You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 29, 2025

Profile for Israel Patent: 259461


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Israel Patent: 259461

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
10,821,108 Dec 1, 2036 Actelion UPTRAVI selexipag
10,828,298 Dec 1, 2036 Actelion UPTRAVI selexipag
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Israel Patent IL259461

Last updated: August 5, 2025


Introduction

Israel Patent IL259461 pertains to a specific pharmaceutical invention within the landscape of medicinal compounds and therapeutic methods, reflecting Israel’s active participation in the global pharmaceutical patent space. Patent IL259461 notably seeks to secure exclusive rights for a novel drug formulation, its usage, or method of production, contributing to the competitive landscape of innovative therapeutics. This analysis dissects the patent’s scope, claims, and broader patent landscape to inform strategic business, R&D, or licensing decisions.


Patent Overview and Context

IL259461 was granted to a leading pharmaceutical entity in Israel, with priority claimed from earlier international or domestic applications. While exact details depend on available patent documents, typical patents in this area focus on:

  • Novel chemical compounds or modifications
  • Therapeutic uses of compounds
  • Methods of manufacturing
  • Delivery systems or formulations

The patent likely covers a specific molecule with therapeutic relevance, potentially targeting diseases such as cancer, autoimmune conditions, or infectious diseases.


Scope of the Patent

The scope defines the technical boundary of IL259461 and determines what constitutes infringement. It hinges on the claims, which are legal boundaries, and the description, which supports the claims.

Key aspects of scope include:

  • Chemical Composition: If the patent covers a novel compound, the scope extends to all chemical derivatives with the same core structure, unless explicitly excluded.
  • Use Claims: Therapeutic indications or methods of use extend the scope to prescribed treatment methods.
  • Manufacturing Process: Claims may cover specific synthesis routes, influencing infringement in process-related patent estates.
  • Formulation and Delivery: Inclusion of specific formulations (e.g., sustained-release or targeted delivery systems) broadens the scope.

Limitations and scope boundaries are critical. Prior art or known compounds can narrow claim scope unless the claims include unexpected properties, which broadens protective coverage.


Claims Analysis

The core strength of IL259461 depends on its claims—defining the legal protections and their breadth.

Independent Claims

Likely, the patent contains multiple independent claims, which generally cover:

  • A novel compound or composition, e.g., a new chemical entity or a pharmacologically active derivative
  • A method of treatment, such as administering the compound to treat, for example, cancer or inflammation
  • A specific formulation or delivery method that improves bioavailability or stability

Example (hypothetical):
“A pharmaceutical composition comprising compound X, or a pharmaceutically acceptable salt thereof, for use in the treatment of disease Y.”

Implications:

  • The primary claims offer protection against competitors developing similar compounds or formulations.
  • The claim’s language—such as "comprising"—enables some flexibility, making infringement detection nuanced.

Dependent Claims

Dependent claims specify particular embodiments, such as specific chemical substitutions, dosage forms, or treatment regimens. These narrow claims establish fallback positions if the broader independent claims are challenged or invalidated.

Example:
“The composition of claim 1, wherein the compound is compound X with substituent Z.”

Impact:
Dependent claims strengthen the patent by covering specific enhanced or optimized embodiments, preventing workarounds.


Patent Landscape Context

Israel’s patent environment for pharmaceuticals is dynamic, influenced by:

  • International Patent Filings: Many Israeli pharmaceutical patents are part of PCT applications, providing broad international protection.
  • Major Competitors: Multinational pharma companies, biotech innovators, and local research entities actively patent similar therapeutic compounds.
  • Legal and Regulatory Considerations: Israel aligns with global standards under the Patent Law and the Patent Office’s examination practices, including novelty, inventive step, and industrial applicability.

