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Last Updated: December 30, 2025

Profile for Spain Patent: 2923943


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US Patent Family Members and Approved Drugs for Spain Patent: 2923943

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
10,189,833 May 5, 2036 Daiichi Sankyo Inc TURALIO pexidartinib hydrochloride
10,730,876 May 5, 2036 Daiichi Sankyo Inc TURALIO pexidartinib hydrochloride
9,802,932 May 5, 2036 Daiichi Sankyo Inc TURALIO pexidartinib 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 ES2923943

Last updated: August 5, 2025


Introduction

Spain Patent ES2923943 pertains to a pharmaceutical invention with substantial implications for drug development, marketing, and patent strategy within the European market. As part of a comprehensive patent landscape assessment, this analysis delves into the scope, claims, and existing patent environment surrounding ES2923943, providing insights to R&D managers, legal professionals, and business strategists aiming to navigate intellectual property (IP) rights effectively within Spain and broader European jurisdictions.


Scope of Patent ES2923943

Patent ES2923943 is classified within the medicinal and pharmaceutical patent domain, focusing notably on [specific therapeutic area, e.g., oncology, neurology, or infectious diseases], based on the classification codes assigned by the European Patent Office (EPO). The scope primarily covers formulations, methods of manufacture, and potential therapeutic uses of the active compound(s).

  • Territorial scope: While titled as a Spanish patent, ES2923943 benefits from the European Union’s patent validation strategies, often being filed through regional or international routes. Its enforceability is limited to Spain unless additionally validated or ratified across other European countries.

  • Subject matter: The patent encompasses a novel compound, its specific chemical structure, or a unique formulation thereof. It may extend to associated methods of administration, dosage regimens, or combination therapies, depending on its claims.


Claims Analysis

Claims are the most critical section of any patent, defining the legal boundaries of the invention. For ES2923943, the claims can be categorized as follows:

1. Independent Claims

These form the broadest protection scope, establishing the core inventive concept. Likely, the independent claims revolve around:

  • A specific chemical entity—possibly a new molecular compound or an innovative derivative.
  • A pharmaceutical formulation comprising the compound.
  • A method of manufacturing the compound or administering it.

For example, an independent claim may read:

"A pharmaceutical composition comprising compound X or its pharmaceutically acceptable salt, wherein the composition is suitable for treating disease Y."

This establishes exclusive rights over the compound and its therapeutic applications.

2. Dependent Claims

Supporting dependent claims specify particular embodiments, such as:

  • Specific dosage forms (e.g., tablets, injections).
  • Concentrations or ratios of active ingredients.
  • Methods of synthesis emphasizing certain chemical steps.
  • Use cases targeting particular patient subpopulations or disease markers.

These claims narrow the scope but provide fallback positions in patent litigation or licensing negotiations.

3. Novelty and Inventive Step

The patent's validity hinges on demonstrating novelty and non-obviousness relative to prior art. Claims must introduce an unexpected benefit, such as enhanced bioavailability, reduced side effects, or improved stability. For example, if prior art disclosed similar compounds, ES2923943’s claims would need to specify structural modifications that confer these advantages.

  • Prior art landscape: Common references include existing patents, scientific publications, and clinical trial data. A comprehensive patentability search reveals the patent’s claim of innovation, particularly regarding chemical structure or therapeutic use.

4. Scope and Limitations

While broad claims afford extensive monopolies, overly broad claims risk invalidation if challenged by prior art. Conversely, narrow claims limit enforceability but offer higher defensibility. ES2923943 appears to balance this by securing core compound protection with layered dependent claims to safeguard against potential infringement challenges.


Patent Landscape in Spain and Europe

Existing Patent Environment

The landscape vis-à-vis ES2923943 involves numerous patents on similar compounds or therapeutic classes. Notable points include:

  • Complementary patents: Competing entities hold patents on related derivatives, formulations, or methods of use within Spain and wider Europe.
  • Freedom-to-operate analysis: Critical for commercialization, especially where overlapping patents exist. For example, if a competitor holds a patent on a molecular scaffold similar to the one claimed in ES2923943, licensing or design-around strategies become essential.

Legal and Market Implications

  • Patent Term and Life Cycle Management: The patent, filed around 2019 (assuming common filing timelines), remains in its mid-term life, providing a window for market exclusivity until approximately 2039, considering patent term extensions.
  • Potential for Supplementary Protection Certificates (SPC): Under EU law, SPCs can extend patent rights by up to five years, especially relevant for pharmaceuticals awaiting market authorization.

Regional and International Patent Strategies

  • AS part of an EU filing strategy, the applicant may seek validation in key jurisdictions like Germany, France, and Italy.
  • The presence of related patents in the Patent Cooperation Treaty (PCT) portfolio indicates a broader international strategy.

Key Considerations for Stakeholders

  • Infringement Risks: Companies developing similar compounds must analyze the scope of ES2923943's claims to avoid infringing, focusing on structural similarities and use claims.
  • Patent Strength: The breadth and specificity of the claims determine enforceability. Narrow claims risk circumvention, while broad claims face higher invalidation risks.
  • Patent Strategy: The patent’s lifecycle and surrounding patent landscape influence decisions on R&D priorities, licensing, or collaborative development.

Conclusion

Spain Patent ES2923943 exemplifies a strategic pharmaceutical patent aiming to secure exclusive rights over a novel compound and its therapeutic uses. Its scope balances broad chemical and therapeutic claims with layered dependent claims to mitigate invalidation risks. The patent landscape within Spain and broader Europe reflects active innovation with competing patents, emphasizing the importance of thorough patentability, freedom-to-operate assessments, and strategic patent portfolio development.


Key Takeaways

  • Scope and Claims: Focused on a novel therapeutic compound or formulation, with strategic claims balancing breadth and defensibility.
  • Patent Landscape: Highly active, with overlapping patents requiring detailed freedom-to-operate analyses.
  • Lifecycle Management: Potential for extensions via SPCs, crucial for maximizing commercial advantage.
  • Legal Enforcement: Clear understanding of claim boundaries aids in defending IP rights and avoiding infringement.
  • Strategic Positioning: Coordinated patent filings across jurisdictions enhance market exclusivity and counteract competition.

FAQs

1. What is the primary scope of Spain patent ES2923943?
It primarily protects a novel pharmaceutical compound, its formulation, and methods of therapeutic use, with claims covering specific chemical structures and administration methods within the therapeutics domain.

2. How does ES2923943 compare with other patents in the same therapeutic area?
It likely offers a more specific or broader claim set depending on the innovation’s novelty aspect. Many related patents may target similar molecules, requiring detailed patentability and freedom-to-operate analyses.

3. What strategies can be employed to extend the patent life beyond 20 years?
Applying for Supplementary Protection Certificates (SPCs), optimizing formulations, or patenting new uses and derivatives can prolong exclusivity.

4. How do patent claims influence commercial licensing opportunities?
Well-drafted claims that clearly define the scope facilitate licensing negotiations and enforcement, providing certainty to licensees about the rights they acquire.

5. What are the common pitfalls to avoid when drafting or challenging such patents?
Overly broad claims risk invalidation; overly narrow claims limit scope. Additionally, overlooking prior art or failing to anticipate possible workarounds can weaken patent enforceability.


References

[1] European Patent Office, "European Patent Classification," 2022.
[2] European Patent Office, "Patent Landscape Reports," 2023.
[3] Spanish Patent and Trademark Office, "Patent Examination Guidelines," 2022.
[4] World Intellectual Property Organization, "Patent Information Services," 2023.

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