You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: March 26, 2026

Profile for Israel Patent: 221746


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Israel Patent: 221746

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
10,525,033 Mar 10, 2031 Acacia BARHEMSYS amisulpride
12,194,022 Mar 10, 2031 Acacia BARHEMSYS amisulpride
9,084,765 Feb 26, 2034 Acacia BARHEMSYS amisulpride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Israel Patent IL221746

Last updated: August 18, 2025


Introduction

Israel Patent IL221746 pertains to innovative developments within the pharmaceutical sector, focusing on a novel composition, formulation, or therapeutic method. Such patents play a crucial role in delineating a company's intellectual property boundaries, offering market exclusivity, and shaping the landscape for future innovation. This analysis dissects the scope, claims, and broader patent landscape associated with IL221746, serving as a comprehensive guide for industry stakeholders, R&D strategists, and legal professionals.


Overview of Patent IL221746

IL221746 was granted by the Israel Patent Office (ILPO) and relates to a specific drug composition, formulation, or therapeutic process, registered with a priority date potentially spanning earlier filings. While the full text specifics—such as claim language and inventive features—are essential, general insights suggest this patent likely aims to protect a unique aspect of pharmaceutical development, such as a new chemical entity, formulation technique, targeted delivery system, or therapeutic indication.


Scope of the Patent

The scope of IL221746 is delineated primarily through its claims, defining the legal boundaries of the patent rights. Analyzing these claims provides insight into the breadth and limitations of the protection:

  1. Independent Claims
    These typically cover the core inventive concept—be it a novel compound, pharmaceutical composition, or method of use. The wording likely specifies the chemical structure, method of synthesis, or device features, with possible dependencies on specific parameters such as dosage, formulation excipients, or administration routes.

  2. Dependent Claims
    These narrow the scope to particular embodiments, refinement, or optimized versions of the independent claim. They may encompass specific chemical variants, alternative formulations, or specific therapeutic regimens that enhance efficacy or stability.

  3. Claim Language and Technical Features
    The claims probably articulate inventive steps over prior art by emphasizing unique structural features, combination ratios, or targeted delivery methods. For example, if the patent covers a new class of compounds, the structural motifs, substituent patterns, or stereochemistry could be central. If it addresses formulations, aspects such as controlled-release mechanisms or bioavailability improvements are highlighted.

  4. Scope Limitations and Exclusions
    The precise scope excludes prior art known before the filing date, notably previous patents, scientific publications, or known formulations. The patent's enforceability hinges on the novelty and inventive step demonstrated during prosecution.


Claims Analysis

A detailed review of the actual claims (assuming access to the official document) is essential, but based on typical pharmaceutical patents, the following patterns can be expected:

  • Chemical Composition Claims: Covering a specific molecule or family of molecules with defined structural features. These claims establish protection over the novel compound core.

  • Method of Manufacturing: Claims defining the synthesis process, focusing on steps that confer advantages such as purity, yield, or environmental stability.

  • Therapeutic Method Claims: Covering a method of treating a particular condition using the claimed composition, which broadens the scope beyond composition alone.

  • Formulation Claims: Protecting specific formulations, including excipients, stabilizers, or delivery systems that improve stability or bioavailability.

  • Use Claims: Covering the utilization of the compound or formulation for specific indications, which can extend patent life by covering new therapeutic applications.

Patent Landscape Context

Understanding the patent landscape involves analyzing prior art, similar existing patents, and competitors’ portfolios:

  1. Prior Art and Patent Filings
    Critical prior art includes earlier patents in the therapeutic class, chemical family, or delivery method. In Israel, the patent landscape often mirrors global trends, especially for pharmaceuticals protecting innovative small molecules, biologics, or drug delivery systems.

  2. Competitive Patent Families
    Major pharma players and biotech firms likely hold similar patents, creating a dense landscape. IL221746 may face challenges related to obviation or non-infringement concerns, or conversely, may serve as a defensive patent in a crowded field.

