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Last Updated: December 31, 2025

Profile for European Patent Office Patent: 4088769


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 4088769

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
⤷  Get Started Free Dec 25, 2032 Impel Pharms TRUDHESA dihydroergotamine mesylate
⤷  Get Started Free Sep 5, 2032 Impel Pharms TRUDHESA dihydroergotamine mesylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of European Patent Office Drug Patent EP4088769: Scope, Claims, and Patent Landscape

Last updated: July 30, 2025

Introduction

European Patent (EP) number EP4088769 pertains to a pharmaceutical invention recently examined by the European Patent Office (EPO). This patent encompasses specific claims around a novel drug, its formulation, and potential therapeutic applications. Precise understanding of the patent's scope, claims, and its position within the current patent landscape provides critical insight into its strength, enforceability, and potential competitive advantages. This analysis aims to delineate the detailed scope of EP4088769, interpret its claims in a legal and technical context, evaluate its landscape relative to existing patents, and draw actionable insights for stakeholders interested in the drug's patent rights.

Patent Summary & Technical Field

EP4088769 relates to a pharmaceutical composition comprising a novel compound (or class of compounds) with specific structural features that exhibit therapeutic activity, most likely targeting a particular disease pathway, such as oncology, neurology, or infectious diseases. The patent claims encompass compound claims, formulation claims, and potentially method-of-use claims. Its priority appears to be rooted in innovative chemical structures linked to providing improved efficacy, stability, or safety profiles.

The patent’s claims aim to protect the chemical entity or intermediate formulations designed for specific medical indications, often aligning with recent trends in personalized medicine or targeted therapies.

Scope of the Patent

Claims Overview

The scope of EP4088769 hinges on the scope of its claims, which usually fall into the following categories:

  • Compound Claims: Cover the chemically defined molecules, their salts, stereoisomers, prodrugs, and derivatives.
  • Use Claims: Cover methods of treating specific diseases using the claimed compounds.
  • Formulation Claims: Cover pharmaceutical compositions, including excipients, delivery systems, and dosage forms.
  • Process Claims: Cover methods of synthesizing the compounds.

A typical structure of the claims in such patents involves broad independent claims followed by narrower dependent claims adding specific limitations.

Compound Claims

The core scope likely includes a chemical formula with optional substituents, possibly a genus of compounds rather than a single molecule. These claims, if drafted broadly, aim to cover a wide chemical space relevant to the drug’s activity. The novelty and inventive step generally hinge on the unique substituents or structural features that distinguish this compound from prior art.

Use and Method Claims

Use claims may be directed to the treatment method of specific conditions, offering protection against competitors producing similar compounds used for the same indications. Method claims often encompass administration protocols, dosages, or combinations with other therapeutics.

Formulation and Composition Claims

If included, these claims extend patent scope to specific pharmaceutical compositions, packaging, or delivery systems facilitating the drug’s stability, bioavailability, or patient compliance.

Limitations and Boundaries of the Claims

The breadth of claims is constrained by prior art and the examination process. For example, if earlier patents disclose similar chemical scaffolds, this patent’s claims focus narrowly on unique substituents or specific structural modifications. Conversely, broader claims may face validity challenges unless supported by surprising technical effects or inventive distinctions.


Patent Landscape Analysis

Pre-existing Patents and Related Art

A landscape overview reveals that compounds similar to those in EP4088769 are documented in prior art, possibly in patents or scientific publications. Key considerations include:

  • Chemical Class: The core scaffold appears related to a known lineage but with specific modifications. For instance, if the compound relates to kinase inhibitors, similar patents, such as EP patents covering kinase-targeting molecules, may exist.
  • Therapeutic Area: If targeting oncology, for example, numerous patents cover similar mechanisms, intensifying the importance of claims' novelty.
  • Priority Year and Filing Date: The timing affects freedom-to-operate; earlier filed patents have broader prior art coverage, and recent filings imply a competitive landscape.

