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Last Updated: December 19, 2025

Profile for Israel Patent: 249651


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US Patent Family Members and Approved Drugs for Israel Patent: 249651

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
8,420,645 Jun 5, 2031 Novartis Pharm TABRECTA capmatinib hydrochloride
8,901,123 May 20, 2029 Novartis Pharm TABRECTA capmatinib hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Israel Drug Patent IL249651

Last updated: July 31, 2025


Introduction

Israel patent IL249651 pertains to a specific pharmaceutical invention, with implications for both market competition and therapeutic innovation. A comprehensive understanding of its scope, claims, and the broader patent landscape informs stakeholders—pharmaceutical companies, legal practitioners, and investors—on the innovation's strategic value and potential infringement risks.


1. Patent Overview and Filing Context

Patent IL249651 was filed in Israel, a jurisdiction known for a robust patent system aligned closely with international standards such as the Patent Cooperation Treaty (PCT). The patent's filing date, priority claims, and prosecution history shape its enforceability and expiration timeline. While publicly available data on this patent is limited, typical patent lifecycle information suggests it was filed in the last decade, aligning with recent therapeutic innovations.


2. Scope of the Patent

The scope of IL249651 covers a specific pharmaceutical compound, formulation, or method of use. The breadth depends on how claims are drafted — broadly, they may encompass:

  • Chemical Composition: Specific molecular structures or subclasses.
  • Use Claims: Therapeutic indications, such as treatment of a disease or disorder.
  • Manufacturing Processes: Unique methods of synthesis or formulation.
  • Combination Therapy: Use alongside other drugs or in specific dosing regimens.

In general, Israeli patents are expected to follow a balance between broad claims and detailed specific embodiments to safeguard against workarounds while maintaining enforceability.


3. Detailed Claims Analysis

Although the full content of IL249651 is proprietary, typical claims in such pharmaceutical patents often exemplify:

  • Independent Claims: Broadly defining the novel compound or therapeutic method. For instance, “A compound of formula X, or a pharmaceutically acceptable salt or ester thereof, for use in treating condition Y.”
  • Dependent Claims: Narrower, elaborating specific embodiments, such as particular dosage forms, combinations, or methods of synthesis.

The strength of these claims hinges on their novelty, inventive step, and clarity. For IL249651, key claims likely focus on:

  • Structural Novelty: The unique chemical scaffold or modifications.
  • Therapeutic Efficacy: Demonstration of improved efficacy or reduced side effects.
  • Method of Treatment: Novel administration protocols or combination therapies.

From a legal perspective, highly specific claims protect against infringers but risk narrowing patent scope, while broader claims increase territorial and functional protection but may face validity challenges during examination or litigation.


4. Patent Landscape Analysis

The patent landscape surrounding IL249651 depends on several factors:

  • Prior Art Searches: Identification of existing patents, publications, or clinical data that predate IL249651. The landscape includes patents from major jurisdictions such as the US, EPO, and PCT filings.
  • Competitor Patents: Other patents targeting similar chemical entities or therapeutic targets. For example, if IL249651 covers a novel kinase inhibitor, related patents in cancer therapy may be relevant.
  • Freedom-to-Operate (FTO): Assessments conducted to evaluate whether IL249651 infringes on existing patents or whether others might infringe upon it.
  • Patent Families & Continuations: Related filings expand or narrow patent rights, affecting global protection.
  • Expiration and Maintenance: Patent lifespan influences market exclusivity. Typically, Israeli patents last 20 years from filing, with some extensions.

It’s noteworthy that the Israeli patent landscape mirrors global trends, especially considering Israel’s active participation in biotech and pharmaceutical innovation, with notable patent filings in oncology, neurology, and metabolic disorders.


5. Strategic Implications for Stakeholders

  • Pharmaceutical Companies: IL249651 could represent a key barrier or a licensing opportunity if the patent covers a promising therapeutic candidate.
  • Legal Practitioners: Patent claims' scope directly impacts patent validity and enforcement strategies.
  • Investors/Innovators: Understanding patent landscape dynamics informs risk assessments, licensing negotiations, and R&D investments.

Conclusion and Future Outlook

Patent IL249651 exemplifies the intricate balance between protecting innovative pharmaceutical compounds and navigating a complex patent landscape. Its claims likely aim to secure broad but defensible rights, influencing competitive dynamics within the Israeli and global markets.


Key Takeaways

  • Scope of IL249651 hinges on detailed structural and therapeutic claims designed for robust protection.
  • Claim Breadth influences enforceability; narrow claims offer strong protection but limited coverage, whereas broad claims risk validity challenges.
  • The Israeli patent landscape is active, especially in biotech sectors, with IL249651 positioned within this vibrant innovation ecosystem.
  • FTO analyses are essential to prevent infringement and identify licensing opportunities.
  • Patent lifecycle management, including expirations and continuations, directly impacts market exclusivity strategies.

Frequently Asked Questions (FAQs)

Q1: How does the scope of claims in IL249651 compare to similar patents in the biotech field?
A1: Typically, biotech patents aim for broad chemical or method claims to maximize protection; however, they face validity scrutiny if overly broad. IL249651's scope likely balances these considerations, providing substantial coverage while maintaining specificity.

Q2: What are common challenges faced during patent examination of pharmaceutical patents like IL249651?
A2: Challenges include demonstrating novelty over prior art, inventive step (non-obviousness), adequate disclosure, and clarity of claims. Patent examiners scrutinize whether the invention is sufficiently distinct and well-supported.

Q3: Could IL249651 potentially face infringement issues?
A3: Yes, if other entities develop similar compounds or methods within the patent’s claims. Conversely, patent holders must monitor the landscape to prevent infringement and enforce their rights.

Q4: What strategies can companies adopt around patents like IL249651?
A4: Strategies include securing complementary patents (e.g., formulations, methods), licensing, or challenging patent validity through post-grant proceedings if warranted.

Q5: How does Israeli patent law influence the enforceability of IL249651?
A5: Israeli law offers strong patent protections similar to the European system, with clear procedural frameworks for enforcement. Patent validity can be challenged via opposition or litigation, requiring robust patent drafting and maintenance.


References

  1. Israel Patent Office, Official Gazette, Patents Section.
  2. World Intellectual Property Organization (WIPO), Patent Landscape Reports.
  3. Global patent databases (e.g., Espacenet, Patentscope).
  4. Israeli Patent Law, 1967 (as amended).

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