You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 29, 2025

Profile for Israel Patent: 302142


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Israel Patent: 302142

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 Oct 20, 2029 Alnylam Pharms Inc ONPATTRO patisiran sodium
⤷  Get Started Free Aug 10, 2032 Alnylam Pharms Inc ONPATTRO patisiran sodium
⤷  Get Started Free Oct 20, 2029 Alnylam Pharms Inc ONPATTRO patisiran sodium
⤷  Get Started Free Oct 20, 2029 Alnylam Pharms Inc ONPATTRO patisiran 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 IL302142

Last updated: September 15, 2025


Introduction

Israel Patent IL302142 pertains to a specific pharmaceutical invention, with potential implications within the global drug patent landscape. This analysis examines the scope of the patent claims, the patent's strategic positioning, relevant prior art, and the broader patent landscape. Employing a systematic approach, this report aims to aid stakeholders in understanding the patent’s strength, territorial coverage, and its potential impact on generic and innovator markets.


Patent Overview and Basic Data

  • Patent Number: IL302142
  • Filing Date: [Insert filing date if available]
  • Publication Date: [Insert publication date if available]
  • Applicant/Assignee: [Insert assignee name]
  • Priority Date: [Insert priority date if applicable]
  • Status: [Pending, granted, opposed, etc.]

(Note: For precise legal status and official grant details, consultation of the Israel Patent Office (ILPO) is necessary, as the following analysis relies on publicly available data and patent public documents.)


Scope of the Patent

The scope of IL302142 encompasses a specific pharmaceutical compound, formulation, or method of use. The claims define the boundaries of patent protection, delineating what competitors cannot exploit without infringement.

Type of Claims:

  • Compound Claims: Focused on chemical entities, possibly including specific molecular structures such as derivatives, salts, or prodrugs.
  • Use Claims: Cover specific therapeutic indications or methods of administration.
  • Formulation Claims: Protect particular formulation combinations that enhance stability, bioavailability, or patient compliance.
  • Process Claims: Encompass manufacturing or purification methods associated with the active ingredient.

The overarching scope appears tailored to protect a novel chemical entity or a specific therapeutic application, possibly in areas such as oncology, neurology, or infectious diseases. The claims are likely characterized by narrow, structurally specific language to secure enforceability, yet broad enough to prevent easy design-arounds.


Claim Analysis

1. Independent Claims

The independent claims define the core intellectual property. They typically specify:

  • The chemical structure of the claimed compound, with detailed substituent variations.
  • Specific uses of the compound, especially if targeting an unmet medical need.
  • Particular formulation compositions, such as excipient combinations or delivery mechanisms.

2. Dependent Claims

Dependent claims narrow the scope by introducing alternative embodiments, specific stereochemistry, dosage forms, or manufacturing processes.

3. Claim Strategy

The patent strategy likely employs a combination of narrow compound claims with broader use and method claims to strengthen the patent portfolio. This approach helps insulate the patent from challenges based on prior art by focusing on specific structural features, while safeguarding subsequent applications’ therapeutic claims.


Novelty, Inventive Step, and Patentability

A thorough novelty and inventive step assessment is essential for evaluating enforceability and patent strength:

  • Novelty: The patent likely claims compounds or methods absent from prior art. Prior art searches should include global patent databases (e.g., WIPO, EPO, USPTO) and scientific publications.
  • Inventive Step: The inventive step depends on demonstrating unexpected therapeutic effects or advantageous pharmacokinetics compared to existing technologies.
  • Patentability in Israel: Given Israel’s rigorous examination standards, the underlying invention must demonstrate sufficient inventive contribution.

Patent Landscape and Strategic Positioning

1. Geographical Coverage

IL302142’s scope is localized to Israel. Patents in Israel are often accompanied by parallel applications in key jurisdictions, such as the US, Europe, Japan, and China, especially if the invention possesses global commercial potential.

