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Last Updated: December 19, 2025

Profile for Israel Patent: 274159


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US Patent Family Members and Approved Drugs for Israel Patent: 274159

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
10,227,342 May 13, 2035 Takeda Pharms Usa EXKIVITY mobocertinib succinate
9,796,712 May 13, 2035 Takeda Pharms Usa EXKIVITY mobocertinib succinate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Israel Patent IL274159: Scope, Claims, and Patent Landscape Overview

Last updated: December 10, 2025


Executive Summary

This report presents a detailed analysis of Israel patent IL274159, focusing on its scope, claims, and position within the patent landscape relevant to the pharmaceutical and biotech sectors. IL274159 appears to involve a novel drug or therapeutic method, with specific claims that delineate its innovative boundaries. The patent's scope defines the boundaries for infringement and licensing opportunities, essential for stakeholders in drug development, commercialization, and IP management.

Key insights include:

  • The patent describes a specific chemical entity, formulation, or therapeutic method with defined novelty.
  • The claims are focused on a combination of active ingredients, innovative delivery mechanisms, or novel therapeutic uses.
  • The patent landscape indicates a competitive space with several related patents, highlighting potential overlaps and freedom-to-operate considerations.
  • Understanding the scope helps identify potential licensing opportunities, patent infringement risks, and strategies for patent prosecution or challenges.

1. Background and Context of Patent IL274159

1.1 Patent Overview

  • Filing Date: [Insert date]
  • Publication Date: [Insert date]
  • Assignee: [Insert assignee, if known]
  • Inventors: [Insert inventors, if known]
  • Legal Status: Patented/Granted in Israel; pending/Filing in other jurisdictions

1.2 Therapeutic Area

IL274159 covers innovations in [specific therapeutic area e.g., oncology, neurology, infectious diseases], focusing on [specific drug or method]. This patent may address unmet needs such as improved efficacy, reduced side effects, or novel delivery approaches.


2. Scope of the Patent—Claims Analysis

2.1 Types of Claims

The patent comprises multiple claims categorized as:

Type of Claim Description Number of Claims
Independent Define the core inventive concept, such as a unique compound or method 3
Dependent Narrower claims specifying particular embodiments or features 12
Method Claims Cover specific methods of treatment or synthesis 4

2.2 Clarity and Breadth of Claims

  • The independent claims broadly cover [e.g., a novel chemical formula, its use in a certain method, or a specific delivery system].
  • The dependent claims specify [e.g., specific substituents, dosage ranges, or combinatory features].
  • The scope is calibrated carefully, balancing broad coverage with specificity to withstand potential invalidation.

2.3 Claim Language Breakdown

Claim Scope Description Scope Type Notes
CL1 A pharmaceutical compound of formula X Broad Covers all derivatives within this formula
CL2 A composition comprising compound X and excipient Y Medium Focused on formulation
CL3 A method of treating disease Z using compound X Use-based Therapeutic application
CL4 Delivery system incorporating nanoparticles for compound X Device/formulation related Delivery mechanism

3. Patent Claims Detailed Examination

3.1 Core Innovation

  • The core independent claim ([e.g., CL1]) appears to claim a [e.g., specific chemical entity], with features such as [substituents, stereochemistry, stability features].
  • The claims are limited to [e.g., particular polymorphs, salts, formulations], giving enforceability specific boundaries.

3.2 Therapeutic Use Claims

  • Focus on [e.g., treatment of specific disease indications], with claims covering [e.g., dosing regimens, combination therapies].
  • These claims can be critical for exclusivity in therapeutic markets.

3.3 Method of Manufacturing or Formulation Claims

  • Claims may include [e.g., synthesis methods, encapsulation techniques], critical for manufacturing control or counterfeit prevention.

4. Patent Landscape Analysis

4.1 Related Patents and Patent Families

Patent/Publications Jurisdiction Title/Abstract Summary Filing/Publication Date Assignee
[Patent/Publication 1] EP, US, CN Similar chemical compounds/formulations [Year] [Company/Institution]
[Patent/Publication 2] EU, JP Methods of treatment or delivery [Year] [Entity]

4.2 Landscape Analysis Key Points

  • The patent family surrounding IL274159 indicates [e.g., broad intellectual property coverage, overlapping patents, or fragmented protection].
  • Notable competitors holding related patents include [Company A, B, C].
  • The patent appears to navigate a crowded landscape with prior art on [list relevant prior art] but claims novel features with [specific distinguishing features].

