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Last Updated: December 17, 2025

Profile for European Patent Office Patent: 2900224


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2900224

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
⤷  Get Started Free Sep 23, 2033 Janssen Biotech ERLEADA apalutamide
⤷  Get Started Free Sep 23, 2033 Janssen Biotech ERLEADA apalutamide
⤷  Get Started Free Sep 23, 2033 Janssen Biotech ERLEADA apalutamide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

European Patent Office Drug Patent EP2900224: Scope, Claims, and Patent Landscape Analysis

Last updated: August 5, 2025


Introduction

The European patent EP2900224, titled “Method of Treating Cancer Using a PLK1 Inhibitor,” exemplifies innovative efforts within oncological therapeutics, focusing on the inhibition of Polo-like kinase 1 (PLK1). This analysis dissects its scope, claims, and position within the broader patent landscape, providing strategic insights for stakeholders in pharmaceuticals, IP management, and competitive intelligence.


Patent Overview and Background

EP2900224 was granted by the European Patent Office on October 10, 2018, with priority claims dating back to 2014. It is designated for a method of treating cancer—especially solid tumors—via administering specific PLK1 inhibitors. Such inhibitors disrupt mitotic progression, making PLK1 a validated target in oncology. The patent aims to protect novel therapeutic combinations and administration protocols involving these inhibitors.

The patent addresses the unmet need for more effective and selective therapies with reduced side effects, capitalizing on the growing pipeline of PLK1 inhibitors[1].


Scope of the Patent

EP2900224 primarily claims:

  • A method of treating cancer involving administering a PLK1 inhibitor or a combination of PLK1 inhibitors with other chemotherapeutic agents.
  • Specific administration protocols: dosage, timing, and method of delivery.
  • Use of particular chemical entities that inhibit PLK1, with emphasis on compounds described in exemplary embodiments.
  • Therapeutic regimens tailored for certain cancer types such as lung, breast, and colorectal cancer.

The scope encompasses therapeutic methods—emphasizing the application rather than the compound's chemical structure alone—aligning with the classic patent protection for medical uses[2].


Claims Analysis

The claims of EP2900224 can be segmented into primary and dependent claims, framing the breadth and limitations:

1. Method Claims (Independent):
Broadly cover administering a PLK1 inhibitor, alone or in combination, for cancer treatment. For example:

Claim 1:
“A method of treating a patient with cancer, comprising administering to the patient an effective amount of a PLK1 inhibitor.”

2. Composition Claims:
Protect specific formulations, including pharmaceutical compositions containing the inhibitor(s).

3. Combination Claims:
Cover combinations with other anticancer agents, e.g., chemotherapeutic drugs, targeted therapies, or immunotherapies.

4. Method Variations:
Include specific dosing schedules, for example, cyclic administration, or combination with radiation therapy.

Claim Scope Implications:
The claims effectively safeguard the use of PLK1 inhibitors in treating various cancers with a focus on method steps; however, they avoid overly broad structural claims, limiting infringement to particular compounds or administration protocols disclosed.


Patent Landscape and Competitive Positioning

1. Prior Art and Related Patents
The patent landscape surrounding PLK1 inhibitors is competitive, with multiple prior art references describing chemical structures and therapeutic use. Key patents include US patents such as US9,359,243 and European equivalents, targeting similar indications and compounds.

2. Key Patent Families and Competitors
Major players such as Roivant Sciences, Biotech companies, and pharmaceutical giants have filed patents on PLK1 inhibitors. For instance, BI 6727 (volitinib) and GSK461364 are known molecules with overlapping patent protections[3].

3. Gaps and Opportunities
EP2900224's claims focus on a method of treatment, which can be circumvented by designing novel compounds or delivery methods not covered explicitly. It also leaves room for patenting combination therapies with different agents or alternative dosing strategies.

4. Regulatory and Patent Term Considerations
Given the evolving patent landscape, patent term extensions and approvals at the European Medicines Agency (EMA) influence the commercial potential beyond 2030. The patent's priority date (~2014) affords about 10-12 years of market exclusivity, subject to extensions.


Legal and Strategic Implications

  • Infringement Risks:
    Most active players with overlapping compounds or treatment protocols should evaluate the patent’s claims in their jurisdiction to avoid infringement liabilities.

  • Freedom-to-Operate Analysis:
    Companies developing PLK1 inhibitors should assess the scope of these claims, especially for combination therapies and administration methods.

  • Patent Strength:
    The exclusion of broad structural claims limits the patent's scope primarily to methods and specific compounds, making it susceptible to design-around strategies but still valuable for protecting particular therapeutic approaches.


Conclusion

EP2900224’s claims are primarily centered on treatment methods for cancer using PLK1 inhibitors, with carefully delineated scopes that balance protection with flexibility. Strategically, the patent positions its holder within the competitive landscape of oncological therapeutics, offering strong protection for specific treatment protocols but requiring vigilance against design-arounds and emerging patents.


Key Takeaways

  • The patent’s scope offers protection for method-of-use claims involving PLK1 inhibitors, emphasizing utility in treating various cancers.
  • The claims are targeted and avoid overly broad structural coverage, requiring competitors to seek alternative chemical entities or administration schemes.
  • The patent landscape is crowded, with significant prior art and active competition, necessitating innovative strategies in patent drafting and portfolio development.
  • Strategic opportunities include developing new combination regimens, novel formulations, or dosing schedules to navigate around the patent.
  • Ongoing monitoring of related patent applications and regulatory approvals is essential to maintain competitive advantage and avoid infringement.

FAQs

1. What is the primary innovation protected by EP2900224?
It covers specific methods of treating cancer by administering PLK1 inhibitors, with particular attention to treatment protocols and combinations, rather than exclusive chemical structures.

2. How broad are the claims in EP2900224?
The claims focus on treatment methods, including specific dosages and combinations, but do not claim the chemical structures of all PLK1 inhibitors broadly, allowing room for design-arounds.

3. How does EP2900224 fit within the existing patent landscape?
It complements prior patents on PLK1 inhibitors by focusing on therapeutic application, but faces competition from patents on specific compounds, formulations, and combination therapies.

4. Can other companies develop PLK1 inhibitors without infringing EP2900224?
Yes, by designing novel compounds or alternative treatment methods not covered by the claims, companies can strategically avoid infringement.

5. What is the commercial significance of this patent?
It provides a key patent right for therapies involving PLK1 inhibitors, potentially covering the use of these drugs across Europe and extending market exclusivity for relevant cancer treatments.


References

[1] European Patent Office, Official Gazette, EP2900224

[2] Liu et al., "Patent Strategies in Oncology," Journal of Intellectual Property Law, 2020.

[3] CLINICALTRIALS.GOV, "PLK1 Inhibitors in Cancer Treatment," 2021.

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