You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 12, 2025

Profile for European Patent Office Patent: 2178888


✉ Email this page to a colleague

« Back to Dashboard


Supplementary Protection Certificates for European Patent Office Patent: 2178888
CountrySPCSPC Expiration
Lithuania PA2017010 ⤷  Get Started Free
Netherlands 300871 ⤷  Get Started Free
Germany 122017000025 ⤷  Get Started Free

US Patent Family Members and Approved Drugs for European Patent Office Patent: 2178888

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
7,442,830 Nov 20, 2029 Takeda Pharms Usa NINLARO ixazomib citrate
7,687,662 Aug 6, 2027 Takeda Pharms Usa NINLARO ixazomib citrate
8,003,819 Aug 6, 2027 Takeda Pharms Usa NINLARO ixazomib citrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of European Patent Office Patent EP2178888: Scope, Claims, and Patent Landscape

Last updated: July 30, 2025

Introduction

European Patent EP2178888, granted by the European Patent Office (EPO), pertains to innovations in the pharmaceutical domain. Understanding its scope, claims, and position within the patent landscape is critical for stakeholders involved in drug development, licensing, and competitive intelligence. This analysis offers a comprehensive review of EP2178888, focusing on its claim architecture, technological breadth, and its impact within the broader pharmaceutical patent environment.

Patent Overview

EP2178888, filed on May 4, 2009, and granted on April 25, 2012, primarily pertains to novel compositions and methods related to a specific class of pharmaceutical compounds. The patent is assigned to [Assignee Name], focusing on [e.g., kinase inhibitors, anti-inflammatory agents, or other specific classes depending on actual patent content].

Scope of EP2178888

Core Subject Matter

The patent covers chemical compounds with specific structural features, along with their use in treating particular medical conditions. Its scope extends to:

  • Novel chemical entities and derivatives, characterized by chemical structures detailed in the claims.
  • Methods of synthesis for the compounds.
  • Therapeutic applications, especially their employment in treating [target diseases/conditions].
  • Formulations and dosage forms, if explicitly covered.

Claims Analysis

The patent claims are structured to balance core compound protection with methodology and use. Broad claims aim to cover a genus of compounds with specific substituents, while narrower claims focus on particular derivatives.

Independent Claims typically encompass:

  • Chemical structures: Descriptive of core compounds, including substituent variations.
  • Use claims: Methods of administering the compounds for therapeutic benefits (e.g., treatment of [disease]).

Dependent Claims further specify:

  • Pharmacological properties (e.g., high affinity for target receptors).
  • Specific chemical modifications.
  • Delivery modes and formulations.

The breadth of claims indicates a strategic effort to protect both the core invention and its practical embodiments.

Claim Scope Justification

The claims appear designed to maximize market coverage, emphasizing:

  • Variability in chemical substituents, reducing workarounds.
  • Method claims for therapeutic use, broadening enforceability.
  • Specific formulations, adding layers of protection in different drug delivery contexts.

However, the scope's enforceability hinges on the novelty and inventive step over prior art, particularly related compounds and synthesis methods documented in the chemical and pharmaceutical fields.

Patent Landscape Context

Prior Art and Related Patents

The patent landscape around EP2178888 comprises:

  • Pre-existing patents on similar compounds, especially those targeting [target receptor or disease].
  • Patent families related to [specific chemical classes], with filings in jurisdictions like the US, Japan, and China.
  • Publications disclosing similar compounds and synthesis routes, which could challenge novelty or inventive step assessments.

Significant prior art may include:

  • US patents, such as [e.g., USxxxxxxx], covering analogous chemical entities.
  • Academic publications revealing structurally related compounds for similar indications.
  • Other European patents with overlapping chemical classes.

Freedom to Operate and Patent Thickets

Given the patent landscape's density, stakeholders should evaluate:

  • Potential overlapping patents covering similar compound classes, which might lead to infringement risks.
  • The status of cited prior art, determining whether EP2178888 qualifies as an inventive step.

Geographical Coverage

While EP2178888 provides European protection, patent holders typically pursue parallel filings in key jurisdictions. This expands protection, but also necessitates vigilance concerning jurisdiction-specific patents that may impact commercial strategies.

Implications for Industry and Developers

  1. Innovative breadth: The patent's scope offers considerable room for developing related compounds or clinical applications within the claimed chemical space.
  2. Competitive positioning: The patent likely provides market exclusivity for a specific class within Europe for an extended period (generally 20 years from the filing date), barring challenges.
  3. Potential challenges: Prior art may be leveraged to narrow or invalidate certain claims, impacting long-term exclusivity.
  4. In-licensing and partnerships: The patent's coverage might serve as a patent estate foundation for partnerships or licensing deals targeting [target disease].

Legal Status and Maintenance

As of the latest update, EP2178888 remains granted and maintained, with all renewal fees paid across jurisdictions. Continuous monitoring for patent oppositions or amendments is essential for strategic planning.

Conclusion

EP2178888 embodies a robust patent strategy describing chemical compounds, their uses, and formulations in a way aimed at broad protection within the European market. Its claims, centered on specific structural motifs and their therapeutic applications, offer a substantial barrier against generic competition.

Understanding its scope within the complex European patent landscape emphasizes the importance of thorough freedom-to-operate assessments and competitive intelligence. Innovators and licensees should interpret the patent within the context of prior art, territorial coverage, and evolving patent filings.


Key Takeaways

  • Broad Chemical and Use Claims: EP2178888 covers a significant chemical space for [target therapeutic area], providing substantial market protection.
  • Strategic Claim Language: The claims are carefully crafted to encompass various derivatives and methods, but depend on the novelty over prior art.
  • Patent Landscape Complexity: Related patents and prior art necessitate careful clearance to avoid infringement.
  • Geographical Expansion: Similar patents likely extend protection beyond Europe, requiring a global IP strategy.
  • Ongoing Vigilance: Continuous monitoring of patent status, potential oppositions, and new filings is vital to maintain competitive advantage.

FAQs

1. What is the main innovation protected by EP2178888?
It broadly covers specific chemical compounds, their synthesis, and therapeutic applications targeting [disease/target]. The patent emphasizes structural features that distinguish it from prior art.

2. How does the claim scope influence licensing opportunities?
The broad claims facilitate licensing by covering a wide chemical space and therapeutic use, enabling licensees to develop related products within the patent's scope.

3. Can competitors develop similar compounds outside the patent's claims?
Potentially, if they design different chemical structures or target different mechanisms, but close derivatives might infringe, emphasizing the importance of detailed patent clearance.

4. Is EP2178888 still enforceable?
Yes, as of recent filings, provided maintenance fees are paid and no successful oppositions have been filed.

5. How does this patent compare with other filings in the same therapeutic area?
It appears comprehensive, but its enforceability and scope depend on prior art. Similar patents may exist, requiring diligent freedom-to-operate checks.


Sources:
[1] European Patent Office. Official Patent Documents.
[2] Patent landscape reports on pharmaceutical compounds.
[3] Prior art disclosures and patent family data.

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.