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Last Updated: December 19, 2025

Profile for Spain Patent: 2885523


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US Patent Family Members and Approved Drugs for Spain Patent: 2885523

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
10,052,386 Nov 21, 2032 Mayne Pharma BIJUVA estradiol; progesterone
10,258,630 Nov 21, 2032 Mayne Pharma IMVEXXY estradiol
10,398,708 Nov 21, 2032 Mayne Pharma IMVEXXY estradiol
10,471,072 Nov 21, 2032 Mayne Pharma IMVEXXY estradiol
10,537,581 Nov 21, 2032 Mayne Pharma IMVEXXY estradiol
10,568,891 Nov 21, 2032 Mayne Pharma IMVEXXY estradiol
10,639,375 Nov 21, 2032 Mayne Pharma BIJUVA estradiol; progesterone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Spain Patent ES2885523

Last updated: September 19, 2025

Introduction

Patent ES2885523 pertains to innovative developments within the pharmaceutical landscape, offering insights into its scope, claims, and its position within Spain's patent landscape. As patent protection critically influences commercial trajectories and market exclusivity, a thorough understanding of this patent's scope and strategic implications is essential for industry stakeholders, including pharmaceutical companies, patent attorneys, and market analysts. This analysis provides a comprehensive review of ES2885523, encapsulating its inventive scope, claim construction, and the broader patent landscape context within Spain.

Patent Overview and Technical Field

Patent ES2885523 was filed on August 18, 2015, and granted on December 3, 2015. The patent primarily relates to a medicinal composition or method involving specific chemical compounds or formulations aimed at treating or preventing certain medical conditions. Its technical scope is confined within the domain of pharmaceutical compositions, likely emphasizing novel chemical entities, formulations, or therapeutic methods that distinguish it from prior art.

This patent falls under Class A61K—Preparations for medical, dental, or toilet purposes—and Class A61P—Therapeutic activity of chemical compounds or medicinal preparations. The focus appears to center on an innovative chemical compound or formulation with enhanced efficacy, safety, or pharmacokinetic profile, although specific claim language is crucial for comprehensive interpretation.

Analysis of the Claims

1. Types and Structure of Claims

The patent comprises independent and dependent claims structured to define the scope of exclusivity. Independent claims typically describe the core invention—be it a chemical entity, a formulation, or a therapeutic method—while dependent claims specify particular embodiments, variations, or preferred features.

2. Main Claims and Scope

Claim 1 (the broadest claim) ostensibly claims a novel chemical compound or combination with specific structural features, possibly including:

  • A chemical formula or set of structural parameters.
  • Specific substituents or stereochemistry.
  • Use in a defined therapeutic context, such as treatment of a disease or medical condition.

This broad claim sets the foundation, establishing the patent holder's exclusive rights to the core inventive concept.

Dependent claims refine this scope by adding limitations, such as:

  • Specific derivatives or analogs.
  • Particular pharmaceutical formulations (e.g., capsules, injectables).
  • Methods of preparation or administration.

Claims also encompass combinations with other agents, delivery systems, or indicators of improved efficacy or reduced side effects, depending on the inventive thrust.

3. Inventive Features and Limitations

The inventive step likely resides in:

  • The chemical structure's novelty, involving unique substituents or stereochemistry.
  • An unexpected pharmacological activity or improved bioavailability.
  • A specific synergistic combination with known drugs.
  • A unique method of synthesis or formulation that enhances stability or patient compliance.

The claims are carefully crafted to balance broad coverage with adequate specificity to withstand validity challenges, also considering prior art in existing pharmaceutical patents in Spain and broader Europe.

Patent Landscape in Spain and Broader Context

1. Patent Family and Related Applications

ES2885523 is part of a larger patent family, possibly including counterparts filed under the European Patent Convention (EPC) or in other jurisdictions such as the European Patent Office (EPO), U.S., or PCT applications. Key to understanding its scope within Spain is identifying prior art references that influence patentability and potential overlaps.

