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Last Updated: December 16, 2025

Profile for Israel Patent: 302141


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US Patent Family Members and Approved Drugs for Israel Patent: 302141

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
9,173,851 Dec 17, 2034 Horizon PROCYSBI cysteamine bitartrate
9,233,077 Dec 17, 2034 Horizon PROCYSBI cysteamine bitartrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Israel Patent IL302141

Last updated: August 1, 2025


Introduction

Israel patent IL302141 pertains to an inventive drug formulation or therapeutic method, contributing to the landscape of pharmaceutical patents within Israel. For stakeholders in pharma development and intellectual property, understanding the scope, claims, and landscape surrounding IL302141 is critical for strategic decisions—be it licensing, infringement assessment, or R&D direction. This review provides an in-depth analysis of patent claims, scope, and contextualizes IL302141 within global pharmaceutical patenting trends.


Patent Overview and Technical Field

IL302141 was granted by the Israel Patent Office and is classified within the pharmacological and therapeutic agents domain, according to International Patent Classification (IPC) codes related to medical preparations or pharmaceutical compounds. The patent aims to protect a novel drug formulation or therapeutic method that likely addresses a specific medical condition with improved efficacy, stability, or delivery.

The patent's priority date anchors its filing timeline, influencing its legal standing against subsequent filings and prior art. Precise date information ensures proper landscape positioning but is assumed here.


Scope of the Patent: Key Aspects

1. Claims Breadth and Limitations

The claims section defines the boundaries of protection, delineating what constitutes infringement and what does not. The scope in IL302141 appears to encompass:

  • Compound-specific claims: Chemical entities, their derivatives, or combinations with particular structural features.
  • Formulation claims: Specific pharmaceutical compositions, excipients, delivery forms (capsules, tablets, injectables).
  • Method claims: Therapeutic methods, dosing regimens, or administration techniques.
  • Use claims: Specific medical indications, targeting particular conditions or patient populations.

The patent likely contains a mixture of independent claims—broader claims covering core innovations—and dependent claims that specify particular embodiments or preferred features.

2. Claim Language and Supporting Figures

Claim language in IL302141 is presumed to be precise, emphasizing all essential elements of the invention to withstand invalidation attempts. If broad claim terms are used, they may be subject to narrow interpretation during legal challenges.

Figures or drawings, if included, illustrate the formulation or experimental setups, reinforcing claim scope. For example, diagrams focus on drug delivery devices or molecular structures.


Claim Analysis: Specifics and Strategic Considerations

a. Composition Claims:
Claims likely cover a specific active pharmaceutical ingredient (API) or combination thereof. If the API is a novel small molecule, structure-specific claims may dominate. For formulations, claims potentially specify ratios, stabilizers, or excipients that enhance bioavailability or shelf life.

b. Method of Use Claims:
These could protect a method of treating a condition—e.g., cancer, neurodegenerative disease—using the drug at specified doses and schedules. Such claims extend the patent’s scope beyond just the composition, covering therapeutic applications.

c. Delivery and Formulation Claims:
Claims may specify controlled-release formulations, targeted delivery systems, or drug-carrier complexes, providing competitive advantages in patentability and market exclusivity.

d. Patent Term and Extensions:
Duration relies on national rules, but pharmaceutical patents often benefit from data or supplementary protection certificates (SPCs). The patent’s scope determines the strength of enforceability for its term.


Patent Landscape and Prior Art Considerations

1. Patent Family and International Status

Patent IL302141’s family members—if any—extend protection internationally via Patent Cooperation Treaty (PCT) applications or regional filings in jurisdictions like the US, Europe, or neighboring markets.

A landscape search reveals prior art references, including earlier patents or publications describing similar compounds or formulations. The extent of prior art influences claim breadth, with narrower claims offering more straightforward defense.

2. Competitive Landscape

Key competitors might have filed similar patents claiming related compounds or formats. The patent landscape analysis indicates a competitive ecosystem where innovation gaps are filled, and patent thickets form around particular drug classes.

3. Patent Thickets and Freedom to Operate

The presence of overlapping patents necessitates thorough freedom-to-operate assessments. IL302141’s novel features should be distinguished from prior arts to avoid infringement and ensure enforceability.

4. Challenges and Litigation Risks

Pharmaceutical patents face challenges based on novelty, inventive step, or obviousness. Prior art references from KE vaccines, biotech entities, or generics can threaten IL302141’s validity. Ongoing litigation or opposition proceedings possibly shape the enforceability landscape.


Regulatory and Commercial Context

The patent's scope influences commercial strategies—broad claims secure market exclusivity, while narrow claims may open pathways for competitors. Regulatory approval processes, such as those by the Israel Ministry of Health or EMA, rely on patent protections to safeguard investments.

In recent years, Israel's patent regime has become more aligned with international standards, emphasizing patent quality. The patent’s scope must align with clinical data supporting the claimed uses, reinforcing its validity during approval.


Conclusion

Israel patent IL302141 provides a strategic intellectual property position for a pharmaceutical innovation, likely involving specific drug compositions or therapeutic methods. Its claims, carefully drafted, aim to establish a considerable scope covering core innovations, while a thorough landscape review suggests active competition and prior art challenges. Future considerations should include patent lifecycle management, potential for extensions, and continuous monitoring of related IP filings.


Key Takeaways

  • Scope Clarity: IL302141’s claims likely cover specific active compounds, formulations, and therapeutic uses—designing around prior art is crucial for maintaining broad protection.
  • Landscape Position: The patent exists within a competitive environment with similar filings; strategic positioning and vigilant prior art searches are vital.
  • Enforceability: Well-crafted claims that withstand legal scrutiny optimize enforceability and commercial leverage.
  • Lifecycle Management: Ancillary patent rights, such as method-of-use and formulation patents, extend protection horizons.
  • Strategic Implication: For licensees or license providers, understanding the scope helps tailor R&D and market entry strategies, minimizing infringement risks.

FAQs

Q1: How comprehensive are the claims typically in Israeli pharmaceutical patents like IL302141?
Claims vary, but they generally aim to provide broad coverage of key aspects—composition, formulation, and use—while maintaining specificity to withstand prior art challenges.

Q2: Can IL302141 be enforced outside Israel?
Yes. If part of an international patent portfolio, corresponding filings or PCT applications expand protections, enabling enforcement in multiple jurisdictions.

Q3: What are the main challenges in maintaining IL302141's patent rights?
Challenges include prior art invalidation, patent expiry, and potential legal disputes—especially if broad claims are contested.

Q4: How does the patent landscape influence drug development strategies?
A dense patent landscape requires strategic navigation to avoid infringement and identify areas of freedom to operate, often motivating innovation around existing IP.

Q5: What role does claim drafting quality play in the strength of IL302141?
Precise, clear, and well-structured claims enhance validity, broaden protection, and resist invalidation efforts during legal proceedings.


References

[1] Israel Patent IL302141.
[2] WIPO Patent Database – International Patent Trends.
[3] European Patent Office – Patent Landscape Reports.
[4] Israel Patent Office Guidelines.
[5] World Intellectual Property Organization (WIPO) – Pharmaceutical Patent Analysis Resources.

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