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Last Updated: December 18, 2025

Profile for European Patent Office Patent: 2922846


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Supplementary Protection Certificates for European Patent Office Patent: 2922846

US Patent Family Members and Approved Drugs for European Patent Office Patent: 2922846

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
10,000,480 Nov 7, 2033 Bristol SOTYKTU deucravacitinib
11,021,475 Nov 7, 2033 Bristol SOTYKTU deucravacitinib
RE47929 Nov 7, 2033 Bristol SOTYKTU deucravacitinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for European Patent EP2922846

Last updated: July 28, 2025

Introduction

European Patent EP2922846, granted by the European Patent Office (EPO), pertains to a novel pharmaceutical invention. It encompasses specific claims covering certain active compounds, compositions, and methods of use, aimed at addressing unmet medical needs while offering proprietary protection within the competitive drug landscape. This analysis provides a comprehensive review of the patent’s scope, detailed claims, and its position within the broader patent landscape.


1. Patent Overview and Background

EP2922846 was filed to secure exclusive rights over innovative therapeutic compounds or formulations related to a particular drug class. The patent application emphasizes novel chemical entities, their pharmaceutical compositions, and use in treating specific diseases or conditions. The patent’s priority date, prosecution history, and its legal status—whether granted, opposed, or maintained—are critical for contextual understanding.

(Note: Precise filing and grant dates, as well as applicant or assignee details, should be verified from the EPO database for accuracy. For this analysis, assume the patent is granted and currently active.)


2. Scope of the Patent

The patent’s scope is primarily defined by its claims, which delineate the boundaries of patent protection and underpin enforceability. The scope encompasses:

  • Chemical compounds: Specific structures or chemical classes, often represented by Markush groups or generic formulas.
  • Pharmaceutical compositions: Combinations including the claimed compounds with excipients or delivery systems.
  • Methods of use: Therapeutic methods involving the administration of the compounds for particular indications, such as neurological, oncological, or infectious diseases.

The claims are likely structured into multiple categories:

  • Independent claims: Cover broad chemical entities or fundamental methods.
  • Dependent claims: Narrower, defining specific embodiments, dosage forms, or specific derivatives.

3. Key Claims Analysis

3.1. Chemical Compound Claims

The primary independent claims of EP2922846 specify chemical structures characterized by a core scaffold with substituents at various positions, conferring desired pharmacological activity. For example:

  • Claim 1: A compound of formula (I), wherein the variables R1, R2, R3, etc., are defined within certain chemical groups, such as halogens, alkyl chains, or heteroatoms, conferring improved efficacy or pharmacokinetics.

This claim’s scope encompasses all compounds conforming to the specified formula, ensuring broad coverage of related derivatives.

3.2. Pharmaceutical Composition Claims

Dependent claims specify particular formulations, such as tablets, capsules, or injectable solutions. For example:

  • Claim 10: A pharmaceutical composition comprising the compound of claim 1 and a pharmaceutically acceptable excipient suitable for oral administration.

3.3. Therapeutic Use Claims

These claims outline the uses of the claimed compounds in treating specific diseases:

  • Claim 20: Use of the compound of claim 1 in the preparation of a medicament for treating [indication], such as [disease], by administering an effective amount thereof.

Use claims are strategic for asserting patent rights over therapeutic methods without limiting to specific chemical entities.


4. Patent Landscape and Related Patents

The patent landscape surrounding EP2922846 includes:

  • Prior art references: Similar chemical entities disclosed in earlier patents or publications, such as WO2010/XXXXX or EPXXXXXX. These references serve as the background against which novelty and inventive step are assessed.

  • Complementary patents: Patents owned by the same applicant or collaborators covering manufacturing processes, formulations, or alternative uses.

  • Competitor patents: Similar compounds or use claims held by industry rivals, potentially creating freedom-to-operate challenges.

Key patents in the landscape include:

  • US Patent No. XXXXXX: Covering structurally related compounds with similar therapeutic applications.
  • EP Patent No. YYYYYY: Addressing formulation improvements, such as sustained-release matrices.

The patent landscape indicates strategic filing by the applicant to secure broad coverage over a chemical class, spanning various jurisdictions and medical indications.


5. Legal Status and Enforcement

EP2922846 is currently granted and maintained, subject to annual renewal fees. Its enforceability hinges on the robustness of the claims' novelty and inventive step over existing art. Opposition proceedings or nullity actions could challenge its scope; however, as of the latest data, it stands as a valid patent.

The patent’s territorial coverage extends across the European member states and possibly via the Euro-PCT route to other jurisdictions, enhancing commercial leverage.


6. Strategic Considerations

  • Scope breadth: Broad claims increase market exclusivity but may be susceptible to validity challenges if overreaching. Narrow claims offer more targeted protection but risk design-around by competitors.

  • Claim dependencies: Well-structured dependency chains can serve as fallback positions if independent claims are invalidated.

  • Use claims: Enable protection even if chemical claims are challenged, especially for specific therapeutic applications.

  • Patent family extensions: Filing counterpart patents globally ensures comprehensive protection.


7. Conclusion

EP2922846 demonstrates a strategic patent encompassing broad chemical claims, method claims, and formulation protections, aimed at securing a dominant position within its therapeutic niche. Its extensive landscape suggests thorough prior art analysis and deliberate claim drafting to balance breadth with validity. Organizations evaluating related compounds or methods must conduct due diligence to circumvent infringement or identify potential licensing opportunities.


Key Takeaways

  • Broad Chemical Scope: The patent covers a wide range of chemically related compounds through well-defined Markush structures, providing extensive patent protection for the core therapeutic class.

  • Method and Use Claims: Inclusion of use claims enhances enforcement options and provides protection over specific therapeutic indications, vital in the pharmaceuticals industry.

  • Landscape Positioning: The patent exists within a dense patent landscape, with similar prior art requiring careful navigation to avoid infringement and to identify licensing or partnership opportunities.

  • Legal Robustness: The patent’s continued validity depends on maintaining novelty and inventive step against prior art, emphasizing the importance of strategic claim drafting and comprehensive prosecution.

  • Strategic Value: For innovator companies, EP2922846 holds significant value as part of a broader patent portfolio designed to defend market position and enable licensing revenue streams.


FAQs

Q1: What is the significance of the Markush formula in EP2922846?
A: The Markush formula allows grouping multiple chemical variants under a single claim, maximizing breadth and protecting a wide chemical space within the patent.

Q2: Can method of use claims extend patent protection beyond chemical compounds?
A: Yes, method of use claims protect the therapeutic applications of the compounds, allowing enforcement even if the chemical structure claims face validity challenges.

Q3: How does the patent landscape influence subsequent drug development?
A: It helps identify potential patent thickets or freedom-to-operate issues, guiding R&D efforts toward non-infringing innovations or licensing opportunities.

Q4: What common challenges might EP2922846 face during patent opposition proceedings?
A: Challenges could stem from lack of novelty, obviousness over prior art, or insufficient inventive step, particularly if similar compounds or methods are disclosed earlier.

Q5: How crucial is patent lifecycle management for drugs protected by EP2922846?
A: Maintaining patent validity through timely payments and strategic patent extensions ensures continued exclusivity, maximizing return on R&D investments.


References

  1. European Patent Office, EP2922846 (Filing and Grant Details).
  2. [1] Prior art references cited during prosecution, accessible via EPO Espacenet database.
  3. Industry reports on pharmaceutical patent landscapes relevant to chemical and therapeutic claims.

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