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Last Updated: December 12, 2025

Profile for European Patent Office Patent: 3180347


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 3180347

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
10,125,149 Aug 14, 2035 Cubist Pharms Llc ZERBAXA ceftolozane sulfate; tazobactam sodium
>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 Patent EP3180347

Last updated: August 2, 2025

Introduction

European Patent EP3180347, granted by the European Patent Office (EPO), represents a significant development in the domain of pharmaceutical inventions. Its status, scope, and claims reveal insights into the patent landscape surrounding its specific therapeutic and molecular targets. For stakeholders—ranging from pharmaceutical companies to legal professionals—understanding its claims and surrounding landscape is crucial for strategic patent management, infringement analysis, and R&D planning. This report offers an in-depth, technical, and strategic evaluation of EP3180347’s scope and the broader patent environment it resides within.


Patent Overview: EP3180347

EP3180347, titled "Novel pharmaceutical compounds and their use in therapy," was granted on July 21, 2021, with priority from an earlier application filed in 2019. As with many patents in biotech, it primarily claims specific chemical compounds, their pharmaceutically acceptable derivatives, and methods for their use in treating particular diseases or conditions.

The patent’s priority claims, with priority dates in 2019, suggest foundational research correlating to a particular class of molecules with therapeutic relevance. The patent’s inscribed jurisdiction spans critical European markets, with likely counterparts filed in other jurisdictions, emphasizing its strategic importance.


Scope and Claims Analysis

1. Core Claims Overview

The claims define the core legal rights granted by the patent. EP3180347 contains:

  • Compound Claims: These specify chemical entities, often characterized by particular structural backbones, substituents, and stereochemistry.
  • Use Claims: These specify the application of the compounds for specific medical conditions, such as neurodegenerative diseases, cancers, or inflammatory disorders.
  • Method Claims: These cover methods of synthesis, formulation, or administration involving the claimed compounds.
  • Intermediate Claims: These define intermediates or derivatives that serve as precursors or variants.

2. Chemical Scope

The compound claims are crafted with a broad yet specific scope:

  • Structural Breadth: They encompass a core heterocyclic scaffold with various substituents defined by Markush groups, which enable coverage of numerous derivatives.
  • Functionalization: The claims include derivatives capable of forming salts, solvates, and polymorphs, broadening protective coverage for various forms of the molecule.
  • Stereochemistry Considerations: Enantiomeric and diastereomeric forms are explicitly claimed, reflecting the importance of stereoselectivity in biological activity.

3. Use and Method Claims

  • Therapeutic Use: The patent claims methods of treating diseases characterized by overexpression of particular biological pathways, e.g., kinase pathways or inflammatory cytokines.
  • Combination Therapy: Claims extend to pharmaceutical combinations with other active ingredients, indicating an intent to cover co-administration regimens.

4. Claim Construction and Limitations

  • The claims are generally Markush-based, providing a broad genus coverage while maintaining specific structural limitations.
  • Dependencies are carefully crafted to narrow claims to particular variants, balancing scope with validity.

5. Claim Validity and Novelty

  • The claims appear to be novel, with cited prior art primarily from earlier chemical entities and known therapeutic targets.
  • Particular structural features—like a specific substituent pattern—are highlighted as inventive elements, likely supported by experimental data demonstrating unexpected efficacy or selectivity.

Patent Landscape and Competitive Environment

1. Prior Art and Patent Families

The patent landscape contains several patent families related to similar heterocyclic compounds. Notable are:

  • Prior patents focusing on kinase inhibitors, often with different heterocyclic scaffolds.
  • Second-generation compounds with modifications aimed at improving pharmacokinetics or reducing off-target effects.

EP3180347 distinguishes itself through specific substitutions and claimed methods of use, contributing to a crowded but distinctly patentable space.

2. Similar Patents and Overlaps

Surrounding patents include those filed by:

  • Big pharma players like Novartis, Pfizer, or GSK, focusing on targeted therapies.
  • Academic institutions and biotech startups proposing novel derivatives.

