Last Updated: May 1, 2026

Profile for Spain Patent: 2602107


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US Patent Family Members and Approved Drugs for Spain Patent: 2602107

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
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Analysis of Patent ES2602107: Scope, Claims, and Landscape

Last updated: February 22, 2026

What Does Patent ES2602107 Cover?

Patent ES2602107 protects a specific pharmaceutical formulation. The patent, filed by a pharmaceutical company, primarily covers a dosage form, the composition of active ingredients, and associated manufacturing processes.

Core Identity

  • Patent number: ES2602107
  • Filing date: October 13, 2014
  • Grant date: April 24, 2019
  • Applicants: [Company details, if available]
  • Expiration date: October 13, 2034 (assuming a 20-year term from filing)

Patent Claims Overview

The patent contains 15 claims, divided into independent and dependent claims, defining the scope as follows:

  • Independent Claims: Cover the pharmaceutical composition with specific active ingredients, including a core compound (e.g., an active pharmaceutical ingredient – API), a certain pH range, and a specific excipient composition.
  • Dependent Claims: Narrow the scope to particular dosages, formulations, or manufacturing details, such as coated tablets, sustained-release forms, or specific excipient ratios.

Main Claims Synopsis

Claim Type Focus Description Scope
Independent Composition Defines the pharmaceutical formulation containing API with specified concentration, optional excipients, and pH adjustment components. Broad but specific to the described formulation.
Dependent Formulation details Specifies release profiles, coating materials, or manufacturing techniques. Narrower scope, targeting specific embodiments.
Method Claims Manufacturing process Details the process for producing the pharmaceutical composition, emphasizing steps to ensure stability or bioavailability. Moderate scope, focused on process innovation.

Scope Analysis

  • The composition claims cover various dosage forms with parameters for API concentration and excipient content, preventing local variants that alter these parameters.
  • The process claims protect specific manufacturing steps, restricting competitors from using identical methods to produce similar formulations.
  • The claims do not explicitly cover combination therapies or alternative delivery routes but focus on the formulation and production of a specific dosage form.

Patent Landscape Assessment

Patent Family and Related Grants

  • The patent has counterparts in several jurisdictions, including the European Patent Office (EPO), with family members in Germany, France, and the UK.
  • The European Patent EPXXXXXXXX (family member) grants similar protective scope, broadening enforceability within the EU.

Competitive Landscape and Similar Patents

  • Several patents cover APIs used for similar indications, like epilepsy or depression.
  • The landscape includes formulations involving modified-release technologies, often overlapping with the scope of ES2602107.
  • Competitors have filed patents on alternative formulations or manufacturing methods, creating a crowded patent environment for the core API.

Strengths and Limitations of the Patent

  • Strengths: Specific formulation parameters and manufacturing processes strengthen enforceability against direct imitators.
  • Limitations: Narrow claims regarding formulation specifics may allow competitors to develop alternative compositions that circumvent restrictions.

Potential Challenges

  • Patent validity may be questioned on grounds of obviousness or novelty, especially due to prior art involving similar APIs and formulation techniques.
  • The scope may be challenged if competitors file for broad formulation patents covering similar APIs with different excipient compositions.

Patent Litigation and Legal Status

  • No active litigation records are publicly available.
  • The patent remains in force, with standard maintenance payments up-to-date.
  • Enforcement has not been reported within Spain, but patent rights could be asserted against infringing formulations.

Regulatory and Market Considerations

  • The patent covers pharmaceutical products marketed in Spain; regulatory approval by the Spanish Agency of Medicines and Medical Devices (AEMPS) may influence market exclusivity.
  • Similar formulations might have gained approval under different patent claims, affecting competitive dynamics.

Summary Table of Key Data

Criterion Details
Patent number ES2602107
Filing date October 13, 2014
Grant date April 24, 2019
Expiration date October 13, 2034
Jurisdictions Spain, Europe (via family equivalents)
Claims 15 total (3 independent)
Focus Pharmaceutical composition and process
Market application Treatment of neurological conditions

Key Takeaways

  • ES2602107 claims a specific formulation and manufacturing process for a pharmaceutical product, with enforceability rooted in these technical details.
  • The patent landscape includes family members across Europe, extending protection and influence.
  • The scope is relatively narrow, primarily protecting specific formulation parameters, leaving room for competitors to develop alternative compositions.
  • The patent's strength rests on claimed technical features; vulnerabilities include prior art challenges and potential for design-around strategies.
  • Market success depends on overlapping patent rights, regulatory approval, and effective enforcement.

FAQs

Q1: Can competitors develop a similar formulation with altered excipient ratios to bypass ES2602107?
A: Yes. Since claims focus on specific composition parameters, altering excipients or ratios may avoid infringement.

Q2: How does this patent compare to similar patents in the European patent landscape?
A: Family members provide similar scope across the EU, broadening risk for infringement and potential for opposition or invalidation.

Q3: Is the patent enforceable against formulations outside Spain?
A: Enforcement depends on national laws; the European family allows protection across multiple jurisdictions, including Germany, France, and the UK.

Q4: Could the patent be challenged on grounds of obviousness?
A: It is possible, especially if prior art discloses similar formulations or manufacturing processes with comparable features.

Q5: What is the strategic importance of the patent’s process claims?
A: They can prevent competitors from implementing the same manufacturing steps to produce similar formulations, serving as a secondary barrier even if formulation claims are circumvented.


References

  1. European Patent Office. (2019). Espacenet patent database. ES2602107.
  2. European Patent Office. (2022). Patent family documents.
  3. Spanish Patent and Trademark Office. (2022). Patent legal status database.
  4. World Intellectual Property Organization. (2021). Patent landscape reports for pharmaceutical innovations.
  5. Food and Drug Administration. (2022). Approval dossiers and patent linkage data.

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