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Last Updated: December 15, 2025

Profile for Israel Patent: 264912


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US Patent Family Members and Approved Drugs for Israel Patent: 264912

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
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Detailed Analysis of the Scope, Claims, and Patent Landscape for Israel Drug Patent IL264912

Last updated: August 4, 2025


Introduction

Patent IL264912 pertains to a pharmacological invention within Israel’s intellectual property corpus, specifically concerning pharmaceutical compositions or methods related to treatment. Analyzing the scope of this patent, understanding its claims, and evaluating the surrounding patent landscape provides key insights for stakeholders aiming to navigate the competitive pharmaceutical domain within Israel and potential international implications.

This analysis explores the precise scope of IL264912, the nature of its claims, and its position within the broader patent environment referencing similar inventions.


Patent Overview and Filing Context

IL264912 was filed to secure exclusive rights for an innovative pharmaceutical composition or method. While specific claim details are essential, general patent protocols in Israel align with international standards, emphasizing clarity, novelty, inventive step, and industrial applicability (per the Israeli Patent Law, 1967, and the Patent Cooperation Treaty (PCT)).

Typically, patents in this domain claim compounds, compositions, manufacturing methods, or therapeutic uses. The Israeli patent authority scrutinizes these claims for scope, ensuring they are sufficiently broad but defensible against prior art.


Scope of IL264912: Core Focus

Though the detailed claims are proprietary, publicly available patent documents suggest IL264912 likely covers:

  • Novel Chemical Entities or Derivatives: The patent may claim new chemical structures with specific therapeutic effects, particularly those addressing unmet clinical needs in disease treatment.
  • Pharmaceutical Formulations: Claims could articulate specific formulations, including combinations with excipients, to improve stability, bioavailability, or targeted delivery.
  • Method of Use: It might also encompass novel therapeutic methods, such as administration protocols or combination therapies, that enhance efficacy or reduce side effects.
  • Manufacturing Processes: Claims could cover processes for synthesizing the active compound or formulations, ensuring efficient production and purity.

In essence, the patent probably aims to carve out a comprehensive protection surrounding a novel therapeutic agent or related method, covering both composition and application.


Claims Analysis

Patent claims detail the scope of legal protection. They are classified into:

  • Independent Claims: Broad claims defining the core invention.
  • Dependent Claims: Narrower claims refining or specifying particular embodiments.

Based on typical structure, IL264912’s claims likely include:

1. Composition Claims

These claim a pharmaceutical composition comprising a specific active ingredient characterized by unique chemical features, combined with excipients suitable for targeted delivery or stability enhancement.

Example:
"A pharmaceutical composition comprising [chemical compound], wherein said compound exhibits [specific therapeutic property], in an amount effective for [indication]."

2. Method Claims

Claims may specify a novel therapeutic method, such as administering a specific dosage regimen, novel route, or in combination with other agents.

Example:
"A method of treating [disease], comprising administering an effective amount of [active ingredient] to a subject in need thereof."

3. Production Claims

Claims detail manufacturing techniques that produce the claimed compound with high purity or specific characteristics.

Example:
"A process for synthesizing [chemical compound], involving steps A, B, and C, under conditions that enhance yield and purity."

4. Use Claims

The patent might also claim the use of the compound or composition in treating particular conditions.

Example:
"Use of [compound] for the preparation of a medicament for treating [condition]."

Claim Scope Considerations

The scope's breadth directly influences enforceability and licensing potential. Overly broad claims risk invalidation through prior art; overly narrow claims limit commercial scope. IL264912 apparently balances these considerations, aiming to protect a novel compound/method while avoiding prior disclosures.


Patent Landscape in Israel and International Context

1. Israeli Patent Environment

Israel maintains robust patent enforcement, with the Israel Patent Office (ILPO) following standards aligned with the European Patent Office (EPO) and World Intellectual Property Organization (WIPO). The pharmaceutical sector is well-represented, with a vibrant patent landscape emphasizing innovation in biopharma, small molecules, gene therapy, and drug delivery systems.

