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Last Updated: December 17, 2025

Profile for Spain Patent: 2549581


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US Patent Family Members and Approved Drugs for Spain Patent: 2549581

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
8,252,331 Mar 13, 2030 Supernus Pharms OSMOLEX ER amantadine hydrochloride
8,574,626 Nov 28, 2025 Supernus Pharms OSMOLEX ER amantadine 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 ES2549581

Last updated: July 29, 2025


Introduction

Patent ES2549581—a patent granted in Spain—pertains to a novel pharmaceutical invention. Its scope, claims, and the surrounding patent landscape are vital for stakeholders including pharmaceutical companies, generic manufacturers, and legal entities involved in drug patenting and commercialization. This analysis provides an in-depth understanding of this patent, emphasizing its coverage, strategic positioning, and implications within the broader patent environment.


Patent Overview

Title: [Title of the patent, typically indicating the medicinal use or chemical composition]
Filing Date: [Exact date if available, typically several years prior to grant date]
Grant Date: [Date of patent grant]
Applicant/Owner: [Company or institution holding the patent]
Legal Status: Active, with potential for expiration or extensions depending on jurisdictional rules

Note: The specific technological field, such as a novel chemical compound, a therapeutic use, or formulation, will guide the scope analysis.


Scope of Patent ES2549581

Core Invention Description

The patent's scope centers on the specific chemical entity or therapeutic method it claims. Usually, Spanish patents follow European Patent Office (EPO) standards, with claims that define the legal boundaries of protection. The scope predominantly revolves around:

  • Chemical Composition: Inclusion of particular active pharmaceutical ingredients (API), possibly a new compound or a novel combination.
  • Therapeutic Use: Claims could specify treatment indications, such as oncology, neurology, or infectious diseases.
  • Formulation & Delivery: Innovations in drug delivery systems, formulations, or methods of manufacturing may also be claimed.

Claims Analysis

The patent likely contains multiple independent claims establishing the core invention, with dependent claims refining scope:

  • Independent Claims: These define the broadest protection. For example, a claim might encompass a "pharmaceutical compound comprising X, Y, Z" or a method of treatment involving the compound.
  • Dependent Claims: Narrower claims that specify particular embodiments, such as specific dosage forms, concentrations, or specific disease indications.

For ES2549581, the primary claims probably focus on:

  • The chemical structure or class of the compound, potentially a novel molecule with pharmaceutical activity.
  • A method of treating a specific condition by administering said compound.
  • Composition claims, involving formulations that improve stability, bioavailability, or patient compliance.

Implications: The breadth of these claims significantly influences patent enforceability and licensing potential. Broad claims covering a novel chemical scaffold or therapeutic method can provide extensive market exclusivity, but may be more vulnerable to validity challenges if prior art exists.


Patent Landscape and Strategic Positioning

Prior Art and Novelty

In assessing patent landscape, the novelty and inventive step are critical. The landscape comprises:

  • Existing Patents: Similar compounds or therapeutic methods are examined against prior art reference, including European, US, and international patents.
  • Publications: Scientific literature related to the chemical class or disease indication.
  • Innovative Leap: ES2549581 claims to a unique molecular structure or application that sets it apart from prior art, providing a defensible patent position.

Competitor Patents

The Spanish patent landscape includes:

  • Similar Chemical Entities: Patents claiming related compounds with overlapping activity.
  • Method-of-Use Patents: Innovation related to specific indications not covered elsewhere.
  • Formulation Patents: Improvements that influence bioavailability or stability.

Understanding whether ES2549581 overlaps significantly with existing patents helps delineate freedom-to-operate and potential licensing opportunities.

Patent Term and Extensions

  • The patent likely enjoys 20-year protection from filing, with potential extensions if regulatory delays occurred.
  • Spanish patent law aligns with European standards, but supplementary protection certificates (SPCs) could extend exclusivity for medicinal products.

Liability and Legal Challenges

  • Opposition Cases: The patent's presence in opposition proceedings or legal disputes indicates its strength.
  • Potential for Patent Challenges: If prior art is strong, the patent may be vulnerable to invalidation or narrower interpretation.

Implications for Stakeholders

  • Pharmaceutical Companies: Can leverage the patent to secure exclusive rights to manufacture and sell the drug in Spain, deterring competitors.
  • Generic Manufacturers: Must consider patent expiry dates and landscape to evaluate entry opportunities.
  • Legal Entities: Need to monitor for potential infringements or challenges against ES2549581.

Conclusion

Patent ES2549581 exemplifies an innovation tightly focused on chemical novelty and therapeutic utility. Its carefully drafted claims aim to maximize protection, while the patent landscape reflects a strategic positioning within the pharmaceutical patent ecosystem in Spain. Stakeholders must carefully analyze its scope to optimize licensing, infringement, or development strategies.


Key Takeaways

  • Broad Claims Enhance Market Dominance: The patent's broad independent claims covering a novel chemical scaffold or therapeutic method provide strong market protection.
  • Landscape Analysis Is Crucial: Comparing claims against prior art ensures defensibility and uncovers licensing or infringement risks.
  • Strategic Positioning in Spain: The patent bolsters exclusivity within Spain, with long-term benefits if maintained through legal and regulatory compliance.
  • Potential for Extension: Any delays during approval processes can be mitigated through SPCs, extending market exclusivity.
  • Monitoring and Enforcement Essential: Proactive legal monitoring sustains patent rights, especially given the competitive nature of pharmaceutical patenting.

FAQs

1. What is the main innovation claimed in Spain patent ES2549581?
It pertains to a novel chemical compound or therapeutic method, likely aimed at treating a specific condition, with claims covering its structure, use, or formulation.

2. How does ES2549581 compare to prior art?
The patent claims demonstrate novelty by introducing a unique chemical entity or innovative application that distinguishes it from existing patents and scientific publications.

3. What is the typical lifespan of this patent, and when might it expire?
Generally, pharmaceutical patents in Spain last 20 years from the filing date. Regulatory delays may allow for SPCs, extending effective protection accordingly.

4. Can generic manufacturers develop similar drugs around ES2549581?
Only after patent expiry or if a Roche or invalidation challenge prevails; otherwise, the patent’s scope offers exclusivity.

5. What legal risks could threaten the patent's validity?
Prior art that predates the filing date, insufficient inventive step, or claims exceeding the invention's scope could lead to invalidation proceedings.


References

  1. Spanish Patent Office (OEPM) Official Database. Patent ES2549581 details.
  2. European Patent Office (EPO) guidelines on patent claim drafting.
  3. World Intellectual Property Organization (WIPO) patent landscape reports.
  4. Spanish Patent Law (Ley de Patentes), applicable statutory framework.
  5. Industry reports on pharmaceutical patent strategies in Spain.

Note: Specific details such as inventors, filing date, and precise claims should be verified through the official patent documentation for exhaustive accuracy.

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