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Last Updated: March 26, 2026

Profile for Israel Patent: 185924


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US Patent Family Members and Approved Drugs for Israel Patent: 185924

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
10,588,975 Mar 13, 2026 Pf Prism Cv TYGACIL tigecycline
7,879,828 Feb 5, 2029 Pf Prism Cv TYGACIL tigecycline
8,975,242 Oct 24, 2028 Pf Prism Cv TYGACIL tigecycline
9,254,328 Mar 13, 2026 Pf Prism Cv TYGACIL tigecycline
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Israel Drug Patent IL185924

Last updated: August 18, 2025

Introduction

Israel patent IL185924 constitutes a significant intellectual property asset within the pharmaceutical domain. This patent appears to encompass innovative drug compositions, formulations, or methods with potential therapeutic utility. An in-depth understanding of its scope, claims, and the broader patent landscape is essential for stakeholders including pharmaceutical companies, generic manufacturers, and legal professionals seeking to navigate patent expiry, infringement risks, or licensing opportunities. This analysis delineates the scope and claims of IL185924 and contextualizes its position within the current patent landscape.


Patent Overview and Context

Patent IL185924 was granted in Israel, offering legal exclusivity for the inventor or assignee within the jurisdiction. While the full text isn’t accessible here, patents of this nature typically cover:

  • Novel chemical entities or drug compounds
  • Specific pharmaceutical formulations or delivery mechanisms
  • Methods of treatment or use claims related to specific medical indications

Understanding the scope involves examining the claims’ language, which defines the legal boundaries of the patent rights.


Scope of Patent IL185924

1. Technical Field and Relevance

Most drug patents like IL185924 fall within the realm of medicinal chemistry, pharmacology, or drug delivery systems. Such patents aim to protect:

  • A new molecule or a novel derivative
  • Unique formulations that enhance bioavailability or stability
  • Innovative methods of synthesis or synthesis pathways

2. Patent Term and Geographic Scope

As a national Israeli patent, IL185924 grants exclusive rights within Israel, typically for 20 years from the filing date, subject to patent maintenance. While the patent is specific to Israel, similar or related patents might exist internationally, covering broader territories via patent families or PCT (Patent Cooperation Treaty) applications.

3. Elements of the Patent’s Claims

The scope is primarily dictated by independent and dependent claims:

  • Independent Claims: Define the core invention, often covering a new compound, a crystalline form, or a method of manufacture.
  • Dependent Claims: Narrow the scope, adding specific embodiments, compositions, or method details.

Without the exact claim language, one can infer standard patent strategies for drug products:

  • Claims likely cover the chemical structure of the active pharmaceutical ingredient (API)
  • Claims may specify dosage forms, delivery routes, or formulations
  • Additional claims could encompass methods of synthesis or use for particular indications

The breadth of claims directly impacts the patent’s enforceability and potential for blocking generic equivalents.


Claims Analysis

1. Claim Structure and Focus

Typical pharmaceutical patents aim for broad claims to maximize scope, balanced with narrower dependent claims for fallback positions. For IL185924:

  • Broad Claims: Encompass the core chemical structure or class of compounds with demonstrated or proposed activity
  • Narrow Claims: Specify particular substituents, stereochemistry, or specific uses

2. Claim Language and Limitations

Precise claim language dictates scope:

  • Use of "comprising" suggests open-ended claims covering compositions containing the claimed compound plus other ingredients.
  • Limitations such as "wherein" or "consisting of" restrict scope.

Legal robustness depends on claim novelty, inventive step, and non-obviousness.

3. Strategic Considerations

Patent claims tend to be written with:

  • A focus on innovative features—e.g., improved stability, bioavailability.
  • Incorporation of specific therapeutic uses, possibly broadening exclusivity.

