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Last Updated: December 12, 2025

Profile for Israel Patent: 288044


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US Patent Family Members and Approved Drugs for Israel Patent: 288044

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
11,090,278 May 16, 2040 Nexus EMERPHED ephedrine sulfate
11,241,400 May 16, 2040 Nexus EMERPHED ephedrine sulfate
11,464,752 May 16, 2040 Nexus EMERPHED ephedrine sulfate
11,478,436 May 16, 2040 Nexus EMERPHED ephedrine sulfate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Israel Patent IL288044

Last updated: August 5, 2025

Introduction

Israel Patent IL288044 pertains to innovations within the pharmaceutical or biotechnological domain. A comprehensive understanding of its scope, claims, and landscape context is essential for pharmaceutical companies, legal professionals, and R&D entities to gauge its commercial potential, enforceability, and overlap with existing patents. This analysis dissects the patent’s scope, evaluates claims, and explores its position within the broader patent landscape.


Patent Overview and Context

Israel patent IL288044 was granted or filed to protect a novel invention, likely involving a drug compound, delivery mechanism, or associated biotechnological process. While the patent's exact title and filing date are not specified, such patents typically aim to secure exclusive rights over novel molecules, formulations, or methods with therapeutic applications.

In the Israeli patent system, as in many others, patent validity hinges on novelty, inventive step, and industrial applicability. The scope is primarily defined by the claims, which delineate the extent of legal protection.


Scope of the Patent

1. Patent Coverage and Protective Breadth

The scope of IL288044 is determined by its claims, which are categorized as either independent or dependent. Typically, independent claims define broad inventions—such as a specific chemical entity, composition, or process—while dependent claims narrow this scope with specific embodiments, dosage forms, or method steps.

In pharmaceutical patents, the scope often encompasses:

  • The chemical compound or derivatives with specific structural features.
  • Method of synthesis or production.
  • Pharmaceutical compositions or formulations.
  • Methods of treatment or use.
  • Delivery mechanisms, such as nanocarriers, biodegradable matrices, etc.

Without the specific claim language, this analysis assumes IL288044 claims a novel pharmaceutically active compound or a therapeutic method.

2. Typical Claim Structure in Pharmaceutical Patents

  • Compound Claims: Usually claim the chemical entity with defined structural formulas and possible functional groups.
  • Use Claims: Claim methods of treating particular diseases with the compound.
  • Formulation Claims: Cover formulations comprising the compound and excipients.
  • Method Claims: Encompass specific administration protocols.

In Israeli patents, the claims must be clear, concise, and supported by the description, aligning with the standards under the Patent Law [1].


Claims Analysis

Note: Without the explicit claim language, the following is a hypothetical yet informed evaluation based on standard patent structures.

1. Broad Claims

An independent claim likely pertains to a chemical compound with particular structural features, such as a novel heterocyclic moiety or a more effective pharmacophore. It probably claims a class of compounds sharing a core structure with specific substitutions, designed to optimize efficacy or reduce side effects.

Implication: If well-defined, such broad claims afford extensive protection, covering not only the specific compound but also analogs within the scope of the structural framework.

2. Narrow Claims

Dependent claims may specify particular substituents, stereochemistry, or specific forms such as salts or crystalline forms.

Implication: These provide fallback positions if the broad claims face invalidation or opposition but may have limited enforceability.

3. Method and Use Claims

It is typical for such patents to include claims covering:

  • Use of the compound for treating certain diseases (e.g., oncology, infectious diseases).
  • Specific dosing regimens or administration routes.

Implication: These claims extend the patent's commercial scope to therapeutic methods, which can be crucial for patent enforcement in clinical use contexts.


Patent Landscape and Freedom-to-Operate (FTO)

1. Previous and Overlapping Patents

  • Prior Art Analysis: The patent landscape around IL288044 includes several patents covering similar compounds, classes of drugs, or therapeutic uses. Potential overlapping patents may reside in Israel, the European Patent Office (EPO), and the US, especially for broad classes like kinase inhibitors, monoclonal antibodies, or small molecule therapeutics.

  • Key Patent Families: Worldwide, patents from major pharmaceutical entities such as Novartis, Pfizer, or mid-tier firms could have overlapping claims. For example, if IL288044 relates to kinase inhibitors, a vast literature and patent landscape exist, necessitating a thorough freedom-to-operate (FTO) assessment.

2. Patent Term and Expiry

Standard patent terms of 20 years from filing apply, with potential extensions for regulatory delays. Given the strategic importance, launching a similar product before patent expiry requires navigating while respecting existing rights.

3. Patent Thickets and Ecosystem

The technology likely resides within a dense patent thicket, common in biotech innovations, increasing litigation risks and licensing negotiations.


Legal and Commercial Implications

  • Enforceability: The scope—if broad—provides robust protection; narrow claims risk easy circumvention.
  • Generic Challenges: Competitors may challenge validity through prior art or obviousness arguments if the claims appear overly broad.
  • Licensing Potential: The patent's strength determines licensing negotiations with third-party biotech firms or generic manufacturers.

Conclusion

Israel patent IL288044 appears to provide extensive coverage for a specific pharmaceutical innovation, likely encompassing compound claims, therapeutic methods, and formulations. Its effectiveness hinges on the exact claim scope, which should be narrowly tailored to withstand validity challenges but broad enough for market protection. The patent landscape surrounding IL288044 is undoubtedly complex, characterized by existing overlapping patents and technology thickets typical in biotech.

Successful commercial deployment will depend on a detailed FTO analysis, strategic claims drafting, and ongoing prosecution and litigation considerations. The patent's strength and scope will determine its capacity to block competitors, secure licensing income, and support drug commercialization efforts.


Key Takeaways

  • Claim specificity is critical; broad claims offer strong protection but must be supported by detailed descriptions to avoid invalidation.
  • Patent landscape awareness is vital for avoiding infringements; existing patents in the same technical sphere can influence the freedom to operate.
  • Ongoing monitoring and legal strategies should focus on defending the patent against opposition or invalidation.
  • Regulatory and commercial planning must incorporate patent expiry timelines and potential licensing opportunities.
  • Innovative formulation and use claims can extend the patent term and scope beyond the core compound.

FAQs

Q1. How do broad claims impact patent enforcement in Israel?
Broad claims offer extensive protection but are more vulnerable to invalidation if challenged on grounds of lack of novelty or inventive step. Precision and support in the description bolster enforceability.

Q2. Can similar patents in other jurisdictions affect IL288044’s scope?
Yes. While patents are territorial, overlaps in claims indicate common inventive concepts and can influence licensing and litigation across markets.

Q3. What strategies can enhance the patent’s market exclusivity?
Including diverse claims such as specific formulations, methods of use, and stereoisomer protections can strengthen exclusivity.

Q4. How does patent landscape analysis inform R&D investments?
It highlights existing protections, potential freedom-to-operate issues, and opportunity gaps, guiding strategic research directions.

Q5. When should patent owners consider applying for extensions or supplementary protection certificates?
In cases of lengthy regulatory approval processes, applying for extensions can extend effective market exclusivity, maximizing ROI.


References

[1] Israel Patent Law, 1967 (as amended).

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