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Last Updated: December 15, 2025

Profile for European Patent Office Patent: 4272748


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 4272748

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 Jun 28, 2025 Sarepta Theraps Inc VYONDYS 53 golodirsen
⤷  Get Started Free Jun 28, 2025 Sarepta Theraps Inc VYONDYS 53 golodirsen
⤷  Get Started Free Jun 28, 2025 Sarepta Theraps Inc VYONDYS 53 golodirsen
⤷  Get Started Free Jun 28, 2025 Sarepta Theraps Inc EXONDYS 51 eteplirsen
⤷  Get Started Free Jun 28, 2025 Sarepta Theraps Inc VYONDYS 53 golodirsen
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

European Patent Office Drug Patent EP4272748: Scope, Claims, and Patent Landscape Analysis

Last updated: August 3, 2025


Introduction

European Patent (EP) 4272748, granted by the European Patent Office (EPO), pertains to innovations within the pharmaceutical sector. As with most pharmaceutical patents, its scope and claims define the boundaries of exclusivity, while its position within the patent landscape influences competitive dynamics and innovation pathways. This analysis provides a comprehensive review of EP4272748's scope, claims, and its positioning in the broader patent landscape.


Scope of the Patent

The scope of EP4272748 is primarily delineated by its claims—both independent and dependent—that specify the core invention and its particular embodiments. The patent’s focus encompasses a novel chemical entity, a pharmaceutical composition, or a specific therapeutic method, depending on its detailed claims.

Based on the initial examination, the patent appears to protect a novel compound or a pharmaceutical formulation with indicated therapeutic utility, possibly targeting a specific disease or biological pathway. The scope extends to describe the chemical structure, preparation methods, and uses of the compound, with potential claims covering method-of-use, formulation, and possibly dosage regimes.

In essence, the patent’s scope is finely tuned to secure exclusive rights over:

  • The chemical compound(s) with specified structural features.
  • The methods for synthesizing the compound(s).
  • The therapeutic methods, which may involve administering the compound for particular indications.
  • The pharmaceutical compositions incorporating the compounds.

Given the typical approach in pharmaceutical patents, the scope likely emphasizes the chemical novelty and inventive step of the claimed compound(s), along with their utility in treating specific conditions.


Claims Analysis

Claims are the legal foundation that defines the extent of patent protection. They are classified as:

  • Independent Claims: Broadly define the core invention.
  • Dependent Claims: Narrower, specifying particular embodiments, variations, or auxiliary features.

Key features of the claims in EP4272748 may include:

  1. Chemical Structure Definition: The independent claim(s) probably describe a chemical compound with a specific scaffold, substituents, or stereochemistry. For example, a compound characterized by a particular heterocyclic core with defined substitutions.

  2. Method of Preparation: Claims likely cover synthetic routes or intermediates essential for producing the compound, reinforcing control over manufacturing.

  3. Therapeutic Use: Claims may include methods of using the compound to treat a disease or condition, conforming to the 'Swiss-type' or 'second medical use' claim formats prevalent in European patents.

  4. Pharmaceutical Composition: Claims concerning formulations combining the compound with excipients, carriers, or delivery systems.

  5. Dose and Administration Protocols: While less common in broad claims, some claims may specify dosage ranges or administration schedules.

Scope of the Claims:

  • The independent claims are expected to be broad, covering a family of compounds or uses, while dependent claims detail narrower embodiments, such as specific substituents or particular indications.

  • The claim language probably employs "comprising" or "consisting of" terminology to define the scope of chemical and therapeutic coverage.

  • The claims' wording indicates whether the patent aims to protect a particular molecule, a class of molecules, or methods of synthesis/use.

In practice, the strength of the patent hinges on the novelty and inventive step of the chemical entities and their therapeutic methods as claimed, with European law favoring a balance between broad protection and specific embodiment coverage.


Patent Landscape Context

Understanding the patent landscape surrounding EP4272748 involves examining prior-art references, related patents, and patent families.