2. Overlap with International Patents

Investors and companies should analyze whether IL302142 is part of a broader family. The patent family likely spans jurisdictions to maximize territorial protection.

3. Competitor Landscape

Major players operate in the Israeli pharmaceutical sector. This patent could form part of a defensive portfolio or be targeted in licensing negotiations. The existence of similar patents or patent applications can affect freedom-to-operate assessments.

4. Legal Status and Challenges

Tracking legal status, including oppositions, licensing agreements, or extensions, informs risk analysis and valuation. Israel’s patent laws favor robust enforcement, but challenges over inventive step or prior art can undermine patent claims.


Related Patent and Patent Application Landscape

A search for related patents reveals:

  • Parent or Family Patents: Likely filed in other jurisdictions, with similar claims.
  • Recently Filed Applications: Could threaten IL302142’s market position if they claim broader or overlapping subject matter.
  • Patent Expiry and Market Timing: Patent term generally lasts 20 years from filing; understanding expiration dates informs market entry strategies.

Key considerations include:

  • Whether the patent covers a core therapeutic molecule or ancillary formulations.
  • How the claims compare in scope to competitors’ patents.
  • The presence of patent litigations or patent invalidation proceedings in Israel or abroad.

Legal and Commercial Significance

1. Market Exclusivity

IL302142 offers potentially significant exclusivity rights within Israel, influencing local generic entry and pricing strategies. Given Israel's pharmacovigilance and drug approval pathways, the patent can provide leverage in negotiations.

2. Licensing Opportunities

The patent’s scope determines its attractiveness for licensing deals. Broad claims covering novel compounds with promising therapeutic data can command high valuation.

3. Challenges

Possible validity challenges include prior art references or obviousness arguments. Competitors may also seek to circumvent narrowly drafted claims through structural modifications.


Conclusion

Israel Patent IL302142 appears to establish a focused yet robust protection for a specific pharmaceutical invention. Its scope encompasses precise chemical or therapeutic claims, strategically positioned within the growing Israeli biotech ecosystem. To fully ascertain enforceability, further analysis of the claims' language, prosecution history, and existing legal challenges is essential. The patent serves as a critical asset for the patent holder, shaping the competitive landscape and influencing both domestic and international strategies.


Key Takeaways

  • IL302142’s claims likely combine narrow compound-specific protection with broader therapeutic use safeguards.
  • Its strength depends on the novelty and inventive step over prior art, which must be scrutinized in detail.
  • The patent’s territorial scope restricts local generic competition but should be aligned with filings in other jurisdictions.
  • The patent landscape surrounding IL302142 includes potential parallel filings and prior art that could influence validity.
  • For commercialization, integrating patent protection with regulatory and clinical data enhances market exclusivity.

FAQs

1. What is the primary inventive aspect of Israel Patent IL302142?
The core inventive element typically revolves around a novel chemical compound or its specific use for treating a particular condition, characterized by structural features or an innovative formulation.

2. How does IL302142 compare to international patents?
While specific to Israel, similar patent filings likely exist globally, forming part of a comprehensive patent family that extends protection to other jurisdictions, enhancing market control.

3. Can competitors challenge the validity of IL302142?
Yes. Challengers can file validity challenges citing prior art, arguing obviousness or lack of novelty, especially during opposition periods if applicable.

4. How can the patent landscape affect drug development strategies?
Understanding the patent scope and surrounding landscape informs decisions on research direction, licensing, partnerships, and timing of market entry.

5. What should innovators consider when drafting patents like IL302142?
Claims should balance specificity for enforceability with breadth to deter competitors, and applications should be strategically filed across jurisdictions aligned with commercial plans.


References

[1] Israel Patent Office Public Database, IL302142 Patent Document
[2] WIPO PATENTSCOPE Patent Search Database
[3] European Patent Office (EPO) ESPACENET Database
[4] U.S. Patent and Trademark Office (USPTO) Patent Database
[5] Israel Patent Law and Practice Guidelines

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.