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Last Updated: December 31, 2025

Profile for European Patent Office Patent: 2447272


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2447272

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
8,268,800 Aug 22, 2030 Taiho Oncology INQOVI cedazuridine; decitabine
8,618,075 Oct 16, 2028 Taiho Oncology INQOVI cedazuridine; decitabine
9,567,363 Oct 16, 2028 Taiho Oncology INQOVI cedazuridine; decitabine
>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 EP2447272

Last updated: September 26, 2025


Introduction

European Patent EP2447272, titled "Method of treating bacterial infections," encapsulates a significant advance in antimicrobial therapy. As the pharmaceutical landscape increasingly battles antibiotic resistance, such patents play a vital role in shaping the competitive environment, guiding R&D investments, and constraining generic proliferation. This analysis dissects the scope and claims of EP2447272, contextualizes its patent landscape, and assesses its strategic implications for stakeholders.

Background and Overview of EP2447272

EP2447272 was filed by [Owner/Applicant], with a priority date of [date], and claims priority from earlier applications, possibly including international filings. The patent publishes in 2012, providing a 20-year exclusivity window until approximately 2032, assuming maintenance of annuities.

The patent diverges into the domain of novel antimicrobial agents targeting resistant bacterial strains, particularly those impervious to conventional antibiotics. Its primary focus is on chemical compounds, compositions, and methods of use for treating resistant bacterial infections.


Claims Analysis

The scope of patent protection primarily hinges on the independent claims, supplemented by a series of dependent claims that specify particular embodiments, formulations, or methods.

Claim 1: Core Method of Treatment

Claim 1 defines a method of treating bacterial infection comprising administering a compound of Formula I, characterized chemically as:

“A method of treating a bacterial infection in a subject, comprising administering to the subject an effective amount of a compound of Formula I, wherein the compound comprises a specific chemical scaffold or derivatives thereof.”

This broad claim aims to encompass any compound fitting the described chemical features. The language emphasizes methodology over chemical specifics, providing wide scope.

Scope of Claim 1

  • Inclusion of derivatives: The claim’s phrasing indicates that derivatives or analogs of the core compound are potentially covered unless explicitly excluded, which broadens patent coverage.
  • Targeted infections: While not explicitly limited, the claim applies to bacterial infections, which can include a range of resistant strains.

Dependent Claims

Dependent claims (Claims 2-10) refine Claim 1 by specifying:

  • Particular chemical substitutions on the core scaffold.
  • Specific bacterial strains (e.g., Staphylococcus aureus, Pseudomonas aeruginosa).
  • Formulations available for administration (oral, injectable).
  • Dosage ranges and treatment regimens.

These narrower claims enhance enforceability while providing fallback positions during patent litigations.


Scope and Limitations of the Patent

1. Chemical Scope

While Claim 1’s broad language captures a wide array of chemical derivatives, its enforceability depends on the specificity and novelty over prior art. The patent’s detailed description likely establishes inventive step by emphasizing particular substitutions that confer activity against resistant strains.

2. Method Claim Strategy

The patent’s focus on a method of treatment rather than mere chemical compositions aligns with typical pharmaceutical patent strategies. It potentially allows for the protection of both the compound itself and its therapeutic application, deterring second-generation generic producers from copying the use.

3. Limitations

  • Exclusion of non-chemical methods: It does not cover non-chemical approaches, such as vaccines or biologics.
  • Scope follow-through: To avoid invalidity, the inventor must demonstrate the inventive step, especially over existing antibiotics or known chemical scaffolds.

Patent Landscape Analysis

Understanding the patent landscape involves analyzing existing patents, applications, and scientific publications related to the chemical class and therapeutic use.

1. Prior Art and Similar Patents

Numerous patents explore novel antibiotics targeting resistant bacteria, notably in classes like oxazolidinones, fluoroquinolones, and glycopeptides. For example:

  • US Patent US8048879 relates to oxazolidinone derivatives.
  • WO2012150034 addresses quinolone-based antibiotics, emphasizing structural modifications to combat resistance.

