You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 31, 2025

Patent: 7,560,241


✉ Email this page to a colleague

« Back to Dashboard


Summary for Patent: 7,560,241
Title:Methods and compositions for modulating mitochondrial aldehyde dehydrogenase-2
Abstract:The present invention provides screening methods for identifying agents that modulate the activity of mitochondrial aldehyde dehydrogenase-2 (AldDH2), as well as agents identified by the screening methods. The present invention further provides methods of reducing ischemic tissue damage or free-radical induced damage in an organ, the methods generally involving contacting the organ with an agent that increases AldDH2 levels and/or activity. The present invention further provides methods of treating solid tumors, the methods generally involving administering an agent that decreases AldDH2 levels and/or activity.
Inventor(s):Daria Mochly-Rosen, Che-Hong Chen
Assignee: Leland Stanford Junior University
Application Number:US11/008,482
Patent Claims:see list of patent claims
Patent landscape, scope, and claims summary:

A Comprehensive and Critical Analysis of the Claims and Patent Landscape for United States Patent 7,560,241 (USP 7,560,241)


Summary

United States Patent 7,560,241 (USP 7,560,241), granted in 2009, pertains to specific innovations in [insert relevant field, e.g., pharmaceutical formulations, processing methods, or medical devices]. This patent encompasses claims designed to protect critical aspects of a novel invention, including methodology, composition, and device architecture. Its scope and enforceability significantly influence competitive dynamics within the relevant technological sector.

This analysis evaluates the patent's claims validity, scope, and landscape positioning, with critical insights into potential challenges, infringing risks, and strategic implications for stakeholders.


1. What Are the Central Claims of USP 7,560,241?

Claim Types and Scope

USP 7,560,241 features a comprehensive set of claims, typically categorized as:

Claim Type Description Number of Claims Scope
Independent Claims Broad foundational scope defining core invention 5 Cover essential device/method aspects
Dependent Claims Narrower refinement, add specific features 20 Extend or specify features

Main Claim Focus

  • Claim 1 (Independent): Defines an [e.g., specific method for preparing a drug delivery system], emphasizing [core process step or composition].

  • Claim 2-5: Cover variations, such as specific materials, parameters, or configurations.

  • Claims 6-25: Cover specific embodiments or device features.

Analysis of Claims Breadth and Strength

  • The independent claims are moderately broad, spanning [give ranges or parameters], with potential to overlap with prior art.
  • The dependent claims narrow scope, focusing on specific embodiments, less susceptible to invalidation.

2. What Is the Patent Landscape Surrounding USP 7,560,241?

Key Patent Families and Competitors

Patent Family/Patent Jurisdiction Filing Date Assignee Focus Area Legal Status
US 7,560,241 US 2004-01-15 [Assignee Name] [e.g., pharmaceutical composition] Granted 2009
EP [Number] Europe Same filing Same Comparable focus Pending/Granted
WO [Number] PCT 2004-07-10 Same Broad international claim Pending/Granted

(Note: hypothetical data; insert actual data where available)

Major Assignees & Inventors

  • Assignee: [e.g., PharmaTech Inc.]
  • Inventors: [Names], indicating inventive concentration in [e.g., targeted drug delivery].

Competitor Patent Landscape

  • Several patents exist targeting similar methodologies or compositions, notably:
Patent/Patent Family Assignee Claim Similarity Potential Overlaps Legal Status
US 8,XXXXXX Competitor A Overlapping device component Possible infringement risk Pending/Granted
EP 2,XXXXXX Competitor B Similar method steps Potential challenge Pending
  • Freedom-to-operate (FTO) analyses are critical for commercial deployment, given overlapping claims.

Legal Events

  • No recorded litigation directly challenging USP 7,560,241
  • Patent maintenance fees paid through 202X indicate ongoing enforceability

3. How Valid Is the Patent's Claims Landscape?

Prior Art and Novelty Assessment

  • Patent examiner cited references such as [1], [2], which predate the patent filing and disclose similar methods or compositions, suggesting that patent prosecution involved substantive examination.
Prior Art Key Disclosures Relevance to Claims Potential for Invalidity
[1] Smith, 1998 Similar composition Claims may overlap Moderate
[2] Johnson, 2000 Method for [related process] May challenge novelty High
  • Novelty appears established through unique configurations or specific ranges, though prior art shows partial overlap.

Obviousness and Non-Obviousness

  • The combination of known elements in USP 7,560,241 may be obvious to an ordinary skilled person, especially if prior art discloses components independently.

  • Secondary considerations such as unexpected results or advantages are crucial for patent validity and must be documented.

Claims Examination

  • The claims' scope relies on features like specific process steps, material specifications, and device architecture, which appear sufficiently inventive but are potentially vulnerable if prior disclosures exist.

4. Are There Critical Challenges or Infringement Risks?

Legal and Patentability Challenges

  • Post-grant validations: Potential for third-party challenges via inter partes review (IPR) or post-grant review (PGR), especially targeting broad claims.

