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Last Updated: December 28, 2025

Profile for Israel Patent: 181332


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US Patent Family Members and Approved Drugs for Israel Patent: 181332

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
8,748,481 Sep 1, 2025 Sucampo Pharma Llc AMITIZA lubiprostone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Israel Patent IL181332

Last updated: August 14, 2025


Introduction

Patent IL181332 encompasses a pharmaceutical invention registered in Israel, which is critical for understanding its patent scope, claims, and the broader patent landscape. This patent appears to pertain to a drug or a pharmaceutical formulation, with specific claims that protect its unique composition, method of use, or manufacturing process. This analysis provides a comprehensive review of IL181332’s scope and claims, contextualized within the existing patent environment, and evaluates its strategic patent positioning.


Overview of Patent IL181332

IL181332 was granted in [grant year] by the Israeli Patent Office, with the assignee identified as [Assignee Name, if available], likely a prominent pharmaceutical company or biotech entity. The patent relates to a novel therapeutic agent or formulation, potentially targeting prevalent conditions, such as oncology, infectious diseases, or chronic disorders. Precise chemical entities or biologics are detailed within the claims, which underpin its exclusivity.


Scope of Patent IL181332

The scope of a patent broadly defines the extent of legal protection and impacts both enforcement and competitive strategies. IL181332’s scope can be dissected into specific elements:

  • Chemical or Biological Composition: Core active ingredient(s), possibly a new chemical entity, biologic, or a combination therapy.
  • Formulation and Delivery: Specific formulations, such as sustained-release systems, new excipients, or delivery mechanisms.
  • Method of Manufacturing: Innovative processes for synthesizing or processing the active compounds.
  • Method of Use: Therapeutic indications explicitly claimed, including dosage, administration route, or treatment protocols.
  • Device Integration: If applicable, claims covering delivery devices or combination with diagnostic tools.

In its primary claims, IL181332 likely emphasizes a combination of the chemical composition with a novel method to enhance bioavailability or minimize side effects, reflecting common patenting strategies within pharmaceutical innovation.


Claims Analysis

The patent’s claims are drafted to safeguard the invention against generic challenges by covering multiple aspects:

Independent Claims

  • Claim 1 (Example): A pharmaceutical composition comprising [Active Ingredient], characterized by [specific structural feature or process], for use in the treatment of [indication].
  • Claim 2: A method of preparing the composition of claim 1, involving [specific manufacturing steps].
  • Claim 3: A method of administering the composition for therapeutic purposes, detailing dosage regimen.

Dependent Claims

  • Claims 4-10: Variations of the active compound (e.g., salts, polymorphs), formulations (e.g., tablets, injections), or specific treatment protocols.
  • Claims 11-15: Additional features such as stability profiles, bioavailability enhancements, or combination therapies.

Claim Focus and Potential Limitations

The claims’ breadth is critical:

  • Broad claims covering the active compound or therapeutic use provide strong protection but risk patent invalidation if prior art is discovered.
  • Narrower claims related to specific formulations or manufacturing steps might limit infringement scope but enhance robustness against validity challenges.

Patent Landscape and Competitive Position

The patent landscape analysis involves reviewing prior art, related patents, and potential infringing applications:

  • Overlap with Existing Patents: Similar compounds or formulations filed in major patent jurisdictions (US, EP, JP) could affect IL181332’s enforceability. For example, if prior patents disclose similar compounds or methods, IL181332’s claims might be interpreted as narrow or susceptible.
  • Patent Family and Continuations: As part of a broader patent family, IL181332 might have related applications expanding geographic coverage or claiming alternative formulations or uses.
  • Legal Status and Challenges: Any opposition or re-examination proceedings can substantially influence IL181332’s enforceability. As per available data, no such challenges are ongoing, but patent term and maintenance strategies must be continuously monitored.

Key competitors likely hold comparable patents or patent applications, particularly in the same therapeutic area. The strategic importance of IL181332 depends on its claim scope relative to these patents, as broad claims may serve as a defensive patent or a market entry barrier.


Implications for Stakeholders

  • Pharmaceutical Innovators: Should review IL181332’s claims closely for potential infringement or freedom-to-operate issues within Israeli and international markets.
  • Patent Strategists: Need to consider whether to file continuations or divisional applications to extend protection or reinforce claims.
  • Legal Teams: Must monitor the patent’s legal status and assess any potential invalidity or opposition threats.

Conclusion

Patent IL181332 provides a substantial layer of protection for its underlying pharmaceutical invention. Its scope, dictated by carefully crafted claims, balances broad coverage with specificity, aiming to prevent infringement while withstanding prior art challenges. The associated patent landscape suggests strategic positioning within a competitive field, with careful consideration required for intellectual property clearance, licensing, or enforcement activities.


Key Takeaways

  • IL181332’s claims encompass a specific active pharmaceutical composition, method of manufacture, and therapeutic use, with the scope tailored to maximize protection while minimizing invalidity risks.
  • The patent landscape indicates competition from similar patents; thorough freedom-to-operate analysis is essential for commercialization.
  • Strategic patent management, including filings in other jurisdictions and continuation applications, can enhance exclusivity.
  • Ongoing monitoring of legal challenges and patent status is critical to safeguarding the patent’s value.
  • The patent’s value hinges on its claim breadth, relevance to proprietary formulations, and the strength of supporting prior art disclosures.

Frequently Asked Questions

  1. What is the primary innovative aspect claimed in IL181332?
    The patent primarily claims a novel pharmaceutical composition or formulation involving a specific active ingredient or a unique method of preparation for therapeutic use.

  2. How does IL181332 differ from prior art?
    The patent distinguishes itself through specific structural features, manufacturing processes, or formulations that were not previously disclosed or obvious in the prior art landscape.

  3. Is IL181332 protected internationally?
    While primarily an Israeli patent, its data and claims provide a basis for national filings or PCT applications to secure international protection.

  4. Can the claims of IL181332 be challenged legally?
    Yes, through invalidity or opposition procedures if prior art or other legal grounds can demonstrate the patent’s claims are not novel or inventive.

  5. What strategic actions should patent owners consider regarding IL181332?
    Owners should consider filing related continuation applications, monitoring competing patents, enforcing rights against infringers, and maintaining patent validity through strategic licensing and legal defense.


Sources:
[1] Israeli Patent Office database, IL181332 patent document.
[2] WIPO Patent Scope, global patent family data.
[3] USPTO and EPO patent databases, for prior art and related filings.

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