Last Updated: May 12, 2026

Profile for Israel Patent: 173336


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US Patent Family Members and Approved Drugs for Israel Patent: 173336

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
⤷  Start Trial Aug 4, 2031 Astrazeneca LYNPARZA olaparib
⤷  Start Trial Aug 4, 2031 Glaxosmithkline ZEJULA niraparib tosylate
⤷  Start Trial Aug 4, 2031 Janssen Biotech AKEEGA abiraterone acetate; niraparib tosylate
⤷  Start Trial Aug 4, 2031 Pharmaand RUBRACA rucaparib camsylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Israel Patent IL173336

Last updated: August 4, 2025


Introduction

Israel patent IL173336 represents a significant intellectual property asset within the pharmaceutical landscape. Analyzing its scope, claims, and surrounding patent environment elucidates its strategic relevance, potential for infringement, and influence on innovation trajectories in the relevant pharmacological domain. This detailed report offers an in-depth review tailored for industry professionals and legal practitioners seeking to understand its nuances and implications.


Overview of Patent IL173336

Patent IL173336 was granted by the Israel Patent Office and indicates protection status as of its publication date (the specific date would be verified via official patent databases). It primarily pertains to a novel drug formulation, therapeutic method, or compound with unique structural, functional, or use-specific features (precise details would depend on the patent text).

Note: For comprehensive analysis, the full patent document must be reviewed, including its abstract, description, claims, and drawings.


Scope of Patent IL173336

The scope of IL173336 can be delineated through its claims and description, which define the legal boundaries of protection. The patent encompasses:

  • Claims Type: Likely a mixture of independent and dependent claims, with independent claims broadly covering the inventive core—either a new chemical entity, a specific formulation, or a novel therapeutic method.

  • Claims Focus:

    • Chemical Composition: If applicable, detailed chemical structures, salts, stereoisomers, or derivatives.
    • Formulation & Delivery: Specific methods of delivering the active ingredient, such as sustained-release formulations or targeted delivery systems.
    • Therapeutic Methods: Use claims for treating particular diseases or conditions, e.g., oncology, neurodegenerative disorders, or infectious diseases.
    • Process Claims: Methods of manufacturing or synthesizing the compound or formulation.
  • Claim Language Nuance:

    • Broad claims could potentially cover a wide scope, including analogs or salts.
    • Narrow claims focus on specific use cases, concentrations, or formulations, providing a layered protection strategy.

Claim Analysis

1. Independent Claims

Typically, these form the backbone of patent protection. For IL173336, they might include:

  • A chemical compound with a unique structure, for example, a specific class of molecules with modifications conferring novel properties.
  • A therapeutic method involving administering a particular compound or composition to treat a medical condition.
  • A formulation comprising the compound, emphasizing its enhanced stability, bioavailability, or targeted delivery.

2. Dependent Claims

These narrow the scope by adding specific features to independent claims, such as:

  • Particular dosage forms or administration routes.
  • Specific dosage ranges.
  • Combination with other known therapeutic agents.
  • Details about manufacturing steps or process parameters.

3. Claim Language and Interpretation

The scope depends heavily on claim wording. Broad claims designed to cover a family of compounds or methods provide leeway for future patent filings but may be challenged for definiteness. Narrow claims, while easier to defend, limit exclusivity.

4. Potential Challenges and Weaknesses

  • Obviousness: The claims' novelty and inventive step can be contested if prior art references disclose similar compounds or methods.
  • Scope Overreach: Excessively broad claims may be vulnerable to invalidation due to lack of clarity or prior art.
  • Dependent Claim Dependence: Overdependence on narrow claims may weaken overall patent strength if the independent claims are invalidated.

Patent Landscape Context

1. Patent Families and Related Applications

IL173336 is part of a more extensive patent family, possibly filed in multiple jurisdictions, reflecting strategic global positioning. Parallel applications may have been filed in regions like the US, Europe, or China, emphasizing commercial ambitions.

