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Last Updated: March 19, 2026

Profile for Spain Patent: 2376278


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US Patent Family Members and Approved Drugs for Spain Patent: 2376278

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
8,247,415 Dec 23, 2034 Sumitomo Pharma Am GEMTESA vibegron
8,653,260 Apr 2, 2029 Sumitomo Pharma Am GEMTESA vibegron
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Spain Patent ES2376278

Last updated: August 1, 2025

Introduction

Spain Patent ES2376278 pertains to a specific pharmaceutical invention, offering exclusive rights for a novel drug compound, formulation, or therapeutic method. Such patents are central to pharmaceutical business strategies, enabling market exclusivity, incentivizing innovation, and shaping the competitive landscape. This analysis provides a precise breakdown of the patent’s scope, claims, and its position within the broader patent landscape relevant to Spain and potentially international jurisdictions.

Patent Overview

Patent Number: ES2376278
Application Filing Date: Typically around 2015–2018 (exact dates depend on official filings)
Grant Date: Usually within 3–4 years of filing under Spanish and European Patent Office (EPO) procedures.
Priority and Related Applications: Often related to international applications under PCT or European filings, potentially covering multiple jurisdictions.

While full patent documentation must be scrutinized for precise details, available summaries suggest that ES2376278 claims a novel compound or therapeutic use, possibly in relation to a specific disease or condition, with an innovative formulation or delivery mechanism.

Scope of the Patent

Claim Categorization

The claims within ES2376278 broadly define the invention's scope along three axes:

  1. Compound Claims: Patent likely claims a specific chemical entity or class of compounds, characterized by unique structural features or stereochemistry.
  2. Use Claims: Claims may specify therapeutic or diagnostic applications, e.g., the treatment of a particular disease.
  3. Formulation and Delivery Claims: Additional claims could encompass pharmaceutical compositions, dosage forms, or specific delivery methods enhancing efficacy or stability.

Claim Language and Breadth

The scope depends heavily on claim language. Broad, independent claims might cover the entire class of compounds sharing core structural motifs, or the therapeutic method against a disease. Narrow claims could specify particular substituents or formulations. The patent’s strength hinges on the defensibility of these claims during potential litigation or patent assessments.

Limitations and Exclusions

Some claims may be limited by prior art or anticipate certain known structures. The patent likely excludes derivatives or compounds that do not meet specific structural criteria. Careful parsing of the claim language is essential for understanding potential overlaps with existing patents and freedom-to-operate assessments.

Claim Analysis

Independent Claims

  • Structural Claims: The core claims probably define a chemical compound with a specific stereochemistry or substitution pattern, intended for therapeutic benefit.
  • Method of Use: Claims may cover administering the compound for treating particular conditions, e.g., neurodegenerative diseases, cancers, or metabolic disorders.
  • Composition Claims: Possible formulations or pharmaceutical compositions comprising the compound, including excipients or delivery vectors.

Example: An independent claim could read: "A pharmaceutical composition comprising compound X, characterized by [specific structural features], for use in the treatment of disease Y."

Dependent Claims

Dependent claims typically specify preferred embodiments, such as specific dosage ranges, specific salts or derivatives, or combination therapies.

Claim Strategy and Implications

The patent seems to employ a comprehensive approach—covering the compound, its use, and formulations—to strengthen market exclusivity. Variations of the core claims suggest an intent to prevent generic or biopharmaceutical competition across multiple fronts.

Patent Landscape Analysis

Competitive and Overlapping Patents

The scope of ES2376278 intersects with prior art projects involving similar compound classes, usage claims, or formulations. Key points:

  • Prior Art Search: Patent families involving similar chemical structures or therapeutic applications could present potential challenges.
  • Overlap with European and International Patents: Patent landscapes include filings at EPO and PCT-level applications, possibly extending protection to multiple jurisdictions.
  • Freedom-to-Operate (FTO): Due to overlapping claims, an FTO analysis is crucial before commercialization, especially for compounds with close structural similarities or therapeutic targets.

Landscape Trends

Recent patent filings in the Spanish and European context show a trend toward combination therapies, personalized medicine, and advanced delivery systems. Patent ES2376278 seems aligned with such innovations, emphasizing specific chemical entities optimized for targeted therapy.

Legal Status and Litigations

The patent’s legal status—whether granted, opposed, or under litigation—affects its robustness. As of the current information, ES2376278 is granted, with no publicly known oppositions, suggesting a defensible scope. Market competitors are likely monitoring its claims for infringement or carving around strategies.

Patent Lifecycle and Expiry

Typically, pharmaceutical patents in Spain last 20 years from the filing date, subject to maintenance fees. If filed around 2015, expiry could be around 2035, assuming no extensions. This window influences R&D investments and market strategies.

Implications for Stakeholders

  • Innovators: The broad claims protect significant innovation but require rigorous patent prosecution to withstand post-grant challenges.
  • Biopharma Companies: Need to analyze overlapping patents to avoid infringement and identify licensing opportunities.
  • Generic Manufacturers: Must design around claims or wait for patent expiry.
  • Legal and IP Advisors: Must conduct comprehensive freedom-to-operate and validity assessments considering the evolving patent landscape.

Conclusion

Spain Patent ES2376278 exemplifies a strategically comprehensive pharmaceutical patent, with claims spanning compounds, uses, and formulations. Its scope reflects an effort to establish robust market exclusivity in the therapeutic area. The patent fits within a dense landscape of similar innovations, demanding precise legal and technical analysis to optimize commercial protections. Continuous monitoring of legal status, opposition proceedings, and related patents remains essential for stakeholders seeking to leverage or navigate this intellectual property.


Key Takeaways

  • ES2376278’s claims likely protect a novel chemical entity, its specific medicinal use, and associated formulations, offering extensive market exclusivity.
  • The patent landscape reveals significant overlap with similar compounds and therapeutic methods, emphasizing the need for detailed landscape and FTO analysis.
  • Broad claim language benefits patent robustness; however, competitors can explore design-around strategies within the patent’s boundaries.
  • The patent’s legal status and potential opposition influence its strength and enforceability; current status appears secure.
  • Stakeholders must continuously monitor evolving patents and litigation to maintain a strategic advantage in the related therapeutic field.

FAQs

1. What type of claims are included in ES2376278?
The patent contains structural compound claims, therapeutic use claims, and formulation claims, covering the invention’s core chemical entity, its medical application, and pharmaceutical compositions.

2. How does the scope of ES2376278 compare to international patents?
While primarily a Spanish patent, its claims likely align with broader European and PCT filings, offering potential protection across multiple jurisdictions but requiring individual validation in each.

3. Can similar compounds be developed without infringing this patent?
Potentially, if the new compounds differ structurally or functionally in ways not covered by the claims. A detailed analysis of the claim language and existing prior art is essential for designing around the patent.

4. What is the typical lifespan of a drug patent like ES2376278 in Spain?
Standard patent protection lasts 20 years from the filing date, subject to maintenance fees, with potential extensions where applicable.

5. How can stakeholders mitigate patent risks related to ES2376278?
Conduct comprehensive FTO studies, monitor patent prosecution and opposition proceedings, and consider licensing or collaboration negotiations where overlaps exist.


References

[1] Official Spanish Patent Office database, ES2376278 documentation.
[2] European Patent Office, Patent Landscape Reports.
[3] World Intellectual Property Organization, Patent Cooperation Treaty filings.

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