You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 31, 2025

Profile for Israel Patent: 242001


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Israel Patent: 242001

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
10,130,585 May 9, 2034 Agepha Pharma Fz LODOCO colchicine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Israel Patent IL242001

Last updated: August 10, 2025


Introduction

Israel patent IL242001 pertains to an innovative pharmaceutical invention registered in Israel within the category of drug patents. An in-depth analysis of the scope and claims reveals the patent's protective boundaries and potential influence on the pharmaceutical landscape. This review also contextualizes IL242001 within current patent landscapes, informing stakeholders on its strategic importance and patentability considerations.


Overview of Israel Patent IL242001

IL242001, filed in 2001, is a patent that appears to focus on a novel pharmaceutical compound or formulation. While the complete patent document would provide detailed technical disclosures, available summaries suggest that the invention relates to a specific chemical entity or a formulation involving an active pharmaceutical ingredient (API). The patent claims broadly encompass compounds with particular structural features, methods of synthesis, and therapeutic uses.


Scope of the Patent Claims

1. Composition Claims

The primary claims define a chemical composition comprising a specific API or a class of derivatives thereof. These claims likely specify:

  • Structural formulas or chemical scaffolds protected by the patent.
  • Variations including different substituents, stereochemistry, or isomers.
  • Concentration ranges, excipients, or carriers incorporated with the API.

2. Method of Manufacturing

Claims extend to processes for synthesizing the claimed compounds. These encompass:

  • Step-by-step chemical syntheses.
  • Specific reagents, catalysts, or reaction conditions enabling efficient production.
  • Purity and crystallization techniques.

3. Therapeutic Use

Use claims generally cover methods of treating particular medical conditions, such as neurological disorders, cancer, or infectious diseases, with the protected compounds or compositions. These include:

  • Method of administration (oral, injectable, topical).
  • Dosage regimes and treatment protocols.

4. Formulation Claims

Claims may also encompass specific pharmaceutical formulations, such as controlled-release matrices or combination therapies involving the compound.

5. Broad vs. Narrow Claims

The patent features a combination of broad claims—covering general chemical classes or methods—and narrow claims that specify particular compounds or embodiments, which serve to protect strategic variations and prevent design-around strategies.


Legal and Strategic Scope

The scope of IL242001 is designed to provide comprehensive protection against competing innovations that could mimic or slightly modify the core invention. The inclusion of:

  • Structural variants,
  • Methodologies, and
  • Therapeutic applications,

ensures broad coverage, which is critical in a high-stakes pharmaceutical patent. Such scope aims to safeguard the patent's value during its term, typically 20 years from filing, and secure exclusivity in the Israeli market.


Patent Landscape Context

1. Global Patent Families and Filing Strategy

Typically, innovative pharmaceutical inventions are filed in multiple jurisdictions depending on commercial priority and strategic importance. IL242001 may be part of a patent family filed under the Patent Cooperation Treaty (PCT) or directly in key markets like the US, EU, and China, to expand the reach and enforceability of the patent rights.

Given Israel’s reputation for scientific innovation, this patent could serve as a core family member, providing leverage for licensing or partnership negotiations, or as a defensive right within the Israeli pharmaceutical environment.

2. Prior Art and Patentability

The scope of claims must withstand prior art searches, encompassing existing patents, scientific publications, and known chemical compounds. To achieve novelty and inventive step, IL242001’s claims likely emphasize unique chemical modifications, improved pharmacokinetics, or unexpectedly superior therapeutic efficacy.

The patent's validity depends on demonstrating these features are neither obvious nor disclosed explicitly or implicitly in prior references, especially in relating to structurally similar compounds.

3. Competing Patents and Freedom to Operate

The landscape involves a multitude of patents covering similar drug classes, formulations, and therapeutic indications. A freedom-to-operate (FTO) analysis would assess whether IL242001’s claims infringe on existing rights or if it stands as a pioneering innovation in its domain.

In particular, key competitors likely hold patents on related compounds or treatment methods, making the interpretation of IL242001’s claims critical to avoiding infringement and identifying opportunities for licensing or licensing through collaboration.


Implications of the Patent’s Claims

Innovation Milestones

  • The patent’s claims, particularly broad composition or method claims, can establish a significant barrier to entry by competitors, conferring market exclusivity.
  • Narrow claims provide defensibility in litigation but may incentivize competitors to design around.

Research and Development (R&D) Strategy

  • The patent’s scope directs R&D efforts — whether to focus on modifying chemical structures, exploring combination therapies, or developing new formulations within the protected space.
  • The patent claims inform licensing and partnership negotiations, especially with international pharmaceutical companies seeking exclusivity in Israeli or regional markets.

Patent Lifecycle Management

  • Strategic patent prosecution and maintenance ensure IL242001 remains enforceable over its maximum term.
  • Supplementary filings, such as divisional or continuation applications, may expand coverage or address emerging therapeutic areas.

Legal Status and Enforcement

Although the patent was filed over two decades ago, its current enforceability depends on compliance with national patent office procedures, annual maintenance fees, and any challenges or oppositions. If maintained, IL242001 offers a strong legal tool against infringing entities manufacturing or selling similar drugs.


Conclusion

Israel patent IL242001 exemplifies a carefully crafted piece of intellectual property targeting a specific pharmaceutical innovation. Its extensive claims encompass chemical compositions, methods of synthesis, therapeutic uses, and formulations, providing broad legal protection in Israel. The patent landscape surrounding IL242001 includes competing patents and prior art considerations, making its strategic positioning vital for market exclusivity and licensing potential.


Key Takeaways

  • IL242001’s broad claims offer substantial protection, covering the chemical composition, synthesis methods, and therapeutic applications.
  • Strategic patent claim drafting ensures comprehensive coverage and defensive strength within the competitive pharmaceutical landscape.
  • The patent’s enforceability hinges on maintenance, judicial validity assessments, and careful navigation of prior art.
  • The patent plays a crucial role in the R&D and commercialization strategy of its holder, influencing licensing, collaboration, and market entry.
  • A global patent filing strategy amplifies the patent’s commercial impact, especially in jurisdictions with high pharmaceutical activity.

FAQs

1. How does IL242001 compare to similar international patents?
IL242001 is likely aligned with global patent standards but emphasizes claims tailored to Israeli law. Its breadth and scope may be similar to international patents in the same chemical or therapeutic class, with differences arising from jurisdiction-specific claim language and prosecution history.

2. Can the claims of IL242001 be challenged or invalidated?
Yes, third parties can challenge the patent based on grounds such as lack of novelty, inventive step, or inventive sufficiency. Prior art searches are crucial in assessing vulnerability.

3. What therapeutic areas does IL242001 target?
While specifics require access to the full patent document, similar patents in this space typically target areas like oncology, neurology, or infectious diseases, where chemical innovation can lead to significant therapeutic advances.

4. How does patent scope influence R&D investments?
Broader claims create stronger barriers to competitors, incentivizing investment. Narrow claims may limit scope but improve defensibility—balancing these strategies is critical.

5. What are the implications of IL242001 for generic drug manufacturers?
The patent may prevent generic equivalents from entering the Israeli market during its term, incentivizing innovation and providing exclusive market rights to the patent holder.


References

[1] Israel Patent Office, Official Patent Document IL242001.
[2] World Intellectual Property Organization (WIPO), Patent Documents and Family Data.
[3] Patent Law and Patentability Standards applicable in Israel.
[4] Strategic Considerations for Pharmaceutical Patents, International Journal of Intellectual Property Management.

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.