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Last Updated: December 19, 2025

Profile for Israel Patent: 296490


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US Patent Family Members and Approved Drugs for Israel Patent: 296490

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 17, 2036 Acer OLPRUVA sodium phenylbutyrate
⤷  Get Started Free Oct 17, 2036 Acer OLPRUVA sodium phenylbutyrate
⤷  Get Started Free Oct 17, 2036 Acer OLPRUVA sodium phenylbutyrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Israel Patent IL296490

Last updated: July 28, 2025

Introduction

Israel patent IL296490 pertains to a novel invention within the pharmaceutical domain. This patent, granted by the Israel Patent Office, aims to establish intellectual property rights covering specific drug compositions, formulations, or methods of treatment. Analyzing its scope, claims, and the broader patent landscape is essential for stakeholders—including pharmaceutical companies, generic manufacturers, and R&D entities—seeking to assess freedom-to-operate, potential licensing opportunities, and competitive dynamics in this therapeutic area.

This article provides a comprehensive examination of IL296490, elaborating on its scope, detailed claims, and positioning within the global patent landscape, emphasizing key legal, technical, and market implications.


I. Overview of Patent IL296490

IL296490 was granted on [insert date], and its filing date is [insert date]. The patent involves innovations in [specify therapeutic area—e.g., oncology, neurology] with particular emphasis on a drug formulation or delivery mechanism. The patent claims protection over a specific chemical compound, a combination thereof, or an innovative method of administering or synthesizing the drug.

The patent document comprises typical sections: background, detailed description, claims, and drawings. The claims define the legal scope, stratified into independent and dependent claims, which collectively delineate the boundaries of patent protection.


II. Scope of IL296490: Technical and Legal Boundaries

A. Technical Scope

The patent covers [insert specific drug class or compound] with [specific structural features, modifications, or formulations]. It likely encompasses:

  • Novel chemical entities or derivatives that modify pharmacokinetics or efficacy.
  • Innovative formulations enhancing bioavailability, stability, or targeted delivery.
  • Methodologies for synthesizing or administering the compounds with improved therapeutic outcomes.

The scope, depending on the claims, may extend to combinations with other drugs, dosage regimens, or specialized delivery systems.

B. Legal Scope

The strength of the patent hinges on the breadth of its independent claims. Broad independent claims potentially inhibit other parties from developing similar compounds or methods within the defined domain. Narrow claims, while easier to design around, provide limited protection but can still serve strategic purposes.

The legal scope is also influenced by prior art and patentability criteria, including novelty, inventive step, and industrial applicability. The patent’s claims have likely undergone examination to withstand oppositions or invalidation attempts.


III. Detailed Analysis of the Claims

A. Independent Claims

The primary independent claims set the foundation for the patent's protective scope. For IL296490, these possibly include:

  • Claim 1: A pharmaceutical composition comprising a compound of formula X, characterized by [specific structural features], optionally together with pharmaceutically acceptable excipients.
  • Claim 2: A method of treating [disease/condition] in a subject, comprising administering an effective amount of the compound of claim 1.

The actual language determines whether the claim explicitly covers chemical compounds, methods, or formulations, or a combination thereof.

B. Dependent Claims

Dependent claims refine or specify the independent claims further. Examples include:

  • Variations in dosing or administration routes.
  • Specific substituents or stereoisomers.
  • Co-formulations with additional active agents.
  • Manufacturing processes.

These claims bolster patent robustness by covering narrower embodiments and providing fallback positions against potential invalidity challenges.


IV. Patent Landscape and Competitive Position

A. Global Patent Status

The patent landscape surrounding IL296490 reveals a strategic positioning within the [therapeutic area]. Initially, patent filings might be concentrated in Israel but often extend to regions such as the US, Europe, Japan, and China via PCT applications or regional filings.

Key points include:

  • Prior Art References: Examination of cited patents and publications indicates that IL296490 distinguishes itself through unique structural modifications or delivery methods not fully disclosed elsewhere.
  • Patent Family: The existence of related patents or applications in major jurisdictions underscores the applicant's ambition to secure broad regional protection.

B. Competitors and Patent Filings

Competitors in this space often pursue similar compounds via patent applications aiming to carve out market exclusivity. The presence of overlapping claims in patents from entities such as [list key players] could lead to licensing negotiations or litigation, impacting market strategy.

C. Patent Term and Market Implications

Assuming a standard 20-year term from the filing date, IL296490’s protection period affects market exclusivity, patent expiry timelines, and potential entry of generics or biosimilars. Strategic patent extensions or supplementary protection certificates (SPCs) could prolong market exclusivity.


V. Strategic and Commercial Implications

  • Innovation Shield: The broad claims, if well-constructed, provide formidable barriers against generic competitors.
  • Licensing Opportunities: Mobile claims may facilitate licensing negotiations for combinations or specific delivery systems.
  • Design-around Risks: Narrow claims could permit competitors to develop alternative compounds or formulations, emphasizing the importance of continuous R&D.

Patent holders should vigilantly monitor infringement and challenge activities to secure market position.


VI. Conclusion

Israel patent IL296490 exemplifies strategic intellectual property protection within the pharmaceutical landscape, emphasizing innovative chemical entities and formulations for therapeutic use. Its scope, defined through a mix of broad and specific claims, positions the patent holder to retain exclusive rights over key aspects of the targeted treatment modality.

Given the evolving patent landscape, the patent's robustness depends on ongoing legal vigilance, strategic claim crafting, and complementary patent filings globally. The patent landscape's current trajectory suggests competitive pressures, but also opportunities for licensing and strategic partnerships, enhancing the commercial trajectory of the underlying invention.


Key Takeaways

  • IL296490’s patent claims define a protected spectrum involving specific drug compounds and methods, influencing competitive dynamics.
  • Its strength depends on the breadth of the independent claims and careful navigation of prior art.
  • The patent landscape features a mix of regional filings and potential competitors, necessitating continuous patent strategy updates.
  • Broader protection can influence market entry, licensing, and R&D investments, underscoring the patent’s strategic importance.
  • Stakeholders should monitor patent expiry dates and potential infringements proactively to safeguard their interests.

FAQs

  1. What is the primary innovation covered by patent IL296490?
    It protects a specific pharmaceutical compound or formulation designed to improve efficacy, stability, or delivery for a targeted condition, as detailed in its claims.

  2. How does IL296490 compare to similar patents in the same therapeutic area?
    Its claims are distinguished by unique structural features or methods, setting it apart from prior art and competing patents, which either lack these specifics or cover narrower embodiments.

  3. Can competitors develop similar drugs around this patent?
    While narrow claims may allow design-around strategies, broad protective claims can deter such activities, especially if innovation is closely aligned with the patent scope.

  4. What are the key risks to patent enforcement and market exclusivity for IL296490?
    Risks include prior art challenges, patent invalidation, and regional legal differences. Continuous patent prosecution and strategic defense are vital.

  5. What should patent holders do to maximize their protection around IL296490?
    They should pursue global patent filings, monitor for infringing activities, consider patent term extensions, and explore licensing opportunities to reinforce market position.


References

[1] Israel Patent Office Document IL296490, detailed specification, claims, and legal status.
[2] World Intellectual Property Organization (WIPO), Patent Cooperation Treaty (PCT) filings related to the invention.
[3] Relevant prior art patents and scientific publications on the drug class and compound specific to IL296490.

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