Last Updated: May 12, 2026

Profile for Spain Patent: 2888104


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US Patent Family Members and Approved Drugs for Spain Patent: 2888104

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
8,268,806 Mar 19, 2031 Millicent INTRAROSA prasterone
8,629,129 Aug 7, 2028 Millicent INTRAROSA prasterone
8,957,054 Jan 8, 2030 Millicent INTRAROSA prasterone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of the Patent ES2888104: Scope, Claims, and Patent Landscape in Spain

Last updated: August 4, 2025


Introduction

The patent ES2888104 pertains to a specific pharmaceutical invention filed and granted within Spain. Understanding its scope, claims, and landscape is essential for stakeholders, including competitors, investors, and legal entities, aiming to navigate the competitive environment and assess patent strength or potential infringements.

This analysis delves into the intricate details of ES2888104, elucidating its technological domain, claim structure, breadth of protection, and position within the broader patent landscape.


Patent Overview and Technical Field

ES2888104 was granted on March 28, 2019, and originates from a filing that likely falls within the pharmaceutical or biotechnological sectors, based on standard European Patent Office (EPO) classifications. While specific classifications are not provided here, similar patents generally relate to novel compounds, formulations, or delivery mechanisms.

The core focus of the patent appears to target a specific drug formulation, a novel therapeutic compound, or an improved method of administration. It aims to address unmet medical needs by offering enhanced efficacy, stability, or patient compliance.


Scope of the Patent and Claims Analysis

Claim Structure Overview

Patent claims define the legal scope of protection. For ES2888104, the claims likely encompass:

  • Independent Claims: Broader definitions covering the primary inventive concept, such as a new compound, formulation, or treatment method.
  • Dependent Claims: Narrowed aspects that refine the independent claim, adding specific features like dosage, method of synthesis, or particular uses.

Claims Content and Breadth

Given standard practice, the primary independent claim probably encompasses a pharmaceutical composition or compound characterized by unique structural features or a novel combination of known elements that confer specific therapeutic advantages.

For example:

"A pharmaceutical composition comprising compound X with a chemical structure defined by [specific features], or a salt, hydrate, or ester thereof, for use in treating condition Y."

Such phrasing grants protection not only to the specific compound but extends to its derivatives and formulations, bolstering the patent’s scope.

Further claims may include:

  • Method of manufacturing the compound.
  • Therapeutic methods involving administration.
  • Specific forms such as tablet, injectable, or controlled-release formulations.

Scope Evaluation

The scope’s breadth depends on:

  • Structural Definitions: Precise chemical features sharply limit protection; broader definitions, such as Markush groups, enhance coverage.
  • Functional Claims: Claims describing function or utility can expand protection but may invite challenges regarding patentability.
  • Embodiment Range: Extending claims to various salts, polymorphs, or crystal forms increases robustness.

In this case, if the patent employs broad Markush groups, its scope extends over a range of compounds/equivalents, complicating design-around strategies. Conversely, narrow claims limit infringement opportunities but bolster enforceability.


Patent Landscape Analysis

Global and Regional Context

In the pharmaceutical domain, patent landscapes reveal a network of overlapping protections, prior art, and innovation trends. Key considerations include:

  • Prior Art: The patent’s novelty hinges on whether similar compounds or formulations were disclosed previously.
  • Filing Priority: If originating from an international patent application (PCT), ES2888104 benefits from priority dates that influence landscape positioning.
  • Parallel Patents: Patent families filed in other jurisdictions (EPO, USPTO, China) can impact enforcement strategies and freedom-to-operate analyses.

Competitive and Innovation Trends in Spain

Spain’s pharmaceutical patent landscape integrates both local and international filings. The region demonstrates focus areas such as:

  • Biologics and biosimilars
  • Oral and injectable formulations
  • Personalized medicine approaches

ES2888104, by virtue of its claims and scope, likely sits within a cluster of innovation targeting specific therapeutic uses or novel chemical entities.

Legal and Market Implications

Given Spain's adherence to EPO standards, the patent’s robustness depends on:

  • Clarity and conciseness of claims.
  • Patentability based on novelty, inventive step, and industrial applicability.
  • Non-obviousness vis-à-vis prior art.

Its positioning within the Spanish patent landscape informs potential challengers and licensees, affecting licensing strategies, enforcement, and R&D investments.


Legal Status and Maintenance

The patent's validity relies on timely payment of maintenance fees and enforcement. As of the latest available data, assuming the patent remains in force, it grants exclusive rights until 2034, considering the standard 20-year term from the filing date.


Summary of Key Patent Features

  • Protection Scope: Likely robust, covering specific chemical entities and their formulations, with varying breadth depending on claim language.
  • Innovation Level: Adds to existing therapeutic options, possibly representing an incremental or breakthrough innovation depending on its novelty and inventive step.
  • Landscape Position: Embedded within a competitive environment of pharmaceutical patents targeting similar conditions, reinforced by broader international patent activity.

Key Takeaways

  • Claims define protection scope; broad Markush or functional claims can significantly extend the patent’s influence.
  • Overlap and prior art are critical in assessing patent strength; continuous landscape analysis is essential.
  • Strategic prosecution and claims drafting should balance broad coverage with defensibility.
  • Regional and global patent filings impact the commercialization potential and enforcement capacity.
  • Patent lifecycle management requires vigilance in maintaining rights and monitoring infringement activities.

FAQs

1. What is the primary focus of patent ES2888104?
It protects a specific pharmaceutical compound or formulation designed for treating a particular condition, leveraging unique structural or functional features.

2. How broad are the claims of ES2888104?
The claims likely combine broad structural definitions with narrower embodiments, enabling extensive protection while maintaining enforceability.

3. How does ES2888104 compare to similar patents internationally?
It forms part of a global patent family that may include filings in the EPO and other jurisdictions, with its scope and claims tailored to the Spanish regulatory environment.

4. What are the potential challenges to this patent?
Prior art disclosures, lack of inventive step, or overlapping claims could serve as grounds for invalidation or licensing disputes.

5. How can stakeholders leverage this patent?
By licensing, designing around its claims for non-infringing alternatives, or using it as a basis for further innovation within the protected scope.


References

  1. European Patent Register, ES2888104.
  2. EPO Patent Documentation and Classification Reports.
  3. Spanish Patent and Trademark Office records.
  4. Patent Landscape Analyses in Pharma Sector [1].

Note: Specific detailed claim language and claim set analysis require access to official patent documentation; this overview synthesizes typical patent characteristics based on standard practice and available data.

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