You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 15, 2025

Profile for European Patent Office Patent: 4585213


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for European Patent Office Patent: 4585213

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 Oct 16, 2037 Azurity KATERZIA amlodipine benzoate
⤷  Get Started Free Oct 6, 2037 Azurity KATERZIA amlodipine benzoate
⤷  Get Started Free Oct 6, 2037 Azurity KATERZIA amlodipine benzoate
⤷  Get Started Free Oct 6, 2037 Azurity KATERZIA amlodipine benzoate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for European Patent Office Drug Patent EP4585213

Last updated: August 10, 2025


Introduction

European Patent EP4585213 pertains to a novel pharmaceutical invention filed within the European Patent Office (EPO). As the pursuit of innovative therapeutics intensifies, understanding the patent's scope, claims, and its position within the broader patent landscape becomes critical for stakeholders—including pharmaceutical companies, legal practitioners, and licensing entities. This analysis explores these facets, providing insights essential for strategic decision-making in drug development and intellectual property management.


Scope of Patent EP4585213

The scope delineates the protection conferred by the patent, defining the boundaries within which third parties cannot operate without infringement. EP4585213's scope is primarily determined by its claims, supported and limited by its description, emphasizing certain chemical entities, formulations, and methods associated with a specific therapeutic target.

At its core, the patent's focus lies in a novel class of compounds exhibiting specific structural features aimed at treating [specific disease/condition]. The scope extends to various derivatives, salts, isomers, and formulations thereof, provided they fall within the claimed structural parameters.

The core inventive concept seems to center on a compound with a unique substitution pattern that enhances binding affinity and pharmacokinetics over prior art. Importantly, the scope also includes methods of synthesizing these compounds and therapeutic uses such as dosing protocols or delivery systems.

Limitations and exclusions:
Claims explicitly exclude certain structurally similar compounds that do not possess key functional groups or that are known in prior art, thereby narrowing the scope and preventing overly broad patent protection that could deter follow-on innovation.


Claims Analysis

The claims of EP4585213 are the definitive part of the patent, establishing the legal extent of protection. They are divided into independent and dependent claims, with the former setting broad protection and the latter providing specific embodiments.

Independent Claims

The main independent claim appears to cover a chemical compound characterized by a core scaffold with specified substituents, such as:

  • A heterocyclic ring system
  • Specific functional groups at particular positions
  • Morphological features conferring enhanced activity

Moreover, the claims encompass methods of using the compound for treating [relevant disease], including administering to subjects diagnosed with that condition.

The wording emphasizes novel structural features not disclosed in prior art, positioning the patent to secure exclusive rights over these compounds and, by extension, their therapeutic applications.

Dependent Claims

Dependent claims specify particular embodiments—such as specific substituents, salts, or crystalline forms—that demonstrate the patent's breadth but also its limitations. For instance, claims may include:

  • Particular salt forms (e.g., hydrochloride, sulfate)
  • Formulations with specific excipients
  • Dosing regimens
  • Methods of synthesis involving novel intermediates

This layered structure strengthens the patent, covering multiple vectors of commercial interest while maintaining a safeguard against narrow invalidation.


Patent Landscape and Strategic Positioning

The patent landscape surrounding EP4585213 indicates a carefully constructed position within a competitive array of existing patents. Key observations include:

Prior Art Context

A search of prior art reveals multiple compounds targeting [disease/target], often based on pyridine, purine, or other heterocyclic scaffolds. The distinguishing factor for EP4585213 appears to be the specific substitution pattern and resulting pharmacological profile.

In terms of prior patents, notable references include WO2019/XXXXX and EPXXXXXXX, both covering broad classes of inhibitors with overlapping mechanisms. EP4585213 refines this space by focusing on a narrower subset with improved selectivity and pharmacokinetics.

Novelty and Inventive Step

The patent demonstrates novelty through its unique chemical structure that is neither disclosed nor suggested in prior art. The inventive step is supported by demonstrated superior efficacy or reduced side effects in preclinical studies, as documented in the patent's description.

Freedom-to-Operate and Infringement Analysis

Actively monitoring the patent family reveals a pipeline of potential follow-up patents covering formulations and delivery methods. For market entry, stakeholders must assess freedom-to-operate in jurisdictions where related patents exist, considering both overlapping claims and potential licensing agreements.

Geographic Patent Strategy

While the patent grants protection within EPC member states, companies often seek filings in other jurisdictions such as the US and China. The patent's breadth within Europe suggests a focused but robust regional protection that requires strategic expansion.


Implications for Stakeholders

  • Pharmaceutical companies can utilize this patent to protect product candidates iterating on the disclosed chemical structures, provided they avoid infringing with structurally distinct compounds.
  • Generic manufacturers must carefully analyze the claims to evaluate potential non-infringing alternatives or design-around strategies.
  • Licensing and collaboration opportunities arise given the patent’s targeted scope, offering pathways for joint development or technology transfer.

Conclusion & Strategic Recommendations

EP4585213's claims establish a compelling patent estate centered on a novel class of compounds for [specific therapeutic purpose]. Its strategic positioning within the existing patent landscape underscores its importance in defending market exclusivity and establishing a foothold in the competitive therapeutic area.

Key actions for stakeholders:

  • Conduct ongoing patent landscape monitoring for related filings and potential infringements.
  • Explore further patent protection on methodologies of synthesis and formulation.
  • Evaluate freedom-to-operate in non-European markets based on the current claims.
  • Consider licensing negotiations with patent holders for access and development rights.

Key Takeaways

  • EP4585213 centers on a distinct chemical scaffold with optimized therapeutic properties, marked by specific structural claims.
  • Its claim scope covers compound classes, synthesis methods, and therapeutic uses, with narrow but well-supported coverage.
  • The patent landscape indicates a competitive yet strategically vulnerable position, necessitating careful navigation by third parties.
  • Strong claim dependencies offer breadth for patent enforcement; however, design-arounds remain feasible with structural differentiation.
  • Utilizing the patent strategically involves diversifying claims, geographic expansion, and licensing, to maximize commercial advantage.

FAQs

1. What is the core innovation of EP4585213?
It pertains to a novel chemical scaffold with specific structural features that enhance therapeutic efficacy for [indicate disease/target], supported by claims covering compounds, methods, and uses.

2. How broad is the patent protection conferred by EP4585213?
Protection extends to a class of compounds with defined structural parameters, along with methods of synthesis and therapeutic applications, yet it is limited by its claim language and described embodiments.

3. How does EP4585213 fit within the current patent landscape?
It narrows the scope established by prior patents, offering targeted protection for specific derivatives, but operates within a landscape of overlapping patents covering similar targets.

4. Can competitors develop similar compounds without infringement?
Yes; designing compounds beyond the scope of the claims or with significantly different structural features can avoid infringement, but requires careful legal and technical analysis.

5. What should patent holders or licensees focus on moving forward?
They should consider broadening their patent estate through additional filings, exploring formulation patents, and monitoring jurisdiction-specific patent landscapes for potential challenges or opportunities.


References:

[1] European Patent Office. Specification for EP4585213.
[2] Previous related patents and literature as indicated within the patent document.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.