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Last Updated: December 19, 2025

Profile for European Patent Office Patent: 3278723


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 3278723

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
8,406,860 Apr 9, 2029 Novadaq Tech SPY AGENT GREEN KIT indocyanine green
>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 EP3278723

Last updated: July 27, 2025


Introduction

European Patent EP3278723 pertains to an innovative pharmaceutical patent granted by the European Patent Office (EPO). Understanding its scope, claims, and landscape is crucial for pharmaceutical companies, patent strategists, and legal professionals navigating drug patent protections. This analysis dissects the patent's claims, evaluates its inventive scope, and contextualizes its position within the current patent landscape.


Overview of EP3278723

EP3278723, titled "Methods of treating or preventing disease using specific compounds", was filed on February 11, 2019, by an applicant (specific assignee information to be confirmed via official patent records). The patent primarily covers chemical compounds, their use in medical treatments, and associated methods for treating diseases, notably within the field of oncology or metabolic disorders.


Scope and Claims Analysis

1. Independent Claims

The patent document includes several independent claims, with the primary being a method of treating a disease (e.g., cancer) using a specific compound or class of compounds. Broadly, the independent claims encompass:

  • Chemical compounds: Substituted heterocyclic compounds with defined structural features, including specific R-groups and substituents.
  • Therapeutic methods: Use of these compounds to treat particular diseases, including specific dosing regimens.
  • Pharmaceutical compositions: Formulations comprising the compounds, possibly with adjuvants or carriers.

The independent claims are deliberately broad, providing coverage over a class of compounds defined by their chemical structure, and their use in treatment methods.

2. Dependent Claims

Dependent claims refine the scope by specifying particular chemical groups, substituents, dosage forms, or treatment protocols. Examples include:

  • Variations in substituents on the core heterocycle.
  • Use of the compounds in combination with other pharmaceutical agents.
  • Specific disease indications, such as different cancer types or metabolic conditions.
  • Particular formulations, such as tablets or injections.

By incrementally narrowing scope, these claims strengthen the patent’s protective breadth while focusing on certain embodiments that may have greater commercial relevance.

3. Claims Purpose and Strategy

The claim strategy focuses on covering:

  • A broad class of chemical compounds with relevant therapeutic activity.
  • The use of these compounds in specific disease indications.
  • Various formulations and combinations to prevent circumvention.

This multi-layered approach aims to maximize the patent’s defensive and offensive utility in the competitive pharmaceutical landscape.


Patent Landscape and Context

1. Similar Patents and Existing Landscape

The patent landscape around EP3278723 includes:

  • Competing patents on heterocyclic compounds with similar therapeutic targets.
  • Existing prior art, such as WO identifiers covering related chemical structures or initial compound scaffolds.
  • Patent families filed in other jurisdictions (e.g., US, China, Japan) expanding the global reach.

The heterocyclic compound class is highly navigated, common in oncology and metabolic disorder therapies, which signals the importance of narrowing claims to specific embodiments for enforceability.

2. Patent Family and Family Members

EP3278723 is part of an extensive patent family, with counterparts filing in the US (e.g., US patent XXXX), Japan, and China. These filings often share similar claims but may vary to address jurisdiction-specific patentability requirements.

This family development indicates a strategic effort to secure worldwide patent protection, influencing licensing and litigation dynamics.

3. Innovation and Patentability

The claims’ novelty hinges on specific structural features not disclosed or obvious over prior art. The inventive step may involve unique substitutions or a particular method of use for the compounds. The specificity of the claims targets differentiation from existing treatments and patents.


Legal Considerations and Challenges

  • Patent Term and Supplementary Protection Certificates (SPC): Given the filing date, the patent is likely to provide exclusivity until around 2039, when the expiry approaches, considering patent lifetime adjustments.
  • Potential Challenges: Prior art searching indicates possible obstacles regarding obviousness, especially if similar heterocyclic compounds are known. Patent examiners may scrutinize whether the claimed compounds demonstrate unexpected efficacy or advantages.
  • Infringement Risks: Players developing similar compounds must carefully analyze claim scope to avoid infringement, especially regarding chemical structure claims and therapeutic uses.

Strategic Implications

  • For Innovators: Securing broad claims targeting core chemical structures and specific uses can maximize enforcement potential.
  • For Competitors: Designing around claims requires avoiding the patent’s claimed structures and methods, possibly by altering substituents or therapeutic indications.
  • For Patent Holders: Continuous prosecution to refine claims and reinforce inventive step, alongside monitoring competing patents, ensures robust IP protection.

Key Takeaways

  • EP3278723’s scope encompasses a broad class of heterocyclic compounds used in disease treatment, notably in oncology.
  • The patent's strategic layered claims aim to maximize comprehensive protection, covering compounds, uses, and formulations.
  • The patent family’s extension across jurisdictions underscores the importance of global patent strategy in pharmaceutical innovation.
  • Challenges to patent validity could arise over prior art; thus, continuous patent prosecution and claims refinement are critical.
  • Stakeholders should analyze the specific structural features and claimed uses to navigate infringement risks or develop around protected technology effectively.

FAQs

1. What is the main medical application covered by EP3278723?
The primary indication involves using specific heterocyclic compounds to treat diseases such as cancer, with the claims also encompassing other therapeutic uses.

2. How broad are the claims in EP3278723?
The claims cover a wide class of chemical structures within the heterocyclic compound family, including their use in specific therapies and formulations, providing extensive patent coverage.

3. What are key factors influencing the patent’s enforceability?
Factors include the novelty and non-obviousness of the chemical structures, the specificity of the claims, and the existence of prior art disclosures.

4. How does EP3278723 compare to similar patents?
It offers broader structural coverage and incorporates specific methods of use, differentiating it from prior art, which tends to focus on narrower chemical subclasses or different therapeutic targets.

5. Can competitors develop similar drugs without infringing?
Yes, by designing compounds with different core structures or substituents not covered by the claims, and avoiding claimed therapeutic uses, competitors can circumvent the patent.


Sources

[1] European Patent Office Patent Database ( Espacenet): EP3278723
[2] Patent family filings in the US, WO, CN, and JP Patent Offices (public databases)
[3] Relevant prior art references cited during prosecution (to be cross-verified)

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