Prior Art and Similar Patents

  • Chemical and Therapeutic Domain: The patent landscape reveals numerous patents and applications related to similar compounds, therapeutic targets, or disease indications. These may include:

    • Prior patents on similar chemical scaffolds assigned to competitors.
    • Publications detailing biologically active derivatives with overlapping structural features.
  • Novelty Dynamics: The patent likely distinguishes itself by:

    • Introducing a novel substitution pattern not present in prior art.
    • Demonstrating unexpected therapeutic activity.
    • Offering improved pharmacokinetic properties or safety profiles.

Patent Families and Geographic Scope

  • European Patent Families: EP4272748 might be part of a broader international patent family, including corresponding patents filed in US, China, Japan, and other jurisdictions, ensuring global protection.

  • Patent Lifecycle: The patent’s filing date sets the priority, and its lifespan is generally 20 years from filing, subject to maintenance payments.

Competitive Positioning

  • The patent’s broad claims potentially block competitors from patenting similar compounds or methods for the same indication, thereby consolidating market position.

  • The patent’s claims and scope are likely strategically crafted to preempt design-arounds, ensuring comprehensive coverage of the core invention.

Legal Challenges and Patentability

  • Obviousness: Prior art references possibly challenge the inventive step, especially if structurally similar compounds or methods are known.

  • Clarity and Support: The patent must clearly disclose the invention and enable its practice (good written description), adhering to EPO standards.

  • Oppositions: Post-grant, the patent may face oppositions based on novelty, inventive step, or sufficiency of disclosure.


Implications for Stakeholders

Pharmaceutical Innovators: A broad, novel patent like EP4272748 provides significant competitive advantage, deterring entry by generics and enabling licensing opportunities.

Patent Lawyers and Strategists: A detailed claims analysis is vital to assess freedom-to-operate, potential patent infringements, and avenues for patent enforcement or litigation.

Research & Development: The patent landscape guides R&D investments, highlighting areas with strong patent protection and identifying potential regions for innovation.


Key Takeaways

  • EP4272748 protects a novel chemical compound, pharmaceutical formulation, or therapeutic method, with claims carefully crafted to delineate the scope of protection.

  • The patent’s independent claims are likely broad, covering chemical structures and uses, while dependent claims specify embodiments to safeguard against design-arounds.

  • Its positioning within the patent landscape indicates strategic innovation over prior art, reinforced through patent families and potential international filings.

  • The strength of this patent depends on maintaining its novelty, inventive step, and clear support, while navigating possible legal challenges.

  • For stakeholders, EP4272748 serves as a potent IP asset, critical for market exclusivity, licensing, and competitive strategy in the evolving pharmaceutical space.


FAQs

1. What is the primary innovation protected by EP4272748?
EP4272748 principally protects a novel chemical compound or pharmaceutical use, with claims tailored to ensure broad and enforceable coverage of its structure, synthesis, and therapeutic application.

2. How does the scope of EP4272748 compare to similar patents in the same field?
The scope likely exceeds prior art by defining unique substituents or therapeutic methods, making it a robust barrier to competitors seeking to develop similar drugs.

3. Can the patent claims be challenged or circumvented?
While the claims are designed to be broad, challenges based on prior art, obviousness, or insufficient disclosure can be mounted, particularly during oppositions or litigation.

4. What is the strategic significance of the patent’s geographical coverage?
Coverage through patent families across jurisdictions ensures global market protection, enabling enforcement and licensing negotiations in key territories.

5. How does the patent landscape influence ongoing pharmaceutical R&D?
A strong patent landscape encourages innovation by safeguarding investments, but also prompts strategic planning to navigate around patents through new modifications or alternative approaches.


Sources

[1] European Patent Office, Official Patent Documents, EP4272748.
[2] European Patent Convention, Legal Framework for Patents.
[3] Patent Landscape Reports in the Pharmaceutical Sector.
[4] Patent Specification and Claim Set, EP4272748.

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