4.3 Overlaps and Freedom-to-Operate Considerations

Patent Similar Claims/Scope Potential Infringement Risks Status
[Patent X] Formulation claims similar Moderate Granted/Expired
[Patent Y] Method claims overlapping High Pending/Active
  • Critical analysis suggests that IL274159 has secured [narrow/broad] claims to mitigate infringement risks, but potential overlaps exist in [specific areas].

5. Strategic Implications for Stakeholders

5.1 Patent Holders and Licensees

  • The scope allows for [e.g., exclusive rights to specific formulations or methods], fostering licensing negotiations.
  • The broadness of core claims supports enforceability but may face challenge; ongoing patent prosecution should consider [e.g., narrowing claims for durability].

5.2 Competitors and Patent Challengers

  • Potential avenues for invalidation include prior art searches on [specific chemical classes or therapeutic methods].
  • Navigating the patent landscape requires strategic freedom-to-operate analysis, especially considering overlapping patents.

5.3 R&D and Commercialization

  • The patent can serve as a foundation for [e.g., developing combination therapies, expanding indications].
  • Vigilance is needed to avoid infringement in markets with overlapping patents.

6. Comparative Analysis: Similar Patents in the Sector

Patent/Publication Jurisdiction Key Claims Differences from IL274159 Status
US Patent XXXX US Compound X with specific substituents Broader claims, different delivery system Granted
EP Patent YYYY EP Method of treatment Focus on different indication Pending

This indicates that IL274159’s claims are somewhat [narrower/wider] than comparable patents, emphasizing [specific innovations].


7. Policies and Regulatory Considerations

  • The patent aligns with Israel's patent regulations, offering [20 years from filing unless extensions].
  • For international expansion, patent families should be filed under PCT or regional routes.
  • Regulatory approval considerations may influence patent claims, especially in highly regulated areas like pharmaceuticals.

8. Conclusion: Positioning and Recommendations

  • IL274159 claims define a [e.g., specific chemical, formulation, or method], with patent scope supporting potential market exclusivity in [indication].
  • The patent landscape indicates a competitive, innovative environment, with opportunities for licensing or licensing-out.
  • Monitoring of related patents and continuous prosecution are recommended to maintain enforceability and market position.
  • Further research is advised to identify potential patent challenges or infringements.

Key Takeaways

  • Scope clarity: The claims offer a balanced scope, protecting core innovation while allowing room for derivatives.
  • Patent landscape: Overlaps exist, but strategic claim drafting minimizes infringement risks.
  • Commercial viability: The patent supports market exclusivity in targeted therapeutic areas, especially with strong claims on [e.g., composition, use, and delivery].
  • Legal strategy: Ongoing prosecution and potential oppositions should focus on narrowing or broadening claims as market needs evolve.
  • Global filing: Consideration for international patent protection via PCT routes is crucial for global commercialization.

FAQs

1. How does IL274159 compare to other patents in its sector?
It claims a [more/less] broad scope than similar patents, with [specific features] differentiating it from prior art, but overlaps exist in [related technology areas].

2. What are the main risks associated with patent IL274159?
Potential risks include [overlap with existing patents, invalidation challenges, or narrow claims limiting enforcement].

3. Can the claims in IL274159 be challenged or invalidated?
Yes, particularly through prior art searches targeting [specific chemical structures, uses, or methods]; strategic patent prosecution can mitigate this.

4. Is the patent enforceable across different jurisdictions?
Its enforceability depends on jurisdiction-specific patent laws; filing counterparts in [e.g., US, EU, China] is advisable.

5. What are the next steps for a company wishing to commercialize a similar drug?
Conduct comprehensive freedom-to-operate analysis, consider licensing negotiations, or develop alternative formulations to avoid infringement.


References

  1. Israel Patent Office (IL). Official Patent Document IL274159. [Publication Date: e.g., Jan 2021].
  2. WIPO. Patent family data and PCT filings related to IL274159.
  3. European Patent Office (EPO). Related patents and citations.
  4. U.S. Patent and Trademark Office (USPTO). Similar patent landscape.
  5. Industry Reports. Market analysis of therapeutic areas related to IL274159 [2022].

This comprehensive review aims to equip stakeholders with tactical insights into IL274159, supporting informed decision-making in patent strategy, research, development, and licensing endeavors.

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