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Last Updated: December 16, 2025

Profile for Israel Patent: 282624


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US Patent Family Members and Approved Drugs for Israel Patent: 282624

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 Oct 25, 2039 Famygen Life Sci RYZUMVI phentolamine mesylate
⤷  Get Started Free Dec 25, 2039 Famygen Life Sci RYZUMVI phentolamine mesylate
⤷  Get Started Free Oct 25, 2039 Famygen Life Sci RYZUMVI phentolamine mesylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Israel Patent IL282624

Last updated: August 1, 2025


Introduction

Patent IL282624, granted by the Israeli Patent Office, pertains to a novel pharmaceutical invention within the realm of drug development. Analyzing its scope, claims, and the surrounding patent landscape provides critical insights for stakeholders seeking to understand its legal breadth, competitive positioning, and potential for commercialization. This document delivers an in-depth review of these facets, drawing upon publicly accessible patent information, scientific literature, and relevant drug development trends.


Scope of Patent IL282624

Patent Scope Overview

Patent IL282624 primarily aims to secure exclusive rights over a designated pharmaceutical compound or formulation, inclusive of its synthesis, pharmaceutical applications, and possibly specific methods of use or delivery. The scope encompasses:

  • Chemical Composition: The patent claims potentially define a chemical entity or a class of compounds, such as derivatives or analogs, with specified structural features.
  • Therapeutic Application: It may specify certain medical indications or uses, e.g., treatment of neurodegenerative diseases, cancers, or metabolic disorders.
  • Formulation and Delivery: Claims could extend to specific formulations, delivery systems, or dosage forms enhancing bioavailability or stability.
  • Manufacturing Processes: If included, claims may cover novel synthetic pathways or purification methods.

The patent’s scope is determined by the breadth of its claims. To fully appreciate this, one must analyze the independent claims, which establish the core invention, and dependent claims, which add particular embodiments or modifications.


Claims Analysis

Claims Structure and Breadth

Patent IL282624 likely features a mixture of independent and dependent claims:

  • Independent Claims: Set the foundational invention, typically describing a compound or method in broad terms. For example, a claim might cover a chemical compound with specified substituents, without limiting to a particular therapeutic use or formulation.
  • Dependent Claims: Narrow the scope, detailing specific derivatives, doses, formulations, or methods, thus providing fallback positions and extending protection to various embodiments.

Sample Claims (Hypothetical)

While the exact patent document must be referenced for precise claim language, typical pharmaceutical patent claims include:

  • Chemical Compound Claims: “A compound of the formula I, wherein R1, R2, R3 are as defined…”
  • Use Claims: “Use of the compound for treating [disease/condition], in particular...”
  • Process Claims: “A method of synthesizing the compound via [specific process]...”
  • Formulation Claims: “Pharmaceutical composition comprising the compound and a suitable carrier...”

Claim Strategy and Limitations

The claims are strategically crafted to cover a broad chemical space to prevent competitors from developing similar compounds. They may also incorporate Markush structures allowing multiple derivatives within the scope.

Potential limitations include:

  • Narrow claim language restricting to specific derivatives or uses.
  • Lack of claims on alternative routes or formulations—limiting the patent’s broader protective umbrella.

Legal boundaries delineate the scope, with potential for patent invalidation if claims are overly broad or lack novelty and inventive step.


Patent Landscape Analysis

Prior Art and Patent Environment

The patent landscape surrounding IL282624 involves assessing prior patents, scientific literature, and regulatory disclosures:

  • Prior Art: Existing patents on similar compounds, especially from key players in the targeted therapeutic area, can challenge novelty. A thorough search reveals whether IL282624 introduces a non-obvious, novel chemical entity or use.
  • Related Patents: Patent families from international jurisdictions (e.g., US, EP, CN) may exist, offering parallel protections or prior art references. It is crucial to analyze their overlap and differences.
  • Research Publications: Scientific papers on similar compounds or mechanisms may affect patent validity, especially if public disclosures predate or coincide with the patent application.

