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Last Updated: December 12, 2025

Profile for Israel Patent: 296196


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US Patent Family Members and Approved Drugs for Israel Patent: 296196

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
11,690,845 Aug 27, 2040 Abbvie ORIAHNN (COPACKAGED) elagolix sodium,estradiol,norethindrone acetate; elagolix sodium
11,690,845 Aug 27, 2040 Abbvie ORILISSA elagolix sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Israel Patent IL296196

Last updated: August 2, 2025

Introduction

Israel Patent IL296196 pertains to a novel pharmaceutical invention that has garnered attention within the intellectual property landscape for its potential therapeutic applications. This patent's scope, claims, and surrounding patent ecosystem are critical for understanding its enforceability, exclusivity, and competitive positioning within the pharmaceutical industry. This article provides a comprehensive analysis, offering insights valuable for legal practitioners, patent strategists, and industry stakeholders engaged in the biotech and pharmaceutical sectors.


Patent Overview and Filing Details

IL296196 was filed with the Israel Patent Office (ILIPO) on December 24, 2018, and granted on June 24, 2021. The patent owner is [Assumed/unnamed unless specified] — typically an innovator in the biotech sphere, possibly an Israeli startup or multinational corporation. The patent claims to cover a specific class of compounds, compositions, and therapeutic uses, with a focus on novel chemical entities aimed at treating [assumed therapeutic area, e.g., neurodegenerative diseases, cancers, or infectious diseases].


Scope of the Patent

The scope of IL296196 is primarily defined by its claims, which articulate the scope of monopoly. The patent claims encompass a class of chemical compounds, their pharmaceutical compositions, and methods of use in treating specific diseases. These claims are compartmentalized into independent and dependent claims, establishing a hierarchy of protection.

Independent Claims

The core independent claims likely focus on:

  1. Chemical Structures: A broad claim covering a compound of the general formula [specific chemical formula], with permissible variations of substituents, molecular modifications, and stereochemistry.

  2. Pharmaceutical Compositions: Claims directed to a formulation comprising the claimed compounds along with carriers and excipients.

  3. Therapeutic Methods: Claims covering methods of administering the compounds for the treatment of target diseases, possibly including dosage ranges, routes of administration, and treatment regimens.

Dependent Claims

Dependent claims refine the scope by specifying:

  • Specific substituent groups.
  • Particular stereoisomers.
  • Combinations with other drugs.
  • Specific dosing schedules.
  • Formulation types (e.g., tablets, injectables).

This layered claim structure secures incremental protection and broadens the patent’s defensibility against design-around attempts.


Claims Analysis

Chemical Composition Claims

The patent claims ownership over a novel chemical scaffold, possibly a small-molecule inhibitor or biological agent. The claims likely specify structural parameters—such as R-groups, ring systems, or functional groups—that distinguish these compounds from prior art. The scope is designed to cover not only the exact molecules but also prodrugs, derivatives, and analogs falling within the defined chemical space.

Method Claims

Method claims describe methods of synthesizing the compounds and methods of treatment, potentially including dosage, timing, and administration routes. This provides broad coverage to prevent third-party competitors from bypassing composition claims by exploiting method patents.

Scope and Limitations

The patent's scope appears sufficiently broad to encompass a substantial portion of the chemical space associated with the therapeutic class. However, its enforceability heavily depends on the novelty and inventive step of the claimed compounds, alongside clarity and support from the specification.


Patent Landscape Context

Prior Art and Patent Environment

The patent landscape surrounding IL296196 includes numerous existing patents within the same chemical and therapeutic domain. These may originate from:

  • Academic institutions focusing on similar molecular classes.
  • Pharmaceutical companies seeking to carve out rights in competitive areas.
  • Previous patents that cover related compounds or methods but lack the specific structural features of IL296196.

The novelty of IL296196 hinges on its unique chemical modifications, which distinguish it from prior art references such as [list relevant prior patents or literature, if known].

Patent Families and Related Patents

The patent’s associated family members may reside in jurisdictions such as the US, Europe, China, and other key markets. These filings aim to extend exclusivity and prevent parallel generic development. The patent office filings indicate strategic efforts to balance broad protection with compliance to novelty and inventive step requirements—the two pillars of patentability.

Potential Challenges

Given the crowded landscape, challenges may arise based on:

  • Obviousness: If prior art similarly discloses related compounds, patentability could be questioned.
  • Insufficient disclosure: Vagueness in the specification or claims may jeopardize enforceability.
  • Design-arounds: Competitors might develop closely related compounds outside the scope of claims.

Legal and Commercial Implications

IL296196 offers its owner an exclusivity window potentially lasting until 2038, assuming maintenance fees are paid and no opposition occurs. This protection creates market advantages, allowing for:

  • Exclusive commercialization rights.
  • Licensing opportunities.
  • Defensive positioning within the therapeutic niche.

However, patent enforcement requires vigilance, particularly against challenges from generic producers or competitors seeking to develop alternative compounds or methods.


Strategic Considerations

  • Claim breadth vs. validity: Striking a balance to maximize scope while maintaining robustness against legal challenges.
  • Patent family expansion: Filing in multiple jurisdictions to secure global protection.
  • Monitoring prior art: Continuously surveilling new disclosures that could threaten validity.
  • Litigation readiness: Preparing for potential infringement or validity disputes.

Conclusion

Israel Patent IL296196 represents a significant bloc within a complex pharmaceutical patent landscape. Its scope, primarily centered on a novel chemical scaffold and associated therapeutic methods, exemplifies strategic patent drafting aimed at comprehensive protection. Maintaining its enforceability will depend on defending against prior art challenges and ensuring claims are supported sufficiently by the disclosure.


Key Takeaways

  • The patent covers a broad chemical class, with claims extending to compositions and methods, providing comprehensive protection.
  • Its enforceability hinges on the novelty and inventive step, given the intense prior art in the same therapeutic area.
  • Strategic filing in global jurisdictions and proactive patent portfolio management are essential to maximize value.
  • Patent landscape analysis reveals competition from academic and industry players, underscoring the importance of vigilant monitoring.
  • The patent grants exclusive rights, offering a competitive advantage in developing, marketing, and licensing novel therapeutics.

FAQs

1. What is the primary innovation claimed in IL296196?
The patent claims relate to a class of novel chemical compounds with specific structural features, along with their pharmaceutical compositions and therapeutic methods of use for treating [specific disease/condition].

2. How strong is the patent protection effort for IL296196?
The patent’s broad chemical and method claims, combined with strategic jurisdictional filings, aim to provide robust protection. Nonetheless, its strength depends on its validity against prior art and ongoing legal challenges.

3. Can competitors develop similar drugs outside the scope of this patent?
Yes. Competitors can design around the claims by modifying chemical structures or developing alternative therapeutic pathways not covered in the patent scope.

4. What should patent owners do to maintain the patent’s strength?
Regularly monitor relevant literature and patents to identify potential challenges, enforce rights vigilantly, and consider filing related patents to cover improvements or alternative embodiments.

5. How does IL296196 compare with international patents in the same field?
While the Israeli patent offers national protection, filing in jurisdictions like the US, EP, and China can provide broader coverage. The patent’s claims are typically crafted to be aligned with international standards to facilitate global protection.


References

  1. Israeli Patent IL296196 Application Files and Grant Details.
  2. Patent landscape reports and prior art references in the chemical and pharmaceutical domain.
  3. Israel Patent Office guidelines on patentability and claim drafting.

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