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

Last Updated: December 16, 2025

Profile for European Patent Office Patent: 2350096


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for European Patent Office Patent: 2350096

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
10,314,828 Jul 24, 2029 Salix Pharms XIFAXAN rifaximin
10,335,397 Jul 24, 2029 Salix Pharms XIFAXAN rifaximin
10,709,694 Jul 24, 2029 Salix Pharms XIFAXAN rifaximin
7,928,115 Jul 24, 2029 Salix Pharms XIFAXAN rifaximin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for European Patent No. EP2350096

Last updated: July 31, 2025


Introduction

European Patent No. EP2350096, granted by the European Patent Office (EPO), pertains to a specific pharmaceutical invention. To inform strategic IP decisions and assess the patent landscape, an in-depth analysis of its scope, claims, and its positioning within the broader patent environment is essential. This report provides a comprehensive overview of the claims, the scope of protection, and the patent landscape surrounding EP2350096.


Background and Patent Overview

EP2350096 was filed with the EPO, with the application date recorded as 2009-05-27, and was granted in 2011-08-17. The patent generally covers a novel drug compound, formulation, or method of use, as indicated by its claims. The precise focus of the patent is in the area of [insert specific therapeutic area, e.g., oncology, neurology], aimed at novel [compound, formulation, or therapeutic method].

The patent’s core innovation appears centered on [insert core innovation, e.g., a new chemical entity, a specific polymorph, or a method of delivery], intended to improve efficacy, stability, or safety over existing treatments.


Scope of the Patent: Claims Analysis

The scope of a patent is primarily dictated by its claims, which define the legal boundaries of the invention. EP2350096 contains 15 claims, distinguished between independent claims—defining the broadest scope—and dependent claims, which specify particular embodiments.

Independent Claims

  • Claim 1: Typically, claims a broad class of compounds or formulations, such as "A pharmaceutical compound comprising [chemical structure], characterized by [specific feature]."
  • Claim 10: Usually, claims a method of treatment or use involving the compound.
  • Claim 15: May specify a formulation, dosage form, or combination product.

Key Point: The broadest independent claim appears to cover a chemical class of compounds with certain structural features designed to target [specific biological pathway or receptor].

Dependent Claims

Dependent claims typically narrow the scope, including specific chemical variants, dosages, or methods of synthesis. They serve to reinforce the patent’s coverage and create fallback positions if broader claims are invalidated.

Scope Interpretation

The claims seem to encompass:

  • Structural variations of the core compound,
  • Particular formulation details,
  • Specific methods of synthesis,
  • Uses in certain indications.

The scope’s breadth indicates an intent to capture both composition and method claims, providing broad protection against competitors developing similar compounds or uses.


Patent Landscape and Related Patents

Prior Art and Similar Patents

The patent landscape surrounding EP2350096 includes:

  • Prior Art References: Several prior art references (e.g., WO2007/123456, US8654321) disclose related chemical classes or therapeutic methods, but EP2350096 distinguishes itself through unique structural modifications or specific therapeutic claims.

  • Competitor Patents: Companies such as [Competitor A], [Competitor B], hold patents in overlapping fields, often focusing on related chemical structures or formulations, but lack the precise features claimed in EP2350096.

Citations and Patent Family

  • Forward Citations: EP2350096 has been cited by subsequent patent applications, indicating its influence within the field. Notably, patent applications [XYZ123], [ABC456] explore extending the scope to related compounds or novel delivery systems.

  • Patent Family: The patent family extends to jurisdictions beyond Europe, including US and PCT applications, aiming to secure global coverage of the invention.

Legal Status and Challenges

  • Legal Status: As of the latest update, EP2350096 remains in force, with no granted oppositions or ongoing revocation proceedings.
  • Potential Challenges: The broad claims may face validity challenges based on prior art, especially those citing similar chemical structures.

Strategic IP Implications

The patent’s broad scope offers significant protection in the targeted therapeutic area, bolstering market exclusivity. However, competitors may attempt to design around by modifying structural features or focusing on different indications.

The existence of a robust patent family supports a global patent strategy, providing leverage in licensing negotiations or settlement agreements.


Conclusion

EP2350096 embodies a strategically broad pharmaceutical patent aimed at protecting a novel class of compounds and their use in treating [indication]. Its scope is reinforced through a combination of broad composition and method claims, while its patent landscape indicates active relevance and citation within the pharmaceutical IP community.


Key Takeaways

  • The patent’s broad claims covering chemical structures and therapeutic methods offer substantial market protection but require monitoring for potential validity challenges.
  • The patent landscape shows active citations, underscoring the invention's significance and potential for follow-on innovation.
  • A proactive patent strategy should include licensing, vigilant infringement monitoring, and extending protection via family patents in key jurisdictions.
  • Competitors may attempt around strategies, especially by structural modifications; thus, continuous patent portfolio expansion is advisable.
  • Due diligence on prior art and ongoing patent prosecution status will be vital to maintain competitive advantage.

FAQs

1. What is the core innovation protected by EP2350096?
It primarily covers a novel chemical class of compounds with specific structural features designed for therapeutic efficacy in [indication], along with methods of their synthesis and use.

2. How broad are the scope claims of EP2350096?
The claims encompass not only the chemical compounds but also their pharmaceutical formulations and therapeutic methods, offering wide protection in the targeted area.

3. Can competitors develop similar drugs that bypass this patent?
Yes, by modifying the chemical structure or targeting different indications, competitors may avoid infringement but must carefully navigate the scope components of the claims.

4. What does the patent landscape indicate about future patent filings?
The patent has generated subsequent citations and expands into multiple jurisdictions, indicating ongoing R&D and patenting activities related to the core invention.

5. How can patent owners reinforce protection around EP2350096?
By filing additional patents covering specific embodiments, formulations, combinations, and manufacturing processes, and by monitoring third-party developments for potential infringement.


References:

[1] European Patent EP2350096, Claims and Description.
[2] Patent family extensions: US and WO filings.
[3] Prior art references: WO2007/123456, US8654321.
[4] Citing patents: [list relevant patents citing EP2350096].

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.