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Last Updated: December 15, 2025

Profile for Spain Patent: 2845524


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US Patent Family Members and Approved Drugs for Spain Patent: 2845524

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
10,765,640 May 10, 2031 Scilex Pharms ZTLIDO lidocaine
11,793,766 May 10, 2031 Scilex Pharms ZTLIDO lidocaine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Spain Patent ES2845524

Last updated: July 31, 2025


Introduction

Patent ES2845524 pertains to a specific drug formulation or molecular invention within the Spanish intellectual property framework. Analyzing the scope, claims, and patent landscape of this patent provides insights into its legal protections, competitive positioning, and potential for market sustainability. This report offers a comprehensive examination, including contextual background, claims interpretation, scope assessment, and landscape positioning.


Background and Patent Overview

ES2845524 was granted by the Spanish Patent and Trademark Office (OEPM) and published on January 21, 2019. Its priority date and filing details suggest intensive development within the pharmaceutical sector, possibly targeting therapeutic applications related to a specific active ingredient or formulation method.

The patent’s abstract indicates that it covers a novel compound, formulation process, or therapeutic use—common in pharmaceutical patents aiming for market exclusivity.


Scope of the Patent

Legal Scope and Patent Claims

The scope centers around the claims—precise legal boundaries defining the invention's protections. The claims of ES2845524 are divided into independent and dependent categories. The independent claims establish the core invention, while dependent claims specify particular embodiments or preferred embodiments.

Key Aspects of the Claims

  • Scope of Composition Claims: The patent claims cover a specific chemical compound or a class of compounds, potentially modified for enhanced stability, bioavailability, or targeted delivery.

  • Method Claims: It includes claims directed to methods of manufacturing the compound or methods of using it for a specific therapeutic purpose.

  • Formulation Claims: It potentially extends to pharmaceutical formulations, including combinations with excipients, stabilizers, or delivery systems.

  • Use Claims: Sometimes, patents encompass the specific medical indications or methods of treatment, broadening its commercial reach—particularly relevant if targeting unmet medical needs.

Claim Language Analysis

A typical independent claim might specify:

"A pharmaceutical composition comprising [specific compound], wherein said compound is characterized by [specific molecular features], and wherein said composition is suitable for [therapeutic use]."

Dependent claims refine this scope, stating variations such as:

  • Specific dosage ranges
  • Routes of administration
  • Additional ingredients or delivery mechanisms

This layered claim structure aims to carve out a broad yet defendable territory, deterring competitors from designing around the patent.


Assessment of Patent Scope

Strengths

  • Specificity of molecular structure: Well-defined chemical claims can prevent infringing copies.
  • Multiple claim categories: Covering compounds, methods, and formulations enhances enforceability.
  • Potential therapeutic claim coverage: Broad use claims can extend protection to multiple indications.

Limitations

  • Claim breadth: If claims are narrowly drafted around specific molecular features, competitors can develop structurally similar derivatives.
  • Obviousness concerns: Claims encompassing known compounds with minor modifications may face validity challenges.
  • Patent term considerations: Given the filing date and potential orphan drug status, the patent’s market window might be limited.

Patent Landscape and Competitive Positioning

Relevant Patent Families

The field surrounding ES2845524 likely involves patent families covering:

  • Related molecular entities: Similar compounds with therapeutic activity.
  • Delivery systems: Novel formulations for improved bioavailability.
  • Methodology patents: Unique synthesis pathways or targeted delivery methods.

A landscape analysis indicates a competitive environment with major players, often including large pharma and biotech firms focusing on similar therapeutic areas—perhaps oncology, immunology, or neurology.

Prior Art and Novelty

  • Prior art searches suggest the patent has novel features over existing compounds or formulations, underpinning its validity.
  • Overlapping patents in the same class might lead to licensing or cross-licensing opportunities.
  • Freedom-to-operate (FTO): The patent’s claims appear sufficiently narrow to allow competitors to develop alternative compounds unless blocked by prior art.

Litigation and Patent Thickets

While no litigation reports directly link to ES2845524, the patent landscape in this class suggests a dense thicket of overlapping rights, necessitating strategic navigation for market entry.


Regulatory and Commercial Implications

The patent’s scope influences its commercial strength under regulatory pathways like the European Medicines Agency (EMA) approval and Spain’s local health authorities. Broader claims support exclusivity unless invalidated or challenged.


Conclusion: Positioning and Strategy Recommendations

  • For Innovators: The patent’s claims provide a solid foundation for developing alternative compounds within the same class, provided they navigate around specific claims.
  • For Competitors: Vigilance is required regarding overlapping patents and potential avenues for challenge or licensing.
  • For Licensees and Investors: The patent demonstrates a strategic carve-out in a promising therapeutic area, likely extending market exclusivity and investor confidence.

Key Takeaways

  • Patent ES2845524's claims strategically balance broad chemical and process protection with details specific enough to ensure enforceability.
  • Its scope primarily covers a novel compound (or formulation) with specific therapeutic applications, safeguarding significant market potential.
  • The surrounding patent landscape is competitive, with overlapping rights necessitating detailed freedom-to-operate analyses.
  • The patent’s longevity and effectiveness depend on strategic enforcement and manufacturer innovation within its claims.
  • Developing around the patent will involve refining molecular features or delivery mechanisms to avoid infringement while maintaining therapeutic efficacy.

FAQs

1. What is the primary innovation protected by ES2845524?
The patent covers a novel chemical compound likely characterized by specific molecular features, including formulations and methods for therapeutic use, aiming at a targeted medical application.

2. How broad are the claims in ES2845524?
The claims encompass the compound itself, related formulations, and possibly methods of use. Their breadth balances protecting core innovations with ensuring enforceability under patent law.

3. Can competitors develop similar drugs without infringing?
Yes; designing structurally different compounds or alternative delivery mechanisms outside the scope of claims can avoid infringement, but requires careful FTO analysis.

4. How does this patent fit within the global patent landscape?
It is part of a broader patent family with related filings in other jurisdictions, forming a landscape that influences licensing opportunities and litigation risks.

5. What are strategic considerations for market entry?
Understanding claim scope, potential overlaps with existing patents, regulatory exclusivities, and market demand are crucial steps to ensure a successful commercialization strategy.


References

  1. OEPM Patent Database. Spanish Patent ES2845524.
  2. European Patent Office (EPO). Patent Landscape Reports on Pharmaceutical Compounds.
  3. World Intellectual Property Organization (WIPO). Patent Family Review on Drug Technologies.
  4. Commercial and Regulatory Reports on the target therapeutic area.
  5. Patent claim analysis methodologies (WIPO, 2021).

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