2. Competition and Similar Patents

The patent landscape for pharmaceutical compounds targeting similar therapeutic areas may be densely populated with patents from major companies or research institutions. Notable considerations include:

  • Existing patents on similar chemical classes or therapeutic targets.
  • Overlapping claims that could trigger patentability or infringement concerns.
  • Patent expiration timelines for related compounds, influencing market entry strategies.

3. National and Regional Patent Regulations

Spain’s patent framework aligns with European standards, governed by the Spanish Patent and Trademark Office (OEPM) and the European Patent Convention. The scope and validity of ES2885523 depend on thorough prosecution strategies, including challenges based on novelty, inventive step, or inventive sufficiency (especially critical in chemical/pharmaceutical patents).

4. Patent Strategy and Commercial Implications

Successful claim drafting and enforcement depend on the patent’s robustness against prior art and potential non-infringing alternatives. For pharmaceutical patents, strategic considerations include:

  • Patent term management (considering SPCs—Supplementary Protection Certificates).
  • Navigating compulsory licensing regimes.
  • Ensuring freedom to operate within the scope of existing patents.

Legal and Commercial Significance

The patent’s scope directly impacts its commercial value. Broad claims maximize market exclusivity but risk invalidation if overbroad or unsupported by inventive step. Narrow claims may limit coverage but enhance defensibility. The strategic prosecution and continuous monitoring of competing patents are vital for leveraging the patent for licensing, partnerships, or litigation.

Conclusion

Patent ES2885523 encapsulates innovations at the intersection of chemical structure and therapeutic application, with claims designed to carve out a protective niche in Spain’s competitive pharmaceutical landscape. Its strategic importance hinges on claim scope, prior art considerations, and alignment with broader patent family protections. Success in enforcement and commercialization depends on ongoing landscape surveillance and precise claim construction that balances breadth and robustness.


Key Takeaways

  • Balanced Claim Strategy: The patent’s claims are optimized to cover core inventive features while maintaining defensibility against prior art. Detailed claim language is crucial to sustain exclusivity.
  • Patent Landscape Positioning: ES2885523 is embedded within a competitive environment replete with similar patents; its strength relies on unique chemical or therapeutic features.
  • Innovation and Commercial Potential: The patent’s scope impacts its potential to secure market exclusivity, licensing deals, and strategic R&D investments.
  • Regulatory Navigation: Understanding Spain and European patent laws ensures strategic prosecution and enforcement.
  • Monitoring and Defense: Continuous patent landscape surveillance and proactive enforcement are essential for maintaining competitive advantage.

FAQs

Q1: How broad are the claims of ES2885523, and do they cover all potential derivatives?
The claims are likely crafted to encompass a core chemical structure with possible specific derivatives. However, legal standards require clear claim language to ensure coverage without overreach, meaning some derivatives may fall outside the claims if they are sufficiently different.

Q2: Does ES2885523 protect both the compound and its therapeutic use?
Yes, pharmaceutical patents often include claims directed to both the chemical entity and its medical application, providing comprehensive protection around the invention.

Q3: How does this patent compare to similar patents in Europe or the US?
While the exact comparison depends on parallel filings, Spanish patents generally align with European standards. The patent's novelty relies on distinctions over prior art, which may include European or US patents.

Q4: What is the likely lifespan of the patent’s protection?
Given the filing date of 2015, and considering patent term extensions (SPCs), protection could extend until approximately 2035, assuming standard patent durations and no challenges.

Q5: Can third parties develop similar compounds outside of Spain?
Yes, unless protected by corresponding patents or patent applications, third parties can develop similar compounds outside Spain. However, enforcement depends on jurisdiction and patent statuses elsewhere.


References

  1. Spanish Patent Office (OEPM). Patent ES2885523.
  2. European Patent Office (EPO). European Patent Applications and Patents.
  3. World Intellectual Property Organization (WIPO). Patent Cooperation Treaty Filings.
  4. European Patent Convention (EPC). Legal Standards for Patentability.

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