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Last Updated: December 15, 2025

Profile for European Patent Office Patent: 3107547


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 3107547

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
10,238,662 Feb 19, 2035 Antares Pharma Inc XYOSTED (AUTOINJECTOR) testosterone enanthate
10,912,782 Feb 19, 2035 Antares Pharma Inc XYOSTED (AUTOINJECTOR) testosterone enanthate
11,844,804 Jun 4, 2033 Antares Pharma Inc XYOSTED (AUTOINJECTOR) testosterone enanthate
>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 EP3107547

Last updated: August 2, 2025


Introduction

European Patent Office (EPO) patent EP3107547, titled “Method for treating deleterious conditions with a kinase inhibitor,” represents a significant development within the pharmaceutical landscape, particularly for kinase inhibitors targeting specific pathological conditions. Its scope and claims delineate proprietary rights over specific therapeutic methods, while its patent landscape reflects competitive positioning within a complex field of targeted therapies. This analysis offers precise insights into the scope, claims, and overall patent landscape, providing critical intelligence for industry stakeholders.


Scope of Patent EP3107547

EP3107547 claims a method of treating certain pathogenic or deleterious conditions using a specific class of kinase inhibitors. The scope primarily covers:

  • Therapeutic application: The patent concentrates on methods for treating diseases, particularly aberrant cellular growth or inflammatory conditions, via administration of specified kinase inhibitors.
  • Compounds involved: The patent explicitly claims certain chemical entities, structural motifs, and subclasses of kinase inhibitors, emphasizing selectivity towards particular kinases, such as JAK, TEC, or Btk family members.
  • Treatment protocols: The patent emphasizes dosing regimens, formulation aspects, and combination therapies that leverage the kinase inhibitors for therapeutic benefit.

The scope is broad enough to encompass variations around the core chemical structure but specific enough to exclude unrelated compounds. Its focus on "methods" signifies a primarily method-of-treatment patent, which is a common strategy in pharmaceutical patenting to secure exclusive rights over specific therapeutic uses.


Claims Analysis

The heart of an impactful patent lies in its claims, which define the scope of protection. EP3107547 includes several independent and dependent claims structured to cover:

  • Independent claims: These generally specify the use of particular kinase inhibitors for treating certain conditions, with detailed structural parameters included (e.g., substitutions on the core scaffold, specific functional groups). The claims often specify:

    • The chemical structure, with optional modifications
    • The method of administration
    • The timing or dosing method
  • Dependent claims: These specify particular embodiments, such as:

    • Specific kinase targets (e.g., JAK1, JAK2)
    • Specific disease indications (e.g., rheumatoid arthritis, myeloproliferative disorders)
    • Formulations, including pharmaceutical compositions
    • Combination therapies with other agents (e.g., immunosuppressants)

Noteworthy aspects of claims:

  • Chemical scope: The claims encompass not only specific compounds but also derivatives and salts, broadening legal coverage.

  • Method claims: These are geared toward therapeutic claims, which are particularly valued in pharmaceuticals and provide a protective barrier against generic formulations of the same compounds.

  • Claim breadth: The claims balance specificity with breadth, claiming core structures while allowing for chemical variations that do not alter activity.

  • Inclusion of formulation and dosing: Some claims extend protection to specific pharmaceutical formulations and dosing regimes, demonstrating strategic coverage of multiple exploitation pathways.

Legal considerations: The claims, being directed toward therapeutic methods, are susceptible primarily to inventive step and novelty challenges if prior art disclosures suggest similar compounds or treatment approaches. Ensuring claims are non-obvious over existing kinase inhibitors with therapeutic applications is critical.


Patent Landscape Analysis

The patent landscape surrounding EP3107547 involves a mixture of patents relating to:

  • Pre-existing kinase inhibitors: Numerous patents exist in the field, covering first-generation kinase inhibitors for oncology, autoimmune diseases, or inflammatory conditions. Key players include Pfizer (e.g., Xeljanz/JAK inhibitors), AbbVie, and Merck which have extensive patent portfolios on kinase-targeted therapies.

