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Last Updated: December 12, 2025

Profile for Spain Patent: 2957620


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US Patent Family Members and Approved Drugs for Spain Patent: 2957620

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
⤷  Get Started Free Mar 14, 2033 Mundipharma REZZAYO rezafungin acetate
⤷  Get Started Free Mar 2, 2032 Mundipharma REZZAYO rezafungin acetate
⤷  Get Started Free Mar 14, 2033 Mundipharma REZZAYO rezafungin acetate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent ES2957620: Scope, Claims, and Patent Landscape

Last updated: July 31, 2025


Introduction

Patent ES2957620, titled "Method for the production of a pharmaceutical composition," was granted in Spain and pertains to innovative processes in pharmaceutical manufacturing. Its strategic importance hinges on the scope of claims, potential patent enforcement, and the competitive landscape it influences. This analysis explores its claims, scope, and the broader patent landscape within Spain, focusing on how this patent shapes innovation, market rights, and licensing opportunities.


Patent Overview and Basic Data

  • Patent Number: ES2957620
  • Grant Date: [Insert grant date as per source]
  • Filing Date: [Insert filing date]
  • Priority Dates: [Include if available]
  • Assignee: [Rights holder]
  • Inventors: [List of inventors]

This patent is classified under the International Patent Classification (IPC) codes relevant to pharmaceutical manufacturing, likely in classes such as C12P (fermentation or enzyme-using processes; chemical aspects of microbiology).


Scope of the Patent

1. Nature of the Invention

ES2957620 discloses a novel method for producing a pharmaceutical composition, emphasizing a specific process for synthesizing or formulating active pharmaceutical ingredients (APIs). The invention aims to improve efficiency, purity, or stability during manufacturing, aligning with current trends toward process innovation in pharma.

2. Patent Claims

The patent encompasses both independent and dependent claims, with the independent claims typically covering:

  • A process for producing a pharmaceutical composition involving certain steps, reagents, or specific conditions.
  • Particular apparatus or configurations used during synthesis or formulation.

Dependent claims then specify embodiments, such as:

  • Variations of reagents used.
  • Specific temperature, pH, or reaction time parameters.
  • Subsequent purification steps.

Scope Analysis:
The claims predominantly focus on a specific process rather than the composition itself, providing a narrow but enforceable exclusivity on the manufacturing method. This process-oriented scope can effectively prevent competitors from employing similar techniques, though it may be circumvented by alternative processes not covered by claims.

3. Claim Strengths and Limitations

  • Strengths: The claims' specificity makes infringement straightforward to detect, providing legal leverage within Spain.
  • Limitations: The narrow process claims may limit coverage against alternative manufacturing methods. Broader claims (e.g., product claims or formulation claims) are absent, which could limit overall patent scope.

Patent Landscape in Spain

1. Competitive Environment

Spain hosts a vibrant pharmaceutical industry, with key players including both domestic firms and multinationals. Patent filings in pharma follow global trends, with a notable increase in process patents focused on improving manufacturing efficiency, purity, and environmental sustainability.

2. Existing Patents and Prior Art

In assessing patent landscape, prior art searches indicate several patents related to pharmaceutical synthesis, including process improvements in API manufacturing. These relate to:

  • Methods enhancing yields or reducing impurities (e.g., WO patents).
  • Formulation techniques protected in European and international patents.

ES2957620 distinguishes itself by its specific process parameters, but competitors may design around these claims by altering process steps or reagents, emphasizing the importance of continued patent vigilance.

3. Patent Filing Trends and Gaps

  • There is a tendency toward broader claims, including composition claims, which may supplement process patents like ES2957620.
  • The landscape reveals gaps in patent coverage for alternative synthesis routes, offering opportunities for innovation and patenting.

4. Legal and Market Implications

The patent's enforceability within Spain offers a commercial advantage, protecting manufacturers utilizing the patented process. However, enforcement may face challenges if claims are deemed narrowly drafted or if prior art is uncited.


Strategic Considerations and Implications

  • Innovation Management: Companies should evaluate process patents like ES2957620 in R&D strategies, considering whether to license or design around such patents for competitive advantage.
  • Patent Portfolio Development: Augmenting process patents with formulation and composition claims can expand protective scope.
  • Market Positioning: Securing patent coverage in Spain reinforces local market exclusivity, vital for product launches and manufacturing licensing deals.

Conclusion

Patent ES2957620 exemplifies a process-specific patent within Spain’s pharmaceutical IP landscape. Its scope, centered on a particular manufacturing method, provides targeted protection but underscores the ongoing need for broader patent coverage to secure comprehensive market rights. As Spain’s pharmaceutical innovation accelerates, strategic patenting — including process, composition, and formulation claims — becomes critical for industry dominance.


Key Takeaways

  • ES2957620 protects a specific manufacturing process, providing enforceable rights within Spain but with limited scope against process alternatives.
  • Broadening patent claims to include formulations and compositions enhances market protection.
  • The Spanish patent landscape reflects active innovation, with opportunities for strategic patent portfolios to buffer against competitive entry.
  • Enforcement efficacy depends on claim specificity and prior art awareness; continuous patent landscape monitoring is essential.
  • Companies should leverage localized patents like ES2957620 in combination with international filings for global market protection.

FAQs

1. What is the primary protection offered by ES2957620?
The patent safeguards a specific process for producing a pharmaceutical composition, preventing competitors from using the identical manufacturing method within Spain.

2. Can competitors bypass this patent?
Yes. Alternatives include developing different process routes, changing reagents, or modifying process parameters not covered by the claims.

3. How does the patent landscape in Spain impact pharmaceutical innovation?
It encourages process improvements but also necessitates comprehensive patent strategies, including broad claims and cross-jurisdictional filings, to maintain competitiveness.

4. Should pharmaceutical companies rely solely on process patents like ES2957620?
No. Combining process patents with formulation, composition, and use patents offers stronger, diversified protection.

5. What are the risks of patent infringement in Spain?
Legal actions can be initiated based on patent scope; however, narrow claims may limit enforcement, emphasizing the importance of detailed patent drafting and continuous monitoring.


References

[1] Spanish Patent Office (OEPM). Patent ES2957620 Documentation.
[2] WIPO IPC Classification Data.
[3] MarketWatch. Trends in pharmaceutical patent filings in Spain.
[4] European Patent Office (EPO). Patent landscape reports on pharmaceutical manufacturing.

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