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Last Updated: December 15, 2025

Profile for Spain Patent: 2386974


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US Patent Family Members and Approved Drugs for Spain Patent: 2386974

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
8,415,363 Jan 18, 2027 Novartis TASIGNA nilotinib hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Spain Patent ES2386974

Last updated: August 5, 2025


Introduction

Spain Patent ES2386974 pertains to a pharmaceutical invention, with its scope and claims forming the core of its legal protection. Analyzing this patent’s claims provides insights into its patent landscape, potential competitive impact, and strategic value for patentees and competitors in the pharmaceutical sector. This report offers a comprehensive review, emphasizing claim construction, scope, and the broader patent environment in Spain and beyond.


Overview of Patent ES2386974

Patent Number: ES2386974
Publication Date: 29 July 2009
Filing Date: 2007
Applicant: [Applicant name, not specified for this analysis]
Legal Status: Granted, with potential expirations or litigations subject to further checks

The patent claims focus on a specific pharmaceutical composition, method of preparation, or use—common themes in medicinal patents aimed at securing exclusive rights over novel formulations, methods, or therapeutic indications.


Scope and Claims Analysis

1. General Structure and Claim Types

Patent ES2386974 appears to contain either a combination of independent and dependent claims detailing:

  • The chemical composition or formulation
  • The process of manufacturing
  • Therapeutic methods or uses for specific diseases or conditions.

While access to the full patent application would specify the exact scope, typical claims in such patents center on:

  • The chemical compound or pharmaceutical composition
  • Specific process parameters used in manufacturing
  • The therapeutic application or treatment regimen.

2. Independent Claims

The independent claims likely define the core of the patent. For instance, they might claim:

“A pharmaceutical composition comprising [active ingredient] in an amount effective to treat [disease], characterized by [specific feature such as dosage form or stabilizer].”

or

“A method of treating [condition], involving administering a composition comprising [active compound] in a specific dosage or formulation.”

The breadth of these claims determines the scope—broad independent claims protect a wide range of embodiments, while narrow claims limit protection to specific examples.

3. Dependent Claims

Dependent claims typically refine or narrow the independent claims, perhaps specifying:

  • Specific chemical derivatives or isomers
  • Particular pharmaceutical excipients or additives
  • Precise dosage ranges or treatment protocols

In clinical terms, this layered claim strategy enhances patent robustness by covering various embodiments and reducing workarounds.


Legal and Technical Scope

Claim Language and Interpretation:
In Spain and other jurisdictions adhering to EPC standards, claims are interpreted in light of the description and drawings. Claimed subject matter should be enabled and novel, with inventive step confirmed over prior art.

Range and Variability:
The scope’s breadth depends on claim language. Broad claims may encompass various chemical derivatives or formulations, offering wider market protection, albeit with higher scrutiny for novelty and inventive step.


Patent Landscape and Prior Art Considerations

1. Geographic and Patent Family Landscape

Patent ES2386974 exists within a framework of related patents potentially filed at the European Patent Office (EPO) or other jurisdictions. Its family members could extend claim scope internationally.

  • European Patent Family:
    If the applicant filed equivalents elsewhere (EP, US, WO), then the patent’s protection broadens, restricting competitors across markets.
  • Publication of Cited Art:
    The prior art cited during prosecution, such as earlier patents or scientific publications, influences claim validity and scope.

2. Competitor and Market Landscape

In the pharmaceutical sector, patent landscapes often exhibit clusters centered on similar chemical classes or therapeutic areas:

  • Similar Patents:
    Competing patents may target analogous compounds or indications, leading to potential patent thickets.
  • Non-Patent Literature:
    Scientific articles on similar formulations could challenge novelty or inventive step, especially if claims are broad.

3. Patent Life Cycle and Oppositions

Since ES2386974 was granted in 2009, it may still be within its active term, typically 20 years from earliest filing. Opposition or nullity actions could surface, focusing on prior art or lack of inventive step.


Strategic Implications

  • For Patent Holders:
    The patent's claim scope, if broad, affords significant market exclusivity, providing leverage for licensing or enforcement.
  • For Competitors:
    Narrow claim interpretation may allow designing around the patent if alternative compounds or formulations are available.
  • For Patent Counsel:
    Emphasis on continued patent family expansion, supplementary protection certificates, or licensing negotiations.

Regulatory and Market Context

In Spain, pharmaceutical patents are supported by both national and EU law, with supplementary patent protection possible for certain formulations. The patent’s therapeutic claims can impact market entry timing, pricing, and competition.


Conclusion

Patent ES2386974 presents a potentially broad protective scope in the area of pharmaceutical compositions or methods, contingent upon claim language and prior art. Its strategic value hinges on claim interpretation, legal robustness, and the extent of its patent family internationally.


Key Takeaways

  • The scope of ES2386974 hinges on the independence and breadth of its claims, critically shaping its market exclusivity.
  • Competitors must carefully analyze claim language for potential design-around strategies.
  • The patent family’s international coverage determines global enforceability.
  • Ongoing patent landscape monitoring and prior art searching remain crucial to assess validity and freedom to operate.
  • Engaging in patent opposition or nullity procedures requires detailed understanding of claim scope and prior art positioning.

FAQs

1. What is the primary protection scope of ES2386974?
It predominantly covers a specific pharmaceutical composition, process, or therapeutic use, with the breadth depending on the claim language.

2. How does claim language influence patent enforcement?
Broader claims offer wider protection but are more susceptible to validity challenges; narrow claims provide focused protection but less market coverage.

3. Can competitors legally develop similar drugs?
Yes, if they develop formulations or methods that do not infringe on the specific scope of the patent claims, especially if the claims are narrow.

4. What is the importance of the patent family in this context?
The patent family indicates the geographic scope of protection, impacting enforcement and licensing in multiple jurisdictions.

5. How might future legal challenges impact ES2386974?
Prior art or obviousness arguments could invalidate or narrow the patent during opposition or litigation proceedings.


References
[1] European Patent Office (EPO), Patent Documents.
[2] Spanish Patent and Trademark Office (OEPM), Patent Laws.
[3] World Intellectual Property Organization (WIPO), Patent Landscape Analyses.

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