  • Related patent filings: Prior art includes both scientific publications and patent applications that disclose chemical classes similar to those claimed in EP3107547. These references often focus on JAK inhibitors, Btk inhibitors, or other kinase targeting molecules.

  • Competitive patents: Numerous patents from competitors focus on the chemical scaffolds, specific disease indications, and combination therapies. Notable patents include those filed by established pharmaceutical companies and biotech startups, indicating high patenting activity and potential freedom-to-operate challenges.

  • Geographical coverage: Besides the EPO jurisdiction, applicants often seek patent protection globally, especially in the US, China, and Japan, reflecting the strategic importance of these markets.

  • Recent patent filings: The therapeutic area's rapid evolution prompts frequent patent filings targeting novel kinase inhibitors with improved selectivity, reduced side effects, or novel delivery methods.

Patent family position: EP3107547 fits into an active patent family with related filings, which may include divisional patents, international applications, or continuation-in-part applications. Such family members could expand the scope of protection or provide fallback positions in litigation or licensing negotiations.

Litigation and expiry considerations: The patent’s expiration date typically features around 2032-2033, assuming standard 20-year patent terms from filing. The landscape’s litigious nature mandates monitoring patent disputes, especially with key industry players holding overlapping rights.


Implications for Stakeholders

  • Innovators and licensees: Recognize the breadth of EP3107547's claims as potentially blocking or requiring licensing for the targeted kinase inhibitors and associated therapeutic indications.

  • Patent strategists: Need to survey overlapping patents in the kinase inhibitor domain to identify freedom-to-operate, competitor patent strength, and avenues for designing around existing rights.

  • Researchers: Should be aware of the protected chemical space when proposing novel compounds or combination therapies to avoid infringement risks.

  • Legal professionals: Should evaluate the validity of the claims based on prior art, potential for infringement, and opportunities for oppositions or patent challenges.


Key Takeaways

  • Scope excellence: EP3107547 covers specific kinase inhibitors used in therapeutic methods, with claims well-structured to encompass both compounds and their medical application.

  • Claim breadth and specificity: The patent balances detailed structure-based claims with method-of-use protections, likely to withstand certain validity challenges but requiring vigilant monitoring.

  • Litigational landscape: The patent resides within a densely populated patent environment characterized by extensive prior art related to kinase inhibitors and targeted therapies.

  • Strategic positioning: Effective market entry or licensing requires detailed freedom-to-operate analysis and possibly designing compounds outside the scope of existing patents.

  • Future considerations: Ongoing patent filings, especially in jurisdictions like China and the US, require continuous landscape monitoring to sustain competitive advantage.


FAQs

1. What therapeutic areas does EP3107547 primarily target?
It primarily targets autoimmune diseases, inflammatory conditions, and certain cancers where kinase pathways like JAK, Btk, or TEC are implicated.

2. Are method-of-use patents like EP3107547 enforceable against generic competitors?
Yes, method-of-treatment patents can prevent generics from marketing the same treatment protocols, although enforcement varies depending on jurisdiction and specific claims.

3. How does EP3107547 compare with existing kinase inhibitor patents?
It offers a narrower scope focusing on specific chemical structures and treatment methods, but overlaps are common given the extensive prior art in kinase inhibitors.

4. What challenges could EP3107547 face during patent examination?
Potential novelty or inventive step rejections, especially if prior art discloses similar compounds or treatment methods, could arise. Clear demonstration of novel structural features or surprising therapeutic effects is crucial.

5. How should companies position themselves around EP3107547’s patent?
They should conduct thorough patent landscape analyses, consider designing around claims by modifying chemical structures or treatment methods, or seek licensing agreements where necessary.


References

[1] European Patent Office, Patent EP3107547, “Method for treating deleterious conditions with a kinase inhibitor,” assigned to [Assignee], filed [date], published [date].

[2] Literature on kinase inhibitor patents, including filings from Pfizer, AbbVie, Merck, and others.

[3] Prior art disclosures on JAK inhibitors and related kinase-targeted therapies in scientific journals and patent filings.


This analysis aims to equip pharmaceutical and biotech professionals with a strategic understanding of EP3107547’s patent scope, claims, and competitive landscape to inform decision-making regarding R&D, licensing, and intellectual property strategy.

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