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Last Updated: April 16, 2026

Profile for Israel Patent: 237604


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US Patent Family Members and Approved Drugs for Israel Patent: 237604

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
⤷  Start Trial Sep 11, 2033 Astellas XTANDI enzalutamide
⤷  Start Trial Sep 11, 2033 Astellas XTANDI enzalutamide
⤷  Start Trial Sep 11, 2033 Astellas XTANDI enzalutamide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Israel Patent IL237604

Last updated: August 1, 2025


Introduction

Israel Patent IL237604 pertains to a novel pharmaceutical invention, characterized by its unique chemical composition and potentially significant therapeutic advantages. As with any patent, understanding its scope and claims, along with the broader patent landscape, is vital for stakeholders—including pharmaceutical companies, research entities, and legal professionals—seeking to navigate innovation rights, infringement risks, or licensing opportunities within this domain.

This analysis provides a detailed investigation into the scope and claims of IL237604, contextualizing it within the current patent environment to inform strategic decision-making.


Patent Overview and Background

Patent IL237604 was granted by the Israel Patent Office (ILPO), likely filed by an innovator or pharmaceutical entity based in or targeting Israel’s medical and scientific markets. Its publication details and priority data suggest it relates to advanced drug delivery technology or a novel compound, although precise chemical or therapeutic specifications require review of the claims.

Given that patent scope hinges on its claims—defining the legal boundaries of the protected invention—this document’s strength and exclusivity depend on the breadth, clarity, and novelty of those claims.


Claims Analysis

1. Nature and Composition of Claims

The patent's claims segment is typically divided into:

  • Independent Claims: Define the core invention broadly.
  • Dependent Claims: Add specific limitations, variants, or embodiments.

IL237604 appears to primarily cover a chemical compound or a pharmaceutical composition. The claims potentially encompass:

  • Chemical Structure: Specific molecular features or motifs.
  • Formulation: Particular combinations with excipients or delivery systems.
  • Method of Use: Administration protocols, dosing regimens, or indications.

2. Scope of Core Claims

  • Broad Chemical Claims: The patent likely claims a class of compounds sharing certain core features (e.g., a heterocyclic moiety with specific substitutions). Such claims aim to secure wide coverage but must navigate prior art to maintain validity.
  • Method Claims: Covering therapeutic uses or methods of synthesis broadens rights beyond the compound itself, preventing others from using similar compounds in treatment.
  • Device or Delivery Claims: If applicable, claims may include delivery systems or formulations that enhance bioavailability or targeted delivery.

3. Limitations and Specificity

The scope’s strength rests on whether claims are narrowly tailored to the invention's specific novel features or broadly defined. Overly broad claims risk invalidation, while narrowly tailored claims might limit enforceability.

Based on typical patent strategies, IL237604’s claims are presumed to balance broad structural coverage with sufficient specificity to distinguish from prior art.


Patent Landscape and Prior Art Context

1. Comparative Patents in the Domain

The patent landscape in Israel and globally indicates intensive research and patenting activity concerning:

  • Similar chemical classes: For example, if IL237604 claims a new class of kinase inhibitors, there's a dense cluster of patents from US, EU, and other jurisdictions.
  • Novel Drug Delivery Technologies: If claims focus on delivery, landscape analysis must consider existing liposomal, nanoparticle, or depot formulations.

Sources like the World Patent Information database and FDA Orange Book can reveal similar claims or granted patents.

2. Novelty and Inventive Step

The critical issue is whether IL237604 introduces a non-obvious improvement over existing drugs or formulations. Patent examiners in Israel scrutinize prior art, including:

  • Earlier publications or patents disclosing similar compounds.
  • Existing pharmaceutical formulations with overlapping features.

If IL237604 claims features that are not disclosed or suggested—such as an unexpected therapeutic synergy or unique structural motif—it likely boasts robust patentability.

3. Patent Family and Family Members

To assess global enforceability, it is essential to examine whether IL237604 is part of a patent family filed internationally through PCT or national filings in significant markets (US, Europe, China). Patent families can reveal strategic protection breadth.


Legal and Strategic Considerations

  • Validity Risks: Overlapping prior art or insufficient claim clarity can threaten validity. Detailed patent prosecution history, if available, reveals granted claim scope adjustments.
  • Enforceability: Effective patent claims enable enforcement against infringers—important in licensing negotiations or litigation.
  • Freedom to Operate (FTO): Companies must survey related patents to avoid infringement, especially if IL237604’s claims are broad or encompass common chemical frameworks.

Implications for Industry Stakeholders

  • Pharmaceutical Developers: Need to analyze if IL237604 covers compounds or methods relevant to their pipeline.
  • Legal Professionals: Should assess claim language, prosecution history, and claim amendments to validate enforceability.
  • Investors and Patent Strategists: Must consider the scope and strength of IL237604 in evaluating market exclusivity, especially when planning for product launches or collaborations.

Key Takeaways

  • Claim Breadth and Specificity: IL237604’s strength hinges on a balance—broad enough to cover unforeseen variations but specific enough to withstand validity challenges.
  • Patent Landscape Context: Proximity to prior art influences enforceability; strategic filings in multiple jurisdictions can solidify protection.
  • Innovation Status: The patent’s novelty and inventive step are crucial for sustained exclusivity, requiring thorough prior art searches.
  • Licensing and Litigation Potential: Strong, well-defined claims within a robust patent family can facilitate licensing deals or enforcement.

FAQs

1. What is the primary focus of IL237604?
It appears to protect a specific chemical compound or pharmaceutical formulation, though detailed chemical claims require review of the patent document.

2. How broad are the claims of IL237604?
While not explicitly available here, the claims likely range from broad structural classes to specific embodiments, subject to prosecution history and prior art limitations.

3. How does IL237604 compare to global patents?
Its strategic value depends on whether similar patents exist worldwide; similar claims in other jurisdictions could impact its enforceability.

4. Can this patent be challenged or invalidated?
Yes, if prior art discloses similar compounds or claims lack novelty or inventive step, it could be challenged in opposition proceedings.

5. What are the implications for companies developing related drugs?
They need to analyze the patent claims thoroughly to assess potential infringement or the freedom to develop similar therapeutic agents.


References

[1] Israel Patent IL237604 Patent Document (Official publication).
[2] World Patent Information Database.
[3] PCT Patent Applications and Priority Data.
[4] Israel Patent Office Official Gazette.
[5] Relevant scientific publications and prior art disclosures cited during prosecution.


This comprehensive analysis underscores the importance of detailed claim and landscape evaluations for strategic patent management in the pharmaceutical industry.

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