Patent Families and Filing Strategies

The applicant may have filed corresponding patent applications under the Patent Cooperation Treaty (PCT) or in specific jurisdictions, expanding protection globally. The timing of these filings influences patent strength and enforceability, especially considering patent term calculations and potential for patent hurdles.

Legal and Commercial Significance

  • Patent IL282624’s position within the landscape influences the enforceability and freedom to operate.
  • If part of a broader patent portfolio, it provides a strategic legal barrier against competitors.
  • Its expiration, typically 20 years from the priority date, affects future research and commercialization plans.

Innovative Aspects and Potential Challenges

  • Novelty and Inventive Step: The core of IL282624’s attractiveness lies in its innovative contribution—whether it represents a new chemical entity, unexpected pharmacological activity, or a synergistic combination.
  • Claims Validity: Facing challenges from prior art may require narrowing claims or justifying inventive step through unique structural features or applications.
  • Regulatory and Patent Life Cycle: Patents expanding into formulations, methods, or new uses often enjoy supplementary protection or extension opportunities, contingent upon regulatory pathways.

Implications for Stakeholders

  1. Pharmaceutical Developers:

    • Should review the claims to assess freedom to operate.
    • May pursue design-around strategies if the patent’s scope is narrow or challenged.
    • Consider licensing negotiations if the patent covers a promising therapeutic candidate.
  2. Legal Professionals and Patent Strategists:

    • Need to evaluate potential infringement risks and validity threats.
    • Could recommend filing continuation or divisional applications to broaden coverage.
  3. Investors and Business Executives:

    • Must consider patent strength as part of valuation, particularly for licensing or partnership opportunities.
    • Should monitor patent landscapes for potential competition or patent cliffs.

Conclusion

Patent IL282624 exemplifies a strategically drafted pharmaceutical patent, designed to protect a novel drug compound or use. Its scope hinges on well-crafted claims that balance breadth and defensibility. The surrounding patent landscape, characterized by prior art and related patents, influences its strength and enforceability. Successful commercialization depends on a clear understanding of these legal boundaries, ongoing patent prosecution, and potential challenges.


Key Takeaways

  • The patent’s scope is primarily defined by its independent claims, which likely encompass chemical entities, therapeutic methods, and formulations related to a novel pharmaceutical compound.
  • Broad claim language enhances protection but must withstand validity challenges based on prior art and inventive step.
  • The patent landscape includes global filings and scientific disclosures that could impact IL282624’s enforceability.
  • Strategic analysis of this patent informs licensing, R&D, and competitive positioning within the pharmaceutical industry.
  • Continuous monitoring and potential patent prosecution strategies are vital for maintaining a competitive edge around this IP asset.

FAQs

1. What is the typical lifespan of Israeli pharmaceutical patents like IL282624?
Patent protection generally lasts 20 years from the filing date, subject to maintenance fees. Extended protections or supplementary certificates can sometimes prolong effective exclusivity.

2. How can competitors challenge the validity of IL282624?
Through patent examinations, oppositions, or invalidity proceedings based on prior art, lack of novelty, or obviousness. Challenges often occur during national phase entries or patent term extensions.

3. Does IL282624 cover just the chemical compound, or does it include formulations?
If the claims are broad, they might cover the compound itself, specific use methods, or formulations. The actual scope depends on the granted claims' language.

4. How does the patent landscape influence drug development decisions?
A robust patent landscape can serve as a barrier to entry, protecting investment in R&D. Conversely, overlapping patents may necessitate licensing agreements or design-around strategies.

5. Can this patent protect multiple therapeutic indications?
Yes, if claims specify a use, a patent can cover multiple indications. If the claims are product-specific, protection extends to the compound regardless of therapeutic application.


References

  1. Israeli Patent Office, Patent IL282624.
  2. WIPO Patent Database. (for related patent families and international filings).
  3. Scientific literature databases for prior art.

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