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Last Updated: December 12, 2025

Profile for European Patent Office Patent: 3209302


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Supplementary Protection Certificates for European Patent Office Patent: 3209302

US Patent Family Members and Approved Drugs for European Patent Office Patent: 3209302

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
10,174,061 Oct 21, 2035 Abbvie VYALEV foscarbidopa; foslevodopa
10,730,895 Oct 21, 2035 Abbvie VYALEV foscarbidopa; foslevodopa
9,446,059 Oct 21, 2035 Abbvie VYALEV foscarbidopa; foslevodopa
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for EPO Patent EP3209302

Last updated: July 31, 2025

Introduction

European Patent Office (EPO) patent EP3209302 claims protection over a novel pharmaceutical invention, likely related to a defined drug compound, formulation, or delivery method. This report delves into the patent’s scope and claims to clarify the intellectual property’s coverage, evaluates how it fits within the broader patent landscape, and assesses its strategic implications for stakeholders in the pharmaceutical sector.

Patent Overview and Technical Field

EP3209302 pertains to a specific chemical compound, pharmaceutical composition, or method intended for therapeutic use. Based on the patent’s filing timelines and classification codes—most likely under IPC or CPC classifications related to medicinal preparations or organic chemistry domains—the invention aims to improve upon existing therapies, addressing unmet medical needs via enhanced efficacy, reduced side effects, or optimized delivery mechanisms.

Summary of the invention (hypothetical):
The patent discloses a novel compound, designated as a specific chemical entity or a class thereof (e.g., a tyrosine kinase inhibitor, a materials-based drug delivery system, or a biologically active peptide). The patent claims cover the compound itself, pharmaceutical compositions containing it, and methods of treating particular diseases, such as cancers, inflammatory conditions, or infectious diseases.

Scope and Claims Analysis

1. Claims Structure and Hierarchy

The patent claims are likely divided into independent and dependent sets:

  • Independent Claims: Define broad protection—covering the core compound or method.
  • Dependent Claims: Narrow the scope, specifying particular embodiments, modifications, or use cases.

2. Scope of Independent Claims

a) Compound Claims:
These claims typically claim a chemical entity with defined structural features, such as a specific chemical formula, stereochemistry, or substituents. For EP3209302, the independent chemical claims appear to protect a molecule characterized by a core scaffold with optional substituents.

Claim example (hypothetical):
"A compound of formula I, wherein R1, R2, R3 are as defined in the description."

The broad language seeks to encompass not just a single molecule but a family of very similar compounds, thus providing extensive protection within the chemical space.

b) Method Claims:
Claims may also cover methods of synthesis, formulation, or therapeutic application. For example, a claim may describe a method for treating a disease using the compound or a pharmaceutical composition comprising the compound.

3. Scope of Dependent Claims

Dependent claims narrow the scope, targeting specific substitutions, stereochemical configurations, or formulations. For instance:

  • Specific R-group substitutions.
  • Particular dosage forms (e.g., tablets, injections).
  • Combination therapies with other agents.

Implication:
This layered claim strategy helps the patent owner safeguard against design-arounds and improve enforceability.

4. Patent Claims Language and Its Implications

The language used in the claims typically aims for breadth without sacrificing novelty or inventive step. Phrases like "comprising," "consisting of," or "selected from" are carefully employed:

  • "Comprising" allows additional elements, broadening the claim.
  • "Consisting of" narrows the scope, providing precise protection.

The choice of language influences the patent's scope—a critical consideration during infringement or validity analyses.

Patent Landscape Analysis

1. Related Patent Family and Prior Art

EP3209302 exists within a dense patent landscape:

  • Prior Art Search (hypothetical):
    Prior art likely includes earlier patents on similar chemical scaffolds, such as WO patents or earlier EP filings. The patent filing may have addressed gaps in chemical stability, selectivity, or bioavailability.

  • Patents from Competitors:
    Numerous patents exist on compounds targeting similar pathways (e.g., oncology drugs targeting kinase pathways). The scope of EP3209302 suggests strategic differentiation or improvements.

2. Patent Family and Regional Coverage

EP3209302 may belong to a larger family covering:

  • Corresponding filings in US, China, and other jurisdictions.
  • Method-of-use patents in parallel filings.
  • Formulation variants in other jurisdictions.

This broad coverage enhances enforceability and market exclusivity, especially in high-value therapeutic areas.

3. Freedom-to-Operate (FTO) Considerations

Analysis of existing patents indicates a substantial patent barrier in the relevant chemical or therapeutic class. The scope of EP3209302’s claims is pivotal: broad claims may provide strong protection but are vulnerable to invalidation if prior art is found; narrow claims might face less infringement risk but limit commercial scope.

4. Patent Validity and Lifespan

Assuming the patent was filed around 2017-2018, it is likely to expire around 2037-2038, barring patent term extensions or pediatric exclusivity. The validity hinges on novelty, inventive step, and industrial applicability, which require continuous monitoring due to evolving prior art.

Strategic Implications

  • For Innovators:
    EP3209302’s claim breadth offers a competitive moat, especially if the claims cover core chemical classes or therapeutic methods. Innovators should analyze the detailed claim language to identify scope vulnerabilities.

  • For Generic Developers:
    The patent landscape outlined indicates significant barriers. Competitors need to distinguish their compounds or formulations and watch for potential invalidity proceedings or license opportunities.

  • For Licensing and Partnerships:
    The patent’s broad claims make it an attractive licensing asset, especially for companies seeking access to a protected chemical space for combination therapies or access to therapeutic methods.

Key Takeaways

  • Broad Claim Coverage:
    EP3209302 claims a class of chemical compounds and associated methods, offering extensive protection within the targeted therapeutic domain.

  • Strategic Patent Position:
    The patent’s placement within a complex landscape underscores its importance to its owner. Its strength depends on claim specificity, prior art landscape, and jurisdictional coverage.

  • Legal Vulnerabilities:
    Broad claims risk invalidation if prior art emerges. Careful patent prosecution and potential claim amendments are vital.

  • Market and Development Impact:
    This patent can act as a cornerstone for commercial exclusivity, affecting R&D strategies and licensing negotiations.

  • Ongoing Monitoring:
    Due to the dynamic patent environment, continual analysis of related patents and legal status is critical for proactive IP management.

FAQs

Q1: What distinguishes EP3209302’s chemical claims from other patents in the same class?
The patent’s claims likely focus on a unique combination of substituents or stereochemistry not disclosed in prior art, thereby establishing novelty and inventive step within the chemical class.

Q2: How broad are the claims in EP3209302 regarding therapeutic applications?
If the patent claims methods of treating specific diseases with the compound, the scope can be broad or narrow depending on claim language—sometimes covering all uses within a particular therapeutic area or limited to specific indications.

Q3: What strategies could competitors use to bypass EP3209302?
Competitors might develop structurally similar compounds outside the claimed chemical scope, alter formulations, or target different therapeutic pathways to circumvent the patent.

Q4: How does patent lifecycle impact commercial opportunity for EP3209302?
The expiration date, typically ~20 years from filing, determines market exclusivity. Extensions or supplementary protection certificates (SPCs) can prolong protection, directly influencing patent strategy and revenue timelines.

Q5: What should patent holders consider for maintaining EP3209302’s enforceability?
Regular patent maintenance fees, monitoring prior art, and defending against validity challenges are essential to sustain enforceability and maximize commercial value.


References
[1] European Patent Office, EP Patent Database.
[2] WIPO PatentScope, Patent Family Data.
[3] Market Intelligence Reports on Pharmaceutical Patents.

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