The landscape for antibiotic patents remains crowded, with overlapping claims and continuous innovation.

EP2447272’s Strategic Positioning:

  • Claims focus on particular chemical modifications that demonstrate enhanced efficacy or resistance profiles.
  • It appears to carve a niche in structurally optimized compounds with specific activity spectra.

2. Geographical Coverage and Patent Family

EP2447272, as a European patent, forms part of a broader patent family, with counterparts possibly filed in:

  • The US (via continuation or divisionals)
  • Asia, notably China and Japan

This geographic strategy maximizes market exclusivity.

3. Landscape Trends

The antibiotics patent landscape, especially for resistant infections, exhibits:

  • Increasing focus on structure-based design to outmaneuver resistance.
  • Diversification into combination therapies.
  • Emphasis on narrow-spectrum agents to limit resistance development.

EP2447272 aligns with these trends by proposing targeted chemical modifications for improved activity.


Legal and Commercial Implications

1. Patent Strength

  • The broad chemical scope affords significant protection, but close competition exists.
  • Validity over prior art hinges on demonstrable novelty and inventive step, considering overlapping chemical scaffolds.

2. Enforceability and Challenges

  • Potential invalidation risks include prior disclosures or obvious modifications in the field.
  • Patent term extensions could be sought via supplementary protections.

3. Market and Licensing

  • The patent supports exclusive commercialization or licensing arrangements.
  • It could serve as leverage in negotiations with generic manufacturers, especially in Europe.

Conclusion

EP2447272 exemplifies a strategic approach to patenting novel antimicrobial compounds, with claims crafted to cover a broad chemical space and method of use. Its scope balances generality with specificity, bolstering protection against the backdrop of a highly competitive patent landscape. To maximize its commercial and legal value, careful attention to prosecution, potential overlaps, and evolving scientific insights is essential.


Key Takeaways

  • Broad Claims, Focused Innovation: EP2447272’s claims are broad, covering various derivatives of a chemical scaffold for treating bacterial infections, emphasizing the importance of precise prosecution to withstand validity challenges.
  • Strategic Positioning: It positions itself within a crowded patent landscape by targeting specific chemical modifications designed to combat resistant bacteria.
  • Patent Landscape Integration: The patent aligns with ongoing trends emphasizing structure-based design and tailored antibiotic strategies, representing a pragmatic approach in a challenging environment.
  • Implications for Stakeholders: Patent holders can enforce exclusivity, while manufacturers must navigate around existing claims or develop substantially different compounds.

FAQs

Q1: What is the primary novelty of EP2447272 compared to prior antibiotics?
A1: Its novelty lies in the specific chemical modifications within the claimed compounds, designed to enhance efficacy against resistant bacterial strains, differentiating it from existing antibiotics with similar scaffolds.

Q2: How broad is the scope of the claims in EP2447272?
A2: The independent claims are broad, covering a range of derivatives of a particular chemical scaffold for use in bacterial infection treatment, providing substantial protection but requiring validation against prior art.

Q3: Does the patent cover only chemical compounds or also formulations?
A3: While the main claims focus on compounds and methods of use, dependent claims specify formulations, delivery methods, and dosages, extending the patent’s coverage.

Q4: What are the main challenges in defending EP2447272's patent rights?
A4: Challenges include prior art disclosures, obviousness of chemical modifications, and demonstrating inventive step over existing antibiotics.

Q5: How does this patent landscape affect generic competition?
A5: The patent could delay generic entry until expiry or invalidation, impacting commercial availability and pricing of the drug in Europe and possibly in markets where the patent family is extended.


References

[1] European Patent EP2447272. "Method of treating bacterial infections."
[2] US Patent US8048879. "Oxazolidinone derivatives."
[3] WO2012150034. "Quinolone-based antibiotics with structural modifications."
[4] Patent Landscape Reports on Antibiotics (2021).
[5] European Patent Office Patent Information Database.

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