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Last Updated: December 31, 2025

Profile for Israel Patent: 222030


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US Patent Family Members and Approved Drugs for Israel Patent: 222030

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
8,486,975 Aug 30, 2032 Msd Merck Co DELSTRIGO doravirine; lamivudine; tenofovir disoproxil fumarate
8,486,975 Aug 30, 2032 Msd Merck Co PIFELTRO doravirine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Israel Patent IL222030

Last updated: July 29, 2025


Introduction

Israel patent IL222030 pertains to a pharmaceutical invention in the realm of drug innovations, with a focus on a novel compound or formulation. This patent, like others in the pharmaceutical sector, aims to safeguard the inventive step, utility, and exclusivity of the claimed medicinal entity, thereby enabling commercial advantage and fostering innovation. This analysis dissects the patent’s scope and claims while positioning it within the broader intellectual property (IP) landscape.


Patent Overview

IL222030, filed and granted under the Israeli Patent Office, is registered primarily as a pharmaceutical patent. Its registration date places it within the recent wave of drug patent protections, reflecting ongoing innovation in specific therapeutic areas. Although the comprehensive content of the patent claims lies behind patent documentation, standard pharmaceutical patents in Israel generally encompass compositions, methods of use, and manufacturing processes.

Scope of the Patent

The scope of IL222030 extends to:

  • Novel compound or composition: The patent likely claims a specific chemical entity, a combination of active ingredients, or a particular formulation characterized by improved pharmacological properties—such as enhanced bioavailability, selectivity, or stability.
  • Therapeutic applications: It delineates the use of the claimed compounds for treating particular diseases or conditions, possibly including indications like oncology, neurology, or infectious diseases.
  • Manufacturing processes: The patent might cover specific methods of synthesizing or formulating the drug, crucial for demonstrating inventive ingenuity over existing technologies.

The scope aims to be comprehensive yet specific enough to avoid overlaps with prior art, aligning with Israeli patent standards that favor clear, well-defined claims.


Claims Analysis

1. Independent Claims

The independent claims set the broadest legal protection, defining the essence of the invention:

  • Chemical Composition or Compound Claim: Usually the primary claim focuses on the chemical structure, such as a novel molecule with particular substituents or stereochemistry.
  • Method of Use: Claims may specify a therapeutic method, including administering the compound to treat or prevent specific diseases, often linked with a particular formulation or dosage regimen.
  • Manufacturing or Formulation Claims: These might cover innovative processes or formulations that improve drug delivery or stability.

2. Dependent Claims

Dependent claims narrow the scope by specifying particular embodiments, such as:

  • Variations in the chemical substituents.
  • Specific dosages and administration routes.
  • Combinations with other drugs for synergistic effects.
  • Specific formulations or excipients that optimize drug performance.

3. Claim Strategy and Critical Elements

The patent’s robustness hinges on:

  • Novelty: The claims must distinguish the invention from prior art, an essential requirement under Israeli patent law.
  • Inventive Step: They require an inventive step, usually demonstrated through structural uniqueness or unexpected therapeutic advantages.
  • Industrial Applicability: The claims are crafted to be practically applicable in pharmaceutical manufacturing and treatment.

Patent Landscape for IL222030

1. Prior Art Environment

The landscape includes earlier patents and patent applications related to similar chemical entities, therapeutic methods, or formulations. Commonly, the patent examiner conducted a thorough search, referencing:

  • International patents from major players such as the US, Europe, and WIPO.
  • Regional patents within the European Patent Office (EPO) and US Patent and Trademark Office (USPTO).
  • Scientific literature indicating continuous innovation in the targeted therapeutic class.

If IL222030 claims a molecule structurally or functionally distinct from prior art, it benefits from a strong novelty position. Conversely, if overlapping prior art exists, the patent could face limitations or challenges in enforcement.

2. Patent Families and Related Applications

IL222030 may be part of a broader patent family covering:

  • Priority claims originating from earlier publications or domestic applications.
  • International filings via Patent Cooperation Treaty (PCT), which extend protection globally.
  • Derived or divisional applications that protect specific embodiments or manufacturing strategies.

3. Competitor Landscape

A competitive analysis reveals that:

  • Major pharmaceutical companies may hold similar patents, competing within the same therapeutic niche.
  • Smaller biotech firms could be exploring analogous compositions or methods, emphasizing the importance of comprehensive patent claims.
  • The patent’s strength relies on unique structural features, claimed indications, or manufacturing efficiencies that differentiate it from close prior arts.

Legal and Commercial Implications

Enforceability and Market Exclusivity

The scope of IL222030 aims to secure exclusive rights for the claimed drug, preventing generic manufacturers from entering the market for the duration of the patent term (typically 20 years from filing). The breadth of claims determines market control, with broad claims offering competitive advantage but increasing scrutiny for validity.

Patent Challenges and Defense

Potential patent challenges include:

  • Invalidity arguments citing prior art or lack of inventive step.
  • Non-enablement or sufficiency issues, if the patent fails to adequately describe the claimed invention.
  • Obviousness in light of existing therapies or chemical classes.

Israel’s patent system emphasizes patent quality; hence, comprehensive claims and detailed descriptions fortify the patent’s position.


Conclusion

IL222030 encapsulates a strategic effort to protect a novel drug composition or method within Israel, with claims carefully structured to balance broad protection and defensibility. Situated within a complex patent landscape, the patent hinges on the novelty and inventive step over prior art streams. Its strength will influence licensing opportunities, collaboration prospects, and competitive positioning.


Key Takeaways

  • IL222030’s scope likely covers a novel pharmaceutical compound, its therapeutic uses, and manufacturing methods, with claims tailored for broad yet defendable coverage.
  • The patent landscape indicates a competitive environment, with prior art necessitating precise claim drafting to establish novelty and inventive step.
  • Strategic patent filing, including potential international extensions, can maximize market exclusivity and commercial return.
  • Ongoing patent challenges can arise from prior art or obviousness rejections, emphasizing the importance of robust patent prosecution.
  • For stakeholders, understanding the scope and claims aids in assessing infringement risks, licensing potential, and R&D direction.

FAQs

1. What is the primary focus of Israeli Patent IL222030?
It generally encompasses a novel drug compound, formulation, or therapeutic method, with specific claims designed to protect innovative pharmaceutical advancements.

2. How does IL222030 compare with similar global patents?
Its novelty and scope depend on differences from prior art, particularly in chemical structure, therapeutic indication, or manufacturing process—similar to international patent standards.

3. Can IL222030 be challenged or invalidated?
Yes, through prior art invalidity or inventiveness challenges, particularly if prior publications or existing patents disclose similar compounds or uses.

4. What strategic advantages does a broad claim scope provide?
It maximizes market exclusivity by covering multiple embodiments and potential variations, deterring competitors from developing similar products.

5. How does the patent landscape influence the future of IL222030?
A competitive landscape requires continuous innovation and vigilant IP management to maintain advantage amid potential patent challenges and evolving therapeutic needs.

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