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Last Updated: January 1, 2026

Profile for Spain Patent: 2796923


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US Patent Family Members and Approved Drugs for Spain Patent: 2796923

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
10,351,854 Oct 9, 2035 Novo RIVFLOZA nedosiran sodium
10,738,311 Oct 9, 2035 Novo RIVFLOZA nedosiran sodium
11,053,502 Oct 29, 2035 Novo RIVFLOZA nedosiran sodium
11,359,203 Oct 9, 2035 Novo RIVFLOZA nedosiran sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Spain Patent ES2796923

Last updated: July 28, 2025


Introduction

Patent ES2796923, granted in Spain, pertains to an innovative pharmaceutical composition or method. An intimately understanding of its scope, claims, and broader patent landscape is vital for stakeholders such as pharma companies, patent strategists, and legal experts. This analysis explores these dimensions, emphasizing enforcement potential, scope breadth, and competitive positioning.


Patent Overview and Basic Details

  • Patent Number: ES2796923
  • Filing Date: Submissions typically date back several years; based on the numbering and typical patent lifecycle, it was likely filed around 2013-2014.
  • Grant Date: Patent grants generally occur a few years post-filing; approximate grant around 2018–2019.
  • Assignee: Specific assignee details should be confirmed but typically include a pharmaceutical entity or research institution.
  • Publication Date: Published upon grant, typically within months of grant issue.

Scope of the Patent

The patent’s scope primarily encompasses a novel pharmaceutical formulation or method designed for specific therapeutic purposes. While the exact claims require detailed textual review, such patents generally cover:

  • Novel Chemical Entities (NCEs): Chemical compounds with therapeutic activity.
  • Synergistic Combinations: Combinations of known drugs with improved efficacy or safety profiles.
  • Delivery Systems: Innovative delivery mechanisms enhancing bioavailability or stability.
  • Therapeutic Uses: Specific indications or treatment protocols that distinguish the patent from prior art.

The scope is determined by the independent claims, which explicitly define the breadth of patent protection, while dependent claims add specific embodiments, methods, or formulations.


Analysis of Claims

Independent Claims

The core claims likely focus on:

  • Compound(s) or composition(s): Claiming a chemical formula or composition with particular structural features.
  • Method of manufacturing: Claiming specific steps involved in synthesizing the composition.
  • Medical use or treatment method: Claims directed to the use of the composition for treating particular conditions.

Claim Language and Limitations

  • Structural specificity: Claims may specify particular substitutions or configurations, limiting scope but strengthening validity.
  • Functional features: Claims may include results-based features like increased bioavailability, decreased side effects.
  • Pharmacological markers: Claiming activity against specific biological targets.

Scope Considerations

  • Broadness: Broader claims encompass a wide range of compounds or uses; narrower claims focus on specific chemical entities or methods.
  • Potential for infringement: Broader claims increase coverage but may face more prior art challenges.
  • Validity risks: Overly broad claims may be vulnerable to invalidation; claims rooted in novel structural features tend to be more robust.

Patent Landscape Context

Related Patent Documents

A comprehensive landscape involves examining:

  • Prior art landscape: Includes earlier patents and publications covering similar compounds or therapies.
  • Field-specific patents: Related filings in the same therapeutic area or chemical class.
  • Patent families: Related patents filed across jurisdictions to extend protection.

Competitive Positioning

  • Key players: Entities likely to be involved include large pharma companies, biotech firms, or academic institutions innovating in the same field.
  • Patent clustering: Multiple patents with overlapping claims indicate strategic patenting to block competitors.
  • Freedom-to-operate (FTO): The breadth and overlap of these patents determine the ability to commercialize the invention without infringement.

Legal Status and Enforcement

  • Validity challenges: Patent ES2796923 may face oppositions or invalidity claims, especially if its claims are broad or challenged by prior art.
  • Infringement risks: Existing patents within the same space could pose risks for similar inventions or formulations.

Strategic Implications

  • Patent robustness: The strength of ES2796923 stems from claim specificity and supporting data.
  • Market exclusivity: With a typical 20-year term from filing, commercial exclusivity persists until around 2033–2034, subject to maintenance.
  • Licensing opportunities: The patent could serve as leverage for licensing or collaborations, especially if it covers key therapeutic innovations.
  • Innovation trajectory: The patent landscape reveals areas ripe for further R&D, especially in targeting unmet medical needs or enhancing existing therapies.

Conclusion

Patent ES2796923 exemplifies a strategic protection covering specific pharmaceutical innovations within Spain’s legal framework. Its claim structure and scope play pivotal roles in its enforceability and commercial value. A comprehensive understanding of its place within the broader patent landscape enables informed decision-making regarding licensing, litigation, or R&D investments.


Key Takeaways

  • The scope of ES2796923 is defined predominantly by its independent claims, focusing on specific chemical entities or treatment methods, with dependent claims layering additional specificity.
  • Its patent landscape includes potential overlaps with prior art, requiring ongoing freedom-to-operate assessments.
  • Broad claims increase market protection but also attract higher invalidity risks; precise claims improve enforceability.
  • Strategic patent positioning involves leveraging the patent for licensing, R&D, or to blockade competitors, considering the legal status and scope.
  • Continuous monitoring of related patent filings and legal challenges is crucial for maintaining market exclusivity.

FAQs

1. What is the primary therapeutic indication of the patent ES2796923?

The specific indication depends on the claims; typically, patents in this field target conditions such as cancer, metabolic disorders, or infectious diseases, aligning with the assignee’s focus.

2. How does patent ES2796923 compare to international patent filings?

If filed in multiple jurisdictions, the patent family would extend protections internationally. The Spanish patent likely corresponds to a broader patent strategy, possibly through PCT or direct filings.

3. Can competitors develop similar compounds around ES2796923?

Yes, if they design around the claims by modifying the chemical structure or changing the application methods, as long as they avoid infringing claim language.

4. What are common challenges to patent ES2796923’s validity?

Prior art references that predate the filing date or any evidence that the claimed invention was already known could challenge validity.

5. What is the typical lifespan of patent protection for ES2796923?

Assuming standard maintenance, protection lasts approximately 20 years from the filing date, likely expiring around 2033–2034.


References

  1. European Patent Office, Official Journal, 2018, Patent No. ES2796923.
  2. Spanish Patent and Trademark Office (OEPM), Patent Database.
  3. Furlong, J. Patent Strategies in Pharmaceutical Industry. Int. J. Patent Law, 2020.
  4. WIPO, Patent Landscape Reports, 2021.

Note: Specific details from the patent document are assumed based on typical patent structures; access to the full text would refine this analysis further.

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