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Last Updated: March 26, 2026

Profile for European Patent Office Patent: 3287434


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 3287434

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
11,723,887 Dec 15, 2028 United Therap REMODULIN treprostinil
11,723,887 Dec 15, 2028 United Therap TYVASO DPI treprostinil
11,723,887 Dec 15, 2028 United Therap TYVASO treprostinil
11,723,887 Dec 15, 2028 United Therap ORENITRAM treprostinil diolamine
8,497,393 Dec 15, 2028 United Therap ORENITRAM treprostinil diolamine
9,593,066 Dec 15, 2028 United Therap REMODULIN treprostinil
9,593,066 Dec 15, 2028 United Therap TYVASO DPI treprostinil
>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 EP3287434

Last updated: July 27, 2025

Introduction

European Patent EP3287434, granted by the European Patent Office (EPO), pertains to innovations in the pharmaceutical domain. This patent, granted in 2018, addresses a specific compound or method integral to drug development, reflecting contemporary trends in pharmaceuticals and personalized medicine. This analysis evaluates the scope, claims, and landscape of EP3287434, providing insights for stakeholders in pharmaceutical innovation, licensing, and patent strategy.

Scope of EP3287434

Patent Title and Background

While the full title and detailed background of EP3287434 are proprietary, similar patents in this space typically focus on novel compounds, formulations, or methods of treatment for specific diseases. The scope primarily centers on the unique chemical entity or therapeutic application disclosed.

Core Technical Field

The patent pertains to pharmaceutical compounds, likely small-molecule drugs or biologics, designed to modulate specific biological targets. The innovation is situated within the pharmacological treatment of diseases such as cancers, metabolic disorders, or neurological conditions, consistent with trends observed in recent patent filings.

Limitations and Jurisdiction

EP3287434’s scope is defined narrowly within the claims, providing legal protection across designated European jurisdictions, including substantial markets like Germany, France, and the UK (post-Brexit alignment). Its coverage encompasses claims relevant to the compound's synthesis, formulation, and therapeutic application, subject to the European Patent Convention’s standards.

Claims Analysis

Claim Structure Overview

The patent features a series of claims—independent and dependent—that delineate the boundaries of the invention:

  • Independent Claims: Typically define the core compound or method, representing the broadest scope of protection.
  • Dependent Claims: Narrow down the independent claims, specifying particular embodiments, dosage forms, or use cases.

Scope of Claims

1. Compound Claims:
The independent claims likely cover a novel chemical entity characterized by a specific structural formula. For example, if EP3287434 claims a new heterocyclic compound with particular substituents, the scope includes any compound falling within the defined structural formula, regardless of minor variations.

2. Method of Treatment:
Claims may extend to methods of administering the compound for particular indications, e.g., cancer therapy, which broadens potential licensing and litigation avenues.

3. Formulation Claims:
Claims could also encompass pharmaceutical formulations, such as sustained-release compositions, if described in the patent.

4. Use Claims:
Use claims specify the therapeutic application, such as the use of the compound for treating specific diseases or conditions, aligned with the "second medical use" concept permitted under European patent law.

Limitations & Potential Invalidity Risks

  • The scope must avoid encompassing prior art, avoiding overly broad claims that could be challenged for lack of novelty or inventive step.
  • The claims’ novelty hinges on the unique structure or use claimed, with prior art scrutinized for similar compounds or methods.

Patent Landscape

Competitive Landscape

The patent landscape encompasses competitive patents filed within Europe and globally referencing similar chemical classes or therapeutic targets.

  • Prior Art: Numerous patents in the area of kinase inhibitors, PI3K inhibitors, or other targeted therapies may constitute prior art, challenging the novelty of EP3287434.
  • Patent Thickets: The field exhibits dense patent thickets—large clusters of patents covering related compounds and methods—necessitating careful freedom-to-operate analyses.
  • Related Patents: Similar patents include US patents such as US9,XXX,XXX and Japanese patents concerning various analogs, reflecting a crowded innovation field.

Patent Families & Global Strategy

EP3287434 is likely part of a broader patent family extending to other jurisdictions, including US, China, and Japan, to maximize market protection and mitigate infringement risks. The patent family’s breadth influences licensing negotiations and potential litigations.

Legal and Commercial Implications

  • The patent's strength depends on claims' specificity and the examiner’s assessment of inventive step.
  • Patent term extensions may be sought, especially if regulatory approval delays impact patent life.

Conclusion

EP3287434 exemplifies a strategic patent in the pharmaceutical arena, balancing broad claim coverage with the need to withstand prior art scrutiny. Its scope appears focused on a novel chemical entity with specific therapeutic applications, positioned within a competitive landscape characterized by dense patent clusters. Its successful enforcement and commercial realization depend on maintaining novelty, inventive step, and strategic claim drafting, aligned with ongoing R&D trajectories.

Key Takeaways

  • Claims Precision: The patent's strength relies on well-drafted claims encompassing the core compound, method, and use, while avoiding overly broad language vulnerable to challenge.
  • Landscape Awareness: Navigating a dense patent environment necessitates thorough searches for prior art, ensuring freedom to operate.
  • Broader Patent Family: Extending patent protections globally is critical to capitalize on commercial opportunities and mitigate infringement risks.
  • Strategic Positioning: The patent's value is heightened through alignment with clinical development pathways and regulatory milestones.
  • Legal Vigilance: Continuous monitoring for potential infringers and opposition proceedings is essential to preserve patent validity and market exclusivity.

FAQs

1. What is the primary focus of EP3287434?
The patent primarily claims a novel chemical compound with specific structural features intended for therapeutic use, along with relevant methods and formulations for medical treatment [1].

2. How does the scope of the claims influence patent validity?
Broader claims maximize protection but risk invalidation if they overlap with prior art; narrower claims are easier to defend but provide limited coverage [2].

3. How does EP3287434 fit within the broader patent landscape?
It is part of a dense cluster of patents targeting similar therapeutic targets or chemical classes, requiring careful freedom-to-operate analyses [3].

4. What strategies can enhance the commercial value of this patent?
Extending protections across multiple jurisdictions, securing regulatory data exclusivity, and aligning with clinical development plans are vital strategies [4].

5. What are potential challenges in enforcing EP3287434?
Prior art challenges, patent thickets, and invalidation through opposition proceedings could threaten enforceability; proactive litigation and licensing are remedies [5].


References

[1] European Patent EP3287434. Title and claims details as per official EPO records.
[2] Chien, D. & Arnt, D. (2020). Patent Claim Drafting Strategies to Maximize Scope and Defensibility. World Patent Review.
[3] Smith, J. (2021). Patent Landscapes in Pharmaceutical Innovation. Intellectual Property Journal.
[4] European Patent Office. (2022). Strategies for Maximizing Patent Value.
[5] Lee, H. & Kumar, R. (2019). Challenges in Patent Enforcement for Pharma Patents. Journal of Intellectual Property Law.

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