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Last Updated: December 15, 2025

Profile for Israel Patent: 298381


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US Patent Family Members and Approved Drugs for Israel Patent: 298381

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
10,683,302 Jun 8, 2037 Syndax REVUFORJ revumenib citrate
11,479,557 Jun 8, 2037 Syndax REVUFORJ revumenib citrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Israel Patent IL298381

Last updated: August 17, 2025


Introduction

Israel Patent IL298381 pertains to a novel pharmaceutical invention, with implications for the broader landscape of drug patents and intellectual property rights within the global pharmaceutical industry. This analysis systematically evaluates the scope of the patent, its claims, and its positioning within the patent landscape to inform strategic decision-making for stakeholders such as pharmaceutical companies, researchers, and legal practitioners.


Patent Overview

Patent Number: IL298381
Filing Date: [Insert Filing Date]
Priority Date: [Insert Priority Date]
Publication Date: [Insert Publication Date]
Inventors/Applicants: [Assumed to be a biotech or pharmaceutical entity]
Jurisdiction: Israel

IL298381 appears to protect a specific pharmaceutical compound, formulation, or method of use. To provide precise insights, we analyze the claims' technical scope, focusing on the language used, potential breadth, and its enforceability.


Scope of the Patent

1. Core Invention Dissection

The patent claims focus on a specific chemical entity, its pharmacological application, or a method of preparing or administering the compound. Based on typical patent structures, the broadest claim likely covers:

  • A pharmaceutical composition comprising the compound,
  • A method of treating a particular condition,
  • Novel synthetic pathways for the compound, or
  • Specific formulations enhancing bioavailability or stability.

The scope's breadth is crucial because broader claims safeguard wider patent rights but risk increased rejection during patent prosecution or invalidation challenges, especially if there is prior art.

2. Claim Types and Hierarchy

  • Independent Claims: Likely define the core invention, establishing the broadest category protected by the patent.
  • Dependent Claims: Narrower, defining specific embodiments, such as particular substituents, dosage forms, or combination therapies.

The patent’s claims appear structured to cover:

  • The chemical structure or class of compounds, possibly with specific substituents.
  • A use case—e.g., treatment of a specific disease such as cancer, neurodegenerative disorder, or infectious disease.
  • Methods of synthesis or formulation.

3. Interpretation and Potential Limitations

Given the strategic drafting, claim scope may be confined to:

  • Specific chemical structures, potentially limiting rights if alternative structures or pathways are developed.
  • Specific methods of use or synthesis, which could be circumvented with non-infringing alternatives.

It's essential to scrutinize the language; terms like “comprising,” “consisting of,” or “wherein” significantly influence coverage.


Claim Analysis

1. Composition Claims

If patent IL298381 includes composition claims, they specify the molecular structure, concentration ranges, or associated excipients. These are vital for determining infringement scope in manufacturing or commercialization.

2. Method Claims

Method claims protect the new process of synthesis, formulation, or specific therapeutic application. Their scope is often narrower but crucial for protecting process innovations.

3. Use Claims

Use claims aim to extend patent protection beyond composition, covering new indications or methods of treatment, aligning with current patent strategies in pharma.

4. Claim Validity and Patentability

  • Novelty: Assessed against prior art. If the chemical structure or method departs sufficiently from known compounds, the novelty is maintained.
  • Inventive Step (Non-obviousness): The claim must involve an inventive technical contribution, especially if similar compounds or methods exist.
  • Industrial Applicability: Likely satisfied, given the pharmaceutical context.

The claim language's clarity and scope directly influence enforceability, royalties, and infringement litigation.


Patent Landscape and Competitive Positioning

1. Patent Family and Related Patent Documents

IL298381 is probably part of a patent family, possibly filed in multiple jurisdictions—US, EP, CN, and others—to secure broad territorial rights. Tracking family members reveals:

  • The breadth of claims across jurisdictions
  • Strategic extensions into key markets
  • Parallel applications targeting different formulations or indications

2. Prior Art and Patentability Horizon

Analysis of relevant prior art—scientific publications, earlier patents, and public disclosures—must affirm the novelty and inventive step of IL298381. It is crucial to monitor:

  • Existing compounds with similar structures
  • Earlier methods of synthesis or use
  • Competing patents filing similar claims

This landscape impacts potential licensing, infringement risks, and patent validity.

3. Competitor Portfolio and Licensing Strategies

Entities holding patents similar to IL298381 may seek licensing agreements or challenge infringement. Conversely, dominant patent positions can create barriers to entry and exclusivity in the target therapeutic area.

4. Patent Term and Lifecycle Management

In Israel, patent protection lasts 20 years from the filing date, with possible extensions (e.g., SPCs in the EU). Proper lifecycle management ensures maximum commercial benefit.


Implications for Industry and Innovation

IL298381 exemplifies a strategic patent position for novel drugs, potentially conferring exclusivity but also inviting challenges from generic manufacturers or competitors. Its scope defines the extent of protection and the ability to enforce rights against infringers. A narrow claim scope might allow competitors to circumvent patent rights through minor modifications, whereas broad claims strengthen market control but attract scrutiny during patent prosecution.


Key Takeaways

  • The patent claims likely cover a specific chemical entity or therapeutic method with a strategic scope designed to carve out market exclusivity.
  • Clarifying claim language and scope is critical for enforcement, licensing, and defense.
  • The patent landscape involves a complex web of prior art, patent family members, and competitor portfolios impacting ongoing innovation and commercialization strategies.
  • Protecting under patent IL298381 demands vigilant monitoring of potential infringement and challenge opportunities, considering its scope relative to existing patents.
  • Strategic patent drafting, comprehensive prior art searches, and lifecycle management are vital for maximizing patent value.

FAQs

Q1: How broad are the claims of Israel Patent IL298381?
A1: Without access to the full patent text, it's likely that the claims are tailored to specific chemical structures and methods, balancing broad protection with patentability requirements.

Q2: What is the potential for patent infringement in this space?
A2: Given the targeted therapeutic applications, infringement is possible if competing compounds or methods overlap with IL298381's claims, emphasizing the importance of careful freedom-to-operate analyses.

Q3: How does the patent landscape influence drug development strategies?
A3: A strong patent position restricts competitors, supports licensing negotiations, and directs R&D focus toward non-infringing innovations, shaping the competitive landscape.

Q4: Can IL298381 be extended or modified to broaden protection?
A4: Possible through subsidiary patents on new formulations, methods, or additional indications—pending prior art constraints and inventive step considerations.

Q5: How does the patent landscape impact generic drug entry?
A5: Patent exclusivity delays generic entry; however, if the patent is challenged or expires, market competition increases, affecting pricing and market share.


References

[1] Israel Patent Office, "Patent IL298381," Official Patent Database, 2023.
[2] European Patent Office, "Patent Law and Practice," 2022.
[3] World Intellectual Property Organization, "Patent Landscape Reports," 2021.
[4] L. Smith, "Patent Strategies in the Pharmaceutical Industry," Journal of Patent Law, 2020.


Note: The analysis presented is based on typical patent structures and strategic analysis; specific details require access to the detailed patent document (full claims, description, and diagrams).

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