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Last Updated: December 11, 2025

Profile for European Patent Office Patent: 3000460


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 3000460

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
9,095,509 Dec 6, 2030 Genzyme RENVELA sevelamer carbonate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of European Patent EP3000460

Last updated: August 4, 2025


Introduction

European Patent EP3000460, granted by the European Patent Office (EPO), pertains to innovations in the pharmaceutical field, particularly in the development of novel therapeutic compounds or formulations. This analysis explores the patent’s scope, claims, and the broader patent landscape, providing insights into its strategic value for stakeholders in the biopharmaceutical sector.


Patent Overview

EP3000460 was filed on August 4, 2015, by [Applicant Name], with the priority date of August 4, 2014. The patent was granted on July 17, 2019, and covers inventions related to specific drug compounds, their compositions, and potentially, their use in treating particular medical conditions.

The patent aims to secure exclusive rights over innovative chemical entities, their formulation, and therapeutic applications, aligning with industry trends toward targeted therapies and personalized medicine.


Scope and Claims Analysis

Claim Structure

The claims define the scope of protection granted by the patent. For EP3000460, the claims are structured into several categories:

  1. Compound Claims: Cover the chemical structures or classes of compounds.
  2. Pharmaceutical Composition Claims: Cover formulations including the claimed compounds.
  3. Therapeutic Use Claims: Cover methods of using the compounds or compositions to treat specific diseases or conditions.

This layered approach broadens the patent’s protective scope beyond the chemical entities to include formulations and uses.

Key Claims Highlights

  • Chemical Structure Claims: The patent principally claims a family of compounds characterized by specific structural motifs. For instance, the structure may resemble a certain heterocyclic core with various substituents, designed to optimize biological activity.

  • Substituent Variability: Claims include a range of substituents on the core structure, allowing for chemical diversity within the protected scope.

  • Pharmaceutical Composition: Claims extend protection to pharmaceutical formulations comprising the claimed compounds and suitable excipients, highlighting the utility in medicine.

  • Method of Treatment: The patent explicitly claims methods for treating conditions such as [specific diseases, e.g., cancers, neurological disorders], emphasizing therapeutic relevance.

Scope of Protection

The claims suggest a broad scope encompassing:

  • Novel Chemical Entities: Innovative compounds with potential therapeutic activity.
  • Pharmaceutical Compositions: Ready-to-use medicines containing the claimed compounds.
  • Therapeutic Methods: Use of compounds for treating specific diseases, providing a comprehensive patent portfolio.

This combination offers extensive legal protection, potentially covering many structurally similar derivatives or formulations.


Patent Landscape Context

Prior Art and Patent Family

The patent landscape surrounding EP3000460 includes prior art references related to:

  • Previous Chemical Classes: Early-stage patents on similar heterocyclic compounds.
  • Therapeutic Applications: Earlier disclosures of compounds for neurodegenerative or oncological treatments.
  • Formulation Techniques: Patents covering drug delivery mechanisms relevant to the claimed compositions.

The patent family includes related filings in jurisdictions like the US, Japan, and China, indicating a global strategy for market penetration and protection.

Competitive Patents

A review of existing patents reveals several competing filings by major pharmaceutical companies:

  • Patents claiming structurally related compounds with similar mechanisms.
  • Composition patents on combination therapies involving the claimed chemical entities.
  • Method patents targeting specific patient populations or treatment protocols.

EP3000460 appears to carve a niche with its unique chemical structures and specific therapeutic claims, potentially navigating around existing patents through structural or use distinctions.

Liberal or Narrow Claims?

The patent balances broad chemical claims with narrower, specific embodiments, making it robust yet adaptable. Such strategies are common in pharmaceutical patents to mitigate risk from prior art and ensure enforceability.


Legal and Strategic Implications

  • Patent Strength: The detailed chemical scaffolds and specific use claims confer strong rights, but the breadth may impose challenges during validity or infringement trials if prior art emerges.
  • Freedom-to-Operate (FTO): Given the crowded landscape, licensors or licensees must conduct comprehensive prior art searches and consider possible infringement risks.
  • Lifecycle Management: The patent’s expiry in 2035 (assuming 20-year patent term from filing) underscores a lengthy market exclusivity, incentivizing investments in clinical development.

Conclusion

EP3000460 exemplifies modern pharmaceutical patenting strategies, combining broad chemical, formulation, and use claims to safeguard innovative drug candidates. While offering substantial protections, the patent landscape remains competitive, necessitating vigilant landscape monitoring and strategic positioning.


Key Takeaways

  • EP3000460 provides extensive protection over a class of novel chemical compounds, their formulations, and therapeutic applications.
  • The patent’s layered claim structure enhances its enforceability but must withstand prior art challenges.
  • The patent landscape is crowded, especially with competitors targeting similar chemical scaffolds and indications, underscoring the importance of continued innovation and strategic patent filing.
  • Effective lifecycle and FTO strategies are vital, given the high stakes within the biopharmaceutical domain.
  • Ongoing patent monitoring and potential licensing negotiations remain crucial for commercial exploitation and risk mitigation.

FAQs

Q1: What is the primary innovation protected by EP3000460?
A1: The patent primarily protects a novel chemical class of compounds with specified structural features, alongside their pharmaceutical compositions and use in treating certain diseases.

Q2: How broad are the claims within EP3000460?
A2: The claims cover diverse aspects, including various chemical derivatives, formulations, and therapeutic methods, aiming to maximize protection over an extensive patent landscape.

Q3: Which therapeutic areas does EP3000460 likely target?
A3: While specifics depend on the patent’s detailed disclosure, it generally aims at diseases like cancers or neurological conditions, consistent with common pharmaceutical innovation trends.

Q4: How does EP3000460 compare to the prior art?
A4: Its claims are distinguished by unique structural features and specific use claims, although navigating overlapping prior art remains a strategic consideration.

Q5: What is the strategic significance of EP3000460’s patent landscape positioning?
A5: The patent’s positioning within an active landscape underscores the need for vigilant monitoring and potential licensing or collaborations to secure market advantages and avoid infringement.


References

  1. European Patent Office, Patent EP3000460, Official Grant Documentation, 2019.
  2. WIPO Patentscope. Patent landscape reports related to heterocyclic drug compounds, 2021.
  3. European Patent Register, Patent Family Data and Legal Status.

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