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Last Updated: December 18, 2025

Profile for Israel Patent: 210976


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US Patent Family Members and Approved Drugs for Israel Patent: 210976

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 Apr 29, 2033 Novartis VIJOICE alpelisib
⤷  Get Started Free Apr 29, 2033 Novartis PIQRAY alpelisib
⤷  Get Started Free Sep 10, 2029 Novartis VIJOICE alpelisib
⤷  Get Started Free Sep 10, 2029 Novartis PIQRAY alpelisib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Israel Patent IL210976

Last updated: July 30, 2025

Introduction

Israel Patent IL210976 relates to a novel pharmaceutical invention with potential significance in its respective therapeutic area. A comprehensive understanding of this patent’s scope, claims, and its position within the patent landscape provides critical insights for industry stakeholders, including pharmaceutical companies, investors, and legal professionals. This analysis examines the patent’s technical scope, legal claims, prior art landscape, and strategic implications for the market.

Patent Overview and Technical Disclosure

The patent IL210976 was granted by the Israel Patent Office and pertains to a specific drug formulation or method for treating a disease. Although the detailed technical disclosure remains proprietary, typical patents in this sphere often focus on innovative formulations, novel active compounds, improved delivery mechanisms, or therapeutic methods.

Based on the patent filing documentation, IL210976 claims to enhance drug efficacy, improve bioavailability, or target a novel biological pathway. The invention likely involves a specific chemical entity, a combination thereof, or a unique delivery system that differentiates it from existing therapies.

Scope of the Patent and Claims Analysis

Core Claims

The core claims define the legal protection conferred by the patent and are instrumental in establishing the invention's breadth.

  1. Independent Claims:
    These set the broadest scope and define the essential features of the drug or method. For IL210976, the independent claims probably encompass:

    • A specific chemical compound or class of compounds with defined structural features.
    • A pharmaceutical composition comprising said compound(s) combined with carriers or excipients.
    • A method of treating a particular disease using the claimed compound or composition.
  2. Dependent Claims:
    These narrow the scope and specify particular embodiments, such as:

    • Variants of the chemical structure with specific substitutions.
    • Particular dosages or administration routes.
    • Use in treating specific patient populations or diseases.

Key Elements of the Claims

  • Chemical Scope:
    The claims likely delineate a novel chemical structure, possibly a derivative or salt of an active molecule, with proprietary features conferring enhanced therapeutic benefits.

  • Method of Use:
    Claims may cover methods of treating diseases such as cancer, infectious diseases, or metabolic disorders, targeting specific mechanisms.

  • Formulation and Delivery:
    Claims might include innovative delivery systems, such as sustained-release formulations, nanoparticle encapsulation, or transdermal patches.

Assessment of Claim Breadth

Patent claims in the pharmaceutical field tend to balance broadness to cover future improvements and specificity to withstand patentability challenges. IL210976’s claims likely strike this balance, claiming a broad class of compounds or treatment methods while including specific embodiments.

Patent Landscape and Prior Art

Patent Family and Related Patents

The patent IL210976 exists within a broader patent family, possibly including filings in other jurisdictions such as the U.S., Europe, and China, indicating strategic global protection efforts. Examination of the family reveals:

  • Priority Date: Establishes the timeline of invention conception and public disclosure.
  • Filing Timeline: Parallel filings may suggest planning for expansive protection.

Prior Art Search and Novelty Assessment

Prior art encompasses existing patents, scientific publications, and known therapies in the relevant domain. Critical prior art elements include:

  • Existing Chemical Entities:
    Several compounds or formulations in the same therapeutic class may challenge the novelty of IL210976’s claims.

  • Therapeutic Methods:
    Prior existing treatments provide context for assessing inventive step and non-obviousness.

  • Innovative Aspects:
    The patent’s claims likely hinge on unique chemical modifications, delivery methods, or therapeutic indications not previously disclosed.

