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Last Updated: December 30, 2025

Profile for Spain Patent: 2546934


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US Patent Family Members and Approved Drugs for Spain Patent: 2546934

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 Dec 19, 2027 Currax ONZETRA XSAIL sumatriptan succinate
⤷  Get Started Free Sep 15, 2025 Currax ONZETRA XSAIL sumatriptan succinate
⤷  Get Started Free Sep 15, 2025 Currax ONZETRA XSAIL sumatriptan succinate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Spain Patent ES2546934

Last updated: July 30, 2025

Introduction

Patent ES2546934, granted in Spain, addresses an innovative pharmaceutical formulation or method. This patent's scope delineates the proprietary space around a specific drug or therapeutic approach, influencing market exclusivity, licensing opportunities, and competitive dynamics within the pharmaceutical patent landscape. Analyzing the patent’s claims reveals the proprietary boundaries, while understanding the broader patent landscape contextualizes its strategic positioning.

Patent Overview

Patent Number: ES2546934
Filing and Grant Dates: Filed in [date], granted in [date] (accurate dates depend on official records).
Applicants/Applicants: Typically, the originator or patent holder, often a pharma company or research institution.
Priority Data: U.S., EP, or PCT filings may underpin the Spanish application, solidifying the scope.


Scope of the Patent

Claims and Their Legal Scope

The core of patent ES2546934 resides in its claims, which define the legal boundary of the invention. Its scope directly impacts potential infringement, licensing, and research freedom.

1. Independent Claims:

  • Type of Composition/Method: The independent claims likely delineate a pharmaceutical composition, specific formulations, or therapeutic methods.
  • Claim Language: Typically, these specify essential components, their ratios, and specific properties or manufacturing steps, often stating "comprising," "consisting of," or "consisting essentially of."
  • Novelty and Inventive Step: The claims must distinguish from prior art by emphasizing unique combinations, delivery mechanisms, or active ingredient modifications.

2. Dependent Claims:

  • These specify particular embodiments, such as specific dosage forms, excipient types, or administration routes, narrowing scope but providing fallback protections.

Assessment of Claims

  • If broad in scope, the claims could cover versatile formulations or therapies related to a particular drug, potentially extending patent life or licensing flexibility.
  • Narrow claims may limit coverage but strengthen enforceability against specific infringers.
  • The claims likely include a combination of:
    • Specific chemical entities or derivatives,
    • Unique formulations or drug delivery systems,
    • Therapeutic methods with particular dosing regimens.

Understanding the precise wording of the claims is critical to assess enforceability and potential for design-around strategies.


Patent Landscape Analysis

Prior Art and Related IP

1. Pre-existing Patents:

  • The patent landscape shows prior art in [relevant therapeutic area], with key patents in related drug formulations, delivery routes, or compound structures.
  • For example, previous patents covering [related drugs or delivery methods] may influence the scope of ES2546934.

2. Cited and Citing Patents:

  • Citations: These include prior patents that establish novelty or address similar compounds.
  • Cited by: More recent patents that probably extend or build upon ES2546934, indicating ongoing research or commercial interest.

Geographical Patent Families and Extensions

  • The application might be part of a broader patent family, with equivalents in the European Patent Office (EPO), the United States (USPTO), and other jurisdictions.
  • These broader protections can extend market exclusivity beyond Spain and influence global licensing strategies.

Legal Status and Challenges

  • The patent's current status (e.g., active, pending, litigated) impacts its strategic value.
  • Potential for opposition or invalidation exists, especially if prior art claims challenge its novelty or inventive step under European patent law.

Implications for Commercial and Legal Strategy

  • A broad, defensible scope supports market exclusivity and deters generic challenges.
  • Narrow claims may necessitate supplementary patent filings or supplementary protection certificates (SPCs).
  • Understanding competing patent filings informs freedom-to-operate analyses.

Conclusion

Patent ES2546934 exemplifies targeted intellectual property relevant to a specific therapeutic or formulation approach. Its claims, meticulously crafted, define a strategic space in the pharmaceutical landscape. The overall patent landscape underscores a competitive environment with prior art and potential challenges that influence the patent’s strength and scope. A holistic understanding of these facets enables informed decision-making regarding licensing, product development, or patent enforcement.


Key Takeaways

  • The scope of ES2546934 hinges on its claims, which delineate proprietary rights in a specific drug formulation or method.
  • Broad claims enhance market protection but must navigate prior art carefully to withstand validity challenges.
  • The patent landscape includes overlapping patents, family extensions, and potential oppositions, informing strategic positioning.
  • Continuous monitoring of patent status, citations, and legal developments is critical to safeguarding market rights.
  • Strategic patent drafting and prosecution must align with evolving scientific and legal standards to maximize value.

FAQs

Q1. How does the scope of patent ES2546934 influence its market exclusivity?
The scope, defined by its claims, determines the breadth of protection. Broader claims provide extensive exclusivity but require robust novelty and inventive step, while narrower claims may be easier to defend but limit coverage.

Q2. Can existing patents threaten the validity of ES2546934?
Yes. Prior art or earlier patents might challenge its novelty or inventive step, leading to potential invalidation unless the patent demonstrates clear differentiation.

Q3. How does this patent fit within the overall pharmaceutical patent landscape in Europe?
If harmonized with broader patent family filings, ES2546934 contributes to a substantial patent portfolio, possibly extending protection through EPO or PCT filings. It reflects current innovation trends and target therapeutic areas.

Q4. Are there opportunities for licensing or partnerships based on this patent?
Potentially, especially if the patent covers key formulations or methods that industry partners seek to access. Licensing negotiations depend on the patent’s enforceability and commercial relevance.

Q5. What strategies can patent holders employ to maximize the value of ES2546934?
They can pursue continuous patent prosecution to broaden claims, file additional applications covering related inventions, enforce patent rights actively, and monitor competing patents for potential overlaps.


References

[1] Official documentation and publication records for ES2546934.
[2] European Patent Office search tools and databases.
[3] Pharmaceutical patent law and patentability standards (European Patent Convention).
[4] Industry reports on pharmaceutical patent landscapes in Europe.

Note: Specific filing dates, applicants, and precise claim language require direct consultation of patent documents from the Spanish Patent and Trademark Office or Espacenet database.

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