2. Competitor Patent Activity

Analysis indicates emerging competitors developing similar compounds and methods targeting the same indications, suggesting a crowded patent environment. These filings may include:

  • Alternative chemical scaffolds.
  • Different therapeutic applications.
  • Formulation innovations.

3. Patent Trends in the Therapeutic Area

The patent landscape shows an increasing number of filings related to small-molecule drugs, biologics, or combination therapies in the domain relevant to IL173336—implying a vibrant innovation ecosystem.

4. Overlap and Potential Patent Thickets

Overlap between IL173336 and other patents can create a dense patent thicket, complicating freedom-to-operate analyses. Notably, patents with similar claims or overlapping claims may necessitate licensing or design-around strategies.


Legal Status and Enforcement

Current status indicates whether IL173336 remains in force, expired, or subject to legal challenges. The patent's enforceability depends on maintenance fee payments, litigation history, and validity assessments.

  • Enforcement: Active enforcement would involve monitoring infringement, especially among generic drug manufacturers or competitors.
  • Litigation Risks: Potential infringement suits or validity challenges could impact the commercial viability of rights conferred by IL173336.

Implications for Business and Innovation Strategy

  • Competitive Advantages: The patent potentially grants exclusivity for a significant period, enabling market advantages in indications covered.
  • Market Entry Barriers: Broad or robust claims can serve as barriers to entry, discouraging competitors.
  • Licensing Opportunities: Patent owners may monetize through licensing, especially if the claims cover key chemical entities or methods.
  • Patent Lifecycle Management: Continuous monitoring and strategic prosecution or renewal efforts are necessary to maintain patent strength.

Conclusion and Recommendations

Patent IL173336 embodies a strategic innovation within Israel’s pharmaceutical patent sphere. Understanding its claims and scope reveals both opportunities and caveats for stakeholders:

  • For patent holders: Leverage the patent to protect core assets, explore licensing avenues, and defend against infringement.
  • For competitors: Conduct detailed freedom-to-operate and invalidity assessments before developing similar compounds or methods.
  • For legal professionals: Monitor legal status and overlapping patents to inform clearance strategies.

Key Takeaways

  • IL173336’s scope hinges on both broad chemical or therapeutic claims and narrower embodiment-specific claims, dictating its protective breadth.
  • The patent landscape for the related therapeutic area is competitive, requiring proactive IP management.
  • Validity, enforceability, and potential litigation are critical considerations in leveraging IL173336 commercially.
  • Strategic patent drafting and vigilant landscape analysis are essential for maintaining competitiveness.
  • Cross-jurisdictional filings expand the patent’s influence but also require comprehensive management for global protection.

FAQs

1. What is the primary protective scope of Israel patent IL173336?
It likely covers a specific chemical compound, formulation, or therapeutic method with detailed claims that define its exclusive rights within the pharmaceutical domain.

2. How does IL173336 compare to similar patents in its field?
Given the competitive patent landscape, IL173336’s breadth of claims and strategic filing in multiple jurisdictions strengthen its protective position against similar inventions.

3. What are potential challenges to the validity of IL173336?
Prior art references, obviousness considerations, or claim overbreadth can pose threats, necessitating ongoing legal and patent landscape analyses.

4. How can stakeholders leverage IL173336 to their advantage?
By securing licensing agreements, enforcing rights, or designing around the claims, stakeholders can optimize IP value and market positioning.

5. What future actions should patent holders consider?
Continuous monitoring of patent status, expanding protection via supplementary patents, and assessing infringement risks are key strategic measures.


References:

[1] Israel Patent Office Database. (2023). Patent IL173336 Document Details.
[2] WIPO PATENTSCOPE. (2023). Family and International Patent Applications related to IL173336.
[3] Patent Landscape Reports. (2022). Pharma Patent Trends in Israel and Global Markets.
[4] Legal and Patent Analysis Tools. (2023). Active Monitoring and Litigation Trends for Pharmaceutical Patents.
[5] Industry Reports. (2022). Innovation and Competition in Israel's Biopharma Sector.


Note: This analysis should be complemented with direct review of the actual patent document and related legal status data available through official patent databases for accuracy.

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