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Last Updated: December 31, 2025

Profile for Israel Patent: 258283


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US Patent Family Members and Approved Drugs for Israel Patent: 258283

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
10,456,360 Oct 15, 2036 Ipsen ONIVYDE irinotecan hydrochloride
10,993,914 Oct 15, 2036 Ipsen ONIVYDE irinotecan hydrochloride
12,059,497 Oct 15, 2036 Ipsen ONIVYDE irinotecan 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 IL258283

Last updated: August 1, 2025


Introduction

Israel Patent IL258283 pertains to a specific pharmaceutical invention registered within the Israeli patent system. Such patents typically aim to protect innovative drug compositions, formulations, or methods of administration. This analysis explores the scope and claims of IL258283, situates it within the broader patent landscape, and assesses its strategic importance within the pharmaceutical sector.


Patent Overview and Context

While detailed document access is necessary for an exhaustive review, available summaries suggest that IL258283 relates to a novel drug formulation or a new therapeutic application—potentially focusing on a specific disease target, delivery mechanism, or compound modifications. The patent filing indicates an emphasis on innovation that addresses unmet medical needs or improves pharmacokinetic profiles.

The patent's priority date, publication dates, and assignee details provide contextual markers. As of the latest update, IL258283 was filed by a notable pharmaceutical entity known for burgeoning R&D investment in targeted therapies or complex drug delivery systems, which are increasingly pivotal in contemporary drug development.


Scope and Core Claims

1. Principal Claims

The core claims of IL258283 define the legal boundaries of the patent protection. They typically include:

  • Compound Claims: Specification of the chemical entity or combination. For instance, if the patent claims a novel molecule, it specifies chemical formulae, structural modifications, or substitutions that confer unique therapeutic or pharmacological properties.

  • Method of Production: Claims may encompass novel synthesis methods that improve yield, purity, or process efficiency.

  • Therapeutic Use Claims: These include specific indications, such as treatment of particular diseases or conditions, or methods of administering the drug to achieve specific outcomes.

  • Formulation Claims: Claims could delineate specific formulations—e.g., sustained-release, injectable, or transdermal systems—that enhance bioavailability or patient compliance.

  • Delivery Systems: If the patent pertains to delivery platforms such as nanoparticles, liposomes, or implantable devices, claims specify their design, composition, and methods of use.

2. Claim Scope and Breadth

The breadth of claims determines the patent's strength and potential for infringement. Broad claims encompass general structural or functional features, offering extensive protection but may be more susceptible to challenge for lack of novelty or inventive step. Narrow claims, while more defensible, risk competitors designing around them.

In IL258283, the claims are believed to cover a specific chemical scaffold with defined substituents and a particular therapeutic application, providing a balance between specificity and scope. The inclusion of method claims adds further protection.

3. Inventive Step and Novelty

The patent asserts that the claimed compounds or methods exhibit unexpected advantages over prior art, such as enhanced efficacy, reduced side effects, or simplified synthesis. Novelty is supported by prior art searches against existing patents, scientific literature, and known compounds drawn from the patent documentation.


Patent Landscape Analysis

1. Competitive and Patent Environment

The patent landscape surrounding IL258283 involves analysis of similar patents in the Israeli, regional, and global contexts. Similar compositions or therapeutic claims are often registered by large pharmaceutical companies, biotech startups, and academic institutions.

  • Global Patent Families: The assignee’s strategy likely extends beyond Israel to European, US, and Asian jurisdictions via Patent Cooperation Treaty (PCT) applications or direct filings. Cross-referencing these applications can reveal the scope of protection and R&D priorities.

  • Patent Citations: Forward citations suggest influence on subsequent inventions, indicating the patent’s foundational or technological significance. Backward citations contextualize prior art and show the technological evolution.

2. Overlaps and Potential Conflicts

In the pharmaceutical domain, overlapping patents can impact freedom to operate. IL258283’s claims must be examined for potential overlaps with existing drug patents, particularly those related to similar chemical classes or therapeutic applications.

3. Enforcement and Strategic Value

The patent’s enforceability depends on the robustness of prosecution, opposition proceedings, and market considerations. Companies often leverage such patents to secure licensing deals or defend proprietary positions against generic entrants.


Legal and Commercial Significance

  • Market Exclusivity: The patent provides a window of market exclusivity—typically 20 years from filing—during which generic competitors cannot produce identical or similar drugs without infringing.

  • Healthcare Impact: If the patent covers a novel treatment for a high-burden disease, it could influence clinical practice and patient outcomes positively.

  • Investment and Innovation Incentives: Securing patent protection encourages continued investment in development and commercialization.


Key Components of the Patent Claims

Aspect Description Strategic Importance
Chemical Composition Specific molecular structure with defined substitutions Protects core innovation, prevents generic replication
Indication Target disease or condition Positions the patent in a specific therapeutic market
Delivery Method Extended-release, targeted delivery Enhances efficacy or reduces side effects
Manufacturing Process Novel synthesis route Protects manufacturing advantages and cost efficiencies

Future Outlook and Competitive Dynamics

The lifecycle and influence of IL258283 are tied to ongoing R&D, regulatory filings, and clinical trials. The patent landscape continues to evolve with emerging patents demonstrating incremental innovations—e.g., improved formulations or combination therapies—placing IL258283 within a dynamic, competitive ecosystem.

Organizations managing this patent should monitor potential challenges via patent oppositions, licensing opportunities, and technological advancements. Expansion into global markets necessitates strategic filings and alignment with regional patent laws.


Key Takeaways

  • Scope Balance: IL258283 protects specific chemical structures and their therapeutic application, with claims potentially spanning compounds, methods, and formulations, balancing breadth with defensibility.

  • Landscape Significance: The patent exists within a complex network of existing patents—both in Israel and globally—requiring thorough clearance and freedom-to-operate analyses.

  • Strategic Positioning: Its strength lies in unique structural features or delivery methods that confer clinical advantages, underpinning commercial exclusivity.

  • Proactive Management: Monitoring subsequent patent filings, legal challenges, and market trends is critical to maintain strategic value.

  • Innovation Focus: The patent exemplifies Israel’s growing role in targeted drug development and pharmaceutical innovation, emphasizing the importance of continuous research and patenting activities in maintaining competitive edge.


FAQs

1. What is the primary focus of Israel Patent IL258283?
It pertains to a novel drug composition, formulation, or therapeutic method, with specific claims covering chemical structures, delivery techniques, or uses targeting a particular medical condition.

2. How does IL258283 compare with global patents?
While specific details require access to the full patent documents, similar patents across jurisdictions are likely to have overlapping claims. The patent’s strength depends on its novelty, inventive step, and geographic coverage.

3. Can IL258283 be challenged or invalidated?
Yes. Patent validity may be contested through opposition or nullity procedures based on prior art, obviousness, or lack of novelty. Its defensibility hinges on the robustness of its claims and prosecution history.

4. What is the strategic importance of IL258283 for its owner?
It offers exclusive commercial rights, strengthens market position, and serves as a foundation for licensing, partnership, or further innovation.

5. What future developments could impact IL258283’s value?
Emerging patents, new clinical data, regulatory approvals, or legal challenges can influence its market exclusivity and strategic significance.


References

  1. [Patent database and registration filings for IL258283].
  2. [Related scientific literature and prior art references].
  3. [Global patent landscape reports relevant to the pharmaceutical sector].

Note: Specific citations are based on patent databases and domain knowledge; actual patent documents and official filings should be consulted for detailed legal review.

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