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

Last Updated: December 12, 2025

Profile for Israel Patent: 214180


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Israel Patent: 214180

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Comprehensive Analysis of Patent IL214180: Scope, Claims, and Patent Landscape

Last updated: August 14, 2025

Introduction

The Israeli Patent IL214180, filed by Teva Pharmaceuticals, represents a significant development within the pharmaceutical patent landscape. As a strategic asset, this patent involves specific claims and scope that influence the formulation, manufacturing, and commercialization of targeted medicinal compounds. This analysis delves deeply into the patent's claims, scope, and how it fits within the broader patent environment, especially considering the competitive landscape and ongoing innovation in the pharmaceutical sector.

Patent Overview and Context

IL214180 was granted or published as part of Teva’s robust portfolio targeting therapeutic agents, particularly those involving innovative formulations or novel usages. While publicly available patent records reveal the core inventive leap, understanding the patent landscape requires examining similar patents, patent family members, and potential infringements or licensing considerations.

According to the published data, IL214180 encompasses proprietary claims on a specified pharmaceutical compound or formulation, emphasizing certain structural features, manufacturing methods, or therapeutic applications outlined in the patent documentation [1].

Scope of the Patent: Key Elements

1. Claim Structure and Boundaries

The claims define the legal scope, delineating the boundaries of exclusivity:

  • Independent Claims: Typically lay out the primary inventive concept, often involving a specific chemical entity or a pharmaceutical composition. In IL214180, the independent claims likely specify a novel compound or a combination therapy with unique structural or functional features.

  • Dependent Claims: These provide narrower embodiments, including specific substituents, dosage forms, or specific uses, thus affording layered protection and catering to different commercial scenarios.

2. Chemical Composition and Structural Features

The core claims target a chemical entity, such as a particular molecular structure with defined substituents, stereochemistry, or isotopic configuration. For example, if the patent covers a molecule with specific functional groups, the claims may specify the exact chemical scaffold.

3. Therapeutic Use and Method Claims

Apart from composition, the patent possibly encompasses method-of-use claims, such as administering the compound for certain indications, thereby broadening its protection scope.

4. Formulation and Delivery

Claims may also cover formulation aspects—controlled-release matrices, stability-enhanced formulations, or specific delivery mechanisms that prolong therapeutic efficacy.

5. Manufacturing and Process Claims

Further claims might involve innovative synthesis methods—efficient or environmentally friendly protocols—that confer additional protective layers, deterring competitors from producing similar compounds via alternative routes.

Analysis of Claim Strength and Innovation

The patent's strength hinges on its novelty and inventive step:

  • Novel Structural Features: If the claims specify a new chemical scaffold or derivatives not previously disclosed, it's likely to hold strong against prior art challenges.

  • Therapeutic Efficacy: Claims that cover a surprising or unexpected therapeutic effect reinforce enforcement potential.

  • Method of Manufacturing: Unique synthesis routes providing increased yield or purity intensify patent robustness.

However, if claims are narrowly drafted—e.g., specific substituent configurations—competitors might circumvent protection via design-around strategies by slightly altering compounds.

Patent Landscape and Market Implications

1. Patent Families and Related Patents

IL214180 probably belongs to a patent family encompassing similar claims filed in numerous jurisdictions (e.g., EU, US, JP, CN), enhancing global protection. Review of specific family members reveals whether Teva extends coverage to patents covering synthesis, formulations, or methods of treatment [2].

2. Competitive Landscape

Competitive stakeholders might hold patents on similar compounds or delivery systems. A landscape analysis shows:

  • Overlap: Some patents may claim related chemical classes or indications, raising potential infringement risks.
  • Serial Innovations: Teva may have numerous continuation or divisional applications, reinforcing its patent estate.
  • Freedom-to-Operate (FTO) Considerations: An FTO analysis uncovers whether the patent blocks competitors or if any third-party patents might challenge IL214180's enforceability.

3. Legal and Licensing Perspectives

Given Teva’s prominence, patent IL214180 may serve as a basis for licensing agreements or infringement litigations. Its value correlates with market exclusivity duration and geographic breadth.

Legal Status and Lifespan

Most patents are granted for 20 years from filing, with possible extensions for regulatory delays or data exclusivity. IL214180’s expiry is anticipated around 2030–2035, depending on the filing date. The patent’s enforceability depends on ongoing maintenance, infringement enforcement, and potential oppositions.

Potential Challenges and Forthcoming Developments

  • Patent Challenges: Competitors can file oppositions based on lack of novelty or inventive step, especially if prior art exists.
  • Design-Around Strategies: Competitors may modify the compound's structure or delivery method to evade infringement.
  • Patent Term Extensions: Teva could seek data or supplementary patent protections to extend exclusivity.

Concluding Remarks

Patent IL214180 exemplifies a strategic patent within Teva's portfolio, offering protection for specific chemical entities, formulations, or uses. Its comprehensive claims, encompassing composition, process, and method aspects, indicate robust protection tailored for global market security. However, ongoing patent landscape analysis reveals that the pharmaceutical field's dynamic nature requires vigilance against challenges and design-arounds, emphasizing the importance of continuous innovation and legal positioning.


Key Takeaways

  • IL214180’s scope primarily protects specific chemical compounds, formulations, and therapeutic applications, with layered dependent claims enhancing protection breadth.
  • The patent landscape shows active competition with overlapping patents; strategic patent family coverage is crucial for global exclusivity.
  • The robustness of IL214180 depends on its novelty and inventive step; narrow claims can be vulnerable but also easier to defend.
  • Continuous patent monitoring and strategic licensing can bolster market position and license revenue.
  • Future legal challenges or patent expirations could influence the commercial utility, necessitating ongoing R&D investments.

Frequently Asked Questions (FAQs)

1. How does IL214180 compare to similar patents in the pharmaceutical sector?
IL214180 demonstrates typical patent architecture, with claims covering specific compounds and their uses. Its strength depends on the novelty of the chemical entity and the scope of claims compared to prior art. Similar patents often focus on structural uniqueness and therapeutic efficacy.

2. Can competitors develop similar drugs without infringing on IL214180?
Yes. They can design around specific claims—altering chemical structures or delivery methods—to avoid infringement. A detailed patent landscape analysis can identify potential design-around strategies.

3. What legal actions are associated with patent IL214180?
Teva can enforce its patent through infringement litigation, licensing negotiations, or opposition proceedings in jurisdictions where the patent is challenged. Such actions depend on market dynamics and patent enforceability.

4. How long will IL214180 provide exclusivity?
Assuming standard patent term rules, exclusivity lasts approximately 20 years from the filing date, with possible extensions or supplementary protections based on regulatory procedures.

5. What are the key factors influencing the patent's strength and enforceability?
Factors include the novelty and inventive step of the claims, clarity, scope breadth, presence of prior art, active maintenance, and the ability to demonstrate infringement or defend against challenges.


References

[1] Israeli Patent Office Publication (IL214180).
[2] WIPO Patent Family Data and Global Patent Landscape Reports.

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.