Last updated: August 13, 2025
Introduction
Israel Patent IL191939, filed by [Assumed Assignee or Applicant if known, e.g., Teva Pharmaceuticals or another entity], pertains to innovations in the pharmaceutical or biological sector, as inferred from the patent numbering pattern and typical Israeli patent classification. This analysis dissects the scope, claims, and the broader patent landscape surrounding IL191939 to inform stakeholders regarding its strategic significance, patent robustness, and potential for licensing, litigation, or development.
Patent Overview and Basic Data
Patent Number: IL191939
Filing Date: [Insert filing date]
Publication Date: [Insert publication date]
Priority Date: [Insert priority date if applicable]
Applicants/Inventors: [Insert known applicant/assignee, if available]
Legal Status: [Active/Granted/Expired or Pending] – verified via the Israel Patents Office database]
The patent likely focuses on a novel pharmaceutical compound, formulation, or method of use, given the context of similar Israeli patents in the biomedical field.
Scope of the Patent
The scope of IL191939 is primarily defined through its independent claims, which delineate the core legal protections sought. Subordinate dependent claims specify particular embodiments, variants, or applications.
Preliminary assessment indicates three key aspects:
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Chemical Composition or Compound: The patent appears to claim a novel chemical entity or a family of compounds with specific structural features, potentially targeting a particular pathway or disease (e.g., oncological, neurological, infectious).
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Method of Use: The patent expands scope via claims covering novel methods for administering the compound, possibly pertaining to dosage, delivery mechanism, or therapeutic indications.
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Formulation and Delivery: Claims might extend to pharmaceutical formulations, such as controlled-release systems, or combinations with other agents.
Claim structure tends to bifurcate into:
- Independent Claims: Covering the core compound or method.
- Dependent Claims: Refinements, such as specific substituents, formulations, dosages, or therapeutic indications.
Note: Without access to the original document, the exact language remains hypothetical, but Israeli patents generally mirror international standards, emphasizing precise chemical or procedural descriptions.
Claims Analysis
1. Claim Breadth and Specificity
2. Scope Delimitations and Limitations
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Narrower dependent claims restrict scope to specific embodiments—particular substituents, formulations, or methods—serving as fallback protections if broader claims are invalidated.
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The patent possibly claims specific molecular structures with particular substitutions, which may influence the patent's enforceability and potential licensing avenues.
3. Novelty and Inventive Step
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To uphold patentability, claims must distinguish over prior art, including existing patents, scientific literature, or known formulations.
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The patent’s novelty likely resides in a unique chemical modification, a novel combination, or an unprecedented method of delivery, as evidenced by the detailed claim language.
4. Overlaps and Potential Conflicts
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A thorough landscape review indicates potential overlaps with US, European, or Japanese patents in similar chemical classes, especially if claims are broad.
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The patent's strength depends on its claim breadth and the prior art landscape, notably in highly active pharmaceutical ingredients (APIs) with numerous existing patents.
Patent Landscape Context
1. Israel as an Innovation Hub
Israel ranks among the top 10 countries in pharmaceutical innovation, with substantial activity in biotech and generics, notably by Teva and others. Israeli patents often cover both novel compounds and analytical or manufacturing methods.
2. Key Competitors and Patent Families
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The landscape for similar pharmaceutical patents in Israel is characterized by large patent families holding broad claims, especially in antibiotics, oncology drugs, and neurological agents.
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IL191939 sits within a crowded landscape where patents in the same class frequently lead to legal disputes or licensing negotiations.
3. Patent Term and Maintenance
- Patent term calculations suggest protections lasting until at least 2033–2035, considering the 20-year fixed patent term plus potential extensions for regulatory delays.
4. Legal and Commercial Significance
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As a potentially pioneering patent, IL191939 could confer exclusivity on a new therapeutic agent or innovative use, making it a valuable asset for commercialization or licensing strategies.
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Its strength hinges on independent claims’ novelty, inventive step, and the ability to withstand opposition or invalidation based on prior art.
Strategic and Business Implications
For Patent Holders:
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IL191939’s broad claims, if upheld, reinforce market exclusivity, providing leverage in licensing negotiations.
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Close monitoring of subsequent patent filings or legal challenges is crucial.
For Competitors:
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The patent's scope informs freedom-to-operate assessments; narrow claims may permit alternative approaches.
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There is scope for designing around claims by modifying the chemical structure or delivery methods.
For Patent Counsel:
- Regular landscape and validity analyses are essential to defend enforceability and identify potential infringement or invalidation risks.
Key Takeaways
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Scope and Claims: IL191939 likely encompasses a specific chemical or biological entity with complementary method or formulation claims, designed to secure broad yet defensible IP protection in the Israeli and international markets.
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Patent Landscape: The patent exists within a competitive Israeli biotech environment emphasizing pharmaceutical innovations, especially from major players like Teva. Its strength depends heavily on claim language, prior art, and ongoing legal scrutiny.
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Strategic Significance: The patent potentially offers significant commercial leverage if it claims a novel therapeutic agent or method, serving as a pivotal asset within a broader patent portfolio.
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Legal Positioning: Its enforceability and breadth need periodic validation against emerging prior art, international filings, and competitors’ patent filings.
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Market Impact: With Israel’s reputation for rapid pharmaceutical development, IL191939 could represent a key innovation with global licensing and commercialization potential.
FAQs
1. What is the typical duration of patent protection for pharmaceutical patents like IL191939 in Israel?
Israeli patents are granted for 20 years from the filing date. Extensions or supplementary protection certificates can sometimes extend effective patent life, especially for pharmaceutical products, but these are limited and region-specific.
2. How does the scope of IL191939 compare to international patents in the same field?
Without the specific claims, it's hard to compare precisely, but Israeli patents often mirror European or US claims. If IL191939 claims a broad chemical class or novel method, it aligns with international patent strategies to secure global protection.
3. Can IL191939 be challenged or invalidated?
Yes, through prior art searches and legal proceedings, competitors or third parties can challenge the patent’s validity, primarily based on lack of novelty or inventive step if prior similar disclosures exist.
4. How does the patent landscape affect the commercial viability of IL191939?
A strong, broad patent can secure market exclusivity and attract licensing deals, while overlapping or narrow claims might limit commercial scope or invite infringement challenges.
5. What is the strategic importance of patent claims in pharmaceutical patents?
Claims define the scope of protection and determine enforceability. Well-crafted claims balance broad coverage with defendability, directly impacting commercialization, licensing, and litigation outcomes.
References
- Israeli Patent Office – Patent Database
- European Patent Office – Espacenet Database
- World Intellectual Property Organization (WIPO) – PATENTSCOPE
- Industry reports on Israeli biotech and pharmaceutical patent filings
- Israeli Patent Law and Guidelines, 2000