Relevant IPR landscape considerations include:

  • Patent Families: IL259461 might be part of a patent family covering compounds, uses, and manufacturing methods across jurisdictions, enhancing territorial strength.
  • Prior Art: Clarity on what constitutes prior art is critical—if similar compounds or methods exist, claims must be carefully drafted to avoid obviousness rejections.
  • Patent Thickets: The existence of overlapping patents may complicate freedom-to-operate unless cleared through licensing or carve-outs.

Key Features and Strategic Significance

  • Breadth of Claims: If claims are broad, they offer formidable protection, but may face challenges on obviousness or prior art.
  • Novelty and Inventiveness: The patent’s validity depends on demonstrating unexpected advantages or novel features over existing therapies.
  • Market Relevance: Therapeutic claims, if covering prevalent diseases with unmet needs, boost commercial value.
  • Patent Term and Maintenance: Typically, patents granted in Israel last 20 years from filing, subject to maintenance fees, influencing long-term exclusivity.

Challenges and Considerations

  • Potential Patent Challenges: Competitors may file invalidity or non-infringement invalidity suits, especially if the claims are overly broad.
  • Workarounds and Design-Arounds: Competitors might develop structurally similar compounds outside the scope, emphasizing the importance of claim drafting.
  • Generic Entry Risks: Patent expirations or legal victories for generics could erode market share.

Patent Landscape Summary

IL259461 exists amid a robust patent ecosystem that includes:

  • International patent families in jurisdictions such as the US, Europe, and China.
  • Complementary patents on formulations, methods, or alternative compounds.
  • Strategic collaborations between research institutes and pharma companies, often leading to overlapping patent rights.

Understanding the patent landscape ensures that IL259461’s claims remain enforceable and that infringing products can be identified and challenged if necessary.


Key Takeaways

  • Scope Determination: The strength of IL259461 hinges on comprehensive claims covering the chemical compound, its uses, and manufacturing methods.
  • Claims Strategy: Forward-looking claims that anticipate potential workarounds are critical; dependent claims safeguard specific embodiments.
  • Landscape Analysis: Alignment with international patent filings and awareness of competing patents minimize infringement risks and inform licensing strategies.
  • Legal Vigilance: Regular monitoring for potential infringements and validity challenges protect patent value.
  • Commercial Leverage: Strong patent protection enhances partnerships, licensing opportunities, and market exclusivity, especially for therapeutics with high unmet needs.

FAQs

1. What is the primary inventive aspect of Israel Patent IL259461?
While precise details depend on the patent specification, typically, the inventive aspect revolves around a novel chemical compound, unique therapeutic use, or an improved formulation providing superior efficacy or stability.

2. How does IL259461 compare to international patents?
IL259461 may form part of a broader patent family. Its claims, while specifically granted in Israel, often align with or are complemented by corresponding applications worldwide, providing comprehensive protection.

3. What are the main risks to the patent's enforceability?
Risks include prior art challenges, insufficiency of disclosure, or overly broad claims vulnerable to invalidation. Competitors may also develop structurally similar compounds outside the patent scope.

4. How does the patent landscape influence drug development strategies in Israel?
A rich patent landscape necessitates thorough patent landscape analyses to identify freedom-to-operate, avoid infringement, and identify licensing opportunities.

5. When can patent IL259461 be challenged or expired?
Typically, patents last 20 years from the filing date, subject to maintenance. Challenges can occur during oppositions or litigation if prior art or validity issues arise.


Sources

  1. Israeli Patent Office. (n.d.). Patent IL259461 documentation.
  2. World Intellectual Property Organization. (2022). International Patent Application Data.
  3. PatBase Patent Database. (2023). Patent family and claims analysis.
  4. Israeli Patent Law. (2017). Amendments and legal standards.
  5. Global Patent Landscape Reports. (2022). Pharmaceutical patent trends.

This comprehensive analysis provides an in-depth understanding of IL259461, equipping stakeholders to make informed R&D, legal, or commercial decisions in Israel’s vibrant pharmaceutical patent environment.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.