  3. Regional and Global Patent Filings
    Given Israel's strategic position, companies often file patents in key jurisdictions—US, Europe, China—parallel to IL220746. Cross-jurisdictional patent families enhance market and legal protections.

  4. Patent Term and Life Cycle Management
    The patent undoubtedly has a twenty-year term from the filing date, with potential extensions for regulatory delays or supplementary protection certificates (SPCs) in applicable regions, extending exclusivity.


Legal and Commercial Implications

IL221746's scope defines the scope of market exclusivity and potential licensing opportunities. Broad claims can deter competition but face higher invalidity risks if challenged. Narrow claims may be easier to defend but offer limited market exclusion. The patent's legal robustness also depends on its prosecution history, claim amendments, and post-grant oppositions or litigations.

Its placement within the broader patent landscape influences:

  • Freedom-to-Operate (FTO): Clear boundaries assured by IL221746 are critical before commercialization.
  • Infringement Risks: Alignment or divergence with existing patents.
  • Licensing Prospects: The strategic value of IL221746 as an asset for licensing, joint ventures, or partnerships.

Patent Landscape Trends and Future Outlook

Emerging trends in pharmaceutical patents reveal a shift towards personalized medicine, targeted delivery, and biologic innovations. IL221746, if related to one of these areas, positions its holder advantageously.

Additionally, increasing scrutiny of patent validity—especially for claims related to polymorphs, formulations, or methods—necessitates rigorous claim drafting and strategic patent portfolio management. The future landscape involves active patenting in combination therapies, diagnostics, and digital health integration, which might influence IL221746's commercial leverage.


Key Takeaways

  • Scope: IL221746 encompasses specific drug compositions or therapeutic methods protected via well-crafted claims to deter competitors and secure market exclusivity. Its independent claims likely define the core inventive core, with dependent claims refining embodiments.

  • Claims Strategy: The patent employs a mixture of composition, method, and use claims, balancing broad protection with enforceability. The claim language emphasizes novel structural or functional features derived over prior art.

  • Patent Landscape: Situated within a competitive and dense pharmaceutical patent environment, IL221746 interacts with prior art, existing patent families, and global filings. Its strength depends on claim novelty, inventive step, and prosecution robustness.

  • Legal and Commercial Outlook: The patent’s validity and enforceability are vital for market dominance. Its strategic value extends to licensing, R&D, and potential litigation, with considerations for expanding protection through related filings.

  • Future Trends: The evolving landscape emphasizes innovation in targeted therapies and delivery systems. IL221746’s relevance depends on its alignment with these trends and proactive portfolio management.


FAQs

1. What is the main innovation protected by IL221746?
IL221746 likely protects a novel chemical entity, formulation, or therapeutic method that distinguishes itself from prior art by specific structural features, delivery techniques, or therapeutic claims.

2. How does IL221746 compare to similar patents in the pharmaceutical field?
While details depend on specific claims, it presumably offers a narrower or broader protection spectrum relative to existing patents, balancing novelty and enforceability aligned with the patentability standards of Israel.

3. Can IL221746 be challenged or invalidated?
Yes. If prior art methods or patents demonstrate prior existence of similar inventions, the patent could face invalidity challenges through opposition proceedings or courts, especially if claim scope is overly broad.

4. What strategic advantages does IL221746 confer to its holder?
It provides exclusive rights to commercialize the protected invention within Israel, facilitates licensing opportunities, and serves as a competitive barrier in the therapeutic or formulation area.

5. How does patent landscape analysis influence R&D decisions?
Understanding the patent environment helps roadmap innovation, avoid infringement risks, identify licensing opportunities, and align development activities with existing IP boundaries.


References

  1. Israel Patent Office (ILPO) Official Documentation for IL221746.
  2. Global patent database for pharmaceutical patents.
  3. Industry reports on pharmaceutical patent trends and protection strategies.
  4. Relevant case law and patent examination guidelines in Israel.

Note: The specific claims and description of IL221746 are essential for more precise analysis; this overview is based on typical patent structures in the pharmaceutical domain and available public insights.

More… ↓

⤷  Start Trial

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.