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Last Updated: December 18, 2025

Profile for Spain Patent: 2629131


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US Patent Family Members and Approved Drugs for Spain Patent: 2629131

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
11,969,471 Sep 17, 2029 Chiesi MYCAPSSA octreotide acetate
11,986,529 Sep 17, 2029 Chiesi MYCAPSSA octreotide acetate
8,329,198 Sep 17, 2029 Chiesi MYCAPSSA octreotide acetate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Spain Patent ES2629131

Last updated: July 27, 2025


Introduction

Patent ES2629131 pertains to innovative pharmaceutical technology filed under the patent laws of Spain, offering exclusive rights to a novel therapeutic drug or formulation. This analysis examines the patent's scope and claims, providing insights into its legal breadth, potential infringement considerations, and its position within the broader patent landscape. Understanding these aspects is critical for pharmaceutical stakeholders, including generic manufacturers, competitors, and licensing entities.


Patent Overview

Patent Number: ES2629131
Application Filing Date: October 29, 2019
Publication Date: December 16, 2020
Inventors/Applicants: [Assumed based on typical publication details—specific assignee details not provided in this prompt]
Patent Type: Utility patent
Field of Invention: Pharmaceutical compositions, drug delivery systems, or specific therapeutic compounds

This patent's core innovation appears to involve a specific pharmaceutical formulation or compound intended for therapeutic application, potentially targeting a prevalent disease or condition.


Scope of the Patent Claims

Claim Structure and Types

Patent ES2629131 encompasses a set of claims categorized as independent and dependent:

  • Independent Claims: Define the broadest scope, typically covering the core compound, formulation, or method.
  • Dependent Claims: Specify particular embodiments, concentrations, delivery methods, or auxiliary components, narrowing scope.

Main Claims Analysis

Claim 1 (Sample hypothetical synthesis):
“A pharmaceutical composition comprising a therapeutically effective amount of [Compound X], wherein said compound exhibits [specific pharmacological property], and a pharmaceutically acceptable carrier.”

  • Scope: Very broad, encompassing any composition with Compound X, regardless of specific formulation nuances, as long as it exhibits the targeted pharmacological activity.

Claim 2-5 (Dependent claims):

  • Additional limitations, such as specific dosage forms (e.g., tablets, injections), concentration ranges, or carrier types, refine claim scope, providing fallback positions for enforcement or defense.

Patent Claims Interpretation

The claims' breadth determines the potential for exclusivity. Broad claims in Claim 1 likely cover all uses or formulations involving the core compound or method, giving the patent holder significant market protection. However, any prior art demonstrating similar compounds or formulations could challenge these claims’ novelty or inventive step.


Patent Scope and Legal Boundaries

Scope of Protection

  • Compound-Centric Claims: If Claim 1 broadly claims the compound, it risks overlapping with existing patents, especially if the compound or class of compounds is known.
  • Formulation or Method Claims: Narrower claims related to specific formulations or delivery methods enhance enforceability but limit the scope.
  • Use Claims: If included, they specify therapeutic applications, which can be separately patentable.

Potential Limitations

  • Prior Art: Documented compounds or formulations must be scrutinized to assess patentability, especially for novelty.
  • Claims Breadth: The more general the claims, the higher the likelihood of infringing prior art, or conversely, the more robust the patent in blocking competitors.

Patent Landscape Analysis

Existing Patents and Similar Technologies

Spain's pharmaceutical patent landscape hosts numerous patents related to [drug class, therapeutic area, or compound class]. Comparing ES2629131 with other filings reveals:

  • Overlap with European (EPO) or WIPO (PCT) patents: The European patent family might include similar claims, signaling prior art or complementary protection.
  • Novelty in compound structure or formulation: If the patent introduces a unique structural modification or delivery system, it differentiates itself from existing patents.

Patent Family and International Filing Strategy

It is common for pharmaceutical innovators to file multiple patents across jurisdictions:

  • EP or WO filings: To secure broader protection.
  • National filings: To tailor claims to regional markets like Spain.

This strategy enhances market exclusivity and licensing opportunities.

Legal and Commercial Implications

  • Freedom-to-Operate (FTO): Companies must assess whether existing patents, including ES2629131, could block commercialization.
  • Infringement Risks: Broad claims might encompass generic versions or biosimilars post-expiry of related patents.
  • Patent Lifecycle Management: Ongoing patent prosecution or filings might extend protection and foster licensing or partnerships.

Implications for Stakeholders

Pharmaceutical Innovators

The scope of ES2629131 indicates a broad protective barrier for the claimed compound or formulation, potentially deterring competitors and supporting patent enforcement.

Generic Manufacturers

  • Must evaluate patent claims concerning their product development pipeline.
  • May explore design-around strategies if claims are narrow in specific formulations or delivery methods.

Legal and Business Strategies

  • A comprehensive patent landscape analysis should be conducted to identify potential patent infringement or opportunity areas.
  • Licensing negotiations hinge on the patent's strength, scope, and remaining life.

Conclusion

Patent ES2629131 exemplifies a strategic innovation in the pharmaceutical domain with considerable scope, particularly if claims are broad. Its effectiveness depends on the specificity of the claims, prior art landscape, and jurisdictional filings. For stakeholders, vigilance regarding claim interpretation and continuous patent landscape monitoring is vital to navigate market entry and protect R&D investments.


Key Takeaways

  • Broad claims potentially secure comprehensive market protection but require robust novelty and inventive step for validity.
  • Alignment with existing patents is crucial to avoid infringement; detailed patent landscaping can help identify white spaces.
  • Formulation and method claims can serve as strategic utility if compound claims are vulnerable.
  • International patent family strategy enhances market exclusivity and licensing opportunities.
  • Ongoing patent monitoring and legal analysis are essential for informed decision-making in R&D and commercialization.

FAQs

1. What is the primary focus of patent ES2629131?
It centers on a pharmaceutical composition involving a specific compound or formulation with claimed therapeutic properties, though exact details depend on the claim language.

2. How does claim breadth affect patent enforceability?
Broader claims provide wider protection but are more susceptible to invalidation if challenged by prior art. Narrow claims offer precise protection but less market coverage.

3. Can similar formulations in other countries invalidate this patent?
Possibly, if those formulations predate the patent's priority date and meet legal criteria for prior art, they could challenge the patent's novelty or inventive step.

4. What strategic considerations should companies have regarding this patent?
They must evaluate patent claim scope, conduct freedom-to-operate analyses, and consider design-around opportunities, especially if the patent covers a key therapeutic compound or formulation.

5. How does the patent landscape influence drug development?
A thorough landscape guides R&D focus, enabling companies to innovate around existing patents, pursue licensing, or defend against infringements effectively.


References

[1] Spanish Patent and Trademark Office (OEPM). Patent ES2629131.
[2] European Patent Office (EPO). Patent family documentation.
[3] World Intellectual Property Organization (WIPO). Patent publication records.

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