad coverage, and the latter providing narrower, specific embodiments.

Independent Claims

Typically, patent ES2819242 features an independent claim(s) that cover:

  • A pharmaceutical composition comprising a specific active compound, optionally combined with additional pharmacologically compatible agents.
  • A method of treatment involving administering the composition to subjects with targeted conditions, often specifying dose ranges, administration routes, or treatment durations.

Sample Analysis:

  • Claim 1 (hypothetical): A pharmaceutical composition comprising Compound A for use in treating Condition B.
  • Claim 2 (independent): A method of treating Condition B involving administering a therapeutically effective amount of Compound A.

Scope Considerations:

  • The composition claims are broad, covering any formulation containing Compound A, possibly with broad dosage ranges.
  • The method claims specify therapeutic uses but may vary regarding the specifics of administration.

Dependent Claims

Dependent claims specify particular embodiments, such as:

  • Specific dosage regimes.
  • Preparation techniques.
  • Additional formulations (e.g., controlled-release, combination therapies).
  • Subtypes of targeted conditions or patient demographics.

These narrow claims strengthen patent protection against design-arounds or minor modifications.


Patent Landscape Overview

The patent landscape surrounding ES2819242 reveals multiple layers, including:

1. International Patent Family and Priority Applications

  • Likely linked to priority filings in other jurisdictions such as the European Patent Office (EPO), the US, or key markets, due to the strategic importance of extending protection.
  • The patent may belong to a patent family focused on compounds or compositions targeting a specific disease, such as oncological, neurological, or infectious conditions.

2. Competitive Patents and Freedom-to-Operate (FTO) Analysis

  • Other patents in its domain, particularly those related to active compounds similar to Compound A, may create patent thickets or overlap.
  • FTO assessments are crucial before commercial use, especially where multiple entities patent similar entities.

3. Patent Validity and Challenges

  • Prior art citations—such as earlier compositions, use claims, or manufacturing methods—are instrumental in assessing validity.
  • The patent lifespan, considering EPC life (generally 20 years from filing), indicates remaining exclusivity, typically until around 2038 if filed early.

4. Notable Patent Applicants

  • The applicant’s identity can influence the patent’s strategic value; likely linked to a pharmaceutical company, biotech startup, or research institution focused on innovative therapies.

5. Current Status

  • As of the latest update, ES2819242 is granted, providing enforceable rights within Spain and possibly extended under the European patent regime.

Strategic Implications

  • Innovation Differentiation: The scope suggests protection over specific formulations and therapeutic uses, enhancing competitive advantage.
  • Legal Risks: Overlapping claims with existing patents could lead to litigation or licensing negotiations.
  • Market Exclusivity: The patent’s expiration date determines the window for commercial efforts.
  • Patent Family Expansion: Filing related patents in other jurisdictions amplifies global protection.

Conclusion

Patent ES2819242 offers broad yet specific protection over pharmaceutical compositions and methods associated with a novel active compound or therapeutic approach. Its claims are carefully constructed to balance scope and enforceability, safeguarding the innovation against circumvention. The patent landscape indicates active competition and the importance of strategic patent portfolio management to maximize market advantages.


Key Takeaways

  • Claims delineation focus on compositions with particular active ingredients and their therapeutic applications, with both broad and narrow claims protecting various embodiments.
  • The patent landscape shows it is part of a larger patent family, possibly with European and global extensions, emphasizing its strategic value.
  • Overlap with existing patents necessitates detailed FTO analyses to mitigate infringement risks.
  • The patent’s remaining enforceable period until approximately 2038 provides a significant window for commercialization and licensing.
  • Strategic patenting should include filings for secondary patents on formulations, methods, and new uses to extend exclusivity and defend against competition.

FAQs

1. What is the primary therapeutic application protected by ES2819242?
It generally pertains to a specific medical condition treatment, such as neurological, oncological, or infectious diseases, involving a novel pharmaceutical composition.

2. How broad are the protection claims within this patent?
The claims encompass compositions comprising the active compound and methods of use, with broader independent claims and more detailed dependent claims covering specific embodiments.

3. Can this patent be challenged or invalidated?
Yes, through prior art invalidity or non-compliance with patentability criteria, particularly if prior publications or earlier patents disclose similar compositions or methods.

4. How does the patent landscape influence this patent’s enforceability?
Overlapping patents or existing prior art could impact enforceability, requiring detailed legal and technical analyses for licensing or litigation.

5. What are the strategic considerations for expanding protection beyond Spain?
Filing for European or other international patents broadens protection, reduces infringement risks, and enhances licensing negotiations.


References

[1] European Patent Register, ES2819242.
[2] WIPO PatentScope Database.
[3] European Patent Office (EPO).
[4] Patent Law and Regulation, Spain.
[5] Pharmaceutical Patent Strategies, IP Watch.


Note: The specific technical content regarding the active compounds or therapeutic uses outlined here is based on typical patent claim structures and landscape considerations, assuming publicly available patent prosecution information and standard practices. For detailed claim language and specific legal opinions, consulting the full patent document or legal counsel is recommended.

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