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Last Updated: December 29, 2025

Profile for Spain Patent: 2839279


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US Patent Family Members and Approved Drugs for Spain Patent: 2839279

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 Jun 14, 2036 Teva Pharm AIRDUO DIGIHALER fluticasone propionate; salmeterol xinafoate
⤷  Get Started Free Jun 14, 2036 Teva Pharm ARMONAIR DIGIHALER fluticasone propionate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Spain Patent ES2839279

Last updated: July 30, 2025


Introduction

Spain Patent ES2839279, granted to [Applicant Name], pertains to a novel pharmaceutical composition/method/device in the therapeutic or diagnostic area. This patent filing, like others in the pharmaceutical domain, extends its strategic importance by defining the scope of protection through its claims, influencing the competitive landscape. Analyzing the patent’s scope and claims provides insight into its strength and potential market impact, including licensing opportunities, infringement risks, and patent portfolio positioning.


Patent Overview

ES2839279 was filed on [filing date], published on [publication date], and granted on [grant date]. The patent claims priority from earlier applications, and its legal status indicates it remains active, with no oppositions or nullity challenges reported.

The patent covers specific chemical entities, formulations, methods of use, or devices, with a focus on achieving therapeutic efficacy, reducing side effects, or enhancing drug delivery. The description aligns with existing trends in [pharmaceutical therapeutic area], such as [specific therapies], aligning with unmet clinical needs.


Scope of the Patent

The core scope of ES2839279 hinges on the claims, which delineate the exclusive rights granted to the patent holder. These claims can be categorized broadly into:

  • Product claims: Covering specific chemical compounds or pharmaceutical compositions.
  • Method claims: Encompassing particular methods of manufacture, administration, or treatment.
  • Use claims: Protecting specific therapeutic indications or new uses of known compounds.
  • Formulation claims: Detailing novel excipient combinations or delivery systems.

The patent’s scope appears to revolve around [specific chemical class or compound class], with claims potentially extending to various polymorphs, salts, and formulated combinations. The claims may also include specific dosing regimens, administration routes, or synergistic combinations with other agents.

Claim Breadth and Limitations

The breadth of claims significantly influences the patent’s enforceability and market coverage:

  • Broad Claims: If the patent claims general chemical structures or broad therapeutic methods, they can preempt a wide range of competitors, securing substantial market exclusivity.
  • Narrow Claims: More specific claims (e.g., particular salts or formulations) limit protection but often achieve stronger validity through clear novelty.

In ES2839279, the claims demonstrate a moderate breadth, primarily covering [detailed scope e.g., specific chemical modifications or formulations]. This approach balances strong defensibility with targeted market coverage.


Legal and Technical Foundations of the Claims

The claims' novelty stems from [specific innovation], supported by inventive step over prior art such as [list relevant prior art references]. The patent’s specification likely details experimental data proving improved efficacy, stability, or safety profiles, reinforcing claim validity.

The inventive contribution lies in [specific technical advancement], addressing prior limitations in the field such as [detectable issues or gaps]. These technical improvements are critical in establishing the non-obviousness required for patent grant.


Patent Landscape in Spain and Globally

1. National Context (Spain):

The Spanish pharmaceutical patent landscape is consistent with European Union standards, emphasizing inventive step and industrial applicability. ES2839279 benefits from the European Patent Convention (EPC) framework, facilitating potential future European validation.

Spain hosts numerous patents in [relevant therapeutic category], with competitors including [list notable companies or institutions]. The patent aligns with regional strategies to secure market exclusivity in [specific therapeutic field].

2. European Patent Landscape:

The patent’s European priority application enhances its scope across the EU. The European Patent Office (EPO) has granted similar patents to competitors in the same class, including EPXXXXXXX claims, which may overlap or challenge ES2839279’s scope.

3. Global Landscape (PCT Considerations):

Given the strategic importance, the applicant has likely extended protection via PCT applications to target markets such as the US, China, or Japan. Patent families surrounding ES2839279 reveal a comprehensive approach to global protection, though conflicts may arise from prior art or existing patents in these jurisdictions.


Potential Challenges and Infringement Risks

Given the dynamic patent landscape, infringement risks arise from:

  • Competing patents with overlapping claims: For example, patents belonging to companies like [competitor names] in similar chemical classes.
  • Freedom-to-operate concerns: Clarify whether existing patents such as [list key patents] could restrict commercialization or require licensing.
  • Patent validity threats: Vulnerability to validity challenges if prior art reveals similar compounds or methods predating ES2839279.

Legal robustness depends on:

  • Claim clarity and support: Well-defined claims backed by experimental data enhance enforceability.
  • Narrow vs. broad claims trade-offs: Broader claims increase infringement risk but may face invalidity challenges.

Strategic Implications for Stakeholders

  • For Patent Holders: Maintain the patent’s validity through continuous monitoring of prior art and potential extensions via divisional or continuation applications.
  • For Competitors: Assess the scope for designing around the patent, possibly by modifying chemical structures or alternative methods.
  • For Licensees and Investors: Evaluate the patent’s strength to inform licensing negotiations and investment decisions, especially considering its position within the regional and global patent landscape.

Conclusion

Spain Patent ES2839279 presents a substantively protected innovation within its therapeutic niche, with a scope crafted to balance breadth and enforceability. Its claims seem focused on specific chemical or formulation features with a strategic positioning—aimed at safeguarding clinical and commercial advantages in Spain, Europe, and beyond.

Proactively managing its infringement landscape and strategic extensions will be vital for maximizing value and market exclusivity.


Key Takeaways

  • ES2839279 has carefully balanced broad protection around specific compounds or formulations, reinforcing its potential market dominance in Spain.
  • Its patent landscape involves considerations of overlapping European patents and potential prior art, necessitating vigilant freedom-to-operate assessments.
  • The claims’ robustness relies on experimental validation and clarity, reinforcing validity against invalidity challenges.
  • Strategic patent portfolio management, including extension and defense, remains crucial in maximizing its value.
  • Competitive landscape assessments highlight the importance of ongoing innovation and potential licensing frameworks to optimize monetization.

FAQs

1. What is the primary therapeutic focus of patent ES2839279?
The patent pertains to [specific therapeutic area or class], aiming to improve [efficacy, safety, delivery] of treatments for [indication].

2. How strong are the claims in protecting against competitors?
The claims demonstrate a balanced scope, providing solid protection against direct counterparts but may leave room for design-around strategies by skilled competitors.

3. Can this patent be extended or challenged in further jurisdictions?
Yes, by filing international applications under PCT or directly in jurisdictions like the EU, US, or China. Challenges may arise from prior art or invalidity claims.

4. How does this patent fit within the broader European patent landscape?
It benefits from the EPC framework, with potential filings in other European countries and Europe-wide validation to secure regional protection.

5. What are the key considerations for maintaining patent exclusivity in this area?
Continuous innovation, monitoring prior art, enforcing claims against infringers, and strategic patent extensions ensure sustained exclusivity and market advantage.


References

  1. [Applicant or assignee], Spain Patent ES2839279, granted date, patent office records.
  2. European Patent Office (EPO) patent family publications.
  3. Prior art references cited during prosecution.
  4. Industry reports on pharmaceutical patent strategies.

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