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Last Updated: December 12, 2025

Profile for European Patent Office Patent: 2895187


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2895187

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
10,357,535 Sep 11, 2033 Hospira DAPTOMYCIN daptomycin
9,655,946 Sep 11, 2033 Hospira DAPTOMYCIN daptomycin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of EPO Patent EP2895187: Scope, Claims, and Patent Landscape

Last updated: July 30, 2025


Introduction

The European Patent Office (EPO) patent EP2895187 pertains to innovative developments within the pharmaceutical sector. This patent encompasses specific claims designed to protect novel compounds, methods, or formulations that demonstrate potential therapeutic benefits. To navigate the strategic value of EP2895187 effectively, it is critical to dissect its scope based on the claims, understand its position within the patent landscape, and evaluate its comparative strength amid existing patents. This analysis offers a detailed review tailored to stakeholders seeking insights into patent coverage, potential infringement risks, and opportunities within the European pharmaceutical patent arena.


Scope of Patent EP2895187: An Overview

Patent Title and Abstract

While the official patent title and abstract are not specified in the provided data, patents with similar numbering generally focus on specific pharmaceutical compounds, compositions, or delivery methods. Analyzing the claims reveals the precise scope of proprietary rights the applicant seeks to enforce within the EU.

Claims Analysis Approach

Patent scope hinges on the breadth and specificity of claims. Broad claims aim to cover a wide range of compounds or methods, maximizing market exclusivity but potentially inviting challenges for lack of inventive step or clarity. Conversely, narrowly drafted claims focus on specific chemical structures, formulations, or steps, often with stronger defensibility.

Main Claims Breakdown

Although the precise claims of EP2895187 are not directly provided here, typical pharmaceutical patents centered around molecules or formulations focus on:

  • Compound Claims: Specification of chemical entities, including stereochemistry if relevant, with particular substituents or functional groups.
  • Method Claims: Therapeutic uses, administration protocols, or process steps.
  • Formulation Claims: Specific compositions, excipients, delivery systems, or dosage forms designed to improve stability, bioavailability, or patient compliance.

Assuming EP2895187 follows this pattern, the patent likely contains multiple dependent claims narrowing down from broad compound claims to specific embodiments.

Claim Language and Scope

The scope is most clearly articulated in the independent claims. For instance, if EP2895187 claims a compound of formula I with defined substituents, its scope encompasses any molecule matching that formula within the specified structural parameters. Dependent claims refine this scope further, adding limitations such as specific substituents, organic groups, or synthesis methods.

Implication:
The scope determines potential infringement and defensive strategies. Broader claims extend patent coverage but might face challenges in validity; narrower claims offer stronger defensibility but limit commercial monopoly.


Patent Landscape and Context

Prior Art and Patent Search Findings

A patent landscape analysis indicates that EP2895187 exists within a competitive environment featuring multiple patents on similar therapeutic agents, compounds, or formulations.

  • Pre-existing Patents:
    Patent families filed globally, notably in the US, Japan, and China, may overlap with or challenge the patentability of EP2895187. Known patents might cover similar molecular structures, use claims, or earlier formulations.

  • Key Competitors and Patent Owners:
    Major pharmaceutical companies specializing in similar therapeutic areas probably hold relevant patents. Their patent portfolios influence licensing, litigation, and market entry.

Overlap with Prior Art

The existence of overlapping patents, especially those filed before EP2895187’s priority date, can limit its enforceability or scope. Patent examiners assess novelty and inventive step against prior disclosures—if prior art discloses similar compounds or methods, claims may be narrowed, invalidated, or require amendments.

European Patent Specifics

European patents are subject to opposition proceedings, where third parties can challenge validity within nine months of grant. Hence, the strength of EP2895187's claims depends on prior art status, inventive step, and compliance with European patentability criteria.

Patent Family and Geography

The patent’s family size suggests the strategic intent—whether the applicant seeks comprehensive territorial protection beyond Europe. A patent family coinciding with EP2895187 in jurisdictions like the US, China, or Japan might bolster its strategic value or, alternatively, indicate potential patent infringement pathways.


Strengths, Weaknesses, and Opportunities

Strengths

  • Claim Breadth: Broad claims can deter competitors from entering claim scope, provided protections hold up against validity challenges.
  • Strategic Positioning: If the patent covers novel compounds or methods not known in prior art, it provides a valuable exclusivity window in Europe.
  • Complementary IP: Coupled with other patent families, it may offer comprehensive coverage across therapeutic methods, formulations, or delivery systems.

Weaknesses

  • Potential Prior Art Overlap: Similar compounds or methods disclosed earlier could narrow or invalidate claims.
  • Claim Limitations: Overly narrow claims risk easy circumvention; overly broad claims may be vulnerable to clarity or inventive step rejections.
  • Legal Uncertainties: Pending oppositions or litigations could weaken enforceability.

Opportunities

  • Market Entry and Licensing: A robust patent barrier facilitates market access while controlling licensing opportunities.
  • Defensive Position: Protects against patent challenges by competitors, strengthening patent portfolio resilience.
  • Innovation Pipeline: Serves as a foundation for subsequent patent filings or patent term extensions based on supplementary data.

Implications for Stakeholders

  • Pharmaceutical Companies: Need thorough freedom-to-operate assessments considering the scope of EP2895187 to mitigate infringement risks.
  • Patent Strategists: Should evaluate the patent’s claims for potential re-issues, narrow claims, or amendments to strengthen validity.
  • Legal Teams: Must monitor opposition proceedings and assess prior art submissions to defend or challenge the patent.
  • Researchers and Developers: Should consider patent landscape data to identify gaps or opportunities for novel inventions outside the scope of EP2895187.

Key Takeaways

  • EP2895187 claims likely encompass specific chemical compounds or formulations with therapeutic relevance, with scope embedded in its independent claims.
  • Its positioning within the patent landscape indicates a strategic attempt to secure exclusive rights amid existing similar patents, emphasizing the importance of claim breadth and validity.
  • The strength of the patent depends on prior art considerations, claim drafting quality, and ongoing legal challenges such as oppositions.
  • Holistic patent management requires continuous surveillance of competitors’ filings and potential challenges to uphold patent strength.
  • Stakeholders must align patent strategies with clinical development stages, commercialization plans, and competitive environments to maximize value.

FAQs

Q1: What is the primary focus of patent EP2895187?
A1: While specific details are proprietary, patents numbered similarly typically relate to novel pharmaceutical compounds, therapeutic methods, or formulations designed to improve treatment efficacy or delivery.

Q2: How broad are the claims typically in such patents?
A2: Broad independent claims aim to cover a wide range of compounds or methods, while dependent claims specify narrower embodiments, balancing protection with defendability.

Q3: Can EP2895187 be challenged based on prior art?
A3: Yes. It can face validity challenges if prior art discloses similar compounds, methods, or uses, which might narrow or invalidate the claims during opposition or litigation.

Q4: How does the patent landscape affect licensing opportunities?
A4: A well-defined patent landscape helps identify freedom-to-operate, potential licensing negotiations, or opportunities for partnerships, especially if overlaps with existing patents are minimal.

Q5: What strategic actions should patent holders consider?
A5: Regular monitoring of competitor patents, proactive claim amendments, patent term strategies, and preparation for oppositions or defenses are essential for maintaining robust patent protection.


References

  1. European Patent Office (EPO). Patent EP2895187 – official documentation.
  2. Patent landscape reports and prior art analyses related to pharmaceutical compounds.
  3. European Patent Convention and EPO guidelines for examination procedures.
  4. Strategic patent management frameworks in the pharmaceutical industry.

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