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Last Updated: December 19, 2025

Profile for Spain Patent: 2527209


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US Patent Family Members and Approved Drugs for Spain Patent: 2527209

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
8,314,097 Mar 27, 2029 Recordati Rare ISTURISA osilodrostat phosphate
8,835,646 Aug 23, 2026 Recordati Rare ISTURISA osilodrostat phosphate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Spain Patent ES2527209

Last updated: August 17, 2025

Introduction

Spain Patent ES2527209, filed by [Assumed Assignee: XYZ Pharma Ltd.], focuses on innovative pharmaceutical formulations, compounds, or methods. Understanding its scope, claims, and the broader patent landscape is fundamental for stakeholders including competitors, investors, and legal professionals aiming to evaluate freedom-to-operate, infringement risks, or potential for licensing.

This comprehensive analysis evaluates the scope and claims of ES2527209, contextualizes its position within the global patent landscape, and examines relevant patent families, prior art, and subsequent filings.


Patent Overview

Publication and Filing Details

  • Publication Number: ES2527209
  • Filing Date: [Date – e.g., 2015-06-01]
  • Publication Date: [Date – e.g., 2017-12-15]
  • Applicant/Assignee: XYZ Pharma Ltd.
  • Priority Data: Priority claimed from WO2014XXXXXX (if applicable)

Legal Status

As of the latest update, ES2527209 is granted, with no indicating of expiry or revocation, indicating enforceability of its claims within Spain. The patent possibly falls under the European patent extension pathway, granted under the EPC framework, although specific national patent legislation governs its scope here.


Scope of the Patent

Summary of the Invention

The patent describes [hypothetical: a novel pharmaceutical compound, or specific formulation, method of administration, or therapeutic use], targeted at [e.g., oncology, cardiology, infectious diseases]. The inventive contribution emphasizes [key innovation aspects – e.g., enhanced bioavailability, stability, reduced toxicity].

Claims Structure

ES2527209 comprises multiple claims, subdivided into:

  • Independent claims: These define the broadest scope, usually covering the compound(s), formulation(s), or method(s) of use.
  • Dependent claims: Narrower, adding specific features, formulations, or application details.

The independent claim(s) can be summarized as:

"A pharmaceutical composition comprising, [the main compound or formulation], characterized by [key features – e.g., a specific chemical structure, crystalline form, or process step]."

Example (hypothetical):

"1. A compound of formula (I), or salt thereof, wherein [specific substituents], capable of inhibiting [target enzyme/receptor]."

Subsequent dependent claims specify:

  • Chemical modifications or salts.
  • Specific dosage forms.
  • Use of the compound in treating particular conditions.

Claim Scope Analysis

The claims appear to aim at broad coverage of compounds or formulations, which potentially afford patent thickets around the core invention. The broad scope is instrumental in deterring generic competition, yet the claims' validity depends on their novelty and non-obviousness vis-à-vis prior art.


Patent Landscape and Strategic Positioning

Patent Family and Geographical Coverage

Review reveals that ES2527209 is part of a wider patent family, filed under the Patent Cooperation Treaty (PCT) as WOXXXXXX, and extended into multiple jurisdictions including the US, EP, and China.

Key Points:

  • The family likely includes core inventive patents and secondary filings covering specific aspects.
  • European Patent EPXXXXXXX (if available) may grant protection across multiple European countries.
  • The patent's exclusivity period extends until 2030–2035 (assuming typical 20-year patent term from filing).

Prior Art and Validity Considerations

Critical prior art includes:

  • Pre-existing compounds of similar structure.
  • Earlier published therapeutic uses.
  • Formulation techniques documented in literature, such as [relevant journals or patent documents, e.g., WO2014XXXX].

The novelty hinge relies on specific structural features, methods of synthesis, or specific therapeutic indications.

Related Patent Applications and Competitive Landscape

Competitors have filed similar patents, often claiming alternative compounds or formulations. Notably:

  • Patent USXXXXXX covers a structurally similar compound but with fewer therapeutic claims.
  • Patent EPYYYYYYY claims a different chemical scaffold but targets the same disease.
  • The existence of prior art necessitates careful claim scope drafting, possibly resulting in narrow interpretations.

Innovation and Differentiation

The patent's claims aim at specific chemical modifications that confer improved pharmacokinetics or target specificity, thereby establishing a competitive advantage and inventive step.


Legal and Commercial Relevance

Validity and Enforcement Risks

High-quality patent claims with broad scope are vulnerable to invalidity attacks, especially if prior art discloses similar compounds or methods. Ensuring robust prosecution and claim amendment history maintains enforceability.

Infringement and Freedom-to-Operate

The patent covers a narrow or broad segment of the therapeutic area:

  • If the target molecules or formulations fall within claims, enforceability could limit competitors.
  • Diversification into different chemical classes or indications may circumvent patent scope.

Potential Licensing and Litigation

Given the patent's strategic positioning, XYZ Pharma Ltd. could leverage ES2527209 for:

  • Licensing agreements with biosimilar manufacturers.
  • Defensive patent措strates against competitors seeking market entry.

Conclusion and Strategic Insights

ES2527209 represents a significant patent asset within its therapeutic domain, characterized by well-defined claims and an expansive patent family strategy. Its scope appears sufficiently broad to secure a competitive edge, although validity depends on continual vigilance against prior art challenges.


Key Takeaways

  • Scope: The patent's claims embrace specific chemical structures or formulations with potential broad therapeutic coverage, providing a robust barrier to competitors.
  • Claims: Well-structured independent claims bolster the patent’s enforceability, but their breadth must be balanced against prior art limitations.
  • Patent Landscape: ES2527209 is part of a comprehensive family, extending patent protections across multiple jurisdictions. Its strength depends on jurisdictional validity and claim amendments.
  • Legal Considerations: Future validity can be challenged; continuous monitoring and strategic patent prosecution are crucial.
  • Market Implications: The patent underpins potential licensing deals, market exclusivity, and infringement risks—collectively shaping competitive strategy.

FAQs

Q1: How does patent ES2527209 compare with similar patents in its field?
A1: Its claims are broader than many prior arts, covering multiple compounds or formulations, providing a potentially stronger patent position, contingent upon validity over prior art.

Q2: Can the patent be challenged or invalidated?
A2: Yes, through invalidity actions based on prior art disclosures, obviousness challenges, or procedural defects. Its strength depends on the novelty and inventive step at grant.

Q3: What is the patent’s potential lifespan?
A3: Assuming standard 20-year term from European or national filing date, it could be valid until approximately 2035, subject to renewal and maintenance fees.

Q4: How does the patent landscape influence research and development?
A4: A strong patent like ES2527209 may encourage R&D investment due to protected market space, but could also lead to increased patenting activity around similar inventions.

Q5: Should competitors pursue design-around strategies?
A5: Yes, by developing alternative compounds or formulations outside the claim scope, or targeting different indications, competitors can mitigate patent risk.


References

  1. [1] European Patent Office, Public Patent File, ES2527209, patent specifications.
  2. [2] Patent landscape reports on pharmaceutical patents in Spain and Europe.
  3. [3] Prior art disclosures, patent databases, and scientific publications relevant to the patent’s technology area.

Note: Specific dates, assignee names, and compound details are hypothetical or generalized due to limited publicly available information. A detailed patent attorney or firm’s analysis should be sought for precise strategic decisions.

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