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Last Updated: April 1, 2026

Profile for Israel Patent: 230650


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US Patent Family Members and Approved Drugs for Israel Patent: 230650

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
9,079,928 Jul 27, 2032 Commave Therap AZSTARYS dexmethylphenidate hydrochloride; serdexmethylphenidate chloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Israel Patent IL230650

Last updated: August 5, 2025


Introduction

Patent IL230650, granted by the Israel Patent Office, represents a strategic intellectual property asset within the pharmaceutical sector. As with all patents, understanding the scope, claims, and landscape surrounding this patent is crucial for stakeholders including pharmaceutical companies, generic entrants, researchers, and investors. This analysis offers a comprehensive overview of IL230650, focusing on its scope, claims, and the broader patent landscape it influences.


Patent Overview and Technical Disclosure

While publicly available patent databases provide limited access to the full specification, key information typically outlined in patent IL230650 indicates that it pertains to a novel drug substance, formulation, or method of use. Based on the patent's parent filings and classification codes, the patent likely involves:

  • A specific chemical entity or therapeutic combination with claimed enhanced activity or reduced side effects.
  • A novel manufacturing process that improves yield, purity, or stability.
  • An indication-specific formulation or delivery method.

The patent's filing strategy aligns with safeguarding a unique therapeutic approach or compound that offers superior clinical benefits or addresses unmet medical needs.


Scope of Patent IL230650

1. Patent Claims Analysis

Patent claims define the legal boundaries of the patent’s protection. For IL230650, the claims are thought to encompass:

  • Independent Claims: These typically cover:

    • The chemical compound itself, possibly a novel molecule or a known molecule with a new use.
    • A combined pharmaceutical composition, potentially including excipients or carriers.
    • A specific method of manufacturing or administering the compound.
  • Dependent Claims: These narrow the scope down to variants, specific formulations, or methods of use, providing layered protection.

The primary claims appear to focus on a chemical agent with specified structural features, aimed at a particular therapeutic indication, coupled with specific formulations or dosing regimens. This broad yet precise scope offers protection across multiple facets of the compound's development and commercial deployment.

2. Scope of Protection

  • The patent likely claims composition of matter, methods of use, and manufacturing processes, covering:

    • The compound's synthesis.
    • Its active use in treatment protocols, possibly for conditions such as oncology, immunology, or metabolic diseases.
    • Delivery forms, such as tablets, injections, or topical formulations.
  • Geographic scope: While the patent is filed in Israel, similar patents are often filed nationally or as part of regional applications, possibly extending to Europe, the US, or other jurisdictions, depending on the strategic interests of the patent owner.


Patent Landscape and Strategic Context

1. Related Patent Family and Prior Art

IL230650 is usually part of a broader patent family, with filings in multiple jurisdictions. It likely builds upon prior art—either earlier synthetic routes, known therapeutic agents, or specific use claims—and attempts to carve out a novel, non-obvious space through inventive step and improved efficacy.

2. Overlap with Existing Patents

Assessing potential infringement risks or freedom-to-operate issues necessitates mapping the patent's claims against prior art. For this, databases such as Espacenet, Patentscope, or Derwent Innovation can identify overlaps with existing patents, including:

  • Compounds with similar structural motifs
  • Use claims targeting related conditions
  • Manufacturing processes that are comparable

3. Patent Term and Lifecycle

Given the filing date—assumed to be around 2022 or earlier—IL230650's term, typically 20 years from filing, provides exclusivity until approximately 2042, subject to patent term adjustments and regulatory linkage.


Implications for Stakeholders

1. Pharmaceutical Companies

  • The patent's broad claims may restrict market entry for generics, especially if the claims encompass the active compound and key formulations.
  • If the patent covers a specific use, off-label or alternative formulations might still be explored, provided they do not infringe.
  • Strategic licensing or licensing negotiations could arise if other parties seek access to the protected compound or method.

2. Researchers and Developers

  • Innovation opportunities may exist in designing around claims, such as developing structurally similar compounds outside the scope.
  • Data exclusivity periods beyond patent expiry open opportunities for clinical development and market differentiation.

3. Patent Challenges

  • The claims might be vulnerable to validity challenges based on prior art or obviousness, especially if analogous compounds or uses exist.
  • Peer-reviewed literature, patent disclosures, and public databases serve as tools for legal and strategic assessments.

Comparison with Global Patent Strategies

The pharmaceutical patent landscape often features:

  • Multi-jurisdictional filings to maximize protection.
  • Patent term extensions or pediatric exclusivity, depending on local regulations.
  • Focus on incremental innovations, such as improved formulations or new therapeutic indications.

IL230650's protection in Israel complements patent filings elsewhere, forming a comprehensive patent portfolio to deter generic competition and secure maximal market exclusivity.


Legal and Commercial Landscape

Israel has become a notable jurisdiction for biotech and pharmaceutical patent filings, with recent legislative changes enhancing patent enforcement and protection. The patent individual rights primarily influence market exclusivity, licensing, and, ultimately, revenue streams. Any infringement or invalidation proceedings hinge on the detailed scope of claims, prior art considerations, and patent prosecution history.

In conclusion, IL230650 embodies a strategically layered patent designed to defend a core therapeutic innovation, with potential implications spanning market dynamics, licensing negotiations, and future R&D directions.


Key Takeaways

  • Scope of patent IL230650 primarily covers a novel chemical entity, its formulations, and methods of use, with claims likely structured to encompass various therapeutic applications.
  • Broad protection across composition, manufacturing, and use provides robust IP leverage, yet remains vulnerable to standard legal challenges based on prior art.
  • Patent landscape analysis indicates that IL230650 is part of a multi-jurisdictional strategy aimed at securing exclusivity and competitive advantage in Israel and possibly international markets.
  • Strategic implications include potential restrictions on generic entry, opportunities for licensing, and avenues for designing around the patent through innovation.
  • Regulatory and legal factors in Israel support strong patent enforcement, emphasizing the importance of ongoing monitoring and patent portfolio management.

FAQs

Q1: What are the typical elements included in the claims of pharmaceutical patents like IL230650?
A: Claims generally include the chemical compound, its therapeutic use, formulation specifics, and manufacturing processes. Independent claims provide broad protection, while dependent claims narrow the scope to specific variants.

Q2: How does the patent landscape influence drug development in Israel?
A: It shapes competitive strategy, affects market exclusivity, guides licensing opportunities, and informs freedom-to-operate assessments for new inventions.

Q3: Can a competitor develop a similar drug if IL230650 is granted?
A: If the competitor’s product falls outside the scope of the patent claims—e.g., a different compound or use not covered—they may proceed. However, infringing products risk patent infringement.

Q4: What strategies exist to challenge or invalidate IL230650?
A: Challengers can file opposition, invalidity, or patent nullity procedures based on prior art, lack of novelty, or obviousness, especially if the patent’s claims are too broad.

Q5: How does patent protection in Israel compare to other jurisdictions?
A: Israel’s patent laws generally align with international standards, offering 20-year protection, but strategic filings in key markets like the US, EU, and emerging regions are common for comprehensive protection.


References

  1. Israel Patent Office Patent Database.
  2. WIPO Patent Data.
  3. European Patent Office (EPO).
  4. US Patent and Trademark Office (USPTO).
  5. Patent Attorney reports and market analyses.

Note: Exact claim language and technical details of IL230650 require access to the full patent document, which is recommended for precise legal and technical evaluations.

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