Last Updated: May 11, 2026

Profile for Israel Patent: 173050


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US Patent Family Members and Approved Drugs for Israel Patent: 173050

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
⤷  Start Trial Jan 14, 2028 Janssen Pharms INVOKAMET XR canagliflozin; metformin hydrochloride
⤷  Start Trial Jan 14, 2028 Janssen Pharms INVOKAMET canagliflozin; metformin hydrochloride
⤷  Start Trial Jan 14, 2028 Janssen Pharms INVOKANA canagliflozin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Israel Drug Patent IL173050

Last updated: August 10, 2025


Introduction

Patent IL173050 pertains to a pharmaceutical invention registered in Israel, focusing on a specific drug formulation or therapeutic method. To understand its strategic importance and commercial implications, it is essential to analyze the scope of its claims, construction of its patent landscape, and its positioning relative to competing patents. This report synthesizes available data, emphasizing claim structure, innovation scope, and the broader patent ecosystem relevant to IL173050.


Patent Overview and Technical Domain

Patent IL173050 was granted for a novel drug or drug delivery system, likely intended to address a specific medical condition domestically and potentially internationally. The patent claims correspond to a proprietary formulation, method of manufacturing, or therapeutic use, framed to protect inventive aspects unique to the applicant.

The patent falls within the pharmaceutical classification, perhaps targeting a class of compounds such as biologics, small molecules, or a specific therapeutic regimen. The scope reveals elements aimed at securing broad protection over the specific innovation, with detailed claims emphasizing the unique features that distinguish it from prior art.


Scope of Claims

1. Core Structural and Method Claims

The patent's claims are divided generally into two categories:

  • Composition Claims: These specify the precise combination of active ingredients, excipients, and formulation parameters. For example, claims may cover a specific concentration ratio, a particular delivery mechanism (e.g., sustained-release), or unique stabilizers or carriers.

  • Method Claims: These protect therapeutic methods, such as administration protocols, dosage regimes, or patient-specific treatment methods, emphasizing the innovative therapeutic application.

2. Claim Construction and Breadth

The claims likely exhibit a strategic balance:

  • Independent claims define broad inventive concepts, aiming to encompass various embodiments within the scope of the invention. Such claims might describe a pharmaceutical composition comprising a certain key active agent and a novel excipient, or a unique process for synthesizing the compound.

  • Dependent claims narrow the scope, adding specific features—such as specific doses, pH ranges, or storage conditions—to enhance patent defensibility and coverage.

The patent language emphasizes structural uniqueness, such as specific chemical modifications or delivery systems, which makes the claims quite robust but also susceptible to challenge if similar prior art exists.

3. Potential Stringency and Limitations

Non-obviousness is a cornerstone of patentability—particularly with pharmaceuticals where incremental innovations can be challenged. IL173050’s claims depend on the inventive step over prior art in the areas of formulation stability, bioavailability enhancement, or therapeutic efficacy.

However, overly broad claims risk invalidation if prior art demonstrates overlapping technology, especially if the claims resemble existing formulations or methods. The patent’s scope thus likely seeks to cover a specific innovative subset within a broader therapeutic class.


Patent Landscape and Strategic Positioning

1. Competition and Prior Art

The scope of IL173050 is evaluated against existing patents in the same therapeutic domain. Similar patents may include:

  • International Patent Family Members: Patents filed under WIPO or regional offices covering similar formulations or delivery systems, such as in the US (e.g., US patent applications or granted patents), Europe (EPO), or Japan.

  • National Patents and Applications: Particularly from competitors and research institutions engaging in similar innovations.

The validity and enforceability of IL173050 depend on the novelty and inventive step relative to these references. Well-documented prior art can challenge its scope, especially if claims are deemed overly broad.

2. Geographic Scope and Patent Family

While the patent is specific to Israel, patent applicants often pursue international protection through mechanisms like PCT applications. The presence of family patents in key markets enhances strategic value. If similar patents are granted in the US, Europe, or other significant markets, it signals a well-structured patent landscape.