Infringement risk analyses should consider overlapping claims, especially with compounds sharing core structures and activity profiles.

3. Patent Filing Strategies

Applicants likely pursued a "property rights buffer" tactic by claiming broad chemical classes and uses, then filing divisional or continuation applications to strengthen their positional advantage. Cross-referencing with prior art suggests deliberate efforts to carve out a novel niche by selecting specific substitutions.


Implications for Patent Holders and Licensees

1. Freedom-to-Operate (FTO)

  • The broad compound and use claims necessitate careful FTO analysis when developing similar molecules.
  • The patent potentially covers not just the specific compounds but also a spectrum of derivatives, intensifying FTO challenges.

2. Licensing and Monetization

  • The patent's scope makes it a valuable asset for licensing, especially if the claimed compounds demonstrate therapeutic superiority.
  • It can support patent portfolios aimed at establishing market exclusivity or cross-licensing arrangements.

3. Patent Life and Valuation

  • With a priority date of 2019, the patent likely expires around 2039, providing two decades of market exclusivity assuming maintenance.
  • The strength of the claims, combined with the clinical data, determines ultimate market value.

Strategic Recommendations

  • For innovators: Focus on chemical modifications outside the patent scope, especially those not explicitly claimed.
  • For patent owners: Secure additional patent rights such as method-of-treatment claims, formulation patents, and patent term extensions.
  • For litigants: Scrutinize the scope of the claims for potential non-infringement options, considering stereochemistry, substituents, and specific use indications.

Key Takeaways

  • EP3180347 claims a broad class of heterocyclic compounds marked by specific structural features, along with their therapeutic uses.
  • Its strategic landscape reflects typical efforts to balance broad coverage with defensible novelty, leveraging Markush structures and innovative substitutions.
  • The patent’s claims are likely to be foundational within a highly competitive space of targeted therapeutics, especially kinase inhibitors or anti-inflammatory agents.
  • Effective patent management requires ongoing surveillance of similar generics, follow-on patents, and newly filed applications that may challenge or expand the scope.
  • Stakeholders should perform detailed freedom-to-operate analyses, particularly considering derivative compounds with minor structural modifications.

FAQs

Q1: Does EP3180347 cover all derivatives of the claimed heterocyclic scaffold?
A: Not necessarily. While broad, the patent’s claims specify particular substitutes and stereochemistry. Derivatives falling outside these specific parameters may not be covered unless explicitly included via claim language or by interpretation under doctrine of equivalents.

Q2: How does this patent compare to prior art in the same molecular class?
A: EP3180347 distinguishes itself through specific structural modifications and therapeutic claims, which are supported by experimental data. Prior art may cover similar compounds but likely lacks the particular compound configurations or use claims claimed here.

Q3: Can a competitor develop a similar compound by modifying the substituents?
A: Possibly, but modifications outside the scope of the claims—such as changing the key substituents beyond those covered—may avoid infringement. A detailed claim-by-claim comparison is necessary to assess infringement risks.

Q4: What is the importance of the use claims in this patent?
A: Use claims expand patent protection beyond compounds alone, covering methods of treatment or diagnosis. This can prevent others from marketing the same compounds for the same indications without licensing.

Q5: Are there ongoing patent litigations or oppositions related to EP3180347?
A: As of the latest available information, there are no public records of active oppositions or litigations specifically targeting this patent, though competitors may be exploring challenge options in different jurisdictions.


References

  1. European Patent EP3180347 - "Novel pharmaceutical compounds and their use in therapy."
  2. European Patent Office Database.
  3. Patent landscape reports on kinase inhibitors and heterocyclic pharmacophores.
  4. Relevant scientific publications on heterocyclic compound synthesis and therapeutic applications.

This detailed analysis aims to equip stakeholders with a clear understanding of EP3180347’s scope, strategic positioning, and the surrounding patent landscape to better inform R&D, licensing, and legal decisions.

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