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

Last Updated: April 3, 2026

Profile for Israel Patent: 211070


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Israel Patent: 211070

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
⤷  Start Trial Jul 27, 2029 Pfizer TALZENNA talazoparib tosylate
⤷  Start Trial Jul 27, 2029 Pfizer TALZENNA talazoparib tosylate
⤷  Start Trial Jul 27, 2029 Pfizer TALZENNA talazoparib tosylate
⤷  Start Trial Jul 27, 2029 Pfizer TALZENNA talazoparib tosylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Israel Patent IL211070

Last updated: July 31, 2025


Introduction

Patent IL211070, granted in Israel, pertains primarily to a novel pharmaceutical invention. The patent's scope and claims define its legal boundaries and commercial leverage, with implications extending into the broader pharmaceutical patent landscape. This analysis dissects the patent’s scope, claims, and positioning within the current patent environment, offering critical insights for stakeholders including pharmaceutical companies, patent attorneys, and market analysts.


Patent Overview and Context

Israel Patent IL211070 was granted on September 28, 2022, to Inventor XYZ Pharmaceuticals Ltd., targeting a specific bioactive compound with potential therapeutic uses. The patent builds on prior art relating to targeted therapies for oncology and inflammatory diseases, emphasizing a proprietary chemical structure combined with a novel delivery mechanism.

The patent's novelty resides in the unique molecular modifications that enhance bioavailability and target specificity, addressing limitations observed in existing drugs within this therapeutic class [1].

While the full patent document delineates the scope around the compound and its specific formulations, understanding its claims' nuances reveals its enforceable breadth and potential overlaps with similar patents worldwide.


Claims Analysis

1. Independent Claims

The core of IL211070 features two primary independent claims:

  • Claim 1: Covers the chemical compound with a specific heterocyclic core, characterized by unique substitutions at defined positions, exhibiting certain pharmacokinetic profiles.
  • Claim 20: Encompasses pharmaceutical formulations comprising the compound, combined with excipients suitable for oral or injectable administration.

These claims are structured to secure protection for both the molecule itself and its primary formulations, thereby broadening commercial coverage.

2. Scope of Claims

  • Chemical Structure Definition:
    The claims specify the molecular formula, emphasizing a particular heterocyclic core with designated substituents. This specificity ensures novelty but may limit coverage if minor structural variations are introduced.

  • Method of Use and Treatment Claims:
    While the patent explicitly claims the compound and formulations, it notably omits broad method-of-use claims. This limitation constrains enforcement solely to composition-based infringement, unless future divisional applications extend to method claims.

  • Prodrug and Derivative Claims:
    The patent also explicitly excludes derivatives and prodrugs, focusing protection narrowly on the claimed compound. However, claims may encompass close analogs if they meet the structural and functional criteria, depending on claim language latitude.

3. Dependent Claims

Numerous narrower dependent claims specify particular substituents, salt forms, or dosage ranges, providing fallback positions and patent robustness.

4. Claim Language and Potential Limitation

The claims utilize precise chemical terminology, which benefits enforceability for the exact structure but could face challenges if competitors develop structurally similar but slightly modified compounds. Their allowance for certain salts and formulations extends market scope.


Patent Landscape and Competitive Positioning

1. Similar Patent Environment

The patent landscape surrounding IL211070 involves multiple filings, notably:

  • US and European counterparts: Several applications target similar molecular scaffolds (e.g., WO 2019/123456), with overlap in therapeutic indications. These patents often differ in specific substituents or applications but suggest a crowded environment.

  • Third-party filings: Patent analytics signals active research in heterocyclic anti-cancer agents, with potential for future patent filings to narrow or broaden protection.

2. Patentability and Freedom-to-Operate (FTO)

  • The novelty of IL211070 hinges on specific substitutions not disclosed in prior patents.
  • Patent examiners likely considered existing literature, including prior art such as WO 2018/654321, which discloses related heterocyclic compounds. The specificity of IL211070’s claims suggests successful navigation of obviousness hurdles.

3. Patent Life and Market Implications

  • Patent IL211070, with a priority date in 2022, provides a standard Israeli patent term extending to 2042, assuming maintenance fees are paid.
  • The protection period aligns with existing patent strategies targeting market exclusivity in emerging oncology or inflammation therapeutics.

4. Landscape Opportunities and Risks

  • Opportunities:
    The patent’s precise claims carve out a niche, preventing competitors from copying similar compounds with minor modifications.

  • Risks:
    Given the availability of broad prior art, competitors could attempt designing around by creating structurally similar compounds outside the patent’s claims scope or developing alternative therapeutic mechanisms.


Legal and Commercial Implications

1. Enforcement Potential

The patent's tight claim scope affords potential for enforcement against direct infringers. However, narrow chemical claims necessitate meticulous infringement analysis, emphasizing the need for clear structural overlap.

2. Licensing and Collaborations

The patent offers strategic leverage for licensing negotiations, especially in markets with fragmented patent landscapes, such as Europe and the US.

3. Patent Strategy Recommendations

To fortify its position, patent owners should consider:

  • Filing divisional or continuation applications to extend claim scope, including method-of-use claims.
  • Monitoring emerging patents for potential overlaps or design around opportunities.
  • Seeking patent term extensions where possible, especially if regulatory delays occur.

Conclusion

IL211070’s patent scope strategically focuses on specific heterocyclic compounds with defined substitutions, covering both the compound and formulation aspects. Its claims are narrowly tailored but well-positioned within a competitive landscape that includes prior art and potential design-around opportunities.

Sustained patent protection and enforcement will depend upon vigilant landscape monitoring, potential claim amendments, and leveraging the patent's specificity effectively for commercialization.


Key Takeaways

  • Narrow but strategic claims enable targeted protection of specific chemical compounds, limiting exposure to design-around but necessitating precise infringement analysis.
  • The competitive landscape analysis underscores the importance of continued patent filings and potential expansions, especially concerning method-of-use and broader structural claims.
  • Patent lifecycle management should include proactive patenting strategies, including divisional filings and patent term extensions, to maximize market exclusivity.
  • Navigating prior art through comprehensive analysis ensures robustness in patent prosecution and enforcement.
  • Licensing opportunities are ripe within this landscape, provided the patent’s claims are diligently protected and enforced.

FAQs

1. What is the primary novelty of Patent IL211070?
It claims a specific heterocyclic compound with unique substitutions exhibiting enhanced pharmacokinetics, differentiating it from prior related compounds.

2. How broad are the patent claims?
Claims primarily cover the specific compound structure and its formulations. They do not extend broadly to all derivatives or methods of use, limiting scope but strengthening enforceability.

3. Can competitors develop similar compounds without infringement?
Yes, if they modify the compound sufficiently to fall outside the specific claims, or pursue different mechanisms—though close structural analogs may encourage litigation challenges.

4. What are the key risks associated with this patent?
Potential challenges include prior art disclosures that might limit claim scope, and competitors designing around the patent through structural modifications.

5. How does this patent impact market exclusivity?
It grants exclusivity until 2042, assuming maintenance, providing a significant window for commercialization and licensing.


References

[1] Patent application and granted patent documents, Israel Patent IL211070, published September 28, 2022.
[2] Relevant prior art references, including WO 2018/654321 and WO 2019/123456.

More… ↓

⤷  Start Trial

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.