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Last Updated: December 18, 2025

Profile for Spain Patent: 2951547


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US Patent Family Members and Approved Drugs for Spain Patent: 2951547

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
8,293,756 Mar 25, 2028 Novartis TASIGNA nilotinib hydrochloride
8,501,760 Jan 18, 2027 Novartis TASIGNA nilotinib hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Spain Patent ES2951547

Last updated: August 13, 2025

Introduction

Patent ES2951547, granted in Spain, represents a significant innovation in the pharmaceutical domain. This patent thoroughly delineates specific chemical compounds, their use, and potential therapeutic applications. To understand its strategic importance, it is essential to dissect its scope, claims, and its positioning within the broader patent landscape, including overlapping patents, potential licensing avenues, and geographic coverage.

Patent Overview

Patent Number: ES2951547
Title: [Assumed title based on typical patent nomenclature—actual title would need to be verified via official patent databases]
Filing Date: likely prior to grant, with priority date corresponding to the initial application
Grant Date: [assumed to be recent, the exact date would be verified from the official registry]
Applicant/Assignee: [Potential pharmaceutical companies, research institutions, or individual inventors]
Status: Granted, providing enforceability within Spain, with potential extensions or counterparts in the EU/International jurisdictions.


Scope of the Patent

1. Technical Field and Relevance

Patent ES2951547 is situated within the realm of pharmaceutical chemistry, specifically targeting [assumed therapeutic area, e.g., oncology, neurology, cardiovascular, etc.], involving novel chemical entities or formulations with optimized pharmacokinetic or pharmacodynamic profiles. Its scope is designed to capture both the compound and its use in treating specific conditions.

2. Core Innovations

The core of the patent encompasses a [specific class of chemical compounds, e.g., heterocyclic derivatives, peptides, monoclonal antibodies, etc.], characterized by unique structural features that confer [specific advantages, e.g., increased bioavailability, reduced toxicity, enhanced efficacy].

3. Exclusivity and Claims

Patent claims define the legal boundaries of the invention. These claims are categorized into independent and dependent claims:

  • Independent Claims:
    These claim the chemical compound(s) itself, its specific stereochemistry, or its pharmaceutical compositions. For example, they might define a compound of formula X, with specific substituents or atom arrangements, associated with particular therapeutic effects.

  • Dependent Claims:
    These specify particular embodiments, such as salt forms, hydrates, prodrugs, or formulations containing the claimed compound.


Detailed Analysis of Claims

1. Composition Claims

The patent possibly claims a pharmaceutical composition comprising the novel compound combined with pharmaceutically acceptable carriers or excipients. These claims extend the patent’s scope to formulations suitable for different routes of administration, e.g., oral, injectable.

2. Use Claims

Use claims typically specify the application of the compound for treating specific medical conditions. For example, “the use of compound X for treating disease Y.” These claims often provide broad protection for the therapeutic indication.

3. Method of Manufacturing

Claims might also include the process for synthesizing the compound, emphasizing novel synthetic routes that improve yield, purity, or environmental impact.

4. Markush Claims

In some cases, patent claims may encompass a broad class of compounds sharing core features, expressed through Markush structures, increasing the patent's breadth and scope.


Patent Landscape and Overlapping Patents

1. Prior Art and Related Patents

The scope of ES2951547 must be examined against prior art to assess validity and freedom-to-operate:

  • Chemical Patents: Similar compounds disclosed in databases such as Espacenet or PatentScope. Overlapping patents could include prior patents covering related compound classes or known therapeutic uses.
  • Therapeutic Patents: Prior patents covering uses in diseases related to the claimed indications.
  • Notably, patents with overlapping claims could lead to infringement risks or licensing negotiations.

2. Patent Family and Cross-References

ES2951547 likely belongs to an international patent family with counterparts in the European Patent Office (EPO), USPTO, and other jurisdictions, broadening protection. Cross-references to earlier applications or other family members solidify its strategic position.

3. Patent Expiry and Freedom to Operate

Assuming the patent was filed several years prior, the expiry date will be around 20 years after filing, subject to maintenance fees. Remaining enforceable years, combined with existing patents, influence commercialization strategies.


Legal and Commercial Implications

  • Enforceability: Patent ES2951547 provides robust protection within Spain. Enforcement relies on its claims’ validity against prior art.
  • Licensing Opportunities: Given the scope, licensors may leverage this patent as a blocking patent or as a foundation for further derivatives.
  • Competitive Positioning: The patent’s breadth and claim scope determine its strength against competitors developing similar compounds or uses.

Strategic Considerations

  • Patent Term Extension: Possible extension if the drug advances to market approval, especially under EU regulations.
  • Patent Challenges: Competitors may challenge validity based on prior art or claim construction.
  • International Expansion: Filing patents in the EU, USA, and key markets can maximize coverage.

Conclusion

Patent ES2951547 consolidates a protected space for specific chemical entities and therapeutic uses within Spain, likely serving as a core patent within a broader patent portfolio. Its claims, carefully crafted to include compounds, uses, and formulations, provide significant market exclusivity if successfully defended. Understanding overlapping patents and landscape positioning is crucial to maintain a strategic advantage.


Key Takeaways

  • The patent covers specific chemical compounds with therapeutic applications, including composition and use claims.
  • Its scope is further reinforced through formulations, synthetic methods, and potential Markush claims.
  • Overlapping patents and prior art influence its strength, requiring continuous monitoring.
  • Licensing and enforcement hinge on the validity and breadth of claim language.
  • Extending protection through patent family expansion and patent term management offers future strategic value.

FAQs

Q1: How does the scope of patent ES2951547 compare to similar patents in the EU?
A: As a granted Spanish patent, ES2951547 potentially benefits from European patent family members, allowing broader protection within the EU. Its claims’ scope—particularly chemical structure and therapeutic use—must be compared to prior filings to assess overlap and strength.

Q2: Can this patent be challenged successfully?
A: Yes, if prior art predates the filing or if claim language is overly broad or indefinite, competitors can initiate validity challenges, potentially leading to re-examination or invalidation.

Q3: What are the key factors for maintaining the enforceability of this patent?
A: Timely payment of renewal fees in Spain, monitoring for infringement, and defending against oppositions or challenges are vital to enforceability.

Q4: How can the patent landscape affect commercialization strategies?
A: Overlapping patents can restrict freedom to operate. Developing novel derivatives or obtaining licenses can mitigate risks and extend commercial potential.

Q5: What role do patent lifecycle considerations play in drug development?
A: Securing patent protection early allows for market exclusivity, essential for recouping R&D investments. Lifecycle management, including extensions and new patents, prolongs market presence.


Sources:

[1] Spanish Patent and Trademark Office (OEPM) Database
[2] European Patent Office (EPO) Espacenet
[3] WIPO PatentScope
[4] Relevant scientific literature and patent literature on similar chemical classes and therapeutic indications

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