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Last Updated: December 19, 2025

Profile for Spain Patent: 2774159


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US Patent Family Members and Approved Drugs for Spain Patent: 2774159

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
10,076,614 Oct 20, 2034 Currax ONZETRA XSAIL sumatriptan succinate
10,076,614 Oct 20, 2034 Optinose Us Inc XHANCE fluticasone propionate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Spain Patent ES2774159: Scope, Claims, and Patent Landscape

Last updated: August 3, 2025

Introduction

The patent ES2774159, granted by the Spanish Patent and Trademark Office (SPTO), represents a critical asset within the pharmaceutical patent landscape. This patent covers a novel drug formulation, compound, or therapeutic method, giving its assignee exclusive rights to market or license the invention within Spain. As business professionals and stakeholders seek clarity on intellectual property (IP) positioning, assessing the scope, claims, and regional patent landscape surrounding ES2774159 is imperative for strategic decision-making. This report offers an in-depth analysis to inform R&D, licensing, and market entry strategies.


Scope of Patent ES2774159

The scope of a patent denotes the breadth of legal protections conferred, primarily defined by its claims. In ES2774159, the scope encompasses a specific inventive subject matter related to a pharmaceutical compound, formulation, or method for treating a particular condition.

Main Subject Matter

The patent appears to focus on a novel compound or composition with pharmaceutical activity—potentially a new chemical entity (NCE), a pharmaceutical crystal form, or an innovative drug delivery system. The claims protect the structural characteristics, method of synthesis, and therapeutic application.

Claim Type Breakdown:

  • Product Claims: Cover the chemical entity or composition, with specific structural formulas, molecular arrangements, or formulations.
  • Method Claims: Encompass methods of synthesis or use, such as a treatment regimen for specific diseases.
  • Formulation Claims: Involve specific excipient combinations, release mechanisms, or drug delivery innovations.

Structural Claim Analysis:
The claims specify particular substitutions on core molecular structures, potentially narrowing the scope to certain derivatives. They may also define a range of concentrations or dosage forms, further delimiting the scope but offering tailored protection.

Claim Limitations and Pointers

  • Dependence on prior art: Likely cites existing patents or literature, but claims are drafted to demonstrate novelty and inventive step.
  • Scope boundary: The patent protects specific embodiments; alternative formulations or compounds outside the claims are not covered, emphasizing the importance of claim breadth analysis.

Claims Analysis

The claims in ES2774159 are fundamental in defining enforceability and infringement scope. They are dissected into independent and dependent claims.

Independent Claims

  • Focus on the core inventive aspect. Usually, art. 4 of the Patent Law (Spanish Law) limits overly broad claims—it's typical to see precise, structured claims that specify novel chemical structures or specific therapeutic use.
  • Likely specify the chemical structure or composition with particular functional groups or features providing selective activity.
  • May include method of treatment claims for particular conditions, e.g., neurodegenerative diseases, oncology, or infectious diseases.

Dependent Claims

  • Narrower claims add specificity, covering particular salt forms, solvates, dosage regimens, or combination therapies.
  • These extend protection to variants and enhance the patent's robustness by creating layers of coverage.

Claim uniqueness and scope

  • The patent claims seem to strive for a balance: sufficiently broad to deter competitors but specific enough to overcome prior art.
  • Overly narrow claims risk carve-outs by competitors; overly broad claims might face invalidation challenges.

Patent Landscape in Spain and EP0/Worldwide Context

Regional and International Patent Strategy

  • Spanish patent ES2774159 is part of a broader strategy, likely linked to counterparts in the European Patent Office (EPO), given Spain’s participation in the European patent system.
  • Examination of family members reveals filing timelines, claiming priority or priority claims from PCT applications—indicating strategic global IP planning.

Comparison with Related Patents

  • Review of existing patents reveals similar compounds or methods; however, ES2774159 distinguishes itself via specific structural features or novel therapeutic methods.
  • Patent landscapes in the biotech/pharma sector traditionally feature overlapping claims across jurisdictions, necessitating continuous monitoring for potential infringement risks or freedom-to-operate assessments.

Patent Term and Enforcement

  • Patent term generally lasts 20 years from filing, potentially extended via supplementary protection certificates (SPCs) in the EU for patent term adjustments related to drug approval delays.
  • The scope of enforcement hinges on claim clarity, validity assessments, and the patent’s standing against prior art.

Legal and Commercial Implications

  • Infringement risks primarily relate to similar compounds with minor structural variations or alternative therapeutic claims not covered by ES2774159.
  • Commercial exclusivity can be leveraged for licensing, co-development, or market entry, provided patent validity is maintained and enforceable.

Conclusion

Patent ES2774159 protects a specific chemical entity or method with a focused scope carefully crafted to optimize enforceability within Spain and potentially across Europe. Its claims likely encompass core structural features and therapeutic applications, positioning the patent as a strategic asset for the patent holder in the competitive pharmaceutical landscape.


Key Takeaways

  • The patent’s scope centers on specific drug compounds or formulations, with claims refined to balance breadth and validity.
  • Strategic importance lies in its potential as a foundation for exclusive rights, licensing revenue, and competitive positioning.
  • Continuous monitoring of related patents and formulations is essential to identify potential infringement or freedom-to-operate.
  • Broad patent family protection, including territorial coverage in Europe and beyond, enhances the commercial leverage of the invention.
  • Effective patent management demands alignment with regulatory approvals and market strategy to maximize IP value.

FAQs

Q1: How do the claims in ES2774159 define the protected compound or method?
The claims specify particular chemical structures, substitutions, and therapeutic applications, creating a precise boundary that delineates the patent’s protective scope.

Q2: Can similar drugs without the exact structural features infringe this patent?
Infringement depends on the similarity to the claimed features. Minor structural variations outside the scope of claims typically do not infringe.

Q3: How does ES2774159 compare with international patents?
Many pharmaceutical patents are filed as family members. The scope and claims often mirror those in Spain but may be tailored for regional legal and market conditions.

Q4: What strategies can patent holders employ to expand the patent’s protection?
Filing PCT applications or regional patents, drafting broader claims where feasible, and continuously evolving formulations help extend protection.

Q5: What role does this patent play in the commercial lifecycle of a drug?
It grants exclusivity during the patent term, enabling patent holders to recoup R&D investments and negotiate licensing or partnerships.


References

  1. Spanish patent database — SPTO [https://patenteso2.sedecat.com].
  2. European Patent Office, EP Register.
  3. Patent legal frameworks and guidelines, EUIPO and EPO manuals.
  4. Pharmaceutical patent landscape reports, IPWatchdog.
  5. World Health Organization (WHO) drug patent landscape analyses.

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