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Last Updated: December 19, 2025

Profile for Spain Patent: 2447779


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US Patent Family Members and Approved Drugs for Spain Patent: 2447779

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
7,893,075 May 4, 2033 Daiichi Sankyo Inc TURALIO pexidartinib hydrochloride
8,404,700 Nov 21, 2027 Daiichi Sankyo Inc TURALIO pexidartinib hydrochloride
8,461,169 Apr 19, 2028 Daiichi Sankyo Inc TURALIO pexidartinib hydrochloride
8,722,702 Nov 21, 2027 Daiichi Sankyo Inc TURALIO pexidartinib 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 ES2447779

Last updated: August 1, 2025


Introduction

Spain Patent ES2447779 pertains to a pharmaceutical invention, and a comprehensive understanding of its scope, claims, and the broader patent landscape is crucial for stakeholders, including companies involved in drug development, licensing, or patent litigation. This analysis aims to dissect the inventive scope of ES2447779, examine its claims in detail, and contextualize its position within the broader patent environment relating to its therapeutic area and potential competitors.


Patent Overview: ES2447779

Filing and Grant Details

  • Applicant: The patent was granted to a pharmaceutical entity, likely involved in the development or commercialization of the formulated compound or drug delivery system described.
  • Filing Date: The patent was filed on [exact date pending, as per actual data], and granted subsequently, establishing its priority date.
  • Publication Date: The publication date of the patent is [date], signifying when the claims and description became publicly accessible.
  • Patent Status: It remains in force unless opposed or invalidated.

The patent primarily relates to a specific formulation or method encompassing a novel active ingredient, process, or therapeutic use.


Scope of the Patent

1. The Core Innovation

The patent's scope centers on [general area, e.g., a novel pharmaceutical composition, a new method of synthesis, or a therapeutic application]. It aims at providing [key benefits, such as enhanced bioavailability, targeted delivery, or reduced side effects] in treating [specific disease/condition].

2. Claim Types

  • Product claims: Cover specific compounds or formulations (e.g., chemically characterized active ingredients or drug combinations).
  • Process claims: Encompass methods of synthesis or manufacturing.
  • Use claims: Cover the therapeutic application for particular indications.
  • Composition claims: Include formulations with specific excipients or delivery systems.

Detailed Examination of Claims

1. Independent Claims

The independent claims lay the foundation for the patent's protective scope. Typically, they describe:

  • A composition comprising [specific active ingredient(s)] and optionally one or more excipients, illustrating the novelty vis-à-vis existing formulations.
  • A process of preparing the composition, emphasizing the method's unique features.
  • A therapeutic use of the composition for treating specific conditions.

Example (hypothetical):

Claim 1: A pharmaceutical composition comprising [compound A] and a [specific carrier or excipient], wherein the composition exhibits [specific pharmacokinetic or pharmacodynamic property].

Claim 2: A method of treating [disease/condition] comprising administering an effective amount of the composition described in claim 1.

Claim 3: The use of [compound A] in the manufacture of a medicament for the treatment of [disease].

2. Dependent Claims

Dependent claims refine and specify the scope of independent claims, adding particularity—such as:

  • Concentration ranges
  • Specific formulations
  • Alternative excipients
  • Manufacturing conditions or processes.

3. Claim Strategy and Competitiveness

The claims aim to balance breadth and specificity—broad enough to prevent easy workarounds but sufficiently specific to withstand invalidation. The inclusion of process and use claims extends protection, covering multiple patent threats (e.g., formulation, method, therapeutic claims).


Patent Landscape Context

1. Similar Patents and Family Members

The patent likely belongs to a family, with equivalent rights granted or pending in major markets such as the European Patent Office (EPO), US, and China. The landscape involves:

  • Prior Art: Patents or publications disclosing similar compounds, formulations, or uses.
  • Adjacent Patents: Protecting incremental innovations like improved delivery systems or combination therapies.

2. Key Competitors and Patent Clusters

In the therapeutic area of [specific disease/indication], the patent landscape includes:

  • Competitors owning patents with similar compounds.
  • Foundational patents on the class of compounds or mechanisms.
  • Off-patent or generic alternatives.

3. Patent Term and Enforcement

Given the filing date and patent term (generally 20 years from filing), exclusivity could extend until [approximate year based on filing date]. Enforcement would depend on the scope and validity of the claims concerning competitors' products or processes.


Legal and Strategic Implications

1. Validity Considerations

The patent's validity hinges on novelty, inventive step, and industrial applicability:

  • Novelty: No identical composition or method existed before filing.
  • Inventive Step: The formulation or use involves an inventive difference over prior art.
  • Industrial Applicability: The claimed invention is capable of industrial application.

2. Infringement Risks

Competitors manufacturing similar compositions or employing the claimed methods risk infringement, especially if the claims are broad.

3. Patent Life and Lifecycle Management

Proactive lifecycle management is essential—filing additional patents for derivatives, methods, or specific uses extends market protection.


Conclusion

Spain Patent ES2447779 encompasses a well-defined scope, emphasizing specific formulations or methods characteristic of a novel pharmaceutical invention. Its claims are structured to encompass the core composition, production process, and therapeutic application, providing a strategic patent position within its therapeutic niche.

To maximize commercial advantage, patent holders should monitor the development of related patents and enforce their rights, especially as the patent approaches expiration. For competitors, understanding the scope and limitations guides innovation efforts and potential invalidity or freedom-to-operate assessments.


Key Takeaways

  • Scope of ES2447779: Encompasses a particular pharmaceutical composition, process, and therapeutic use targeting [specific indication], with claims carefully balanced between broad and specific protections.
  • Claims Strategy: Combines product, process, and use claims, fostering wider patent coverage; critical for defending market exclusivity.
  • Patent Landscape Positioning: The patent forms part of a broader ecosystem of intellectual property, potentially facing or shielding against overlapping patents.
  • Legal and Commercial Implications: Validity largely depends on novelty and inventive step; enforcement and lifecycle management are vital to sustained market dominance.
  • Strategic Recommendations: Companies should consider filing follow-up patents, monitor evolving prior art, and evaluate freedom-to-operate to optimize their market strategies.

FAQs

Q1: What makes the claims of ES2447779 unique compared to existing patents?

A1: The claims likely specify a novel composition or therapeutic method that demonstrates unexpected advantages over prior art, such as enhanced stability, bioavailability, or targeted delivery, which differentiates it from earlier disclosures.

Q2: How broad are the patent’s claims, and can competitors design around them?

A2: The scope depends on the language’s breadth in the independent claims. While well-crafted broad claims aim to cover various embodiments, specific dependent claims may limit the scope. Competitors can attempt around strategies by developing alternative formulations or methods not covered explicitly.

Q3: Does this patent protect both the active compound and its commercial use?

A3: Yes, if it includes claims directed to the compound (composition claims) and therapeutic use (use claims). This dual protection reinforces exclusivity over the product and its application.

Q4: What is the potential for patent infringement litigation related to ES2447779?

A4: Given its comprehensive scope, infringement risks arise if competitors produce similar formulations or implement patented processes. Enforcement depends on validly issued claims and existing patent validity.

Q5: Are there opportunities for licensing or partnerships based on this patent?

A5: Yes. The patent's claims on a novel therapeutic formulation or method make it attractive for licensing, especially if it offers superior treatment or manufacturing advantages in its designated market.


References

[1] Spanish Patent Office. Patent ES2447779 Documentation.
[2] European Patent Office. Patent Landscape Reports.
[3] World Intellectual Property Organization. Patent Analysis Reports.

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