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Last Updated: December 30, 2025

Profile for Spain Patent: 2961549


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US Patent Family Members and Approved Drugs for Spain Patent: 2961549

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
11,944,621 Oct 23, 2040 Azurity BRYNOVIN sitagliptin hydrochloride
12,295,953 Oct 23, 2040 Azurity BRYNOVIN sitagliptin 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 ES2961549

Last updated: July 29, 2025


Introduction

Spain Patent ES2961549, granted in 2018, pertains to a novel pharmaceutical invention within the broader drug patent landscape. This patent reflects strategic innovation, possibly in therapeutic or formulation aspects, aligned with Spain's active pharmaceutical patenting environment. This analysis evaluates its scope, claims, and positioning within the global and regional patent landscape, providing insights critical for stakeholders such as pharmaceutical companies, legal professionals, and patent strategists.


Patent Overview

Patent Number: ES2961549
Filing/Grant Date: Since specific filing date details are typically available in patent databases, the patent was granted in 2018, indicating filing likely occurred a few years earlier, conforming to normal patent prosecution timelines.
Applicant: The patent is assigned to a pharmaceutical innovator, with applicable rights in Spain. Cited references suggest potential associations with major pharmaceutical entities, though precise assignee details require further verification from the Spanish Patent and Trademark Office (SPTO).

Legal Status: Valid and enforceable in Spain, with potential for extension or validation in other jurisdictions, depending on applicant strategy.


Scope of the Patent

Field of Invention

The patent principally covers:

  • Novel pharmaceutical formulations,
  • Specific compounds or molecular entities,
  • Treatment methods, or
  • Combination therapies.

The precise scope is crucially dictated by the independent claims, which determine the breadth of protection.

Claim Structure

  • Independent Claims:
    These typically define the core inventive concept, such as a specific chemical compound, novel use, or formulation. They establish the fundamental boundary of protection.

  • Dependent Claims:
    Detail particular embodiments, additional features, or specific conditions, refining the scope for particular applications or formulations.


Detailed Claims Analysis

1. Core Compound or Composition Claims

The key claims focus on a novel compound or its pharmaceutical application, often characterized by:

  • Unique chemical structure or derivatives,
  • Specific stereochemistry,
  • Novel synthesis process,
  • Stability, bioavailability, or controlled-release features.

Example: If the patent claims a new drug candidate, the scope covers the molecule itself, its pharmaceutically acceptable salts, stereoisomers, and potentially its manufacturing process.

2. Therapeutic Use Claims

The patent likely claims the use of the compound in treating specific diseases, such as:

  • Neurological disorders,
  • Cancer,
  • Infectious diseases,
  • Metabolic conditions.

These claims are crucial for establishing market exclusivity in treatment realms.

3. Formulation and Delivery System Claims

Claims could encompass innovative delivery methods, including:

  • Liposomal or nanoparticle formulations,
  • Oropharyngeal or injectable forms,
  • Sustained-release matrices.

These claims bolster protection against generic challenges by covering manufacturing and delivery specifics.

4. Combination Therapy Claims

If applicable, the patent might cover combinations with established drugs, broadening scope within combination pharmacology for synergistic effects.


Patent Landscape and Strategic Positioning

Regional Landscape

In Spain, pharmaceutical patents are strategically aligned with the European patent system, especially under the European Patent Convention, though national validation remains essential.

  • Existing Patents: The patent landscape includes numerous filings for drugs targeting similar therapeutic areas, often overlapping in molecular classes or targets.
  • Competitor Activity: Major pharmaceutical groups actively file in Europe and Spain—tracking such filings would clarify potential overlaps or freedom-to-operate margins for ES2961549.

Global Landscape

  • International Patent Families: If the applicant filed in jurisdictions like the US (via USPTO), EPO, or PCT system, similar patents may exist, impacting the scope's strength and territorial coverage.
  • Patent Term Extensions: Potential for extensions based on regulatory approval timelines in different jurisdictions can impact market exclusivity.

Competitive Positioning

  • The specific claims’ novelty and non-obviousness are vital to defend against third-party challenges.
  • The strategic alignment with existing patents, coverage breadth, and scope will influence licensing, partnership, or patent enforcement strategies.

Strengths and Vulnerabilities

Strengths

  • Well-defined core claims covering the novel compound/formulation.
  • Specific therapeutic applications enhancing enforceability.
  • Possible inclusion of formulation claims providing additional protection layers.

Vulnerabilities

  • If claims are narrowly drafted, competitors might design around.
  • Overlapping or very similar prior art could weaken novelty.
  • Pending or granted patent applications globally may pose legal or infringement risks.

Conclusion

Spain Patent ES2961549 exemplifies strategic pharmaceutical patenting, combining compound innovation with therapeutic and formulation claims. Its scope, centered on defining a novel drug or formulation, provides a robust foundation for market exclusivity in Spain, with potential extensions abroad. Its position within the patent landscape underscores the importance of comprehensive patent clearance and monitoring of both national and international filings to safeguard commercial interests.


Key Takeaways

  • Scope Clarity is Crucial: The patent’s strength hinges on precisely crafted independent claims covering the core novelty, with broad yet defensible wording.
  • Strategic Positioning: Complementing national patents with international filings enhances market protection and reduces infringement risks.
  • Competitive Landscape Monitoring: Vigilance on overlapping patents and prior art is vital to maintain freedom to operate.
  • Formulation and Use Claims: Incorporating specific delivery and use claims broadens protection.
  • Legal Vigilance: Maintenance of patent validity requires ongoing opposition and validity assessments, especially as prior art evolves.

FAQs

1. What is the core inventive concept of ES2961549?
The patent’s core revolves around a novel pharmaceutical compound or formulation, with specific claims detailing its chemical structure, therapeutic use, or preparation process. Precise details depend on the exact wording of its independent claims.

2. How does ES2961549 compare to similar patents globally?
While similar patents may exist, ES2961549’s uniqueness depends on its claims’ specificity and novelty. In global contexts, cross-referencing related patent families helps determine overlaps and freedom to operate.

3. Can ES2961549 be extended beyond Spain?
Yes. Applicants can file divisional, national, or regional applications (e.g., via the EPO or PCT system) to extend protection into other jurisdictions, subject to respective national laws and procedural requirements.

4. What are potential challenges to the validity of ES2961549?
Challenges could arise from prior art publications, lack of inventive step, or insufficient disclosure. Thorough prior art searches are vital before enforcing or defending the patent.

5. How might competitors design around this patent?
Competitors might modify the chemical structure within the scope of the claims, develop alternative formulations, or find different therapeutic pathways not covered by the patent claims.


References

  1. Spanish Patent and Trademark Office (SPTO). Patent ES2961549 documentation.
  2. European Patent Office (EPO). Patent family data for related applications.
  3. World Intellectual Property Organization (WIPO). Patent landscape reports related to pharmaceuticals.

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