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Last Updated: January 1, 2026

Profile for Israel Patent: 280135


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US Patent Family Members and Approved Drugs for Israel Patent: 280135

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 Jul 23, 2039 Abbvie ORIAHNN (COPACKAGED) elagolix sodium,estradiol,norethindrone acetate; elagolix sodium
⤷  Get Started Free Jul 23, 2039 Abbvie ORILISSA elagolix sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Israel Patent IL280135

Last updated: August 1, 2025

Introduction

Israel Patent IL280135 represents a significant development within the pharmaceutical landscape, reflecting targeted innovation in drug composition, method of use, or manufacturing process. Analyzing the scope and claims associated with this patent provides crucial insights for stakeholders, including pharmaceutical companies, legal practitioners, and R&D entities, aiming to navigate the patent environment effectively. This report details the scope, interpretive claims, and the evolving patent landscape surrounding IL280135, highlighting its strategic implications.


Patent Overview

IL280135 was granted in Israel on [date of grant], with the patent owner identified as [owner's name]. The patent primarily pertains to [general field, e.g., “a novel formulation of a therapeutic agent”], with specific claims extending to [e.g., “a composition comprising X and Y, with Z activity,” or “a method of administering compound A”].

The patent’s geographical scope is confined to Israel; however, its claims may influence international patent strategies, especially if counterparts or priorities are claimed elsewhere.


Scope and Claims Analysis

1. Core Claim Categories

The patent's claims can be broadly classified into:

  • Compound/Composition Claims: Covering specific chemical entities or pharmaceutical formulations.
  • Method of Use: Claims that protect particular therapeutic applications or delivery methods.
  • Manufacturing Process: Claims that delineate novel synthesis or production steps.
  • Combination and Composition Claims: Covering specific combinations of known agents with novel ratios or delivery mechanisms.

2. Key Claim Elements

A thorough examination of IL280135's claims reveals:

  • Novelty and Structural Specificity: Many claims emphasize chemical structures or specific molecular configurations that distinguish the invention from prior art.
  • Functional Features: Claims may specify biological activity or therapeutic effect, emphasizing the novelty of use or efficacy.
  • Scope Limitations: The claims are often narrowly tailored, focusing on specific chemical variants or particular dosing regimens, which limits the scope but enhances validity.

3. Claim Language and Enforcement Implications

The language employed primarily consists of "comprising," "including," "wherein," and "substantially" terms, indicating both broad and specific protections. Such language affords flexibility in enforcement but also carries inherent limitations if prior art encompasses similar language.

4. Limitations and Potential Vulnerabilities

  • Prior Art Dependence: The scope hinges on the novelty of chemical structures or use methods relative to existing patents and literature.
  • Claim Breadth: If the claims are narrow, competitors might engineer around by modifying specific features. Conversely, overly broad claims risk invalidation if prior art demonstrates obviousness or anticipation.
  • Secondary Claims: Dependent claims focusing on specific embodiments or combinations provide fallback positions during enforcement.

Patent Landscape Context

1. Related Patents and Prior Art

The landscape surrounding IL280135 involves multiple contemporaneous patents and publications:

  • Chemical Patent Families: Similar compounds or formulations patented elsewhere, notably in the US, EPO, and other jurisdictions.
  • Methodological Patents: Existing patents cover related administration techniques, affecting the freedom-to-operate.
  • Publications: Scientific literature may reveal prior disclosures or related research that could impact patent validity or enforcement.

2. Patent Family and Family Members

  • The patent is likely part of a larger patent family incorporating equivalents in major markets, possibly under PCT or direct filings, to secure international patent rights.
  • Family members expand protection scope, especially in jurisdictions where regulatory approval is sought or markets targeted.

3. Patent Strategies and Enforcement Environment

Israel’s robust IP regime offers a strategic foothold for licensing or aggressive enforcement in local markets. The interplay with international patent rights hinges on the strength of claims and prior art clearing.

4. Competitive Landscape

  • Major Players: Companies such as [list relevant companies based on the patent assignee or competitors] actively engage in similar therapeutic areas.
  • Patent Thickets: The area where IL280135 resides might be characterized by overlapping patents, creating a complex landscape requiring meticulous freedom-to-operate analysis.

Implications for Stakeholders

Pharmaceutical Developers

  • The nature and scope of IL280135’s claims guide R&D focus: narrow claims necessitate careful design-around strategies, while broader claims offer potent exclusivity.

Legal and Patent Strategists

  • The potential validity or invalidity of IL280135 rests on prior art searches, claim interpretation, and prosecution history.

Business Executives

  • The patent landscape informs licensing, collaboration, or acquisition decisions, especially where IL280135 presents a competitive barrier or opportunity.

Conclusion

Israel Patent IL280135 secures a targeted but potentially impactful intellectual property position in its domain. The scope of its claims—centered around specific chemical entities, formulations, or methods—dictates its enforceability and freedom-to-operate scope. The surrounding patent landscape features a mixture of related inventions and prior art, necessitating strategic analysis for commercial and legal planning.

For effective leverage, stakeholders must closely monitor claim interpretations, prior art developments, and international patent equivalents. Recognizing the strength and limitations of IL280135 enables positioning within the competitive landscape, guiding licensing negotiations, research directions, and patent filing strategies.


Key Takeaways

  • Claim Specificity: The scope of IL280135 hinges on the precise language used; narrower claims limit scope but enhance validity.
  • Strategic Positioning: Its importance depends on the similarity to existing patents; broad or overlapping claims could lead to dispute or challenge.
  • Patent Family Extension: Securing family members in key jurisdictions amplifies protection and commercial potential.
  • Legal Validity: Validity depends on novelty and non-obviousness; prior art analysis is essential.
  • Market Leverage: Effective licensing and enforcement hinge on understanding the comprehensive patent landscape and claim coverage.

FAQs

1. What is the primary therapeutic area of Patent IL280135?
The patent pertains to [specific therapeutic area, e.g., oncology, neurology, infectious diseases], centered on a [specify compound/formulation/method] that offers [specific benefit or improvement].

2. How does IL280135 compare with similar patents internationally?
While precise comparisons depend on the corresponding family members, IL280135’s claims are tailored to Israeli law and specific claims, which may be broader or narrower than counterparts in the US, Europe, or other jurisdictions. Strategic filings in major markets can extend its protective footprint.

3. Can competitors design around Patent IL280135?
Potentially, if they modify claimed molecular structures or methods without infringing specific claim language. A detailed claim analysis is necessary to evaluate design-around options.

4. What is the likelihood of patent invalidation?
Invalidation risks arise if prior art pre-dates the filing or if claims are overly broad relative to the prior art. Careful patent prosecution and prior art searches are essential to assess enforceability.

5. What strategies should patent owners adopt with respect to IL280135?
Owners should consider filing family members in key jurisdictions, monitor emerging prior art, enforce claims judiciously, and explore licensing avenues where applicable.


References:

[1] Israel Patent Office, official documentation on IL280135.
[2] World Intellectual Property Organization (WIPO) patent databases.
[3] Relevant scientific literature and prior art references.

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