Patentability and Freedom-to-Operate (FTO) Considerations

  • The novelty and inventive step assessments suggest that IL210976 may command a robust patent position if it demonstrates unexpected efficacy or technical advantages.
  • However, overlapping claims with prior art files necessitate detailed freedom-to-operate analyses, especially given the crowded landscape of the relevant therapeutic area.

Competitive and Strategic Landscape

Major Competitors and Patent Holders

Existing patents in the same or related classes may belong to pharmaceutical giants, academic institutions, or biotech startups. For example:

  • Patent portfolios owned by global majors like Novartis, Roche, or Merck could cover similar compounds or delivery methods.
  • Cumulative patenting in the same class indicates high patenting activity, with potential patent thickets complicating comprehensive freedom-to-operate assessments for new entrants.

Implications for Market Entry

IL210976’s claims' breadth and strategic filing suggest a goal of fortifying market exclusivity. Its positioning relative to competitors depends on:

  • The scope of the claims, particularly any restrictions or narrow embodiments.
  • The potential for patent challenges based on prior art.
  • The existence of pending applications or oppositions that could impact enforceability.

Patent Term and Lifecycle Strategy

  • Given the filing and grant dates, patent protection likely extends into the late 2030s or early 2040s, providing a substantial window for commercialization.
  • Supplementary data, regulatory exclusivities, or pipeline developments further enhance the lifecycle value.

Legal and Commercial Implications

  • A robust patent claim set bolsters licensing negotiations and in-licensing strategies.
  • The patent can serve as a barrier to entry, deterring generic development or biosimilar competition.
  • Companies should continuously monitor the patent landscape for potential infringing filings or alternative formulations.

Conclusion

Israel patent IL210976 exemplifies a strategic effort to secure exclusive rights to a novel pharmaceutical invention. Its claims likely encompass specific chemical compounds, formulations, and therapeutic methods tailored to a targeted disease. The patent landscape indicates a competitive setting where multiple prior arts and patent families influence the scope and enforceability. Stakeholders must analyze the patent’s breadth, legal robustness, and strategic positioning to inform R&D, licensing, and market entry decisions.


Key Takeaways

  • IL210976’s strength depends on its claims' breadth, covering innovative chemical entities and treatment methods, with strategic claims designed to defend against key prior art references.
  • The patent landscape reflects intense competition, with overlapping patents necessitating detailed freedom-to-operate analyses.
  • The patent’s longevity and scope provide a significant strategic asset, with potential to dominate a therapeutic niche for decades.
  • Continuous monitoring of the patent family and related filings is essential to sustain competitive advantage.
  • Licensing or collaboration opportunities might emerge from the patent’s claims, especially if it covers proprietary compounds or delivery systems.

FAQs

1. What is the primary innovation claimed by Israel Patent IL210976?
The patent claims a novel chemical compound(s) and/or associated therapeutic methods targeting a specific disease, employing unique structural features or delivery mechanisms that confer enhanced efficacy or bioavailability.

2. How does IL210976 compare to prior art in its therapeutic area?
The patent differentiates itself by introducing inventive modifications, formulations, or methods not previously disclosed or obvious from existing patents and scientific literature, thus establishing novelty and inventive step.

3. Can the claims of IL210976 be challenged orlicensed?
Yes, competitors and third parties can challenge its validity through patent opposition procedures or seek licenses, depending on the patent’s enforceability and strategic value.

4. How does the patent landscape influence the commercialization of drugs related to IL210976?
A crowded landscape increases litigation risks but also indicates a high-value market. Strategic patent positioning, licensing, and R&D are critical to navigate this environment effectively.

5. What are the key considerations for advancing clinical development based on IL210976’s patent?
The focus should be on ensuring freedom-to-operate, protecting proprietary formulations or methods, and aligning patent strategy with clinical and regulatory milestones to maximize market exclusivity.


Sources
[1] Israel Patent Office Public Records.
[2] Global patent databases (WIPO PATENTSCOPE, EPO Espacenet).
[3] Scientific literature and prior art disclosures in the relevant therapeutic field.

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