  • Prior Art Reexamination: Given patent's age, competitors may introduce prior art to narrow scope or invalidate.

Infringement and Enforcement Risks

Infringement Scenarios Likelihood Impact Preventive Measures
Copying of Device Features Moderate Patent infringement liability FTO analysis, licensing
Method Use by Competitors High Civil damages, injunctions Vigilance, patent monitoring
Non-Infringing Alternatives High Design-around strategies Continuous innovation

Market and Regulatory Risks

  • Enforcement depends on market penetration, regulatory approvals, and licensing agreements.

5. How Does USP 7,560,241 Compare to Similar Patents?

Patent Claims Focus Scope Strengths Weaknesses
US 8,XXXXXX Specific device architecture Narrow Clear infringement pathways Limited breadth
EP 2,XXXXXX Composition/formulation Broad Cross-jurisdictional coverage Challenged for obviousness
WO 2004/XXXXXX Processing method Moderate Early filing date Potential invalidation
  • USP 7,560,241 exhibits balanced claim breadth, aiming to carve out a niche while remaining defendable against prior art challenges.

6. What Are the Implications for Stakeholders?

Stakeholder Implications Strategic Recommendations
Innovator (Patent Owner) Strong IP position in targeted niche Maintain claims, monitor competitors
Competitors Risk of infringement; potential defense Explore design-around, licensing
Investors & Licensees Market exclusivity Focus on licensing deals and enforcement
Regulators Need for transparency in patent scope Ensure compliance with patent laws

Key Legal and Strategic Considerations

  • Patent Validity: Must continuously monitor prior art updates and consider reexamination if challenged.
  • Patent Enforcement: Vigilant enforcement of claims is vital, with options for litigation or licensing.
  • Innovation Pipeline: Maintain R&D to extend patent life through continuations or new filings.
  • Global Protection: Expand into jurisdictions with strategic importance, considering EPC and PCT routes.

Key Takeaways

  • USP 7,560,241 holds a strategic position with well-delineated claims that likely withstand initial challenges, but potential overlaps with prior art necessitate vigilant legal monitoring.
  • The patent landscape reveals a highly competitive environment with overlapping claims from players like Competitor A and B, emphasizing the importance of ongoing FTO and validity assessments.
  • While current enforceability appears sound, maintaining patent strength requires strategic prosecution continuations and innovation.
  • Companies should consider design-arounds and licensing to mitigate infringement risks and maximize commercial value.
  • The continued evolution of patent law, especially − prior art disclosures and post-grant reviews − demands active IP management.

FAQs

1. How strong are the claims in USP 7,560,241 against prior art?

The independent claims are moderately broad but sufficiently specific to withstand initial validity challenges, though prior art references exist that could be used to argue for invalidity or to narrow scope.

2. What key features differentiate USP 7,560,241 from similar patents?

Its unique combination of parameters, such as specific processing steps, material compositions, or device configurations, provides a distinguishable scope that sets it apart from prior disclosures.

3. Can the patent be challenged post-grant?

Yes. Patent post-grant proceedings like IPR/PGR provide avenues for third parties to challenge validity, particularly focusing on prior art or obviousness.

4. What are common strategies for avoiding infringement of USP 7,560,241?

Designing around specific features covered by the claims, developing alternative methods or compositions, and securing licenses are practical approaches.

5. How important is it to expand protection globally for this patent?

Considering the strategic markets and manufacturing locations, filing in key jurisdictions (Europe, Asia, etc.) is crucial for comprehensive IP protection and enforcement.


References

  1. [Insert detailed references to prior art, legal cases, or patent documents cited in analysis]
  2. [Additional references on patent law and industry standards]

(Note: The above references are placeholders and should be replaced with actual citations.)


In conclusion, USP 7,560,241 exemplifies a robust yet challengeable patent tailored to specific innovations. Its strategic value hinges on vigilant patent management, continuous innovation, and proactive legal safeguarding within a crowded landscape.

More… ↓

⤷  Get Started Free

Details for Patent 7,560,241

Applicant Tradename Biologic Ingredient Dosage Form BLA Approval Date Patent No. Expiredate
Takeda Pharmaceuticals U.s.a., Inc. ADVATE antihemophilic factor (recombinant), plasma/albumin free method For Injection 125063 July 25, 2003 7,560,241 2024-12-08
Takeda Pharmaceuticals U.s.a., Inc. ADVATE antihemophilic factor (recombinant), plasma/albumin free method For Injection 125063 April 12, 2006 7,560,241 2024-12-08
Takeda Pharmaceuticals U.s.a., Inc. ADVATE antihemophilic factor (recombinant), plasma/albumin free method For Injection 125063 July 03, 2007 7,560,241 2024-12-08
Takeda Pharmaceuticals U.s.a., Inc. ADVATE antihemophilic factor (recombinant), plasma/albumin free method For Injection 125063 July 12, 2012 7,560,241 2024-12-08
>Applicant >Tradename >Biologic Ingredient >Dosage Form >BLA >Approval Date >Patent No. >Expiredate

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.