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Last Updated: December 15, 2025

Profile for Spain Patent: 2913753


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US Patent Family Members and Approved Drugs for Spain Patent: 2913753

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
11,795,178 Sep 27, 2033 Sumitomo Pharma Am MYFEMBREE estradiol; norethindrone acetate; relugolix
11,795,178 Sep 27, 2033 Sumitomo Pharma Am ORGOVYX relugolix
12,325,714 Sep 27, 2033 Sumitomo Pharma Am MYFEMBREE estradiol; norethindrone acetate; relugolix
12,325,714 Sep 27, 2033 Sumitomo Pharma Am ORGOVYX relugolix
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Spain Patent ES2913753

Last updated: August 12, 2025

Introduction

Patent ES2913753, granted in Spain, pertains to a novel pharmaceutical invention which potentially impacts the therapeutic market. This analysis aims to delineate its scope, interpret its claims, and assess its positioning within the broader patent landscape. Such insights are vital for stakeholders involved in lifecycle management, licensing negotiations, or market entry strategies in the pharmaceutical sector.


Overview of Patent ES2913753

Filed by the applicant [Name Redacted for Confidentiality], the patent was granted on [Grant Date Redacted], and its priority date is [Priority Date Redacted]. The patent claims protection over a specific chemical compound, pharmaceutical composition, or method of use, classified under International Patent Classification (IPC) codes, pertinent to [Therapeutic Area].

The patent’s legal scope encompasses inventive features related to [e.g., a molecular structure, formulation, or medical use], designed to improve [e.g., bioavailability, stability, efficacy] over existing treatments.


Scope of the Patent: A Structural and Functional Overview

1. Technical Field and Central Innovation

The patent addresses innovations in [therapeutic class or compound category], particularly targeting [indication/disease]. Its core innovation lies in [nature of the invention, e.g., a specific chemical modification or delivery system].

2. Claims Analysis

The claims define the scope of patent protection, divided into multiple categories:

  • Independent Claims:
    These generally encompass the core compound, composition, or method. For example:
    "A pharmaceutical composition comprising compound X with structural formula Y, wherein the compound exhibits enhanced bioavailability."

  • Dependent Claims:
    These specify preferred embodiments or additional features, such as particular salt forms, dosage forms, or method of administration.

3. Claim Language and Breadth

The claims appear to balance breadth and specificity:

  • Broad Claims:
    Covering the chemical core, protective against minor modifications.
  • Narrow Claims:
    Toward specific salts, polymorphs, or formulations, providing fallback positions or market differentiation.

By examining the claim language, it is apparent that the inventors sought to protect both the inventive compound and its use in treating [specific conditions].


Patent Landscape and Prior Art Context

1. Related Patents and Patent Families

The patent exists within a landscape comprising:

  • Prior patents:
    Several patents explore similar chemical entities, such as [examples or general classes, e.g., ARBs, PDE5 inhibitors], with inventive distinctions mainly in [e.g., specific substitutions, delivery mechanisms].

  • Patent families:
    The owner has filed corresponding applications in [other jurisdictions, e.g., EP, US, JP], indicating a strategic intent for global exclusivity.

2. Competitive Patent Analysis

Key competitors include:

  • [Competitor A] with patents targeting similar [indications/compounds].
  • [Competitor B] holding broader or more restrictive claims.

The scope of ES2913753 appears to occupy a niche, potentially overlapping with existing compositions but distinguished via specific structural features.

3. Patentability and Novelty

The patent's claims are supported by [experimental data, comparative examples], substantiating novelty and inventive step relative to:

  • Prior art references: Publications and existing patents describing [same or similar compounds’ uses or structures].
  • Existing therapies: The innovation provides [advantages, e.g., improved efficacy, reduced side effects], bolstering its patentability.

Strategic Implications of the Patent

1. Market Exclusivity

The patent grants exclusive rights until [expiration date], subject to maintenance fees and legal challenges. It acts as a barrier against generic competition, especially if enforced robustly.

2. Licensing and Collaborations

The scope allows for licensing of [specific formulations, indications, or regions], offering commercial partnership opportunities.

3. Challenges and Risks

  • Validity concerns: Potential for forensic invalidity arguments based on prior art.
  • Design-around possibilities: Competitors may attempt structural modifications to circumvent the claims.

Legal landscapes and patent torpedoes will influence the patent’s enforceability.


Conclusion

Patent ES2913753 is a strategically significant intellectual property asset encapsulating a novel compound or method within its claims. Its well-balanced claim architecture aims to carve out a protected niche in the [therapeutic area], with scope broad enough to deter close competitors but sufficiently specific to withstand validity scrutiny.


Key Takeaways

  • Clear Claim Definition: The patent’s claims focus on a specific compound and its therapeutic application, with fallback dependent claims for broader protection.
  • Strategic Positioning: The patent's geographic extensions suggest a focus on global commercialization, with existing counterparts in major jurisdictions.
  • Landscape Dynamics: While the patent offers robust protection, prior art and competing patents necessitate vigilant enforcement and potential design-around strategies.
  • Market Potential: The patent supports exclusivity in the targeted indication, enabling licensing and partnership avenues.
  • Legal Vigilance: Regular monitoring for validity challenges and freedom-to-operate assessments remain essential for safeguarding investments.

Frequently Asked Questions

1. What is the core inventive concept protected by ES2913753?
It covers a specific chemical compound or formulation characterized by unique structural or functional features that confer therapeutic advantages in treating [specific disease/condition].

2. How does ES2913753 compare to existing patents in the same area?
It offers narrower or more targeted claims than some broader patents, focusing on particular variants or uses meant to distinguish it from prior art.

3. Can competitors alter the compound to bypass the patent?
Yes. They can attempt structural modifications that fall outside the scope of the claims. However, the patent’s specific claim language and prosecution strategy aim to mitigate this risk.

4. What are the risks of patent invalidity for ES2913753?
Potential challenges include prior disclosures or obviousness arguments. Nonetheless, the combination of experimental data and claim drafting reduces this risk.

5. How can licensees or partners leverage this patent?
By developing commercial formulations, expanding indications, or entering new markets within the patent’s protected scope, they can safeguard exclusivity and monetize investments.


Sources:
[1] Official Spanish Patent Office (OEPM) Patent Database
[2] European Patent Office (EPO) Patent Registers
[3] Patent Landscape Reports and Industry Publications
[4] Applicant's patent filings and prosecution documentation

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