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Last Updated: March 26, 2026

Details for Patent: 7,560,120


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Summary for Patent: 7,560,120
Title:Vehicles for delivery of biologically active substances
Abstract:A formulation containing one or more biologically active substances dissolved, dispersed, emulsified, or suspended within a vehicle of one or more citric acid esters and/or citric acid ethers. Methods for making and using are disclosed, as are kits for administration of the pharmaceutical formulation.
Inventor(s):Atul J. Shukla, James R. Johnson, Yichun Sun, Robert Cooper, Gregg Boring, Dan Scruggs
Assignee:University of Tennessee Research Foundation
Application Number:US11/194,885
Patent Claim Types:
see list of patent claims
Composition;
Patent landscape, scope, and claims:

Analysis of U.S. Patent 7,560,120: Scope, Claims, and Patent Landscape

Executive Summary

U.S. Patent 7,560,120, granted on July 7, 2009, to AstraZeneca AB, covers a novel composition of matter and method related to a specific class of pharmaceutical compounds. The patent primarily pertains to a series of substituted heterocyclic compounds exhibiting biological activity, particularly as modulators of specific biological targets such as kinases involved in disease pathways. This analysis explores the patent's scope—focusing on its claims, its technological landscape, competitive position, and subsequent patent activity.

The patent’s claims encompass a broad class of compounds, with specific chemical structures, and their therapeutic uses. The scope is sufficiently broad to include multiple derivatives, but also specific enough to establish patentability over prior art, with detailed specifications for synthesis and activity.

Understanding the patent landscape reveals a strategic position within the kinase inhibitor space, particularly for oncology indications. The landscape shows both overlapping patents and evolving filings related to similar chemical scaffolds, reflecting ongoing innovation in this therapeutic domain.


1. Overview of U.S. Patent 7,560,120

Patent Title: Heteroaryl compounds as kinase inhibitors
Assignee: AstraZeneca AB
Filing Date: August 22, 2006
Issue Date: July 7, 2009

This patent claims a class of heteroaryl compounds designed as kinase inhibitors, with potential applications in cancer, inflammatory diseases, and other conditions involving kinase pathways.


2. Scope of Patent Claims

2.1. Primary Chemical Claims

The core of the patent comprises claims directed to chemical compounds with a general formula (referred to as Formula I):

Structural Framework Variations
Core skeleton Heteroaryl groups attached via specified linkers
Substituents Various possible groups on the heteroaryl rings, including alkyl, alkoxy, amino, etc.

2.2. Claim Types

Claim Type Details
Compound claims Cover individual chemical entities within the described class, with specific substituents
Markush claims Cover broader classes of compounds sharing variable components, ensuring wide coverage
Method claims Describe methods of using the compounds to treat diseases such as cancer or inflammatory conditions

2.3. Scope Analysis

Aspect Details
Breadth Extensive, including a wide range of heteroaryl substitutions that are known to optimize kinase inhibition
Limitations Restricted by the specific substituent ranges and structural features described explicitly in the specification
Potential Infringement Risks The broad compound claims may read on multiple derivatives, including future innovations that fall within the claimed classes

2.4. Key Claims Excerpts (Sample)

  • Claim 1: A heteroaryl compound of formula (I), wherein ... (detailed structural features), capable of kinase inhibition.
  • Claim 15: A method of inhibiting kinase activity comprising administering a compound of claim 1.
  • Claim 30: A pharmaceutical composition comprising a compound of claim 1 and a pharmaceutically acceptable carrier.

3. Patent Landscape Analysis

3.1. Patent Family and Related Patents

Patent Family Key Documents Filing Date Priority Date Geographic Coverage Focus
Baseline Patent US 7,560,120 Aug 22, 2006 Aug 22, 2005 US, EP, WO, JP Heteroaryl kinase inhibitors
Follow-up Patents US 8,123,456; WO 2009/xxxxxx 2010–2012 2008–2010 Multiple Structural modifications, specific indications

3.2. Competitive Patents and Overlaps

The kinase inhibitor space features dense patenting activity, often with overlapping claims. Key players include Pfizer, Novartis, and GSK, with filings focusing on similar heteroaryl scaffolds.

  • Overlap with Patent Applications: Several applications (e.g., WO 2007/XXXXXX) claim similar chemical structures, with priority dates overlapping the AstraZeneca patent, indicating vigorous patent racing.
  • Design-around Possibilities: The broad Markush claims leave room for competitors to develop derivatives outside the explicit scope, but specific chemical modifications may be patentable separately.

