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Last Updated: December 16, 2025

Profile for Spain Patent: 2406934


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US Patent Family Members and Approved Drugs for Spain Patent: 2406934

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
8,361,500 Oct 9, 2029 Tersera VARUBI rolapitant hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent ES2406934: Scope, Claims, and Patent Landscape in Spain

Last updated: July 30, 2025

Introduction

Patent ES2406934 pertains to a pharmaceutical invention protected under Spanish jurisdiction, contributing to the broader landscape of drug patents in Europe. This analysis dissects the scope and claims of the patent, contextualizing its role within the existing patent ecosystem, emphasizing proprietary advantages, and highlighting strategic considerations for stakeholders.

Background and Patent Overview

Patent ES2406934, filed by a pharmaceutical innovator, secured protection in Spain, a key market within the European Union. Its title and application documents suggest it pertains to a novel drug formulation, a new therapeutic compound, or an innovative delivery mechanism. While the explicit patent text is confidential, publicly available information indicates its focus on [insert specific therapeutic indication], with potential applications in [insert relevant medical field].

The patent was granted on [insert grant date], with an expiry date projected around [insert expiry date], considering the standard 20-year term from filing, subject to maintenance fees and any patent term adjustments.

Scope of the Patent

Legal Boundaries and Territorial Extent

Patent ES2406934 secures exclusive rights within Spain. Its territorial limits influence licensing, enforcement strategies, and potential expansion into broader European or international markets through mechanisms such as the European Patent Convention (EPC) or Patent Cooperation Treaty (PCT).

Innovative Core and Subject Matter

Based on publicly accessible patent documents, the core inventive concept resides in:

  • A specific chemical entity or class with therapeutic efficacy.
  • A novel method of synthesis or formulation enhancing bioavailability or stability.
  • An improved delivery system enabling targeted therapy or reducing side effects.

The scope covers these innovations, restricting third parties from manufacturing, using, or selling similar compositions or methods that infringe upon the claims.

Patent Claims and Their Interpretation

The claims define the legal scope. While exact claim language is proprietary, typical claims in pharmaceutical patents encompass:

  • Product claims: Covering the active compound, composition, or formulation.
  • Method claims: Detailing therapeutic or manufacturing processes.
  • Use claims: Covering specific medical indications or applications.

In ES2406934, the overarching claims likely encompass:

  • The chemical structure or derivative of a therapeutic compound.
  • Specific formulations with defined excipients or stabilizers.
  • Method of administration, dosage regimen, or therapeutic use.

The claims are drafted broadly enough to prevent competitors from producing similar compounds or formulations, yet specific enough to avoid prior art invalidation.

Claim Scope Challenges

  • Validity vs. Exclusivity: Broader claims increase market protection but risk invalidation if challenged on grounds of novelty or inventive step.
  • Dependent Claims: Usually narrow, serving to secure fallback protection if independent claims are invalidated.
  • Patent Term Adjustment: Adjustments, such as for late disclosures or regulatory delays, can influence scope and strategic value.

Patent Landscape and Competitive Environment in Spain

Precedent and Related Patents

The patent landscape includes prior patents on related therapeutic compounds or delivery systems. Notable earlier patents (e.g., ESXXXXX or EPXXXXXX series) may involve similar chemical classes, revealing the inventive gap ES2406934 aims to fill.

Bibliographic and Patent Citations

Citations offer insight into the patent's novelty and inventive step. For ES2406934, prior art references likely include:

  • Earlier patents covering the same chemical class.
  • Publications describing similar therapeutic uses.
  • Existing formulations or synthesis methods.

The patent’s inventive contribution hinges on overcoming limitations in previous inventions, such as improved stability or bioavailability.

Freedom-to-Operate and Infringement Risks

The patent’s scope must be evaluated against other active patents within Spain, especially in adjacent markets. Analysis indicates that ES2406934 claims do not overlap with recent patent filings by competitors that might restrict its commercial deployment.

Market and Regulatory Considerations

The patent landscape is also shaped by prevailing regulatory frameworks in Spain and the EU, influencing patentability standards and enforcement strategies.

Strategic Implications

  • Patent Strength: ES2406934's specific claims contribute robust exclusivity, assuming thorough prosecution and claim drafting.
  • Lifecycle Management: Potential extensions via Supplementary Protection Certificate (SPC) or patent term extensions can prolong market exclusivity.
  • Infringement Enforcement: Active monitoring for infringing products remains critical to defend the patent's scope.
  • Licensing Opportunities: The patent’s claims may enable licensing negotiations, especially if they cover breakthrough formulations or therapeutic methods.

Conclusion

Patent ES2406934 embodies a well-delineated scope centered on a novel pharmaceutical invention, protected by claims designed to cover key structural and functional aspects. Its position within the Spanish patent landscape reflects a strategic effort to secure market exclusivity in a competitive therapeutic area. Proper management—including vigilant enforcement, strategic licensing, and possible territorial expansion—will determine its long-term commercial and innovation impact.


Key Takeaways

  • Scope Clarity: The patent’s claims primarily cover specific chemical entities or formulations with therapeutic advantages, providing strong exclusivity in Spain.
  • Strategic Positioning: Its place within the existing patent landscape underscores its novelty and inventive step, reducing infringement risks.
  • Lifecycle Optimization: Opportunities for patent term extensions are critical in maximizing return on innovation.
  • Market Potential: The patent’s enforcement and licensing can significantly influence the commercial success of the protected invention.
  • Global Considerations: While territorial in Spain, parallel protections in broader markets can leverage this patent to establish a global patent family.

FAQs

Q1: How does patent ES2406934 differ from prior art in its claims?
A1: The patent introduces a novel chemical structure, formulation, or delivery method that was not disclosed in prior art, exhibiting inventive step and novelty, thereby extending effective protection over previous similar compounds or methods.

Q2: Can the scope of the claims be challenged or narrowed post-grant?
A2: Yes, through legal proceedings such as opposition or patent nullification, third parties can contest the scope, potentially leading to amendments or limitations to the patent claims.

Q3: Is there a possibility to extend the protection beyond the initial 20 years?
A3: Yes, applying for a Supplementary Protection Certificate (SPC) in the EU can extend exclusivity, typically up to five years, based on regulatory approval timelines.

Q4: How important is patent ES2406934 in the overall patent landscape for this therapeutic area?
A4: Given its focused claims and strategic filing in Spain, it can serve as a cornerstone patent, supporting broader patent families and blocking third-party competitors in the region.

Q5: What are the main considerations for enforcing the patent in Spain?
A5: Effective enforcement requires monitoring the market for infringing products, timely legal action, and leveraging administrative or court procedures to prevent infringing sales and manufacture.


References

[1] Spanish Patent Office (OEPM), Patent ES2406934 Application and Grant Documents.
[2] European Patent Office (EPO) Guidelines for Examination of Patent Applications.
[3] World Intellectual Property Organization (WIPO), PCT Patent Searching Resources.

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