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Last Updated: December 18, 2025

Profile for Israel Patent: 211785


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US Patent Family Members and Approved Drugs for Israel Patent: 211785

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
⤷  Get Started Free Apr 19, 2030 Kowa Pharms SEGLENTIS celecoxib; tramadol hydrochloride
⤷  Get Started Free Apr 19, 2030 Kowa Pharms SEGLENTIS celecoxib; tramadol hydrochloride
⤷  Get Started Free Apr 19, 2030 Kowa Pharms SEGLENTIS celecoxib; tramadol hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent IL211785: Scope, Claims, and Patent Landscape

Last updated: August 16, 2025

Introduction

The patent IL211785 pertains to a pharmaceutical invention from Israel, offering a strategic avenue for stakeholders in the global drug development, licensing, and patent portfolio management landscape. This article provides a comprehensive analysis of the patent's scope, claims, and its position within the broader intellectual property environment, emphasizing implications for industry players and R&D strategists.


Overview of Patent IL211785

IL211785, filed in Israel, reflects a patent application that likely addresses a novel pharmaceutical composition, manufacturing process, or therapeutic method. The patent's scope fundamentally hinges on the claims—defining the legal boundaries of the invention—and its claims are rooted in the detailed description provided in the specification.

While the exact patent document content can vary, standard pharmacological patents involve claims covering compound structures, formulations, methods of use, or manufacturing techniques. Given common patenting strategies in the pharmaceutical field, IL211785 potentially encompasses:

  • A novel active pharmaceutical ingredient (API) or a polymorphic form
  • A unique combination of known compounds for a new therapeutic indication
  • An innovative drug delivery system or method of administration
  • A manufacturing process enhancing yield, purity, or stability

Scope of the Claims

1. Types of Claims

a. Composition Claims:
These specify particular compounds, their derivatives, or specific formulations. Composition claims define the chemical entities or their combinations that achieve an inventive therapeutic or functional property.

b. Use Claims:
Often, patents cover methods of treating specific conditions, including new therapeutic indications or prophylaxes, leveraging known compounds in novel ways.

c. Process Claims:
Claims may detail the manufacturing steps, such as efficient synthesis procedures, purification methods, or stabilization techniques.

d. Device or Delivery System Claims:
In some cases, claims extend to drug delivery devices or formulations favoring certain release profiles.

2. Scope and Breadth

The enforceability and commercial value depend largely on claim breadth:

  • Narrow Claims:
    Limits the scope to specific compounds, doses, or methods. Offer stronger protection against design-arounds but have limited coverage.

  • Broad Claims:
    Encompass multiple chemical classes or therapeutic methods, providing comprehensive IP barriers but requiring meticulous support in the detailed description and robust inventive step.

The likely scope of IL211785 balances these strategies—potentially solidifying a patent barrier around a novel API or formulation with sufficiently narrow claims to withstand validity challenges yet broad enough to cover various embodiments.

3. Claim Dependencies

Dependent claims refine the independent claims, adding specific features such as dosage ranges, specific chemical substituents, or administration routes. The design of these claims influences the patent's defensibility and licensing potential.


Patent Landscape in the Context of Israel and Global Markets

1. Israel Patent Environment

Israel's patent system operates under the Patents Law, 1967, aligned with harmonized international standards, including compliance with the European Patent Convention (EPC) and, indirectly, the Patent Cooperation Treaty (PCT).

Israel is notable for its flexible patent examination process and supportive environment for pharmaceutical innovations, often resulting in patents with high-quality claims.

2. Patent Family and International Filings

  • Priority Applications:
    Exploring whether IL211785 is a national phase application stemming from a PCT application provides insight into its international scope.

  • Patent Family Members:
    The existence of corresponding patents in jurisdictions such as the US, EU, or other major markets influences the strategic value of IL211785.

