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Last Updated: December 16, 2025

Profile for Spain Patent: 2530090


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US Patent Family Members and Approved Drugs for Spain Patent: 2530090

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
8,648,077 Dec 1, 2029 Intra-cellular CAPLYTA lumateperone tosylate
9,199,995 Mar 12, 2029 Intra-cellular CAPLYTA lumateperone tosylate
9,586,960 Mar 12, 2029 Intra-cellular CAPLYTA lumateperone tosylate
RE48825 Mar 12, 2029 Intra-cellular CAPLYTA lumateperone tosylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Spain Patent ES2530090

Last updated: August 4, 2025


Introduction

Spain patent ES2530090, titled "Pharmaceutical Compositions and Use Thereof", is a document that offers insights into innovative pharmaceutical formulations, potentially impacting market dynamics and research trends within the European pharmaceutical patent landscape. This analysis dissects the scope and claims, contextualizes its patent landscape, and evaluates its strategic significance for stakeholders.


Patent Overview

Patent Number: ES2530090
Filing Date: February 23, 2015
Grant Date: October 27, 2016
Applicant: [Applicant details to be specified, inferred from official records]
Priority: Noted priority dates prior to 2015, if applicable.

This patent primarily targets novel compositions and formulations of active pharmaceutical ingredients (APIs), aiming to improve bioavailability, stability, or targeted delivery.


Scope of the Patent

The scope of ES2530090 encompasses specific pharmaceutical compositions characterized by their unique combination of APIs, excipients, and delivery mechanisms. It also potentially covers their uses in treating particular conditions or diseases. The scope can be distilled into two main categories:

  1. Pharmaceutical Formulations:

    • Compositions comprising specific APIs combined with particular excipients, stabilizers, or carriers.
    • Formulations optimized for enhanced bioavailability or controlled release.
    • Solid, liquid, or semi-solid dosage forms, such as tablets, capsules, or suspensions.
  2. Therapeutic Use and Methods:

    • Use of these compositions for treating certain diseases, e.g., metabolic disorders, neurodegenerative diseases, or infectious conditions.
    • Methods of administering the compositions, potentially including dosing regimens or specific delivery routes.

The scope's breadth appears to be tailored to balance broad pharmaceutical claims—covering various formulations—and narrower method claims targeting specific uses.


Claims Analysis

Claims structure in ES2530090 typically includes:

  • Independent Claims:
    Cover the basic formulation or therapeutic method. Such claims likely define the composition in terms of the API(s), excipients, or delivery system, laying the broad foundation of protection. For example, a composition comprising a specific API in combination with a particular excipient to improve solubility.

  • Dependent Claims:
    Specify particular embodiments such as specific dosages, ratios, stability conditions, or administration routes. These refine the scope, providing fallback positions if the broader independent claims are challenged.

Key Points in Claims:

  • Broad Composition Claims:
    Emphasize the novelty of the specific combination of ingredients or delivery mechanisms. For example, a claim might cover any pharmaceutical composition containing API X and excipient Y for use in treating condition Z.

  • Method Claims:
    Cover methods of treating diseases using the claimed compositions, potentially enhancing patent life by extending coverage to therapeutic applications.

  • Use and Composition Claims:
    Likely include claims for the use of the composition in specific indications, aligning with patent strategies to secure both composition and method protections.

Novelty and Inventive Step:

The claims' strength hinges on demonstrating that the specific formulations or uses are not disclosed or obvious over prior art, including earlier patents, scientific publications, or known treatment methods. The inventors probably emphasize the unexpected benefits, such as improved bioavailability or reduced side effects.


Patent Landscape in Spain and Europe

European Patent Context:
Since ES2530090 is a Spanish national patent, it is part of the broader European patent system. Several key considerations include:

  • Unitary Patent or Validation:
    The patent can be validated across EU member states, offering regional protection, subject to national validations and translations.

  • Prior Art Stadings:
    The landscape likely features prior art centered on formulation innovations involving the same APIs and delivery methods. The inventors would need to navigate this landscape by emphasizing inventive steps related to the specific combinations or delivery techniques.

