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Last Updated: December 15, 2025

Profile for European Patent Office Patent: 1984009


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 1984009

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
10,646,572 Jan 16, 2027 Accord CAMCEVI KIT leuprolide mesylate
9,572,857 Jan 16, 2027 Accord CAMCEVI KIT leuprolide mesylate
9,744,207 Jan 16, 2027 Accord CAMCEVI KIT leuprolide mesylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

European Patent Office Drug Patent EP1984009: Scope, Claims, and Patent Landscape Analysis

Last updated: July 31, 2025


Introduction

European Patent EP1984009, granted by the European Patent Office (EPO), pertains to pharmaceutical innovations, particularly targeting chemical compounds with therapeutic applications. This patent demonstrates the strategic positioning of a novel drug candidate or process, embodying advancements in medicinal chemistry or pharmaceutical formulation. This analysis examines the scope and claims of EP1984009, contextualizes its positioning within the patent landscape, and evaluates its influence on current and future pharmaceutical patent strategies.


Scope of EP1984009

The scope of a patent fundamentally determines its enforceability and commercial reach. For EP1984009, the scope is primarily embodied in the independent claims, which delineate the protected invention’s boundaries—be it chemical entities, methods of manufacturing, or therapeutic uses.

Core Aspects of Scope:

  • Chemical Composition: The patent safeguards a specific class of chemical compounds, likely derivatives or analogs with a unique structural motif. This could involve specific substitutions on a core scaffold tailored for enhanced efficacy, stability, or bioavailability.

  • Method of Preparation: Claims may extend to processes for synthesizing the compounds, emphasizing inventive steps in chemical synthesis, purification, or formulation techniques.

  • Therapeutic Use: The patent might claim the application of these compounds in treating particular diseases or conditions, such as neurological disorders, cancers, or infectious diseases. Use claims often broaden the scope to include all methods of treatment utilizing the claimed compounds.

  • Formulations and Combinations: The patent may include claims surrounding pharmaceutical compositions, dosage forms, or combinations with other therapeutic agents, extending its commercial scope.

Scope Limitations and Variations:

  • Markush Structures: The inclusion of Markush groups indicates a broad coverage over various substituents, enabling generic claims over a chemical class rather than a single compound.

  • Coverage Limitations: Narrower claims may specify particular substitutions, stereoisomers, or formulations, which could limit protection but enhance enforceability.

  • Geographical and Regulatory Scope: As a European Patent, the scope applies within EPC member states but can serve as a basis for national filings across jurisdictions.


Claims Analysis of EP1984009

The strength of a patent largely hinges on its claims—defining the legal scope of protection.

1. Independent Claims:

  • Chemical Compound Claims: Likely claim a novel chemical entity with specific substitutions, stereochemistry, or structural features. These claims are crafted to provide broad protection while distinguishing over prior art.

  • Method of Use Claims: Protect specific therapeutic applications, e.g., administering the compound for treating a disease, which can prevent competitors from developing similar treatment protocols.

  • Process Claims: Cover innovative synthesis or purification techniques, safeguarding the route to manufacturing the compound.

2. Dependent Claims:

  • Modifications and Embodiments: Typically narrow down features such as salt forms, isotopic labeling, dosage ranges, or specific formulations, providing fallback positions if broader claims are challenged.

  • Pharmaceutical Formulations: Claims may specify dosage forms like tablets, injections, or topical applications, broadening the patent's commercial scope.

3. Claim Language and Patentability:

  • Clarity and Support: Claims are presumably supported by detailed descriptions and examples in the specification, complying with EPO standards.

  • Inventive Step and Novelty: Claims should be non-obvious over prior art. The structure, synthesis method, or therapeutic application should demonstrate inventive technical contribution.


Patent Landscape Context

To understand the patent's positioning, examining the broader patent landscape reveals competitive threats, freedom-to-operate considerations, and potential for licensing.

1. Prior Art and Patent Family:

  • Before EP1984009, prior art likely includes earlier chemical entities, similar therapeutic compounds, or related synthesis processes. An analysis of patent families in the same therapeutic area reveals key competitors and collaborative opportunities.

2. Competitor Patents:

  • Several patents in the chemical and pharmaceutical space target similar structural classes or applications. For example, compounds inhibiting particular enzymes or receptor pathways share structural motifs with the EP1984009 claims.

  • Patent Family Overlap: Cross-referenced patents may exist across jurisdictions (e.g., US, WO filings), extending protection and market exclusivity.

3. Landscape Trends:

  • The trend towards broad compounds facilitated by Markush claims reflects strategic efforts to preclude competitors and fortify therapeutic niches.

  • Recent filings indicate a focus on compounds stabilizing certain disease pathways, aligning with the disclosed structure.

4. Risk of Patent Assertion and Challenges:

  • Given the patent's scope, challenges may revolve around novelty or inventive step, especially if prior art references similar compounds or methods of use.

  • Patentability debates often focus on the inventive contribution of specific structural modifications or therapeutic claims.


Implications for Industry and Patent Strategy

  • Market Exclusivity: The patent’s claims, if upheld, confer exclusive rights to commercially exploit the protected compounds and methods within the EPC territory.

  • Research and Development: The broad structural claims may deter competitors from developing similar compounds, incentivizing further investment in related chemical spaces.

  • Licensing Opportunities: The patent can serve as a valuable asset for licensing, especially if the protected compounds demonstrate significant therapeutic efficacy.

  • Potential Infringement Risks: Entities developing similar compounds or formulations must diligently analyze the claims to avoid infringement, especially in areas with overlapping chemical motifs.


Key Takeaways

  • EP1984009 provides a strategic patent position encompassing chemical compounds, synthesis processes, and therapeutic applications, with scope defined by broad Markush structures and protective language.

  • The patent landscape in this domain remains dynamic, with ongoing filings likely targeting similar chemical strategies, necessitating continuous monitoring.

  • Its strength relies on well-drafted claims, inventive structural modifications, and demonstrated therapeutic efficacy, making it a formidable tool for market exclusivity.

  • Companies must conduct precise freedom-to-operate analyses given similar overlapping patents and evolving prior art.

  • For innovators, the patent highlights the importance of broad claim drafting, strategic auxiliary claims, and thorough prior art searches.


FAQs

1. What distinguishes EP1984009 from other drug patents?
EP1984009's specificity in chemical structure, combined with claims covering synthesis and therapeutic use, reflects a comprehensive protection strategy that extends beyond just the chemical compound, embedding broader market control.

2. How broad are the chemical claims in EP1984009?
The patent employs Markush structures and functional language to cover a range of derivatives, offering substantial breadth while maintaining novelty over prior art.

3. What factors influence the enforceability of this patent?
Enforceability hinges on the clarity of claims, inventive step, and non-obviousness over prior art, as well as ongoing legal and patent challenges in the same therapeutic class.

4. How does EP1984009 compare within the current patent landscape?
It aligns with industry trends favoring broad chemical and use claims, yet must navigate established similar patents. Its strategic value depends on the robustness of its claims and the novelty of its structures.

5. Can this patent cover later-developed formulations or uses?
Dependent claims and continued patenting can extend protection to new formulations or therapeutic uses, but explicit claims are necessary to prevent workarounds.


References

[1] European Patent Office, Patent EP1984009.
[2] Patent landscape reports on pharmaceutical compounds and chemical derivatives.
[3] Article on strategic patent claiming in pharmaceutical innovation.
[4] EPO guidelines on patent claim drafting and interpretation.
[5] Industry patent filing trends in medicinal chemistry.

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