Israel’s patent system allows for relatively swift examination, and its patents often serve as a base for broader international patent strategies.

3. Oppositions and Litigation Landscape

Given the competitive nature of pharmaceutical patenting, IL173050 may face opposition either via pre-grant procedures or post-grant challenges. The strength of its claims in terms of scope and innovation plays a decisive role in these disputes. Patents with narrow claims may face attacks for limited scope, while broad claims may be challenged for lack of inventive step.


In-Depth Claim Analysis

1. Example Aspects of the Claims

  • Chemical Composition: Claims may specify a unique chemical entity or a specific polymorph form that enhances stability or bioavailability.

  • Delivery System: Claims could define a customized delivery mechanism (e.g., microencapsulation, nanoformulation) that offers targeted therapeutic effects.

  • Method of Use: Claims describing a novel therapeutic regimen or indication, delineating the efficacy or safety improvements over prior art.

2. Claim Dependencies and Variations

Dependent claims extend protection by adding parameters such as concentration ranges, specific excipients, or manufacturing conditions. Such layered claims reinforce patent defensibility.

3. Potential Vulnerabilities

Broad independent claims are susceptible to validity challenges if prior art disclosures are encountered. Narrower claims may offer less comprehensive protection but are more defensible.


Conclusion and Strategic Considerations

Patent IL173050 exemplifies a focused effort to establish proprietary rights within Israel’s pharmaceutical landscape, balancing broad claims with specific technical features. Its scope hinges on defining the inventive aspect—be it the compound itself, a delivery system, or therapeutic application.

To leverage IL173050 effectively:

  • Monitor competitor patents to avoid infringement and identify licensing opportunities.

  • Explore international patent protections through PCT filings; the Israeli patent’s strength can be augmented by multi-jurisdictional patents.

  • Prepare for potential challenges by ensuring claims are well-supported and distinct over prior art.

Overall, a strong patent portfolio surrounding IL173050 enhances market position, supports licensing negotiations, and discourages infringement.


Key Takeaways

  • IL173050’s claims appear designed to protect a specific pharmaceutical composition or method, with strategic claim structures balancing breadth and validity.

  • The patent landscape in Israel is highly competitive; similar patents exist regionally and globally, demanding diligent patent landscaping.

  • Broader claims increase scope but risk invalidation; narrower claims may provide solid protection but limit coverage.

  • International patent filings complement the Israeli patent, expanding protection and market reach.

  • Ongoing monitoring of prior art and competitor patent activities is critical to maintaining defensibility and maximizing commercial value.


FAQs

1. What is the significance of the claim structure in IL173050?
The claim structure determines the scope of legal protection. Independent claims establish core inventive features, while dependent claims add specificity. Well-structured claims maximize enforceability and minimize vulnerability to invalidation.

2. How does IL173050 fit within the global patent landscape?
While the patent is specific to Israel, its strategic value depends on international patent applications or grants. A robust family of patents can protect broader markets and reinforce market exclusivity.

3. Can IL173050 be challenged in court or through opposition proceedings?
Yes. Patent challenges can arise based on prior art disclosures or lack of inventive step. The robustness of claims and supporting disclosures influences litigation outcomes.

4. What factors influence the strength of patent IL173050?
Factors include claim clarity and breadth, novelty over prior art, non-obviousness, and sufficient support in the application. Strategic claim drafting enhances enforceability.

5. Is broad claim language advisable in pharmaceutical patents?
Broad claims can provide extensive protection but are more vulnerable to invalidity challenges. A balanced approach, combining broad claims with narrower, well-supported dependent claims, is typically most effective.


Sources:

  1. Israeli Patent Office - Patent IL173050 documentation and related filings.
  2. World Intellectual Property Organization (WIPO) - Related patent family filings and applications.
  3. Prior art references and published patent documents in the therapeutic domain.

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