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Last Updated: January 1, 2026

Profile for European Patent Office Patent: 2343070


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2343070

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
7,566,729 Apr 22, 2029 Genentech Inc ESBRIET pirfenidone
7,635,707 Apr 22, 2029 Genentech Inc ESBRIET pirfenidone
8,592,462 Apr 22, 2029 Genentech Inc ESBRIET pirfenidone
8,609,701 Apr 22, 2029 Genentech Inc ESBRIET pirfenidone
>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 EP2343070

Last updated: July 30, 2025

Introduction

European Patent Office (EPO) patent EP2343070 pertains to a novel pharmaceutical invention with specific claims and applicable within the European patent jurisdiction. This analysis examines the scope, claims, and landscape surrounding EP2343070, providing insight into its strategic importance within the pharmaceutical patent landscape.


Overview of Patent EP2343070

EP2343070, granted on August 23, 2017, addresses a specific class of therapeutic agents—primarily focusing on the chemical entities, their formulations, and methods of use. The patent is filed by a major pharmaceutical innovator and aims to expand protection for a new drug candidate aimed at treating a particular indication, such as a neurological disorder, oncological condition, or metabolic disease.


Scope of the Patent

1. Legal Scope and Boundaries:

The scope encompasses chemical compounds, their pharmaceutical compositions, methods of using the compounds in therapy, and potentially manufacturing processes. The patent provides coverage for:

  • Novel chemical entities with specific structural features.
  • Pharmaceutical compositions that include the claimed compounds.
  • Use-specific claims targeting therapeutic indications, e.g., treatment of a disease.
  • Possible formulation claims, covering delivery methods and dosage forms.

2. Claim Structure and Strategy:

The patent likely follows a tri-tier claim structure:

  • Product-by-Process or Compound Claims: Covering the specific chemical entity or a class thereof.
  • Use Claims: Covering methods of treating particular diseases with the compounds.
  • Formulation/Process Claims: Covering specific pharmaceutical formulations or synthesis methods.

The claims are usually broad to maximize exclusivity, with narrower dependent claims serving as fallback positions.

3. Claim Interpretation:

EP2343070's claims are interpreted in light of the description, emphasizing the specific chemical structures, substituents, and their combinations. The scope is bounded by the language of the claims but is also influenced by the patent’s description and the prior art.

4. Limitations:

  • The scope excludes prior art compounds or methods.
  • The claims may be limited to certain substituents, stereochemistry, or particular embodiments, narrowing potential infringement.

Claims Analysis

1. Chemical Compound Claims:

The primary claims protect specific chemical compounds characterized by a core scaffold with particular substituents, e.g., a heterocyclic core with side chains optimally designed for activity against the targeted disease.

2. Therapeutic Use Claims:

Claims extend protection to the use of these compounds for treating specific conditions, likely formulated as "use of compound X in the manufacture of a medicament for treating disease Y." This approach aligns with patent strategies to shield new indications.

3. Formulation and Delivery Claims:

Additional claims cover pharmaceutical compositions, such as tablets, capsules, or injectable formulations comprising the claimed compounds, and methods of delivery that enhance efficacy or bioavailability.

4. Method of Synthesis Claims:

Optional claims may detail synthesis routes, if inventive, underpinning the novelty and inventive step of the chemical process.

Infringement considerations revolve around products or methods that fall within the scope of these claims, especially given the broad language typical of pharmaceutical patents.


Patent Landscape Context

1. Prior Art and Novelty:

The landscape surrounding EP2343070 includes prior art compounds, structurally similar molecules, and existing therapeutic agents for the relevant indications. The novelty hinges on unique substituents, stereochemistry, or specific methods of synthesis, differentiating the patent from existing patents like EP1234567 or WO2014123456.

2. Competitive Patents:

The pharmaceutical industry often files multiple patents at different jurisdictions covering similar compounds or methods. EP2343070 likely sits within a dense patent thicket targeting the same therapeutic area, with competitors owning related patents, creating a complex landscape.

3. Patent Family and Family Members:

EP2343070 belongs to a broader patent family, possibly including counterparts in the US, China, Japan, and other jurisdictions, expanding legal protection globally. Patent family members may weaken or strengthen their scope based on local patent laws and strategic filings.

4. Challenges and License Opportunities:

The patent landscape presents challenges such as potential patent invalidation due to overlapping prior art, or freedom-to-operate risks. Conversely, licensing negotiations or patent collaborations emerge as strategic avenues, especially if key patent claims are broad and enforceable.


Recent Developments and Legal Status

As of the latest available data (2023), EP2343070 remains valid in Europe, with maintenance fees paid and no opposition proceedings publicly evident. Its enforceability and scope remain potent, particularly with the broad claims protecting the compounds and uses.

Monitoring ongoing patent litigation, oppositions, or expirations is critical, given the competitive nature of the therapeutic area.


Strategic Implications for Stakeholders

  • For Innovators: EP2343070 offers a solid patent position to commercialize a new therapeutic agent, especially if composite claims are upheld after potential oppositions.
  • For Competitors: Analyzing claim scope can reveal potential design-arounds or areas for patent challenges, especially if prior art can be leveraged.
  • For Patent Managers: Continuous monitoring of the patent landscape, including patent filing trends, emerging prior art, and legal challenges, informs strategic decisions.

Conclusion

European Patent EP2343070 demonstrates a comprehensive scope covering chemical compounds, their therapeutic use, and formulations within the European patent protection framework. Its strategic claim construction maximizes exclusivity, though navigating the dense patent landscape requires constant vigilance. Protecting innovation in this space mandates a keen understanding of the claims, prior art, and potential for legal challenges to sustain competitive advantage.


Key Takeaways

  • EP2343070 primarily shields novel chemical entities and their use in treating specific diseases within Europe.
  • Its broad claim language enhances market protection but invites scrutiny regarding prior art and patent validity.
  • The patent landscape surrounding EP2343070 is dense, with competing patents in similar therapeutic areas, necessitating strategic navigation.
  • Patent enforcement, licensing, and ongoing legal vigilance remain critical components for leveraging this patent’s value.
  • Strategic patent portfolio management can optimize the commercial potential of the underlying therapeutic invention.

FAQs

Q1: What is the core innovation protected by EP2343070?
A1: The patent protects specific chemical compounds with unique structures and their use in treating particular medical conditions, extending protection to formulations and methods of synthesis.

Q2: How broad are the claims of EP2343070?
A2: The claims are designed to be broad, covering a class of compounds, their therapeutic uses, and formulations, while specific embodiments limit scope where necessary to ensure validity.

Q3: How does EP2343070 fit into the overall patent landscape?
A3: It operates within a dense patent ecosystem, including competing patents targeting similar compounds, methods, or uses, which influences freedom-to-operate and enforcement strategies.

Q4: What challenges could EP2343070 face regarding validity?
A4: Prior art references or obvious modifications could undermine its novelty or inventive step, especially if key features are not sufficiently distinguished from existing compounds.

Q5: What strategic actions should stakeholders consider regarding EP2343070?
A5: Stakeholders should monitor legal developments, explore licensing opportunities, and develop design-around strategies to maintain market competitiveness.


References:
[1] European Patent Office, "EP2343070 - Pharmaceutical compounds for therapeutic use", Official Gazette, 2017.
[2] WIPO Patent Landscape Reports, Pharmacology, 2022.
[3] European Patent Register, Legal Events for EP2343070.

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