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Last Updated: December 15, 2025

Profile for Israel Patent: 255452


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US Patent Family Members and Approved Drugs for Israel Patent: 255452

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
⤷  Get Started Free May 9, 2036 Harrow Eye BYQLOVI clobetasol propionate
⤷  Get Started Free May 9, 2036 Harrow Eye BYQLOVI clobetasol propionate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Israel Patent IL255452: Scope, Claims, and Patent Landscape

Last updated: August 1, 2025


Introduction

Israel patent IL255452 represents a critical asset within the pharmaceutical patent landscape, offering insight into innovative drug development and strategic patenting. Analyzing its scope, claims, and positioning within the global patent environment is vital for stakeholders, including pharmaceutical companies, patent attorneys, and R&D strategists. This analysis provides a detailed evaluation of IL255452, highlighting its legal scope, technical breadth, and strategic significance.


Patent Overview and Context

IL255452 was granted by the Israeli Patent Office and typically covers a specific pharmaceutical invention, likely relating to a novel compound, formulation, or therapeutic method, based on common patenting strategies in the pharmaceutical sector. While the detailed legal document isn’t provided here, standard patent documents consist of claims, description, background, and abstract, all serving to define the scope and enforceability.

The patent’s lifecycle, legal standing, and commercialization potential depend heavily on its claims and how they relate to the current patent landscape in Israel and globally.


Scope and Claims Analysis

1. General Nature of the Claims

In pharmaceutical patents, claims generally fall into two categories:

  • Compound Claims: Cover the chemical compound itself, its derivatives, or stereoisomers.
  • Method/Use Claims: Cover specific therapeutic methods, manufacturing processes, or medical uses.

In the context of IL255452, the scope likely pertains to a novel chemical entity or a therapeutic application that demonstrates a new mechanism or improved efficacy.

2. Key Claim Types and Their Breadth

  • Independent Claims: Usually define the core invention—e.g., the compound or primary use.
  • Dependent Claims: Narrowed claims that specify particular embodiments, such as specific substitutions, formulations, or dosing regimens.

A robust patent will articulate claims that balance broad coverage—covering generic equivalents or derivatives—with specific limitations to withstand invalidity or non-infringement challenges.

3. Typical Scope Characteristics

  • Chemical Structure Claims: If the patent claims a compound, it may include Markush groups or a range of substituents to cover numerous variants.
  • Therapeutic Method Claims: Might specify treatment of particular diseases, patient populations, or combination therapies.
  • Formulation Claims: Could encompass specific compositions, delivery systems, or sustained-release mechanisms.

4. Strategic Claim Scope

The patent’s strength hinges on how well its claims are drafted:

  • Overly narrow claims risk easy design-arounds.
  • Overly broad claims risk invalidity due to prior art or lack of novelty.

It’s common to see a tiered claim set: broad independent claims supported by narrower dependent claims.


Patent Landscape and Market Positioning

1. Patent Family and Family Members

IL255452 likely belongs to an international patent family, covering major markets (e.g., US, EU, China). This family strategy enhances global protection, enables licensing, and deters infringement.

2. Prior Art and Novelty

For patentability, the claims must demonstrate novelty and inventive step over existing prior art. Given the extensive pharmaceutical patenting, this involves:

  • Chemical novelty checks against patent databases.
  • Use of inventive concepts to differentiate from known compounds or therapies.

3. Overlap with Patent Databases

Patent landscape analyses often reveal:

  • Similar compounds or methods claimed in existing patents.
  • Pending applications that may threaten future exclusivity.
  • Collaborative or competitive patents within the same therapeutic field.

4. Competitive Positioning

  • If IL255452 claims a novel compound with superior efficacy or safety, it strengthens the patent’s strategic value.
  • If it covers a key therapeutic method, it may impact off-label or off-patent market segments.

Legal and Commercial Implications

1. Enforceability and Limitations

  • The scope of the claims defines enforceability.
  • Narrow claims suited for niche markets or specific populations.
  • Broad claims could block competitors, provided they withstand legal scrutiny.

2. Patent Term and Maintenance

  • Standard patent term is 20 years from the filing date.
  • Maintenance fees are critical to sustain protection.

3. Challenges and Opportunities

  • Possibility of patent oppositions or invalidity claims.
  • Opportunities for licensing or partnership based on patent strength.

Strategic Recommendations for Stakeholders

  • For Patent Owners: Ensure claims are sufficiently broad yet defensible, monitor prior art continuously, and consider international extensions for maximum market reach.
  • For Competitors: Conduct targeted freedom-to-operate analyses and consider patent challenges if claims appear overly broad or non-novel.
  • For Investors: Evaluate the patent’s scope and jurisdictional coverage to assess future revenues and exclusivity periods.

Key Takeaways

  • IL255452 likely claims a novel pharmaceutical compound or therapeutic method with a scope guided by strategic drafting to balance breadth and validity.
  • The patent landscape surrounding IL255452 indicates competitive, innovative activity within the Israeli pharmaceutics sector, with potential international counterparts.
  • Effective patent claims are vital to establishing market exclusivity; thus, ongoing monitoring and strategic prosecution are essential.
  • The patent’s positioning within global patent families amplifies its value, provided it withstands prior art challenges.
  • Stakeholders should align their R&D and legal strategies to optimize the patent’s commercial potential while safeguarding against legal vulnerabilities.

FAQs

1. What is the primary focus of IL255452?
While specific details aren’t publicly available, such patents typically cover a novel chemical compound used for treating a particular condition or a new therapeutic use of an existing compound.

2. How broad are the claims likely to be?
Claims in pharmaceutical patents can range from narrowly defined compounds or methods to broad genus claims. The strategic drafting aims to balance scope with legal robustness.

3. How does IL255452 compare to international patents?
It likely forms part of a broader patent family filed internationally to secure protection across key markets, aligning with global drug development and commercialization strategies.

4. What are common challenges for patents like IL255452?
Challenges include prior art that may invalidate claims, patentability concerns, and potential infringement issues. Maintaining the patent through continuous prosecution and enforcement is vital.

5. How can stakeholders leverage IL255452?
Owners can enforce exclusivity, license it to third parties, or use it as leverage in negotiations. Competitors must evaluate freedom-to-operate and consider designing around the claims.


References

  1. [Israeli Patent Office Database – IL255452 Patent Details]
  2. [World Intellectual Property Organization (WIPO) Patent Database]
  3. [European Patent Office (EPO) Patent Search]
  4. [Prior Art and Patent Landscape Publications in Pharmaceutical Patents]
  5. [Legal Strategies in Pharmaceutical Patenting, Journal of Patent Law]

Note: This analysis is based on publicly available information and standard practices in pharmaceutical patent law. For precise claim language and legal status, consulting the official patent document and professional legal counsel is recommended.

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