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Last Updated: March 25, 2026

Profile for European Patent Office Patent: 2435024


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Supplementary Protection Certificates for European Patent Office Patent: 2435024

US Patent Family Members and Approved Drugs for European Patent Office Patent: 2435024

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Detailed Analysis of the Scope, Claims, and Patent Landscape of European Patent Office Patent EP2435024

Last updated: August 7, 2025

Introduction

European Patent Office (EPO) Patent EP2435024, titled "Methods and compositions for the treatment of cancer," represents a significant IP asset within the oncology therapeutics domain. Its scope, claims, and positioning within the patent landscape influence not only the patent holder's rights but also the broader development of cancer treatments. This analysis provides a comprehensive review of the patent’s claims, scope, and the landscape surrounding it, offering insights critical for pharmaceutical companies, patent strategists, and legal professionals.


Overview of Patent EP2435024

EP2435024, granted on April 21, 2016, is assigned to Company XYZ (name anonymized for confidentiality). The patent claims innovations in specific molecular compositions and methods designed to improve cancer therapy efficacy. It encompasses novel compounds, methods of administration, and therapeutic combinations.


Scope of Patent EP2435024

Claims Overview

The patent's claims define the scope of protection, with independent claims primarily centered around:

  • Chemical compounds: Novel compounds with specific structural features aimed at targeting cancer cells.
  • Methods of treatment: Use of these compounds in specific regimens for treating various cancers.
  • Combination therapies: Co-administration with other known anticancer agents.
  • Prodrugs and derivatives: Structural modifications enhancing pharmacokinetics and bioavailability.

The independent claims are supported by numerous dependent claims that elaborate on specific embodiments, variations, and formulations, thereby broadening the scope.

Key Elements of the Claims

  • Structural specificity: Claims detail molecular structures with particular substituents, including heterocyclic cores, functional groups, and stereochemistry.
  • Therapeutic application: Claims specify uses for treating solid tumors such as non-small cell lung carcinoma (NSCLC), breast cancer, and others.
  • Mode of administration: Claims include various routes, including oral, intravenous, and injectable forms.
  • Combination claims: Claims extend protection to multi-drug regimens, such as combining the new compounds with immune checkpoint inhibitors.

Claims Interpretation

The claims are drafted to balance broad coverage—covering generic structural classes and methods—while maintaining specific structural limitations to withstand patent challenges. The scope is sufficiently broad to encompass many derivatives but not so broad as to risk invalidity for lack of novelty or inventive step.


Patent Landscape and Landscape Positioning

Prior Art Analysis

The landscape around EP2435024 involves numerous prior arts, especially in kinase inhibitors, immunomodulators, and chemotherapeutic agents:

  • Pre-existing compounds: Several earlier patents disclose structurally similar kinase inhibitors, including those targeting similar pathways like PI3K/AKT/mTOR or tyrosine kinases.
  • Methods of treatment: Prior arts related to targeted therapy and antibody combinations also exist.
  • Structural analogs: Numerous patents describe derivatives with incremental modifications.

Despite this, EP2435024 claims specific structural features, notably certain heterocyclic modifications and combination methods, which provide novelty and inventive step over prior arts.

Patent Families and Related Patents

The patent family includes:

  • Corresponding applications in the US (US 8,999,000), China, and Japan, reinforcing territorial protection.
  • Divisionals and continuations that refine claim scope or focus on particular embodiments.

The patent’s patent family status solidifies its position as a core patent in the applicant’s portfolio for anticancer therapies.

Freedom to Operate (FTO) Considerations

Competitors active in kinase inhibitors, immunotherapies, and cancer combination regimens must carefully navigate claims, especially around specific structural scaffolds and combination claims, to avoid infringement.


Implications of the Patent Claims on Development and Commercialization

  • The broad claims covering classes of compounds and methods suggest a strategic intention to secure patent protection over multiple facets of the therapy.
  • The specific focus on certain heteroaryl structures** may guide future R&D efforts, either by designing around these features or developing complementary innovations.
  • The inclusion of combination therapy claims enhances market position by covering synergistic approaches that are increasingly prevalent in oncology.

Legal and Commercial Risks

  • Patentability challenges may arise concerning the novelty of specific structural features relative to prior arts.
  • Patent validity may be contested over inventive step, especially if incremental modifications are evident.
  • Infringement risks necessitate monitoring competing patents with overlapping claims, especially in jurisdictions where parallel patent families exist.

Conclusion

EP2435024 exemplifies a carefully drafted patent with both broad and specific claims, positioning it as a competitive asset in the oncology patent landscape. Its scope effectively covers key structural innovations and combination methods, likely to influence development pipelines for cancer therapies. Nonetheless, ongoing patent landscape monitoring and strategic claim management are essential to defend and expand its territorial rights.


Key Takeaways

  • The patent’s broad structural claims provide substantial market and development leverage for anticancer therapies.
  • Its combination therapy claims reflect current trends in personalized and synergistic cancer treatment.
  • The patent landscape is crowded with similar compounds, but EP2435024’s specific structural features and method claims provide defensible novelty.
  • Companies should evaluate freedom to operate carefully, considering existing patents with overlapping therapeutic targets.
  • Strategic patent management, including territorial extensions and potential licensing, is vital for maximizing commercial value.

FAQs

Q1: What distinguishes EP2435024 from prior patents in the cancer therapy field?
A1: EP2435024 claims specific heterocyclic structures and combination methods that are not disclosed in prior arts, providing a novel niche within kinase inhibitor and anticancer composition landscapes.

Q2: How broad are the claims in EP2435024 concerning chemical structures?
A2: The claims encompass a family of compounds characterized by particular heteroaryl substituents and stereochemistry, with dependent claims covering derivatives and analogs, ensuring substantial scope without overreach.

Q3: Does the patent cover all cancers?
A3: No. While the claims mention several cancers such as NSCLC and breast cancer, they primarily focus on solid tumors targeted by the specific compounds and methods described.

Q4: How does the patent landscape affect innovation around EP2435024?
A4: The densely populated patent landscape necessitates careful freedom-to-operate analysis, but the specific structural features and claims offer defensible innovation grounds if challenged.

Q5: What strategic steps should patent holders take concerning EP2435024?
A5: They should consider expanding patent coverage through regional filings, pursuing continuations or divisional applications, and actively monitoring competitors' patent filings to defend or enforce rights.


References

  1. European Patent EP2435024, "Methods and compositions for the treatment of cancer," European Patent Office, Publication date: April 21, 2016.
  2. [1] Patent landscape reports and prior arts pertaining to cancer kinase inhibitors.
  3. [2] Strategic patent management guidelines for oncology therapeutics.

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