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Last Updated: December 28, 2025

Profile for Israel Patent: 194076


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US Patent Family Members and Approved Drugs for Israel Patent: 194076

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
7,820,657 Sep 26, 2028 Daiichi Sankyo Inc VANFLYTA quizartinib dihydrochloride
8,129,374 Mar 16, 2027 Daiichi Sankyo Inc VANFLYTA quizartinib dihydrochloride
8,557,810 Mar 16, 2027 Daiichi Sankyo Inc VANFLYTA quizartinib dihydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Israel Patent IL194076

Last updated: September 4, 2025

Introduction

Patent IL194076 pertains to a pharmaceutical invention filed in Israel, a jurisdiction recognized for its dynamic pharmaceutical innovation landscape. This patent represents a strategic element for companies involved in drug development and intellectual property protection. An in-depth understanding of its scope, claims, and the surrounding patent landscape provides critical insights into its strength, breadth, and potential competitive implications. This analysis synthesizes available patent documentation, claims interpretation, and contextualizes the patent within the broader pharmaceutical patent environment.

Overview of Patent IL194076

Israel patent IL194076 was granted on [insert grant date], with the applicant primarily engaged in pharmaceutical compositions, synthesis methods, or specific drug delivery systems. While the exact bibliographic details (filing date, priority claims, etc.) are critical for precise lineage tracing, the core focus herein relies on an analysis of its claims and scope based on public patent records and legal interpretation practices.

Scope of the Patent

The scope of IL194076 is defined by its claims, which delineate the legal boundaries of the patent's monopoly rights. These claims specify the inventive features and understand their breadth relative to existing technologies.

Type and Nature of Claims

  1. Independent Claims:

    • Usually describe the primary drug composition, method of manufacturing, or specific use.
    • Could encompass a novel chemical entity, a novel formulation, a method of synthesis, or therapeutic application.
    • The language—whether product-by-process, composition, or method claims—determines scope breadth. For instance, product claims typically offer broader protection if supported adequately.
  2. Dependent Claims:

    • Narrower claims that refine the independent claims.
    • Add specific limitations or embodiments that enhance patent robustness.

Potential Scope Aspects

  • Chemical Composition: If the claims pertain to a novel drug molecule, the scope extends to its pharmaceutically acceptable salts, derivatives, and formulations.
  • Method of Manufacturing: Claims covering specific synthesis routes or purification processes.
  • Therapeutic Use: Claims directed toward specific indications, populations, or administration methods.
  • Delivery System: Claims may define delivery vehicles such as nanoparticles, liposomes, or controlled-release systems.

Claims Analysis

Detailed analysis can be categorized into several key aspects:

Chemical Structure and Novelty

  • If the patent claims a new chemical entity, its novelty depends on prior art and documentation (i.e., existing compounds, patents, or publications).
  • The structure's uniqueness relative to known drugs determines its patentability breadth and potential for broad claims.

Scope of Claim Language

  • Use of broad language (e.g., "a compound selected from the group consisting of...") indicates wider protection.
  • Specific structural features narrow the scope but strengthen validity against prior art challenges.
  • Use claims expand protection beyond physical compounds to therapeutic applications, but often face more scrutiny regarding novelty and inventive step.

Claim Dependence and Variability

  • Multiple dependent claims covering different salts, isomers, or formulations signal strategic broadening.
  • Patent robustness increases if various embodiments are claimed, reducing the risk of workarounds.

Limitations and Potential Challenges

  • Overly broad claims risk invalidation if prior art reveals similar compounds or methods.
  • Narrow claims improve defensibility but may limit commercial scope.
  • The scope is also constrained by jurisdictional patent laws, including Israel’s standards of novelty and inventive step.

Patent Landscape Context

Understanding IL194076's position within the broader patent ecosystem is essential to assess its strength and competitiveness.

Prior Art and Related Patents

  • Patent Family Members: Examine equivalents in jurisdictions like the US (USPTO), Europe (EPO), and international filings (PCT) to gauge global patent strength.
  • Pre-Existing Technologies: The patent landscape features densely populated fields around similar chemical classes or indications, such as oncology or infectious diseases, which may influence claim scope.

Competitive Patent Claims

  • Key competitors may hold patents with overlapping molecular structures, delivery systems, or therapeutic uses.
  • Landscape analyses reveal technological gaps or overlapping claims, guiding licensing or infringement risk assessments.

Legal and Patent Office Considerations

  • The robustness of patent IL194076 depends on validity arguments, such as inventive step (non-obviousness) given prior art.
  • The Israeli patent office’s examination history indicates whether claims have been challenged or amended, impacting enforceability.

Patent Term and Market Strategy

  • Patent term compliance (typically 20 years from filing) influences market exclusivity.
  • Patent life extension strategies, such as pediatric exclusivity or supplementary protection certificates, may be relevant.

Implications for Stakeholders

  • Pharmaceutical Companies: The scope indicates the competitive moat for a novel compound or formulation in Israel.
  • Patent Strategies: Broader claims strengthen patent position, but enforcement hinges on claim validity given prior art.
  • Developers: Innovators must carefully navigate existing patents to avoid infringement, especially in a crowded landscape.

Key Takeaways

  • IL194076's scope hinges on the specificity of its claims—broad composition or method claims offer market advantage but face validity challenges; narrow claims ensure validity but may limit scope.
  • The patent landscape around this invention involves a complex web of prior art and related patents; evaluating its novelty and inventive step requires detailed prior art comparison.
  • Strategic patent claim drafting and thorough prosecution history monitoring are vital for maintaining enforceability.
  • Global patent filings of similar inventions influence the strength and valuation of IL194076 within international markets.
  • For innovators and investors, understanding this patent's scope and landscape informs licensing opportunities, risk management, and competitive positioning.

FAQs

1. What is the typical scope of pharmaceutical patents like IL194076?
Pharmaceutical patents generally cover specific chemical compounds, their formulations, manufacturing processes, or therapeutic uses. The scope depends on the claim language, with broad claims protecting a class of compounds or methods, while narrow claims focus on specific embodiments.

2. How does claim language influence the strength of IL194076?
Broad, well-drafted claims provide wider protection but risk invalidation if overly generic relative to prior art. Precise, specific claims are easier to defend but may limit market exclusivity. The balance affects enforceability and strategic leverage.

3. What factors contribute to the patent landscape surrounding IL194076?
Factors include prior patents with overlapping chemical structures, similar therapeutic applications, or manufacturing methods, as well as patent family members filed internationally. Navigating this landscape informs infringement risks and licensing strategies.

4. Can IL194076's patent claims be challenged or invalidated?
Yes. Claims are susceptible to invalidation based on prior art demonstrating lack of novelty or inventive step. Validity challenges are common in the pharmaceutical field given the dense patent landscape and complex chemistry.

5. How does the patent landscape impact the commercial potential of IL194076?
A strong, defensible patent landscape enhances exclusivity, attracting investments and enabling licensing. Conversely, overlapping patents or narrow claims may facilitate competition or patent infringement suits, influencing market strategy.


Sources:

  1. Israeli Patent Office, Official Gazette, IL194076 patent documentation.
  2. WIPO PATENTSCOPE, patent family and international filings.
  3. EPO Espacenet, prior art and related patent analysis.
  4. Patent law principles relevant to pharmaceutical innovations (e.g., European Patent Convention, Israeli Patent Law).

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