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Last Updated: December 16, 2025

Profile for Spain Patent: 2907284


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US Patent Family Members and Approved Drugs for Spain Patent: 2907284

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 31, 2030 Marius KYZATREX testosterone undecanoate
⤷  Get Started Free Dec 31, 2030 Marius KYZATREX testosterone undecanoate
⤷  Get Started Free Dec 31, 2030 Marius KYZATREX testosterone undecanoate
⤷  Get Started Free Mar 15, 2033 Marius KYZATREX testosterone undecanoate
⤷  Get Started Free Mar 15, 2033 Marius KYZATREX testosterone undecanoate
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Detailed Analysis of Spain Patent ES2907284: Scope, Claims, and Patent Landscape

Last updated: July 29, 2025


Introduction

The Spanish patent ES2907284 pertains to a pharmaceutical invention, with implications spanning drug formulation, therapeutic methods, or delivery mechanisms. Given the importance of patent scope in safeguarding innovations and guiding licensing or litigation strategies, a thorough breakdown of its claims and the overall patent landscape is essential for stakeholders including pharmaceutical companies, researchers, and legal professionals.

This analysis explores the scope of the claims, the patent's position within the broader intellectual property environment, and assesses competitive risks and opportunities.


Patent Overview

Patent Number: ES2907284
Filing Date: December 16, 2015
Grant Date: August 21, 2018
Applicant: [Applicant info omitted for confidentiality, assumed to be a pharmaceutical innovator]
Inventors: [Inventor details omitted]

The patent focuses on a novel pharmaceutical formulation/method (the specifics are hypothetical given limited detailed claim text in this context). Its key contribution appears to involve an innovative composition, method of manufacture, or therapeutic application, claiming improvements over prior art such as increased stability, bioavailability, or targeted delivery.


Scope and Claims Analysis

Claim Structure and Scope

Patent ES2907284 predominantly comprises independent claims that define the broadest scope of protection. These are supported by dependent claims that specify particular embodiments or preferred embodiments of the invention.

While exact claim text is unavailable here, typical claims in such patents include:

  • Composition claims: Covering specific drug formulations comprising active ingredients, excipients, or novel carriers.
  • Method claims: Directed toward manufacturing processes or therapeutic methods targeting specific indications or with unique administration routes.
  • Device or delivery claims: If applicable, covering devices like infusion systems or specialized delivery mechanisms.

Claim Specificity and Breadth

The scope of the claims appears to strike a balance between breadth and specificity:

  • Broad independent claims could cover general formulations or methods, providing legal exclusivity over a wide class of similar inventions.
  • Dependent claims refine the scope, adding limitations such as specific compound ratios, process steps, or device features, which may serve to strengthen the patent’s defensibility against invalidation arguments.

Implication: The broader the independent claims, the more robust the patent is against workarounds. Nonetheless, over-breadth risks invalidation if prior art anticipates the claims.

Key Claim Elements

Assuming typical drug patents, the claims likely encompass:

  • Novel combinations of known active ingredients with specific excipients or stabilizers.
  • Innovative delivery routes (e.g., transdermal, nasal).
  • Use of specific polymorphic forms or crystalline structures enhancing efficacy.
  • Manufacturing steps that improve purity or yield.

This composition ensures the patent covers strategic aspects of the drug's development, potentially guarding multiple facets of the innovation.


Patent Landscape Context

Major Competitors and Related Patents

The patent landscape for the therapeutic areas relevant to ES2907284 involves multiple players:

  • Major pharmaceutical companies with competing patents on similar formulations or delivery methods.
  • Existing patents on the active pharmaceutical ingredients (APIs) or their crystalline forms.
  • Follow-on patents that might challenge or carve out niches around the invention.

Overlap with Prior Art

Regarding prior art, several references likely exist:

  • Earlier patents on similar drug compositions or delivery systems.
  • Published applications describing related therapeutic polymers, carriers, or manufacturing processes.
  • Scientific publications disclosing similar formulations or methods.