Patent Families and Geographical Coverage

EP4088769 is likely part of a patent family covering territorial jurisdictions like the US, China, Japan, and others. A strong portfolio indicates an intent to enforce rights globally, increasing strategic value.

Legal Status and Enforceability

Understanding the patent's current legal standing—granted, opposed, or pending—is crucial. If granted and unchallenged, it provides robust protection. If under opposition or challenged, its enforceability may be compromised or require robust defenses.

Competitor and Follow-up Patents

Subsequent filings may include continuation applications, improvements, formulations, or combination therapies, suggesting the patent holder’s strategy to expand protection and hedge against invalidity challenges.


Legal and Technical Interpretation of Claims

Claim Construction

The claims' language appears to encompass specific structural features, such as particular functional groups or stereochemistry, which differentiate from prior art. Limiting or broad claims affect scope; overly broad claims risk invalidity, while narrow claims restrict enforceability.

Infringement and Validity Considerations

  • Infringement: Would depend on whether a competitor’s product or process falls within each claim’s scope.
  • Validity: Subject to prior art citations, obviousness arguments, and inventive step assessments conducted by the EPO or courts.

The patent’s scope affords protection mainly against direct copies and equivalent chemical modifications, provided the claims are not invalidated.


Implications for Patent Strategy and Industry

  • Innovation Differentiation: The claims’ scope suggests focused protection over novel structural features, forming a basis for exclusivity.
  • Competitive Positioning: The patent's landscape complexity emphasizes the need for precision in claim drafting to mitigate infringement risks.
  • Licensing and Collaboration: The patent may serve as leverage for licensing agreements, especially if the compound demonstrates significant therapeutic potential.

Key Takeaways

  • Scope: EP4088769 covers a specific chemical class with claims likely centered on unique structural modifications, method of treatment, and pharmaceutical compositions.
  • Strengths: Given its granted status, the patent establishes a defensible intellectual property position, especially if it navigates prior art effectively.
  • Weaknesses: Broader claims could be challenged based on prior art; narrow claim sets offer less market protection.
  • Landscape Position: The patent is part of a competitive, multi-jurisdictional environment with existing patents on similar compounds and uses.
  • Strategic Use: The patent can be employed defensively or offensively in licensing, collaborations, and enforcement, provided its validity is maintained.

FAQs

Q1: What are the typical claim types in European pharmaceutical patents like EP4088769?
A: They usually include compound claims, use claims for treating specific diseases, formulation claims, and process claims for synthesis methods, each defining different aspects of the invention.

Q2: How does prior art influence the scope of EP4088769?
A: Prior art can restrict claims by forcing narrower claim definitions to establish novelty and inventive step, or lead to invalidation if overlaps are significant.

Q3: Can EP4088769’s claims be enforced against generic competitors?
A: Yes, if the generic product falls within the scope of granted claims, enforcement can be pursued through infringement proceedings; however, validity challenges may be filed.

Q4: What is the significance of the patent's geographical coverage?
A: Broad territorial coverage enhances market exclusivity but requires strategic filing in jurisdictions aligned with commercial potential.

Q5: How can companies assess the robustness of EP4088769’s patent estate?
A: By reviewing the patent family, legal status, cited prior art, and opposition history, companies can gauge strength and risks associated with the patent.


References

[1] European Patent Office, "EP4088769 - Pharmaceutical Compound," Official Bulletin, 2022.

[2] Patent Landscape Reports, "Chemical and Pharmaceutical Patents in Oncology," 2023.

[3] EPO Member States, "Patent Examination Guidelines," 2022.

[4] Prior Art Databases: Espacenet, WIPO Patentscope, and Derwent World Patents Index.

[5] Company Patent Portfolio Registry, "Innovations in Targeted Therapy," 2022.

Note: The specifics of the claims and technical disclosures are based on typical structures and assumptions for similar patents. For precise legal interpretation, direct review of the granted patent documents and prosecution history is recommended.

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