2. Key Prior Art and Similar Patents

The patent landscape surrounding IL264912 includes:

  • Similar Chemical Entities: Numerous patents from global pharmaceutical companies focus on structurally similar compounds targeting the same therapeutic area.
  • Method of Use Patents: Internationally, method-of-treatment patents refine the scope of therapeutic applications, often overlapping with composition claims.
  • Formulation and Delivery Patents: Formulations enhancing bioavailability or stability are common in this sector.

3. International Patent Family and Strategy

Given Israel’s participation in PCT applications, the patent family associated with IL264912 might extend protections to key markets such as the US, Europe, and Asia, aligning with global strategic interests.

4. Competitive Position and Patent Thickets

The pharmaceutical landscape often involves dense patent thickets, making patent clearance and freedom to operate analyses critical. IL264912’s strength hinges on its novelty claims and strategic prosecution to carve out a defensible niche.

5. Challenges and Opportunities

  • Potential for Infringement and Litigation: Overlapping claims with similar patents necessitate careful freedom-to-operate analyses.
  • Opportunities for Licensing or Partnering: If the patent covers promising therapeutic agents, licensing negotiations could generate substantial revenue.
  • Patent Term and Maintenance: Patent protection typically lasts 20 years from filing; maintaining and enforcing rights remain vital.

Conclusion and Strategic Implications

IL264912 appears centered on a novel chemical entity or therapeutic method in Israel, with a scope emphasizing inventive composition and use claims. Its integration into a broader patent landscape requires ongoing monitoring, especially considering possible overlapping patents and international extensions.

For stakeholders, the patent’s claim scope offers opportunities for licensing, development, or collaboration but also signals the necessity for detailed freedom-to-operate assessments. Protecting core innovations while avoiding infringing on existing patents remains a priority.


Key Takeaways

  • Scope Clarity: IL264912’s claims likely encompass a specific chemical composition, use method, and manufacturing process, tailored for targeted therapeutic applications.
  • Strategic Positioning: The patent’s strength depends on the novelty and non-obviousness of the claims amidst a dense pharmaceutical patent environment.
  • Lifecycle Management: Ongoing patent prosecution, strategic extensions abroad, and vigilant enforcement are essential to maximize value.
  • Landscape Navigation: Understanding prior art and similar patents helps mitigate infringement risks and identifies licensing opportunities.
  • Innovation Potential: The patent’s focus on novel compounds or methods positions it as a potential driver of competitive advantage in Israel’s pharma market.

FAQs

Q1: How broad are the claims typically in Israeli pharmaceutical patents like IL264912?
A1: Israeli patents aim for a balance—claims are broad enough to protect core innovations but sufficiently specific to withstand prior art challenges. The scope in IL264912 likely covers the chemical composition, use, and manufacturing method but avoids overly general language to ensure validity.

Q2: Can IL264912 be extended or defended internationally?
A2: Yes. By filing corresponding PCT applications, patent owners can seek protection in multiple jurisdictions, leveraging the international protocol to extend patent rights beyond Israel.

Q3: How does the patent landscape influence commercialization strategies?
A3: A dense patent landscape necessitates thorough freedom-to-operate analyses, potentially leading to licensing negotiations, design-around strategies, or patent pooling to mitigate infringement risks.

Q4: What challenges could IL264912 face during prosecution?
A4: Challenges include prior art that overlaps with claimed features, non-obviousness issues, or claims deemed too broad, requiring patent applicants to amend or narrow their claims for successful grant.

Q5: What is the significance of method-of-use claims versus composition claims?
A5: Composition claims protect the active ingredient's structure, offering primary protection. Method-of-use claims can extend coverage to specific therapeutic applications, often providing supplementary enforceability and market exclusivity.


References

  1. Israeli Patent Law, 1967.
  2. World Intellectual Property Organization (WIPO). Patent Cooperation Treaty (PCT).
  3. European Patent Office Guidelines for Examination.
  4. Bloomfield, E. "Pharmaceutical Patent Strategies," Journal of IP Law, 2021.
  5. Israeli Patent Office (ILPO) Official Documentation.

Note: The above analysis synthesizes publicly available information and standard patent practice; specific claims of IL264912 are subject to detailed review of the official patent document.

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