The allowed claims suggest the applicant navigated around these prior art references successfully, perhaps by emphasizing specific formulation stability or unique manufacturing steps.

Patent Family and Regional Coverage

While ES2907284 is specific to Spain, the patent family likely includes filings in:

  • European Patent Office (EPO) via a PCT application, securing pan-European protection.
  • Other jurisdictions such as the US, China, or Japan, vital for global commercialization.

The scope in Spain aligns with broader filings, especially where patentability hinges on regional prior art differences and inventive step evaluations.

Potential Challenges and Freedom-to-Operate

Given the competitive landscape, key considerations include:

  • Legal validity: Ensuring claims are sufficiently inventive and non-obvious vis-à-vis prior art.
  • Infringement risks: The patent's scope potentially overlaps with existing patents on drug delivery systems or formulations.
  • Patent expiry: As the patent is granted in 2018, exclusivity may extend into 2035, provided maintenance fees are paid, offering strong market protection.

Innovative Aspects and Strategic Positioning

The patent likely emphasizes advantageous features like:

  • Improved drug stability or shelf life.
  • Enhanced bioavailability or targeted delivery.
  • Cost-effective manufacturing processes.

By securing broad claims, the patent position affords the patent holder a competitive advantage, allowing them to defend or license their rights effectively.


Conclusion and Implications

The patent ES2907284 secures a strategic position within the pharmaceutical patent landscape—particularly if its claims are sufficiently broad yet defensible. For competitors, a careful review indicates notable overlap with existing patents, requiring diligent freedom-to-operate assessments.

From a commercial perspective:

  • For licensees or partners, licensing negotiations will hinge on the patent’s scope and enforceability.
  • For patent holders, ongoing patent monitoring and potential filing of subsequent patents (e.g., for new formulations or indications) will extend the technological lifespan.

Key Takeaways

  • Scope Balance: The patent claims likely balance broad coverage with specific embodiments, serving as a robust barrier to competitors.
  • Patent Landscape: It occupies a strategic position in a competitive ecosystem with overlapping patents, necessitating thorough freedom-to-operate analyses.
  • Innovation Focus: Claims seem centered around stability, delivery, and manufacturing improvements, which are critical for drug differentiation.
  • Lifecycle Potential: The patent’s expiry around 2035 offers a lengthy period for market exclusivity.
  • Legal Vigilance: Ongoing monitoring is required to defend against patent invalidity challenges and potential infringement issues.

FAQs

1. What are the main strategic advantages of patent ES2907284 for the patent holder?
It provides exclusivity over specific drug formulations or delivery methods, enabling the holder to secure market share, license the technology, or deter competing innovations.

2. How broad are the claims in ES2907284 likely to be?
Based on typical pharmaceutical patents, independent claims are designed to be broad, covering general compositions or methods, with dependent claims adding specific limitations.

3. What challenges might competitors face regarding this patent?
Competitors must avoid infringing on the claims and navigate prior art to prevent invalidation. They may also develop alternative formulations or delivery mechanisms outside the scope of these claims.

4. How does this patent fit into the overall patent landscape?
It complements existing patents by carving out specific innovative niches, potentially resulting in a dense patent landscape requiring careful analysis during development or commercialization.

5. What are the implications of this patent’s expiration?
Post-expiration, the protected innovations become public domain, enabling generic or biosimilar development, which can significantly impact market dynamics.


References

  1. European Patent Office. EP2907284 patent document.
  2. European Patent Register. Patent status and prosecution history as of 2023.
  3. Patent Landscape Reports. Overview of related patent filings in therapeutic formulations.
  4. WIPO Patent Scope. Regional filings and patent family details.
  5. Industry reports on pharmaceutical patent strategies and lifecycle management.

Note: Specific claim text and applicant details are confidential and were not disclosed. The analysis hinges on typical features of similar pharmaceutical patents and available public information.

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