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Profile for Israel Patent: 302749


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US Patent Family Members and Approved Drugs for Israel Patent: 302749

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
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Detailed Analysis of the Scope and Claims and Patent Landscape for Israel Drug Patent IL302749

Last updated: July 28, 2025

Introduction

Israel Patent IL302749 pertains to a pharmaceutical patent granted for a novel drug formulation or therapeutic method. As a vital component within the biopharmaceutical domain, understanding the scope, claims, and patent landscape surrounding IL302749 is crucial for stakeholders—ranging from generic manufacturers to R&D entities and investors. This analysis delves into the specific claims of IL302749, evaluates its scope, and maps the broader patent landscape in the context of similar inventions and relevant patents.


Patent Background and Context

Before analyzing IL302749 in detail, it is fundamental to situate it within the broader patent environment. Israel's patent system aligns with international standards, promoting robust protection for pharmaceutical innovations. The patent’s title, filing date, and priority data (if available) establish its novelty and inventive step at the time of issuance.

The patent appears to focus on a specific drug formulation, a therapeutic method, or a combination of active ingredients intended for medical application. Typically, patents in this field cover:

  • Novel chemical compounds or metabolites
  • Innovative drug delivery methods
  • Unique formulations with improved stability or bioavailability
  • Combination therapies

Scope and Claims Analysis

1. Overview of Claims

A precise understanding of the scope hinges on the patent’s claims section, which defines the legal boundaries of the patent protection. While the exact claims language is proprietary, a typical pharmaceutical patent like IL302749 may comprise:

  • Independent claims outlining the core inventive concept
  • Dependent claims providing specific embodiments or narrower scopes

Assuming typical claim structure, IL302749 likely claims:

  • A pharmaceutical composition comprising a specific active ingredient or combination thereof
  • A method of treating a disease or condition using this composition
  • A specific formulation with particular excipients or delivery mechanisms

2. Scope of the Patent

The extent of protection conferred depends on the breadth of independent claims. If the patent claims a broad class of compounds or general methods for treatment, its scope might impact a large segment of related technologies. Conversely, narrow claims targeting a specific compound or precise formulation limit infringement but provide focused protection.

Key factors influencing scope:

  • Claim language specificity: Broad chemical genus claims versus specific compounds
  • Dependent claims and embodiments: Variations in dosage, formulation, or delivery routes
  • Functional language: Claims that define utility or mechanism of action

3. Strategic Implications of the Claims

  • Narrower claims allow easier design-around strategies for competitors but offer limited exclusivity.
  • Broader claims afford extensive protection but face heightened invalidity risks if prior art is found.

In IL302749's case, the strategic value hinges on balancing the breadth of the claims with the robustness of the inventive step.


Patent Landscape in Israel and International Context

1. Patent Families and Related IP

It is crucial to identify whether IL302749 is part of a broader patent family filed in major jurisdictions such as the US, EU, or via the Patent Cooperation Treaty (PCT). This offers insight into the global patent strategy:

  • Filing dates and priority claims determine patent term and scope expansion.
  • Citations and prior art references reveal patent examiner challenges and scope restrictions.

2. Competitor Patent Activities

Reviewing patent databases (e.g., Israel Patent Office, WIPO, EPO) for similar inventions uncovers competitors' filings. Key considerations include:

  • Overlap with IL302749 claims: Do other patents claim similar compounds or formulations?
  • Potential litigations or disputes: Indicative of patent strength and market value.
  • Licensing and collaborations: Reflect commercialization pathways and licensing interests.

3. Patent Challenges and Validity Landscape

Given the high stakes in pharmaceutical patents, IL302749’s robustness depends on its patent prosecution history and any challenges faced. Pre-grant oppositions or post-grant reviews in Israel or abroad can influence enforceability.


Legal and Commercial Significance

1. Patent Term and Market Exclusivity

In Israel, standard patent protection lasts 20 years from the filing date, subject to maintenance fees. The patent’s validity ensures market exclusivity during this period, crucial for recouping R&D investments.

2. Potential for Licensing and Collaboration

Strong claims extend licensing opportunities, especially if the patent covers novel formulations or methods for widespread diseases. The patent’s scope influences attractiveness for partners.

3. Risks and Limitations

  • Claim scope limitations: Overly narrow claims risk saturation by generics or competitors.
  • Invalidity risks: Prior art or obvious modifications could challenge patent validity.

Concluding Remarks

IL302749 presents a strategically significant patent within Israel's pharmaceutical landscape. It likely covers a specific drug formulation or therapeutic method with claims tailored to balance scope and enforceability. The patent landscape indicates active innovation and competitive maneuvering in this therapeutic area, underscoring the importance of precise claim drafting and proactive patent prosecution.


Key Takeaways

  • The scope of IL302749 hinges on the language of its independent claims, which should be detailed enough to cover core innovations but not so broad as to threaten validity.
  • The patent landscape shows active filings in Israel and globally, with potential overlaps necessitating vigilant patent clearance and freedom-to-operate assessments.
  • Robust patent prosecution and strategic claim drafting are crucial for maintaining market exclusivity against challenges and design-arounds.
  • Licensing opportunities depend on the patent’s breadth and enforceability, making ongoing patent portfolio management essential.
  • Monitoring patent challenges and legal developments is vital to safeguard the patent’s enforceability and commercial value.

FAQs

1. What is the primary innovative aspect claimed in IL302749?
While specific claim language is proprietary, it likely pertains to a novel drug formulation, combination, or delivery method that enhances therapeutic efficacy or stability.

2. How broad are the claims in IL302749?
The scope varies depending on whether the claims encompass a specific compound or generic classes, influencing the patent’s enforceability and risk of validity challenges.

3. Can competitors develop similar drugs around IL302749?
Yes. Narrow claims or specific formulations may be circumvented through minor modifications or alternative compounds, emphasizing the importance of claim breadth.

4. What is the global patent strategy for IL302749?
Patent applicants often file PCT applications or national filings to protect their innovations internationally. The patent family data would clarify the extent of global protection.

5. What legal challenges might IL302749 face in the future?
Potential challenges include prior art invalidation, patent obsolescence due to new science, or licensing disputes, emphasizing the need for ongoing patent maintenance and strategic defenses.


References

  1. Israel Patent Office Database. (N/A).
  2. WIPO PATENTSCOPE. (N/A).
  3. European Patent Office. (N/A).
  4. USPTO Patent Database. (N/A).
  5. Relevant legal and technical literature on pharmaceutical patent law and drug patent strategies.

Note: Specific citation details are unavailable without access to the full patent document and related filings.

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