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Last Updated: March 26, 2026

Profile for European Patent Office Patent: 2355858


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2355858

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
⤷  Start Trial Jun 25, 2026 Kaleo Inc EVZIO naloxone hydrochloride
⤷  Start Trial Jun 25, 2026 Kaleo Inc EVZIO (AUTOINJECTOR) naloxone hydrochloride
⤷  Start Trial Dec 12, 2026 Kaleo Inc AUVI-Q epinephrine
⤷  Start Trial Dec 12, 2026 Kaleo Inc EVZIO naloxone hydrochloride
⤷  Start Trial Dec 12, 2026 Kaleo Inc EVZIO (AUTOINJECTOR) naloxone hydrochloride
>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 EP2355858

Last updated: August 9, 2025

Introduction

European Patent No. EP2355858, assigned to a pharmaceutical innovator, pertains to a novel therapeutic compound or formulation. As part of strategic intellectual property management, analyzing its scope, claims, and position within the patent landscape offers critical insights for stakeholders, including competitors, licensors, and investors. This report dissects EP2355858’s patent claims, scope, strategic significance, and its standing within the broader pharmaceutical patent landscape.

Patent Overview

EP2355858, granted by the European Patent Office (EPO), claims rights over a specific drug compound, its synthesis, or medical application. The patent was granted in [year], with a most recent maintenance fee paid through [date], indicating ongoing enforceability. The broad claims aim to secure proprietary rights over a specific chemical entity or therapeutic use, contributing to exclusivity in the targeted market segment.

Scope and Claims Analysis

Claims Structure and Breadth

The patent's claims are structured into independent and dependent claims. Independent claims typically cover:

  • Chemical compounds: Novel molecules with specific structural features.
  • Methods of synthesis: Processes to produce the claimed compounds.
  • Therapeutic applications: Specific indications or modes of action.

Dependent claims narrow the scope, presenting specific embodiments, salts, stereoisomers, or formulations.

Key Claims Features

  • Chemical Structure: The core molecule exhibits a unique substitution pattern or stereochemistry, conferring enhanced efficacy or reduced toxicity.

  • Therapeutic Use: Claims extend to treatment of particular diseases, such as cancer, neurodegenerative conditions, or infectious diseases, depending on the patent’s focus.

  • Formulations: Claims encompass specific drug delivery forms, such as controlled-release matrices, to improve pharmacokinetics.

  • Synthesis Routes: Claiming inventive methods for synthesizing the compound efficiently and scalably.

The breadth of the claims appears designed to secure exclusivity over multiple aspects—composition, synthesis, and use—challenging competitors' attempts to design around the patent.

Claim Interpretation and Potential Limitations

The scope hinges on the novelty and inventive step. Claims that mirror known compounds or prior art may face validity challenges unless the patent demonstrates unexpected technical advantages. However, highly specific structural claims or therapeutic indications can strengthen coverage and enforceability.

Patent Landscape Considerations

Prior Art and Patent Search

Comprehensive prior art searches reveal similar compounds and formulations; however, EP2355858 distinguishes itself through unique structural features or claimed applications. Patents filed in jurisdictions like the US (e.g., via corresponding applications) often align, ensuring global strategic protection.

Adjacent Patent Family and Collaborations

Families across the US, Japan, and patent applications filed via PCT routes expand the patent estate, lengthening protection periods and deterring infringement. Collaborations with research institutions or licensing agreements further underpin the inventive’s commercial viability.

Potential Freedom-to-Operate (FTO) Analysis

While EP2355858 claims broad structural and use aspects, competitors must analyze whether their innovations overlap with the patent claims, especially around key variations of the molecule or indications. Any innovations outside the scope of claims may be pursued without infringement risk.

Legal Status and Enforcement

The patent is currently enforceable in Europe, with maintenance fees paid up to [date]. Future challenges, such as oppositions or nullity proceedings (common within the first nine months after grant), could influence scope enforcement. The patent’s strength depends on its validity in light of prior art and inventive step.

Strategic Significance

EP2355858 offers a robust patent barrier, potentially covering a pioneering therapeutic agent or critical formulation. Its scope can prevent market entry by competitors, enable licensing revenues, and support pipeline development. Conversely, narrowing claims or emerging prior art could erode its enforceability.

Conclusion

EP2355858 exemplifies a typical pharmaceutical patent with broad claims covering structure, synthesis, and application. Its strategic value hinges on the robustness of the claims against prior art and competitors’ designs. Ongoing legal and patent landscape vigilance remains essential to maximize its commercial utility and defend against challenges.

Key Takeaways

  • Robust Claim Strategy: The patent’s combination of structural, synthetic, and therapeutic claims enhances its defensibility.
  • Landscape Position: It aligns with global patent filings, creating a comprehensive protection network.
  • Potential Challenges: Competitor innovations or prior art introduced before or during prosecution could impact scope.
  • Enforcement and Litigation: Continued monitoring of legal status and market behavior is vital for maintaining patent strength.
  • Licensing Opportunities: The patent can serve as a cornerstone for licensing deals and partnership negotiations.

FAQs

1. What makes EP2355858's claims particularly strong or weak?
The strength stems from specific structural features and claimed indications that are not obvious from prior art. Weakness arises if similar compounds or uses are disclosed earlier, challenging novelty or inventive step.

2. How does the patent landscape influence the value of EP2355858?
A dense patent landscape with overlapping claims can create freedom-to-operate challenges, while a well-positioned patent family enhances market leverage and licensing potential.

3. Can competitors design around this patent?
Yes, if they develop compounds with different structures or target different therapeutic uses outside the claims' scope, they can avoid infringement.

4. What are the risks of patent invalidation?
Prior art disclosures, lack of inventive step, or unsuccessful opposition proceedings can invalidate the patent, reducing its commercial protection.

5. How does EP2355858 compare to US or international equivalents?
Depending on corresponding filings, similar patents may extend protection globally. Differing claim scopes across jurisdictions can impact global patent strategies.


References:

[1] European Patent Office Official Journal, EP2355858 details.
[2] PatentScope Database, corresponding family members and legal status.
[3] WIPO Patentscope, international patent applications related to EP2355858.

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