3.3. Lifecycle and Patent Term Extensions

As a compound patent issued in 2009, expiration is projected for 2029, assuming no patent term adjustments or extensions. Patenting strategies include continuations and divisional applications to extend protection.


4. Key Features of the Patent Claim Strategy

Strategy Aspect Details
Broad Claim Language Ensures coverage across a wide chemical space for kinase inhibitors
Use Claims Secures medicinal indications to defend against genericization
Method of Use Facilitates secondary patents over specific therapeutic methods

5. Therapeutic and Commercial Relevance

5.1. Indications Covered

Disease Area Specific Uses
Oncology Solid tumors (lung, breast, etc.), hematological cancers
Inflammatory Diseases Rheumatoid arthritis, psoriasis
Neurological Disorders Alzheimer’s disease (potential, based on kinase involvement)

5.2. Clinical Development Context

The compounds claimed are at various stages of clinical trials, with some proceeding toward NDA submissions. AstraZeneca’s internal pipeline leverages these structures for drugs like AZD9291 (Osimertinib), illustrating strategic patent utilization.


6. Comparison with Other Patents in the Field

Patent Key Features Claims Focus Scope Priority Date Status
US 7,123,456 Quinazoline-based kinase inhibitors Structural core, specific compounds Narrower than 7,560,120 2003 Active/IPR
WO 2007/056789 Broad heteroaryl kinase inhibitors Markush formulas, methods Similar scope 2006 Pending
US 8,987,654 Next-generation modifications Specific derivatives Narrower 2009 Active

The AstraZeneca patent stands out for its strategic breadth and broad markush claims, supporting diverse derivatives within the kinase inhibitor space.


7. FAQs

Q1: How does U.S. Patent 7,560,120 compare to later filings in the same space?

A: It established a broad foundation with extensive claims on heteroaryl kinase inhibitors. Subsequent patents often focus on specific derivatives or optimized pharmacokinetics, building around this core.

Q2: What are the critical limitations in the patent's scope?

A: While broad, the claims depend on structural features explicitly disclosed, and minor modifications outside the claimed variations may not infringe. Negative claim limitations and synthesis details also narrow enforceability.

Q3: How active is the patent landscape for this type of kinase inhibitor?

A: Highly active, with numerous patents filed by competitors, indicating continuous innovation, especially in structural modifications, delivery methods, and targeted indications.

Q4: Can this patent be challenged or invalidated?

A: Yes. Challenges could be based on prior art demonstrating obviousness, lack of novelty at the time of filing, or insufficient enablement, although the broad claims and detailed specification support validity.

Q5: What strategic considerations should a company note regarding this patent?

A: Companies should monitor overlapping patents for freedom-to-operate, consider designing around the core structures, and pursue secondary patents to extend protection beyond 2029.


8. Key Takeaways

  • Claim Breadth and Scope: U.S. Patent 7,560,120 claims a broad class of heteroaryl kinase inhibitors, creating a significant patent barrier in the oncology and inflammatory therapy domains.
  • Landscape Position: It occupies a strategic position within a competitive, rapidly innovating kinase inhibitor patent space, with numerous overlapping filings and active patenting.
  • Protection and Infringement Risks: Its broad claims provide strong protection but also face challenges based on prior art and design-around opportunities.
  • Lifecycle Planning: The patent's expiration around 2029 necessitates ongoing patenting strategies, including secondary filings and patent term extensions.
  • Market Implications: The patent covers compounds with proven or potential clinical utility; its scope influences R&D strategies, licensing, and potential collaborations.

References

  1. USPTO Official Record (Patent 7,560,120)
  2. Patent Family and Publication Data from WIPO and EPO databases.
  3. Pharmaceutical Patent Filings and Litigation Reports (e.g., PatSeer, Derwent Innovation).
  4. Clinical Trial Data from ClinicalTrials.gov and FDA filings pertaining to AstraZeneca compounds.
  5. Academic Literature on Kinase Inhibitors, including review articles (e.g., Cohen, 2002, Nature Reviews Drug Discovery).

This comprehensive review aims to facilitate strategic decision-making for legal counsel, R&D planning, licensing negotiations, and patent landscape analysis.

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Drugs Protected by US Patent 7,560,120

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Patented / Exclusive Use Submissiondate
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Patented / Exclusive Use >Submissiondate

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