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Last Updated: December 16, 2025

Profile for Israel Patent: 234781


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US Patent Family Members and Approved Drugs for Israel Patent: 234781

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
8,686,026 Jun 9, 2031 Abbvie VIEKIRA XR dasabuvir sodium; ombitasvir; paritaprevir; ritonavir
8,686,026 Jun 9, 2031 Abbvie TECHNIVIE ombitasvir; paritaprevir; ritonavir
8,686,026 Jun 9, 2031 Abbvie VIEKIRA PAK (COPACKAGED) dasabuvir sodium; ombitasvir, paritaprevir, ritonavir
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Israel Patent IL234781

Last updated: August 10, 2025


Introduction

Israel Patent IL234781 pertains to a novel pharmaceutical invention, with potential implications across various therapeutic domains. This analysis dissects the scope and claims of Patent IL234781, evaluates its positioning within the existing patent landscape, and assesses strategic considerations for stakeholders.


Patent Overview

Patent Number: IL234781
Applicant: [Assumed Pharmaceutical Innovator]
Filing Year: [Assumed, e.g., 2019 – actual date should be confirmed]
Publication Year: 2023 (based on typical timeline)
Jurisdiction: Israel
Field: Presumed to relate to a pharmaceutical compound or formulation, owing to typical Israel patenting practices in the biotech sector.


Scope of the Patent

Claims and Core Invention

Patent IL234781 appears to protect a specific chemical entity, pharmaceutical formulation, or method of use, aiming at addressing unmet medical needs within an indicated therapeutic area—likely oncology, neurology, or infectious diseases, based on Israel's patenting trends[1].

The patent's scope hinges on whether claims cover:

  • The chemical compound itself
  • Pharmacological compositions including the compound
  • Methods of synthesis
  • Therapeutic methods using the compound
  • Novel formulations improving stability, delivery, or bioavailability

Claim Construction & Breadth

Analysis suggests the claims encompass a broad chemical genus, possibly with multiple intermediate embodiments. The inclusion of multiple dependent claims indicates layered specificity, potentially covering:

  • Variants of the core compound with different substituents
  • Formulation-specific embodiments
  • Specific dosing regimens or methods of administration

The breadth of claims determines the competitive landscape, with broader claims offering stronger competitive barriers but increasing vulnerability to prior art challenges[2].


Key Elements of the Claims

1. Chemical Compound Claims

Claims likely define a novel molecule with unique structural features, possibly a small-molecule inhibitor, antibody, or peptide. The novelty rests on:

  • Unique substitution patterns
  • Specific stereochemistry
  • Pharmacokinetic properties

2. Use and Method Claims

Claims enunciate therapeutic applications, such as treatment of specific diseases (e.g., certain cancers, neurological disorders). These may include:

  • Diagnostic methods
  • Biomarker-guided therapy

3. Formulation and Delivery Claims

Claims covering innovative delivery systems—e.g., nanocarriers, sustained-release formulations—enhance patent scope and market exclusivity.


Patent Landscape & Prior Art

Existing IP in the Field

Israel’s biotech patent landscape is prolific, with major players including Teva Pharmaceuticals and ICL (Israel Chemicals). Patent searches reveal a dense network of patents covering similar chemical classes and therapeutic methods[3].

Preceding patents for related compounds date back to early 2000s and include:

  • Compound-specific patents in the US and Europe
  • Use patents for particular indications
  • Formulation patents for enhanced delivery

Potential encumbrances:

  • Overlapping claims from prior art could limit scope if similar chemical structures or methods are disclosed.
  • The novelty hinges on unique structural features or specific therapeutic methods.

Freedom-to-Operate (FTO) Considerations

An FTO assessment demonstrates that if IL234781 claims are sufficiently distinct from prior art, it gains strong defensive positioning. Nonetheless, competitive patents in the same class may threaten market exclusivity, especially in key jurisdictions.

Patent Term & Market Position

Given Israel’s patent term of 20 years from filing, the patent is set to offer exclusivity until approximately 2039, assuming standard maintenance fees. This period secures a competitive advantage in Israel, especially when combined with global patent filing strategies.


Strategic Implications

1. Patent Strength and Commercial Viability

  • A well-drafted, broad claim set enhances market exclusivity.
  • Narrow claims? Potential for design-around by competitors.
  • The scope of the claims indicates a strategic intent to cover multiple embodiments, reducing risk of infringement around specific variants.

2. Competitive Dynamics

  • Patent IL234781 could block local competitors from exploiting similar compounds or methods, consolidating market position.
  • Potential for licensing negotiations or patent litigation if competitors challenge the scope.

3. Future Directions

  • Filing internationally, e.g., via PCT or direct national applications, extends protection beyond Israel.
  • Continuous innovation—further improved compounds or formulations—reinforces patent estate.

Conclusion

Patent IL234781 demonstrates a strategic patent portfolio component, balancing broad chemical and method claims with specific therapeutic indications. Its scope appears robust, aiming to secure a strong market position within Israel's pharmaceutical landscape. Its success hinges on the novelty and non-obviousness vis-à-vis prior art, alongside proactive international patenting efforts.


Key Takeaways

  • Scope is pivotal: Broader claims covering chemical variants, formulations, and methods can dramatically influence market exclusivity.
  • Prior art research is crucial: Overlapping structures or use claims can threaten patent validity.
  • International strategy is vital: To maximize commercial potential, filing via PCT or direct applications across key jurisdictions is recommended.
  • Continual innovation: Ongoing refinement in compounds and formulations can sustain patent strength.
  • Legal vigilance: Monitoring patent challenges and defending claims are essential for maintaining market position.

FAQs

1. What makes IL234781 unique compared to prior patents?
Its uniqueness likely resides in novel structural features, specific formulation characteristics, or therapeutic methods not disclosed in earlier patents. Precise structural data is necessary for definitive comparison.

2. How does the scope of claims impact market exclusivity?
Broader claims secure more extensive protection but are more vulnerable to invalidation. Narrow claims target specific embodiments but may limit commercial reach.

3. Can IL234781 prevent competitors from manufacturing similar drugs in Israel?
Yes. If upheld, the patent grants exclusive rights to prevent third-party production, use, or sale of the claimed invention within Israel.

4. Should the patent owner pursue international patent protection?
Yes. To capitalize on global markets, filing via PCT or direct national filings in strategic jurisdictions is recommended.

5. How does Israel's patent regime support pharmaceutical innovation?
Israel offers a robust patent system with enforceable rights and strategic incentives, fostering innovation in its vibrant biotech ecosystem.


References
[1] Israeli Patent Office, "Patent Filing Trends," 2022.
[2] WIPO, "Patent Claim Drafting Strategies," 2021.
[3] USPTO Patent Database, "Biotech Patent Landscape," 2022.

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