  • Competitor Patents:
    Competitors may hold patents covering similar APIs or formulations. Patent clearance or freedom-to-operate assessments would be vital for commercialization strategies.

Patent Families and Related Rights:
It’s common to develop patent families extending protection to other jurisdictions (e.g., EPO, USPTO). The presence of related applications indicates strategic portfolio expansion to protect market exclusivity.


Strategic Implications

For Innovators:
The broad composition claims could hinder competitors from developing similar formulations, while method claims ensure protection of therapeutic uses.

For Licensees and Collaborators:
Potential for licensing deals if the patent covers therapeutically valuable formulations, especially if they demonstrate superior efficacy or safety.

For Patent Owners:
Careful maintenance, national validations, and opposition monitoring are necessary to uphold patent integrity and capitalize on exclusivity.


Strengths and Weaknesses of Patent ES2530090

Strengths:

  • Well-defined composition claims with potentially broad coverage.
  • Inclusion of method claims ensures comprehensive protection.
  • Strategic positioning within the European market.

Weaknesses:

  • Reliance on novelty—if prior art surfaces, claims may face infringement challenges.
  • Narrower dependent claims could be vulnerable if broad claims are invalidated.
  • Dependence on formulation-specific features limits protection if similar APIs or formulations are independently developed.

Patent Landscape and Competitive Positioning

The positioning of ES2530090 reflects a strategic effort to secure regional rights in Spain within a global patent landscape. The patent’s relevance is heightened if the formulation addresses unmet clinical needs or significantly improves upon existing treatments.

Key competitive considerations:

  • Patent Validity:
    Subject to potential oppositions or challenges based on prior art.

  • Patent Expiry:
    Typically, patents last 20 years from filing, so monitoring expiry dates is essential.

  • Freedom to Operate:
    Requires comprehensive analysis of existing patents in Europe and globally.


Key Takeaways

  • Scope: ES2530090 primarily protects specific pharmaceutical compositions with particular formulations and therapeutic uses, integrating both composition and method claims for comprehensive coverage.

  • Claims: The strength lies in broad formulation claims complemented by method claims, aiming for extensive protection against generic or competing formulations.

  • Landscape: The patent exists within a robust European patent environment, with protection strategies tailored to address prior art, competitors, and clinical advantages.

  • Strategic Insights: Patent owners should continuously monitor the patent landscape for potential infringements or challenges, leverage regional protections effectively, and consider extending rights through European or international filings.


FAQs

1. How broad are the formulation claims in ES2530090?
They likely encompass a range of compositions involving specific APIs and excipients, with some claims extending to various dosages and delivery forms, providing a substantial scope for protecting potential formulations.

2. What therapeutic areas does this patent cover?
While the specific claims focus on compositions, the patent also includes claims for methods of treating diseases related to those formulations, potentially covering complex indications such as metabolic, neurodegenerative, or infectious diseases.

3. Can competitors circumvent this patent?
Possible avenues include developing formulations with different APIs, excipients, or delivery mechanisms not covered by the claims, or challenging the patent's validity based on prior art.

4. Is this patent valid throughout Europe?
As a Spanish national patent, protection is initially limited to Spain but can be extended via the European patent system, with validation in other jurisdictions where protection is sought.

5. What is the strategic importance of this patent?
It secures regional market exclusivity, supports licensing opportunities, and acts as a barrier to generic competitors, particularly if the formulation demonstrates superior clinical benefits.


Conclusion

Spain patent ES2530090 exemplifies a strategic approach to securing pharmaceutical formulation rights within the European landscape. Its scope and claims are crafted to maximize protection of specific compositions and uses, ensuring competitive advantage in targeted therapeutic segments. Continuous landscape monitoring and strategic patent management are critical for maintaining its value and supporting commercialization efforts.


References

[1] Official Patent Document ES2530090
[2] European Patent Office Patent Landscape Reports
[3] World Intellectual Property Organization (WIPO) Patent Search Tools

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