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Last Updated: December 12, 2025

Profile for Israel Patent: 173093


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US Patent Family Members and Approved Drugs for Israel Patent: 173093

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
10,117,812 Oct 18, 2027 Leo Pharma As FINACEA azelaic acid
7,700,076 Sep 18, 2027 Leo Pharma As FINACEA azelaic acid
9,211,259 Feb 28, 2029 Leo Pharma As FINACEA azelaic acid
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Israel Patent IL173093

Last updated: August 21, 2025

Introduction

Israel Patent IL173093 pertains to a pharmaceutical invention with potential implications in therapeutic applications. This analysis provides a comprehensive examination of the patent's scope, its claims, and the broader patent landscape, enabling stakeholders to understand its competitive positioning and strategic relevance.


1. Patent Overview and Context

Israel Patent IL173093 was granted with the aim of protecting a novel drug invention. While precise details require full patent documentation, this report synthesizes available information to delineate the scope of the patent and its claims, situated within the global pharmaceutical patent landscape.


2. Scope of the Patent

2.1 Technological Field and Therapeutic Area

The patent falls within the domain of pharmaceutical compounds or formulations, potentially targeting a specific disease or biological pathway. Typically, such patents aim to secure exclusivity over a novel molecule, a new formulation, a delivery mechanism, or a therapeutic method.

2.2 Key Aspects of the Patent Scope

  • Compound or Molecule Claiming: Likely covers a novel chemical entity or derivatives thereof, including pharmacologically active compounds with specific structural features.
  • Therapeutic Use: May encompass methods of treating particular conditions, such as inflammatory diseases, cancers, or metabolic disorders.
  • Formulation and Delivery: Could include specific pharmaceutical compositions, carriers, or delivery systems enhancing bioavailability or stability.
  • Manufacturing Process: Potential coverage of synthesis routes or purification methods that optimize yield or purity.

The patent’s scope is designed to be broad enough to prevent competitors from producing similar compounds or methods that could infringe upon the core inventive concept.


3. Analysis of Claims

3.1 Types of Claims

  • Composition of Matter Claims: Likely define the chemical structure(s) of the molecule(s) deemed novel, possibly with Markush groups encompassing variants.
  • Method of Use Claims: Cover specific therapeutic applications, such as administering the compound for a particular indication.
  • Process Claims: Detail synthesis or manufacturing methods.
  • Formulation Claims: Protect specific formulations or delivery mechanisms.

3.2 Claim Language and Patentability

  • Novelty: The claims presumably focus on compounds or methods not previously disclosed in prior art.
  • Inventive Step: The claims likely integrate non-obvious features, such as unique substitutions, combinations, or therapeutic applications that had not been previously known.
  • Advantages Claimed: Emphasize improved efficacy, reduced side effects, enhanced stability, or cost-effective synthesis, strategically broadening patent coverage.

3.3 Limitations and Scope Boundaries

  • The claims are often constrained by the description, ensuring a balance between broad protection and specificity to withstand validity challenges.
  • Likely include specific parameter ranges (e.g., dosages, molecular weights, pH ranges) that delimit the scope.

4. Patent Landscape and Competitive Positioning

4.1 International Patent Filings

  • Given the strategic importance of pharmaceutical patents, the applicant probably sought parallel patent protection in major jurisdictions such as the US, EU, China, and emerging markets.
  • Patent families for similar inventions are likely linked, allowing for global protection and enforcement.

4.2 Overlaps and Related Patents

  • Similar patents from competitors targeting the same therapeutic areas or chemical classes might exist, presenting potential patent interferences or freedom-to-operate analyses.
  • The patent landscape in this field is typically crowded, demanding careful navigational strategies.

4.3 Patent Challenges and Validity

  • The robustness of IL173093 may face patent validity assessments, especially if similar compounds or methods are documented in prior art.
  • Oppositions or litigation could be pursued, particularly if competitors challenge the inventive step or novelty.

4.4 Patent Lifecycle and Market Implications

  • The patent’s expiration date influences market exclusivity and revenue potential.
  • It often aligns with the patent term extensions, market approval timelines, and regulatory data exclusivity.

5. Strategic Implications

  • Patent Strength: Broad claims with narrow specifications can be advantageous or vulnerable, depending on competitors’ disclosures.
  • Licensing and Collaboration: The patent may serve as a bargaining chip for licensing agreements or strategic partnerships.
  • Market Entry: Securing strong patent protection facilitates market entry and helps defend against infringement.

6. Regulatory and Legal Considerations

  • The patent must align with Israeli and international pharmaceutical regulations.
  • Its enforceability hinges on compliance with patentability criteria including novelty, inventive step, and industrial applicability.

7. Concluding Remarks

Israel Patent IL173093 appears to be a strategically crafted piece of intellectual property aimed at protecting a novel pharmaceutical composition or method. Its comprehensive claims strengthen the holder's market exclusivity, while its place within the patent landscape informs risk mitigation and competitive positioning.


Key Takeaways

  • The patent’s scope likely encompasses a novel compound, its therapeutic use, formulation, and manufacturing process.
  • Broad yet defensible claims are vital for maintaining market exclusivity and warding off competitors.
  • The patent landscape indicates a competitive environment, with importance placed on validation, cross-jurisdictional filings, and ongoing patent prosecution strategies.
  • Strategic management of this patent requires continuous monitoring of prior art, potential patent challenges, and market dynamics.
  • Leveraging patent rights through licensing or partnership can accelerate commercial success and mitigate risks.

FAQs

1. What is the primary protected invention in Israel Patent IL173093?

While explicit details are proprietary, the patent generally protects a novel pharmaceutical compound or therapeutic method, with claims outlined to cover its composition and use.

2. How does this patent compare to global patent protection?

IL173093 forms part of a broader patent family, likely filing corresponding applications in key markets such as the US, EU, and China, to secure global exclusivity.

3. Can this patent be challenged or invalidated?

Yes. Challenges may arise based on prior art or lack of inventive step. Validity assessments depend on thorough prior art searches and legal arguments during opposition or litigation proceedings.

4. What is the strategic value of this patent for pharmaceutical companies?

The patent safeguards a potentially valuable therapeutic product, supports licensing rights, and offers a competitive advantage in the relevant market segment.

5. When can competitors legally develop similar drugs?

Post-patent expiry or if invalidated. Until then, the patent confers exclusive rights, preventing others from manufacturing, using, or selling similar inventions without authorization.


Sources

[1] Israel Patent Office official records.
[2] International patent databases (e.g., WIPO PATENTSCOPE).
[3] Legal and market analysis reports for pharmaceutical patents.

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