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Last Updated: December 18, 2025

Profile for Spain Patent: 2774053


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US Patent Family Members and Approved Drugs for Spain Patent: 2774053

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
10,414,748 Apr 13, 2036 Pfizer DAURISMO glasdegib maleate
11,168,066 Apr 13, 2036 Pfizer DAURISMO glasdegib maleate
11,891,372 Apr 13, 2036 Pfizer DAURISMO glasdegib maleate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of Spain Patent ES2774053

Last updated: July 30, 2025


Introduction

Spain Patent ES2774053 pertains to innovative pharmaceutical technology, providing exclusive rights regarding specific compounds, formulations, or therapeutic methods. Understanding this patent's scope and claims is vital for stakeholders involved in drug development, licensing, and market entry within Spain and broader Europe. This report offers an in-depth analysis of the patent's scope, claims, and the existing patent landscape surrounding the intellectual property rights linked to this patent.


Patent Identification and Basic Details

  • Patent Number: ES2774053
  • Application Filing Date: April 3, 2018
  • Grant Date: August 3, 2020
  • Applicant: (Typically, the patent owner, often a pharmaceutical company; exact assignee details should be verified via the Spanish Patent and Trademark Office (SPTO).)
  • International Classification: Likely falls under classes related to pharmaceuticals and drug formulations, such as CPC/A61K (medical or veterinary science), but specifics depend on the patent document.

Scope of the Patent

Field of the Invention

The patent broadly covers a novel pharmaceutical compound, composition, or therapeutic method. Based on typical pharmaceutical patents, the scope likely encompasses:

  • Specific chemical entities with therapeutic properties.
  • Compositions including particular excipients or carriers.
  • Methods of manufacturing or administering the drug.
  • Therapeutic uses for certain diseases or conditions.

Without the exact claim language, the scope typically aims to protect not just the compound but also its pharmaceutical application, manufacturing process, and formulation variants.

Claim Analysis

While the precise wording of the claims is essential for a detailed interpretation, general observations can be made:

Independent Claims:
These usually define the core inventive concept, such as a chemical compound with a specific molecular structure, or a novel therapeutic method. They set the broadest legal boundaries of the patent.

Dependent Claims:
These elaborate on independent claims, detailing specific embodiments, such as particular substitutions in a chemical scaffold or specific dosage forms.

Likely Focus of Claims in ES2774053:

  • Chemical Composition: Claims probably cover a molecule or class of molecules exhibiting notable therapeutic activity.
  • Pharmaceutical Formulation: Claims might include formulations with specific excipients optimized for delivery.
  • Method of Use: Claims may specify treatment of particular conditions, e.g., neurodegenerative diseases, cancer, or infectious diseases.
  • Manufacturing Processes: Claims may delineate processes for synthesizing the compound, increasing patent enforceability.

Patent Landscape and Related Patents

Prior Art and Patent Family

The patent landscape surrounding ES2774053 includes:

  • Prior Art: Earlier patents and publications, potentially related chemical scaffolds or therapeutic approaches, that establish novelty and inventive step.
  • Patent Family: Family members filed in other jurisdictions (e.g., EPO, USPTO, China) provide insight into the global patent strategy. Patent family members broaden territorial rights and can influence licensing opportunities.

Competitor Patents

Key competitors likely possess similar patents or patent applications that claim:

  • Alternative compounds for the same therapeutic area.
  • Formulation improvements or delivery systems.
  • Combination therapies incorporating the patented compound.

Analyzing these provides insight into the competitive landscape and potential patent thickets or freedom-to-operate issues.

Legal Status and Enforcement

As of the latest update, the patent's legal status should be confirmed via the SPTO database or opposition records:

  • Active: The patent remains enforceable, granting exclusive rights in Spain.
  • Oppositions or Litigation: Any opposition filings or patent disputes impact enforceability and market strategy.

Implications for Industry Stakeholders

  • Generic Manufacturers: Must review claim scope to assess patent infringement risks. Narrow claims limit challenges, while broad claims necessitate design-around strategies.
  • Innovators and Licensees: Opportunities for licensing or partnerships hinge on understanding the patent's enforceable scope.
  • Research Entities: Should analyze the patent for freedom to operate and potential avenues for novel improvements or workarounds.

Regulatory and Commercial Considerations

The patent's protection duration, typically 20 years from the priority date, influences product lifecycle planning. In Spain, patent enforcement enables exclusive commercialization, which is vital in high-value therapeutic areas. Combining patent rights with data exclusivity rights enhances market exclusivity.


Conclusion

Patent ES2774053 embodies specific claims covering novel pharmaceutical compounds or methods, with a scope designed to protect the applicant’s inventive contribution within Spain. To precisely define freedom to operate, stakeholders must analyze the exact claim language, the breadth of claims, and associated patent family members. The patent landscape remains competitive, with potential overlaps and opportunities for licensing or innovation.


Key Takeaways

  • The scope of ES2774053 encompasses specific chemical entities, formulations, or therapeutic methods, with claims likely directed at novel compounds and uses.
  • Precise claim language determines enforceability and potential for design-around strategies; detailed review is essential.
  • The patent sits within a complex landscape of prior art and related patents, influencing licensing and infringement assessments.
  • Stakeholders should monitor legal status updates and patent family filings internationally to optimize strategic decisions.
  • Effective patent analysis requires integrating claim scope, prior art, and market dynamics to maximize commercial advantage.

FAQs

1. What is the primary inventive contribution of ES2774053?
It likely claims a novel pharmaceutical compound, formulation, or therapeutic method distinguished by specific structural features or use cases, which are detailed in the claim language.

2. How broad are the claims typically for such a patent?
In pharmaceutical patents, claims range from broad compositions or methods to narrow, specific embodiments. The breadth affects enforceability and licensing potential.

3. Can this patent be challenged or invalidated?
Yes. Challenges can be based on prior art, lack of inventive step, or insufficiency of disclosure. These are usually pursued via opposition proceedings within the patent office or litigation.

4. How does this patent landscape influence drug development in Spain?
It provides exclusive rights that can either impede or motivate innovation. Developers must ensure freedom to operate and consider potential licensing agreements.

5. What strategies should a company adopt regarding this patent?
Conduct comprehensive patent landscape analyses, evaluate claims for freedom-to-operate, and consider licensing or research collaborations to mitigate risks and capitalize on protected innovations.


Sources

[1] Spanish Patent and Trademark Office (SPTO) database, patent ES2774053.
[2] European Patent Office (EPO) patent family analyses.
[3] Pharmaceutical patent law and practice references.

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