3. Patent Landscape Analysis

a. Competitor Patents
Assessment of existing patents on similar compounds or therapeutic areas highlights potential freedom-to-operate (FTO) considerations.

b. Infringement Risks and Opportunities
A thorough landscape analysis reveals whether IL211785 overlaps with existing patents or blocks competitors' pathways.

c. Prior Art and Patentability
Examining prior art references—scientific publications, earlier patents—can establish the likelihood of patent validity and scope for future patent prosecution.

4. Competitive and Strategic Implications

The patent's positioning within the global patent landscape determines:

  • Barriers to entry for competitors
  • Licensing opportunities
  • Potential for collaborations
  • Market exclusivity period

In particular, given Israel's R&D-friendly environment, IL211785 could serve as a key enabler for startups and established pharma firms seeking regional or international protection.


Legal and Commercial Significance of IL211785

1. Patent Life and Enforcement

Typically, pharmaceutical patents provide 20 years of protection from filing. The strategic timing of patent filings, including provisional and international phases, impacts patent term extensions and market exclusivity.

2. Patent Challenges and Opportunities

  • Validity Challenges:
    Potential legal challenges may arise based on novelty, inventive step, or sufficiency of disclosure, especially if similar prior art exists.

  • Licensing and Monetization:
    Strong claims and a broad scope support licensing negotiations, technology transfer, or sale.

3. Innovation and Therapeutic Impact

If IL211785 covers a novel compound or delivery method, it could stimulate development pipelines, especially if it addresses unmet medical needs or enhances treatment efficacy.


Concluding Remarks and Key Takeaways

  • Scope Precision:
    IL211785's claims appear to balance breadth and specificity to maximize enforcement and mitigate invalidation risks.

  • Strategic Positioning:
    The patent's landscape within Israel and its international family will determine its role in global market strategies, especially concerning markets with high pharmaceutical patenting standards.

  • Infringement and FTO:
    Stakeholders should conduct detailed FTO analyses considering existing patents and prior art to identify licensing opportunities or avoid infringement.

  • Future Developments:
    Monitoring subsequent patent family filings, legal challenges, or oppositions remains critical to assessing the patent's longevity and value.


Key Takeaways

  • The scope and claims define the enforceability and commercial potential of IL211785, with typical pharmaceutical patents balancing narrow safety for validity and broad claims for market leverage.

  • Understanding the patent landscape, including prior art and patent family strategies, is essential for effective patent management and business decision-making.

  • IL211785's strategic value hinges on its novelty, inventive step, and international patent family, influencing licensing, R&D direction, and competitive positioning.

  • Proactive monitoring and legal stewardship will be vital in maximizing the patent's commercial life and defending against challenges.

  • For stakeholders, aligning patent strategy with clinical and market developments ensures optimal utilization of IL211785's protected innovations.


FAQs

Q1: What are the most common claim types in pharmaceutical patents like IL211785?
Answer: They typically include composition claims (covering specific drugs or formulations), use claims (indicating indications or methods), and process claims (methods of manufacture or delivery systems).

Q2: How does the patent landscape in Israel influence a global patent strategy?
Answer: Israel's supportive patent laws and enforcement environment serve as a strategic platform for regional protection, and filings often integrate into international patent strategies via PCT routes to secure global coverage.

Q3: What factors determine the strength of IL211785’s claims?
Answer: Claim breadth, novelty, inventive step, and thorough description support strength. Broader claims increase scope but may face validity challenges, while narrow claims are easier to defend.

Q4: How can stakeholders assess the risk of patent infringement relating to IL211785?
Answer: Conducting comprehensive freedom-to-operate (FTO) analyses against existing patents within the relevant jurisdictions helps identify potential infringement issues or licensing opportunities.

Q5: Why is patent family analysis important for IL211785?
Answer: It reveals international protection status, strength, and scope, enabling strategic decisions on patent enforcement, licensing, and R&D investments across markets.


References:
[1] Israel Patent Law, 1967.
[2] World Intellectual Property Organization (WIPO). Patent Cooperation Treaty (PCT) filings.
[3] European Patent Office (EPO). Guidelines for Examination.
[4] IPWatchdog. Pharmaceutical patent claim strategies.

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