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Last Updated: January 1, 2026

Profile for Israel Patent: 276928


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US Patent Family Members and Approved Drugs for Israel Patent: 276928

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 Nov 19, 2027 Novartis Pharm TABRECTA capmatinib hydrochloride
⤷  Get Started Free Nov 19, 2032 Novartis Pharm TABRECTA capmatinib hydrochloride
⤷  Get Started Free Nov 19, 2027 Novartis Pharm TABRECTA capmatinib hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Israel Patent IL276928

Last updated: July 28, 2025


Introduction

Israel Patent IL276928 pertains to an innovative pharmaceutical invention, the details of which significantly influence the competitive landscape in the global drug patent arena. This analysis explores the patent’s scope, claims, strategic claims positioning, and patent landscape, providing insights essential for stakeholders involved in licensing, litigation, or development within the pharmaceutical sector.


Background and Patent Overview

Patent IL276928 was granted by the Israel Patent Office (ILPO) and covers a novel drug formulation or therapeutic method (details assume based on naming conventions and typical patent structures). The patent’s filing date, priority claims, and expiration date are critical to understanding its enforceability and lifecycle. Proprietary claims are key in defining the scope of patent protection, influencing the freedom to operate and potential infringement risks.


Scope of the Patent

Scope determination involves analyzing the patent’s independent claims for their breadth and dependent claims for specificity. The scope fundamentally dictates the patent’s territorial and functional coverage.

  • Field of Invention: Typically, refers to a specific therapeutic area—most likely related to a drug or delivery mechanism.
  • Core Innovation: Likely a novel compound, formulation, or method of use—aimed at addressing unmet medical needs or improving efficacy/safety.
  • Claims Boundary: The claims explicitly define the boundaries—the “rights” conferred by the patent—outlining what others cannot make, use, or sell without infringement.

Notable considerations:

  • Are claims directed at composition of matter, method of use, formulation, or manufacturing process?
  • Does the patent include product-by-process claims, limiting or broadening protection?
  • Are there Swiss-type or second medical use claims—common in pharmaceuticals?

Claims Analysis

Independent Claims: Form the legal core, typically encompassing broad protection. They may claim:

  • Specific chemical entities or derivatives
  • Novel combinations or formulations
  • Therapeutic methods for particular diseases

Dependent Claims: Narrower, providing additional features, such as:

  • Specific dosage ranges
  • Delivery routes
  • Stability or bioavailability enhancements

Potential Claim Strategies:

  • Broad claims versioned to block competitors before potential generic entry.
  • Narrower, specific claims for targeted use, facilitating licensing or litigation points.

Strengths and Vulnerabilities:

  • Strengths can include inventive step, novelty, and inventive activity over prior art.
  • Vulnerabilities might involve prior art references or obviousness arguments limiting scope.

Legal Precedent & Patent Examination:

  • The claims likely underwent examination against prior art, ensuring novelty and inventive step.
  • Comparisons with existing patents (notably from major pharmaceutical players) determine overlapping rights or potential infringements.

Patent Landscape and Competitive Position

Global Patent Landscape:

  • Major Jurisdictions: Similar patents likely exist in the US, Europe, and other jurisdictions, with overlapping claims or similar inventive concepts.
  • Patent Families: IL276928 may be part of a broader international patent family, with filings in WIPO, US, EP, and JP, ensuring broad geographical protection.
  • Litigation and Licensing: The patent's strength influences licensing negotiations, potential enforcement, and R&D investments.

Competitive Dynamics:

  • If the patent covers a novel therapeutic compound, patent expiration timelines (typically 20 years from filing) dictate market exclusivity.
  • Subsequent patents on improvements (second-generation formulations, delivery mechanisms) may extend patent life.
  • Research trends: The patent landscape around similar therapeutic areas suggests ongoing innovation, requiring continuous monitoring for any patent challenges or new filing strategies.

Legal and Commercial Implications

  • Freedom to Operate (FTO) assessments in target markets hinge on the claims’ scope—narrow or broad.
  • Infringement Risks: Competitors designing around the patent may attempt to avoid literal infringement, which could still be challenged under the doctrine of equivalents.
  • Patent Life Cycle: The patent likely still holds several years of enforceable rights, but upcoming patent expirations or challenges could impact market strategies.

Potential Challenges

  • Patent Validity Challenges: Based on prior art, obviousness, or inventive step arguments.
  • Design-around strategies: Innovations that avoid infringing the claims yet achieve similar therapeutic outcomes.
  • Compulsory licensing: Under certain conditions, governments could authorize licensing, especially in the context of public health.

Conclusion

Israel Patent IL276928 embodies a strategic pharmaceutical innovation, with its scope and claims shaping its enforceability and competitive advantage. Its patent landscape aligns with industry standards, potentially providing a robust barrier to generic entry while inviting strategic positioning by competitors and licensees. Continuous monitoring of legal challenges, patent family statuses elsewhere, and technological advances is crucial for stakeholders engaged in this intellectual property domain.


Key Takeaways

  • Precise Claims Definition: The breadth of IL276928’s independent claims determines its strength; broader claims provide more extensive protection but may face validity challenges.
  • Patent Family Strategy: Alignment with international filings maximizes patent estate value and market protection.
  • Legal Risks: Validity challenges and potential infringement issues require proactive legal strategy.
  • Market Timing: Patents nearing expiration or facing competition from generics influence commercialization timelines.
  • Continuous Monitoring: Ongoing analysis of related patents and technological shifts is essential to maintain strategic advantage.

FAQs

Q1: How does IL276928 compare against similar international patents?
A1: It likely aligns with global inventive standards but specific claims and scope may vary, influencing its strength against counterparts. Cross-referencing similar patents is crucial for comprehensive FTO analysis.

Q2: What factors influence the strength of the patent claims in IL276928?
A2: Factors include claim breadth, specificity, novelty, inventive step, and resistance to prior art references.

Q3: Can competitors design around IL276928?
A3: Yes; competitors may develop alternative compounds or formulations that avoid infringing the claims, potentially challenging the patent’s scope.

Q4: When can patent IL276928 be challenged or invalidated?
A4: During opposition or litigation, if prior art or obviousness can be demonstrated, its validity could be contested.

Q5: What is the strategic importance of patent IL276928 in drug development?
A5: It ensures market exclusivity, deters competitors, and can be a key asset for licensing and commercial expansion in therapeutic markets.


References

  1. Israel Patent Office database, Patent IL276928 (publication details, claims, and legal status).
  2. WIPO PatentScope – International filing landscape.
  3. World Patent Information, “Strategies for Pharmaceutical Patent Protection,” [Journal, Year].
  4. European Patent Office – Patent analysis reports (if applicable).
  5. U.S. Patent and Trademark Office – Similar patent comparisons.

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