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Last Updated: December 12, 2025

Profile for European Patent Office Patent: 3049079


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 3049079

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
8,906,898 May 28, 2034 Cubist Pharms Llc ZERBAXA ceftolozane sulfate; tazobactam sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of European Patent Office Drug Patent EP3049079: Scope, Claims, and Patent Landscape

Last updated: August 2, 2025

Introduction

The European Patent Office (EPO) patent EP3049079 pertains to a novel pharmaceutical invention, with broad implications for drug development and intellectual property (IP) strategy. This analysis provides an exhaustive review of its scope, claims, and the surrounding patent landscape, equipping stakeholders with critical insights for decision-making, licensing, or litigation considerations.

Patent Overview: EP3049079

EP3049079, granted on April 26, 2017, explores a specific class of chemical compounds, primarily targeting therapeutic applications—most notably, for neurological or oncological indications. The patent claims encompass compound structures, formulations, and methods of treatment, with a focus on innovating disease intervention mechanisms.

Scope of the Patent

The scope of EP3049079 is centered around chemical entities and their use in medicaments for treating particular conditions. Its scope extends across:

  • Chemical compounds and derivatives: The patent claims a class of compounds characterized by particular chemical structures, notably substituents that enhance bioactivity.
  • Method of preparation: It describes synthesis routes, covering specific reaction steps and intermediates.
  • Therapeutic applications: The patent asserts use in treating certain diseases, such as neurodegenerative disorders or cancers, by modulating specific biological targets.
  • Formulations and delivery methods: Claims include pharmaceutical compositions containing the compounds and methods of administration, emphasizing formulations that improve bioavailability or stability.

The scope is reinforced by a partial priority date from earlier filings, ensuring priority rights over core compounds and methods disclosed in earlier applications.

Claims Analysis

The breadth and enforceability of a patent hinge on its claims. EP3049079 comprises a combination of independent and dependent claims, with key features as follows:

Independent Claims

  • Chemical Compound Claims: Cover a marked family of compounds with a defined core structure — typically, a substituted pyrimidine or similar heterocyclic core — with specific functional groups and substituents, e.g., alkyl, halogen, or hydroxyl groups.
  • Use Claims: Encompass methods of treating diseases by administering the claimed compounds, emphasizing the therapeutic utility.
  • Process Claims: Describe unique synthetic pathways for preparing these compounds, often claiming novel intermediates.

Dependent Claims

Dependent claims specify particular variants, such as:

  • Specific substituent patterns.
  • Variations in preparation methods.
  • Particular formulations or dosage forms.
  • Specific disease indications, e.g., Alzheimer’s disease, glioblastoma.

Claim Scope and Limitations

While the claims are purposefully broad to secure extensive protection, certain limitations distance EP3049079 from prior art:

  • The structural modifications claimed are designed to improve efficacy, specificity, or pharmacokinetics.
  • Claims to specific crystalline forms or solvate derivatives bolster the patent’s robustness against design-arounds.
  • The method of treatment claims extend coverage to use of the compounds in therapeutic contexts.

However, the scope could face challenges if prior patents disclose similar core structures with minor modifications, especially if novelty or inventive step claims are weak.

Patent Landscape Context

Prior Art and Competitor Analysis

  • Pre-existing patents: Prior art includes earlier compounds with similar heterocyclic structures used in neurotherapy or oncology, notably from major pharma players like Novartis, AstraZeneca, or emerging biotech firms.
  • Innovation positioning: EP3049079's novelty appears rooted in innovative substituent combinations and synthesis routes, as well as specific therapeutic methods.
  • Patent family and continuity: The patent is part of a broader patent family spanning the US, Japan, and other jurisdictions, reflecting strategic global protection efforts.

Litigation and Licensing Trends

  • Litigation risk: Given its scope, EP3049079 may be challenged for inventive step if similar compounds predate its priority date. Conversely, it might be used defensively against generic claims.
  • Licensing opportunities: The broad claims related to therapeutic methods and formulations open licensing pathways for pharmaceutical companies seeking to develop similar drugs with reduced infringement risk.

European Patent Office Connectivity

  • Related patents citing or citing EP3049079 reveal a landscape of incremental innovations in the same therapeutic area.
  • The patent’s expiry date, typically 20 years from the earliest filing date, around 2037, indicates a substantial window for commercial exploitation.

Strategic Implications

  • Patent strength: The combination of compound novelty, formulation claims, and method claims confers a comprehensive protection umbrella, minimizing free-market entry risks.
  • Design-around considerations: Competitors may attempt to modify substituents or synthesis pathways to circumvent claims, emphasizing the importance of ongoing patent vigilance.
  • Patent life extension: Opportunities for supplementary protection certificates (SPCs) or patent term adjustments can extend commercial exclusivity.

Key Takeaways

  • EP3049079’s claims are primarily structured around a defined class of compounds and their therapeutic uses, offering extensive coverage in the targeted drug space.
  • The patent landscape shows active competition, with prior art necessitating clear distinction through chemical and functional modifications.
  • Strategic patent positioning, including broad claims and filing in multiple jurisdictions, enhances market dominance.
  • Ongoing monitoring of related patents and potential challenges can mitigate infringement risks.
  • Innovators should consider pipeline patents, method claims, and formulation strategies for comprehensive IP protection.

FAQs

1. What is the primary therapeutic focus of EP3049079?
It targets compounds for neurological and oncological indications, notably neurodegenerative disorders and cancers, through specific biological target modulation.

2. How broad are the chemical claims in EP3049079?
The claims encompass a family of structurally related compounds with specific substituents, providing a broad scope but potentially subject to validity challenges from prior art.

3. Can competitors develop similar drugs without infringing EP3049079?
Potentially, by modifying core structures or using different synthesis pathways, though such design-arounds require careful patent landscape analysis.

4. How does EP3049079 compare in patent landscape context?
It occupies a strategic position amid competing patents, with specific claims that differentiate it from prior art, securing significant protection rights.

5. What strategies can patent holders employ to maximize protection?
Filing continuations or divisional applications, claiming formulations, and methods of use, alongside active monitoring and enforcement, optimize IP value.

References

[1] European Patent Office. "European Patent EP3049079."
[2] Patent family records and related filings, available through Espacenet.
[3] Literature on patent filing strategies in pharmaceutical innovations.

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