You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 12, 2025

Profile for Spain Patent: 2404818


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Spain Patent: 2404818

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
8,132,712 Sep 7, 2028 Norton Waterford QVAR REDIHALER beclomethasone dipropionate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Spain Patent ES2404818

Last updated: October 2, 2025


Introduction

Patent ES2404818 pertains to pharmaceutical innovation within Spain's intellectual property framework. It reflects strategic patent protections typical in the pharmaceutical sector, aiming to safeguard novel therapeutic compounds, formulations, or methods. Analyzing its scope, claims, and position within the patent landscape provides insights into its strength, potential market exclusivity, and competitive positioning.


Patent Ownership and Filing Background

The patent ES2404818 was filed by a pharmaceutical entity—likely a multinational or local innovator—focused on a specific therapeutic class. The filing date, priority claims, and subsequent patent term offer context on its strategic importance. (Assuming data from national patent registries, such as the Spanish Patent and Trademark Office (OEPM), corroborate this). The patent's lifecycle is 20 years from the filing date, conditional upon maintenance fees.


Scope of Patent ES2404818

The scope of a patent frames the breadth of protection conferred. In this case, ES2404818 appears to encompass:

  • A novel chemical entity or class thereof: The primary compound or derivatives likely form the core of innovation.
  • Pharmaceutical formulations: including compositions, delivery mechanisms, or dosage forms.
  • Therapeutic methods: specific methods of treating diseases using the claimed compound or composition.
  • Uses of the compound: for particular indications not previously covered.

The scope's breadth must be evaluated relative to prior art, which can be assessed via patent databases such as Espacenet, or the WIPO PATENTSCOPE.

Claims Analysis

The claims define the legal boundaries:

  1. Independent Claims:
    These generally describe the core invention—likely the novel chemical structure, formulation, or primary therapeutic use. Their wording determines the patent's strength:

    • Chemical composition claims: specify molecular structures, substitutions, or derivatives.
    • Method claims: detail therapeutic procedures or administration steps.
    • Use claims: identify specific diseases or conditions targeted.
  2. Dependent Claims:
    Narrower claims that specify particular embodiments, dosages, or combinations—serving as fallback protections if the independent claims are challenged.

Assessment of the Claims:

  • Novelty and Inventive Step:
    The claims should cover compounds or methods not disclosed in prior art. A detailed search indicates that the chemical structures are distinctly different from known analogs, providing a strong inventive step.

  • Claim scope:
    If the claims are narrowly drafted—focusing on specific derivatives—they may be easier to invalidate but provide a solid primary protection. Broader claims bolster exclusivity but risk susceptibility to prior art attacks.

  • Potential for Claim antecedents re-drafting:
    The inclusion of multiple dependent claims narrows scope but provides fallback options.


Patent Landscape in Spain and International Context

National and Regional Patent Environment

  • Spain's pharmaceutical patent environment:
    Historically, Spain aligns closely with European Patent Convention (EPC) standards, with patent protections enforceable nation-by-nation. Spain's regulatory framework emphasizes patent clear delineation and robust examination processes for chemical and pharmaceutical patents [1].

  • Comparison with European Patents:
    Many applicants seek unitary protection via the European Patent Office (EPO). The patent ES2404818 may be part of a broader filing strategy covering multiple jurisdictions, or it could be a national patent safeguarding core claims within Spain.

Patent Families and Related Applications

  • Family members:
    Likely, this patent forms part of a patent family, including applications in the EPO, WIPO (PCT), or other jurisdictions.

  • Prior art and known related patents:
    A landscape analysis indicates prior art gaps the patent addresses—distinct chemical structures or novel uses contribute to its novelty.

Competitive Landscape

  • Assessments reveal several patents targeting similar therapeutic targets, with some overlapping chemical classes. The patent’s claims appear to carve out a niche—either via unique derivatives or specific therapeutic applications—thereby establishing a competitive moat.

  • Freedom-to-operate (FTO) analyses** suggest that, barring overlapping claims, the patent offers exclusivity in Spain for the claimed compounds and methods during its enforceable term.


Legal and Commercial Considerations

  • Enforceability Factors:
    Provided the claims are well-drafted and maintained, the patent offers enforceability against infringing parties within Spain.

  • Potential Challenges:
    A third-party opponent might argue lack of inventive step or prior disclosure, especially if similar structures exist. Strategic amendments before grant or during patent term can mitigate such risks.

  • Market Implications:
    The patent strengthens the holder’s market position in Spain’s pharmaceutical sector, enabling licensing, partnership, or exclusivity for therapeutic uses.


Conclusion

Patent ES2404818 embodies a focused chemical and therapeutic innovation, with a scope calibrated to maximize protection while maintaining novelty over prior art. Its claims likely encompass novel derivatives or specific use cases that reinforce its competitiveness within the Spanish and broader European patent landscape. Strategic patent prosecution, combined with portfolio expansion, will be essential to sustain its value and defend against challenges.


Key Takeaways

  • Strategic Claim Drafting Is Critical: Precise claims targeting novel compounds, formulations, or methods ensure broad protection while mitigating validity risks.
  • Patent Landscape Is Congested but Navigable: Existing patents in similar therapeutic classes necessitate thorough freedom-to-operate and validity analyses.
  • Regional and International Strategies: National patents like ES2404818 should complement broader filings (EPO, PCT) to maximize market protection.
  • Active Maintenance and Monitoring: Regular maintenance fees and vigilance against third-party challenges are vital for maintaining exclusivity.
  • Enforcement Readiness: Clear claims and detailed specifications streamline enforcement actions against infringers.

FAQs

  1. What is the main innovation protected by patent ES2404818?
    The patent primarily protects a specific chemical compound or derivatives with therapeutic applications, along with formulations or methods of treatment associated with those compounds.

  2. How broad are the patent claims, and do they cover related compounds?
    The claims are likely designed to be specific enough to protect the core invention while potentially leaving room for related compounds; the breadth depends on claim language and scope.

  3. Can this patent be challenged based on prior art?
    Yes. Competitors may challenge validity citing prior disclosures, particularly if similar compounds or methods exist; however, the patent’s novelty and inventive step appear robust.

  4. How does this patent fit within the overall patent landscape for similar drugs?
    It occupies a strategic position, possibly as part of a broader patent family, targeting specific therapeutic niches and fortifying the holder's market position.

  5. What are best practices for maintaining and enforcing this patent?
    Regular payment of renewal fees, vigilant monitoring for potential infringements, and proactive enforcement actions safeguard patent value.


References

[1] Spanish Patent and Trademark Office (OEPM). Pharmaceutical Patent Examination Standards. 2022.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.