Without access to the official patent document, detailed claim-by-claim analysis remains limited, but typical strategies for similar drug patents include:

  • Claiming a new chemical scaffold
  • Claiming specific polymorphs or salts
  • Claims covering specific dosages or formulations

Patent Landscape Analysis

1. Global Patent Families and Related Applications

Most drug-related patents are part of international patent families, with filings in multiple jurisdictions. For IL185924:

  • It is likely part of a global patent family, with equivalents filed under PCT or national patent offices.
  • Similar patents may exist in the US, Europe, or Asia, affecting freedom-to-operate (FTO) considerations.

2. Patentability and Prior Art

The patent’s validity hinges on:

  • Novelty: Chemical structures or uses must be new.
  • Inventive Step: The invention must be non-obvious over prior art.
  • Industrial Applicability: Must have utility.

A thorough prior art search—for example, in patents or scientific literature—would clarify the scope and enforceability.

3. Competitor and Clinical Pipeline Landscape

Identifying active competitors or similar innovations involves reviewing:

  • Patents citing IL185924
  • Patent applications that challenge or circumvent its claims
  • Drugs already approved or in clinical development sharing similar structures or uses

Legal and Commercial Implications

  • Patent Blockade: IL185924’s claims, if broad and robust, could prevent generic entry in Israel.
  • Patent Term and Expiry: Patents generally have 20-year terms, but supplementary protections or patent extensions can influence effective monopoly periods.
  • Licensing Opportunities: Strong claims invite licensing negotiations with generic manufacturers or biotech firms.
  • Infringement Risks: Companies developing similar compounds must carefully analyze claims to avoid infringement.

Conclusion

The efficacy of IL185924’s patent protection depends on the precise scope of its claims and how they address prior art and competitors’ innovations. While exact claim language is critical, typical patent strategies suggest broad compound claims supplemented by narrower use or formulation claims to maximize exclusivity.

Understanding this patent’s position within the patent landscape requires examining related filings, adjacent patents, and opposing literature. This contextual view informs decision-making regarding R&D, licensing, and market entry strategies.


Key Takeaways

  • Scope is Defined by Claims: The breadth and enforceability of IL185924 depend on the specific language used in its claims.
  • Broad Claims Offer Greater Protection: If well-crafted, they can prevent generic competitors in Israel and potentially influence international markets via patent families.
  • Patent Landscape is Complex: Compatibility with existing patents and freedom-to-operate analyses are essential before commercialization.
  • Strategic Positioning: The patent’s strength can provide catalyst for licensing, collaborations, or exclusivity in key markets.
  • Ongoing Legal Monitoring: Vigilant review of patent filings and litigation activity is necessary to maintain competitive advantage.

FAQs

Q1. How does the scope of patent IL185924 compare to similar patents in other jurisdictions?
A1. Without specific claim language, exact comparisons are challenging. Generally, patent scope depends on claim breadth; if similar claims are granted abroad, enforcement and licensing strategies may be aligned across jurisdictions.

Q2. Can IL185924 be challenged or invalidated?
A2. Yes. Challenges can arise from prior art, obviousness, or lack of inventive step. Validity challenges are typical during patent prosecution or post-grant proceedings.

Q3. What is the potential lifespan of IL185924’s patent protection?
A3. Usually 20 years from the application filing date, subject to maintenance fees. Potential extensions or supplementary protections can modify this timeline.

Q4. How do competitor patents impact the enforceability of IL185924?
A4. Overlapping claims or prior art can lead to patent invalidation or design-around strategies by competitors, influencing the patent’s market strength.

Q5. What role does the patent landscape play in drug development?
A5. It guides R&D investments, helps avoid infringement, informs licensing strategies, and identifies opportunities for innovation or patent clearance.


Sources:
[1] Israeli Patent Office, Patent IL185924 Documentation (if publicly available).
[2] WIPO PatentScope, International Patent Family Data.
[3] Patent law and strategy literature relevant to pharmaceutical patents.

(Note: For detailed claim language and legal status, consulting the official patent document and legal counsel is recommended.)

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