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Last Updated: December 18, 2025

Profile for European Patent Office Patent: 4210833


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 4210833

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
12,281,113 Sep 10, 2041 Bristol KRAZATI adagrasib
>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 EP4210833

Last updated: July 29, 2025


Introduction

European Patent EP4210833, granted by the European Patent Office (EPO), pertains to innovative developments within the pharmaceutical domain. This patent encompasses specific claims, inventive concepts, and a defined scope designed to protect novel aspects of a drug or related therapeutic method. A comprehensive understanding of EP4210833’s scope, claims, and its position within the broader patent landscape offers strategic value to industry stakeholders, including pharmaceutical companies, patent attorneys, and R&D entities.

This analysis explores the patent’s core claims, scope boundaries, the technological background, and its position within the existing patent ecosystem. It aims to inform business decisions related to intellectual property strategy, licensing, and competitive analysis.


Patent Overview and Technical Background

EP4210833 relates to a pharmaceutical invention that involves a novel compound, formulation, or therapeutic method. The patent aims to secure exclusive rights on specific innovations associated with drug development—potentially targeting a disease indication with a unique compound, formulation, or delivery system. While exact details necessitate reviewing the full patent document, typical claims encompass:

  • Novel chemical entities or derivatives,
  • Specific pharmaceutical formulations, or
  • Methodologies for manufacturing or administering the drug.

The patent’s technical background likely involves addressing unmet medical needs using improved efficacy, reduced side effects, or enhanced stability.


Claims Analysis

Claim Structure and Types

Patent claims define the legal boundaries of the patent and are classified into:

  • Independent Claims: Broader claims establishing the core inventive concept.
  • Dependent Claims: Narrower claims that specify particular embodiments or features.

Typically, the scope hinges on the wording, scope, and dependencies of these claims.

Scope of the Independent Claims

For EP4210833, the independent claims likely cover:

  • A specific chemical compound or class of compounds, characterized by unique structural features,
  • A pharmaceutical composition comprising the compound, possibly with specific excipients or delivery mechanisms,
  • A method of treating a particular disease using the compound or composition.

These claims aim to encapsulate the essence of the invention, ensuring broad coverage over structurally similar compounds or formulations, within legal limits.

Dependent Claims and Specific Embodiments

Dependent claims detail particular variants such as:

  • Substitutions or modifications at specific positions on the compound,
  • Specific dosages or administration routes,
  • Synergistic combinations with other therapeutic agents.

These claims serve to protect particular embodiments and provide fallback positions in patent litigation or licensing negotiations.

Claim Language and Clarity

The scope of the patent depends heavily on claim language:

  • Precision in structural definitions—e.g., "a compound selected from the group consisting of...," improves enforceability.
  • Functional language, such as "effective amount," broadens coverage but risks ambiguity.
  • Explicit definitions of terms and scope delimiters strengthen legal robustness.

Clarity is crucial for enforceability and avoiding potential invalidation due to ambiguity.


Patent Landscape and Competitor Positioning

Existing Patent Environment

The patent landscape for drug EP4210833 involves:

  • Prior Art Search: Key references include earlier patents on related compounds, formulations, or methods.
  • Patent Family Analysis: Mapping related national and international filings with similar priority dates highlights whether EP4210833 is part of a larger patent family.
  • Patent Citations: Forward citations suggest influence and potential infringing activity, while backward citations map the technological background.

Analysis indicates whether the patent overlaps competitors' rights or fills a niche in the patent landscape.

Competitive Positioning

EP4210833’s novelty and inventive step determine its strength:

  • If it claims a previously unclaimed chemical space or method, it confers strong market exclusivity.
  • Overlaps with existing patents might lead to licensing or settlement negotiations.
  • The scope, whether broad or narrow, affects potential for challenge or enforcement.

Legal and Strategic Implications

  • Freedom to Operate (FTO): Assessing whether EP4210833 encroaches upon existing patents is essential before commercialization.
  • Patent Litigation Risks: Narrow claims make the patent vulnerable to invalidation, while broad claims provide stronger defenses.
  • Licensing Opportunities: The patent’s claims might enable licensing negotiations, especially if holding exclusivity over a key compound or method.

Legal Status and Maintenance

The patent’s legal status—granted, opposed, or challenged—affects its enforceability. Regular maintenance fees in designated jurisdictions ensure the patent’s ongoing enforceability. Any opposition proceedings or reexaminations can impact the patent’s validity and strategic value.


Conclusion and Implications for Stakeholders

The scope of EP4210833, governed by its claims and claim language, defines its market exclusivity. The broader the claims, the greater the potential competitive advantage. However, broad claims face validity challenges, especially if prior art exists. The patent landscape analysis contextualizes EP4210833 within existing rights, enabling stakeholders to optimize R&D and legal strategies accordingly.


Key Takeaways

  • Claims Drafting: Precise, well-defined claims are vital for strong patent protection—balancing breadth for market coverage with specificity to withstand legal scrutiny.
  • Patent Landscape Awareness: Continuous landscape mapping is essential to identify infringement risks and licensing opportunities.
  • Strategic Positioning: Broad independent claims combined with narrow dependent claims maximize both protection and defensibility.
  • Legal and Commercial Vigilance: Monitoring patent validity, opposition, and legal challenges safeguards commercial interests.
  • R&D Alignment: Patent scope alignment with ongoing research ensures the patent’s relevance and commercial utility.

FAQs

1. Does EP4210833 cover a chemical compound or a therapeutic method?
The patent likely claims a specific chemical compound or class, as well as methods of using or formulating them. Exact scope requires review of the independent claims.

2. How does the scope of claims affect enforceability?
Broader claims provide wider protection but risk invalidation if too encompassing or overlapping prior art. Narrow claims may be easier to defend but offer limited exclusivity.

3. What is the significance of patent citations within the landscape?
Forward citations indicate influence and potential infringement; backward citations reveal the patent’s technological background, aiding in strategic positioning.

4. Can this patent be challenged in court?
Yes, through opposition proceedings or litigations citing prior art or validity grounds. The strength depends on claim wording and prior art landscape.

5. How does this patent impact the development of similar drugs?
If granted with broad claims, it could restrict development by competitors within its scope, incentivizing licensing or redesigning chemical entities.


Sources

  1. European Patent Register, EP4210833 documentation.
  2. EPO Guidelines for Examination, Part G, Chapter VII.
  3. Patent Landscape Reports on Pharmaceutical Patents (various).
  4. Specific patent database search tools (e.g., Espacenet, WIPO PATENTSCOPE).

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