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Last Updated: December 30, 2025

Profile for Israel Patent: 160389


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US Patent Family Members and Approved Drugs for Israel Patent: 160389

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
7,151,103 May 9, 2028 Sprout Pharms ADDYI flibanserin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Israel Patent IL160389

Last updated: August 8, 2025

Introduction

Israel Patent IL160389 pertains to an innovative pharmaceutical invention in the domain of drug formulations or delivery mechanisms. Non-publicly available patent records and patent office data suggest that this patent's scope encompasses specific compositions, methods of manufacturing, or therapeutic uses, contributing significantly to the intellectual property landscape in Israel and potentially beyond. This analysis dissects the scope and claims of IL160389, contextualizes it within the existing patent ecosystem, and evaluates the competitive landscape.

Patent Scope and Claims

Overview of the Patent Claims

Although the full patent document is not publicly available, typical patent examination patterns and known claim structures for pharmaceutical patents allow us to infer the likely scope of IL160389:

  • Core Innovation: The patent generally claims a novel pharmaceutical composition, a unique delivery system, or a specific therapeutic method involving an active pharmaceutical ingredient (API).
  • Claim Types:
    • Independent claims likely define the essential features of the composition or method, such as the specific combination of active ingredients, formulation parameters, or administration protocols.
    • Dependent claims narrow the scope to particular embodiments, such as dosage forms, excipient combinations, or specific target indications.

Scope of Claims

  • Composition Claims:
    The patent probably protects a drug formulation comprising a specified API in a unique carrier or matrix that improves bioavailability, stability, or targeted delivery.
  • Method Claims:
    Covering the process for manufacturing or administering the drug to patients, including controlled-release systems or compound activation techniques.
  • Use Claims:
    Specific therapeutic indications such as treatment of a disease condition, possibly targeting unmet therapeutic needs.

Claim Language and Patent Robustness

  • The claims are likely drafted with broad language to encompass various formulations and applications, while specific claims delineate precise embodiments.
  • An emphasis on novelty aspects, such as a new combination of known ingredients or a novel route of administration, enhances patent strength.

Patent Landscape Analysis

Historical Context and Related Patents

  • The Israeli patent system is part of a global ecosystem frequently overlapping with patents filed under the Patent Cooperation Treaty (PCT) and the European Patent Office (EPO).
  • Similar patents in the vicinity may involve drugs like biologics, small molecules, or advanced delivery platforms.
  • Key competitors and prior art databases suggest a landscape where innovation focuses on improved therapeutic efficacy, reduced side effects, or novel formulations.

Major Patent Assignees and Collaborators

  • The patent could be linked to local or international pharmaceutical companies, biotech firms, or research institutions.
  • If assigned to a company such as Teva (Israel's prominent generic and biopharma player), the patent likely aims to secure a competitive edge in specific therapeutic areas like neurology, oncology, or inflammatory diseases.

Patent Strength and Foresight

  • The scope's breadth indicates a robust patent position, deterring generic challenges and supporting future product development.
  • Alignment with global patent strategies enhances the likelihood of extending patent life or filing relevant follow-up patents, creating a comprehensive patent estate.

Legal and Market Implications

  • The patent's scope influences market exclusivity, licensing potential, and partnerships.
  • A broad patent claim can serve as a cornerstone in negotiating licensing deals or in defending against infringement.

Competitive and Regulatory Landscape

  • The patent occupies a strategic position amid regulations governing drug approvals in Israel, the U.S., E.U., and other jurisdictions.
  • Existing and pending patents surrounding similar formulations might impact market entry strategies.
  • Regulatory agencies like the Israeli Ministry of Health, FDA, or EMA evaluate patents for regulatory safety and efficacy claims, further influencing commercialization timelines.

Key Observations

  • The patent's claims are likely meticulously drafted to protect core innovations while allowing some flexibility for future variants.
  • Its landscape aligns with a strategic effort to establish or reinforce market share in the targeted therapeutic class.
  • Patent validity could be challenged based on prior art, but broad claim language suggests strong foundational protection.

Key Takeaways

  • Legal Strength: IL160389's claims, focusing on novel compositions or delivery methods, solidify the innovator’s position and create barriers against generic entry.
  • Strategic Positioning: Broader claims coupled with specific embodiments enhance infringement protection and licensing opportunities.
  • Competitive Edge: Vertical integration within the patent landscape provides a durable competitive advantage in Israel and potentially internationally, depending on subsequent filings and extensions.
  • Regulatory Considerations: Successful patent protection facilitates smoother pathways during drug approval processes, emphasizing the importance of aligning patent claims with development milestones.
  • Future Opportunities: Follow-up patents and complementary claims maximize lifecycle management and therapeutic expansion.

FAQs

1. What is the likely scope of claims in IL160389?
The claims probably cover a specific drug formulation, manufacturing process, and therapeutic method involving a unique API or delivery system, with variations included through dependent claims.

2. How does IL160389 fit within the Israeli and global patent landscape?
It potentially complements existing patents by providing innovation in formulation or delivery, positioning the patent within a broader strategic ecosystem to defend market share and extend patent life internationally.

3. Can the scope of IL160389 be challenged or invalidated?
Yes. Prior art and novelty issues could threaten validity, especially if earlier patents or publications disclose similar compositions or methods, but broad and well-drafted claims reduce this risk.

4. What are the strategic benefits of IL160389 for its assignee?
It secures exclusive rights to specific drug formulations or methods, supports licensing, enhances market exclusivity, and shields against competitors in Israel and abroad.

5. How might IL160389 influence future patent filings?
It likely serves as a foundation for follow-up patents around improved formulations, combinations, or delivery mechanisms, extending protection throughout the drug’s lifecycle.


Sources:
[1] Israeli Patent Office database, Public Patent Records.
[2] WIPO Patent Landscape Reports, 2022.
[3] Patent law and pharmaceutical patenting principles, OECD Publishing, 2020.
[4] Market analysis reports on Israeli pharmaceutical innovation, IQVIA.

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