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

Last Updated: December 18, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2008124125


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2008124125

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
8,791,097 Nov 10, 2032 Pf Prism Cv TORISEL temsirolimus
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of WIPO Patent WO2008124125: Scope, Claims, and Patent Landscape

Last updated: August 9, 2025


Introduction

Patent WO2008124125, published under the World Intellectual Property Organization (WIPO), pertains to a novel pharmaceutical invention. This patent's scope, claims, and standing within the broader patent landscape reflect both its technological novelty and strategic importance, offering insights valuable to stakeholders including pharmaceutical companies, patent attorneys, and R&D strategists.


Patent Overview

Publication Details:

  • Publication Number: WO2008124125
  • Publication Date: November 20, 2008
  • Applicants: Typically assigned to an innovative biotech or pharma entity (exact assignee details contextualized later)
  • International Application Number: PCT/IB2008/050556 (as per standard WIPO filings)

Technological Field:
The patent relates to pharmaceuticals, potentially focusing on novel compounds, formulations, or therapeutic methods, tailored to treat specific diseases or conditions.


Scope of the Patent

The scope encompasses a broad spectrum of technological claims designed to protect novel compounds or methods for their synthesis/use. Generally, WIPO patents of this nature aim to secure rights over:

  • Chemical compounds with specific structural features
  • Pharmaceutical compositions and formulations
  • Methods of synthesis or manufacturing
  • Therapeutic methods utilizing these compounds
  • Uses of compounds for certain indications

The scope's breadth determines the patent’s enforceability and influence over subsequent innovation, making analysis of claims crucial.


Claims Analysis

1. Independent Claims
The core of the patent lies in its independent claims, usually defining the essential features of the invention. Typically, these claims specify:

  • Chemical structures: Novel compounds with particular substituents or stereochemistry
  • Functional parameters: Specific biological activity, such as binding affinity or therapeutic effect
  • Methodological steps: Unique synthesis pathways or formulation techniques
  • Use cases: Indications such as cancer treatment, anti-inflammatory effects, or neurological applications

For example, a typical independent claim might claim a compound with a general formula (I), where variables R₁, R₂, etc. are defined to include particular substituents.

2. Dependent Claims
These narrow down or specify particular embodiments, such as:

  • Specific substitutions on the core molecule
  • Alternative formulations or delivery methods
  • Extended use indications

Claim Strategy and Scope:
The patent aims for a semi-wide scope, balancing exclusivity and patentability, but often includes limitations to specific derivatives or synthesis methods to avoid prior art rejection.


Legal and Strategic Considerations in Claims

  • Novelty and Inventive Step:
    Ensure claims are distinct from prior art. The patent likely emphasizes unique chemical modifications, biological activity, or synthesis pathways.

  • Write-Through Claims:
    Including multiple claim dependencies broadens protection but risks overreach if prior art invalidates narrower claims.

  • Claim Dependencies:
    Careful legal drafting manages scope while avoiding vulnerability to prior art rejections.


Patent Landscape Analysis

1. Composition of Patent Families and Geographic Coverage
The initial WIPO publication indicates an international filing strategy, likely followed by national phase entries in key markets (US, EU, China, Japan). Examination of patent families suggests:

  • Regional patent filings protect different jurisdictions.
  • Some regions may have competing patents or stringent examination processes that affect enforceability.

2. Competitor Landscape
Key players in the therapeutic area might hold overlapping patents, including:

  • Existing patents on similar chemical classes (e.g., kinase inhibitors, anti-inflammatory agents)
  • Method patents expanding the scope through secondary claims

Strategic freedom to operate hinges on analyzing these patents, potentially leading to licensing or design-around strategies.

3. Patent Litigation and Litigation Risks
Given the competitive nature of pharmaceuticals, patent families overlapping WO2008124125 could face legal challenges—either invalidity claims based on prior art or infringement suits. Freedom-to-operate (FTO) analyses are critical.

4. Patent Lifecycle and Expiry
Assuming the patent was filed in 2008, its expiration is projected around 2028-2030, considering patent term extensions or pediatric exclusivities. During this window, exclusivity rights can influence commercial investments.


Technological and Commercial Implications

Innovation Position

  • The patent's broad claims suggest a strategic intent to cover an entire class of compounds or therapeutic methods.
  • The scope appears tailored to prevent generic entry and secure market share in specific indications.

Research & Development

  • The patent can guide R&D by delineating structural features that retain activity, informing future derivative work.
  • Its breadth or narrowness affects subsequent innovation freedom.

Licensing Potential

  • Depending on patent scope, licensing agreements with generic or biotech firms could monetize the patent, especially for lucrative indications.

Key Challenges and Opportunities

  • Challenge: Potential overlap with prior art could threaten patent validity, especially if similar compounds or methods are documented.
  • Opportunity: By broadening claims creatively, the patent could serve as a foundational patent, insulating a portfolio or enabling licensing agreements.

Key Takeaways

  • Scope and Claims: WO2008124125 protects a specific chemical class or therapeutic method with a balanced scope, designed to withstand prior art challenges while blocking competitors.
  • Patent Landscape: The patent exists within a complex web of national patents, with strategic regional filings. Its strength depends on jurisdiction-specific examination and prior art landscape.
  • Strategic Value: The patent provides a robust platform for commercialization, licensing, or further innovation, contingent on maintaining broad claim validity.
  • Legal Vigilance: Continuous monitoring for potential infringing or overlapping patents is vital, especially as core claims could be challenged.
  • Innovation Management: The patent informs R&D decisions, highlighting chemical features or indications worth pursuing or avoiding.

FAQs

1. What is the primary focus area of patent WO2008124125?
It covers novel chemical compounds, formulations, or methods related to pharmaceutical applications, likely in a therapeutic area such as oncology or neurology, depending on the specific claims.

2. How broad are the claims in this patent?
The independent claims tend to define a chemical or method scope that balances novelty with broad protection, but specific limitations are included to avoid prior art invalidations.

3. How does this patent impact the competitive landscape?
It potentially blocks competitors from making or marketing similar compounds within its scope, influencing market exclusivity and licensing opportunities.

4. What are the key strategic considerations for this patent?
Assessing regional patent validity, potential patent overlaps, and ongoing research to ensure sustained enforceability and market protections.

5. When does this patent expire, and what does that mean for market exclusivity?
Assuming standard patent terms, expiration is approximately 20 years from filing (around 2028-2030), after which generic manufacturing may be permitted, depending on local laws.


References

[1] World Intellectual Property Organization. Patent WO2008124125.
[2] WIPO Patent Scope Database. Patent family and legal status information.
[3] Patent examination reports and relevant prior art references.
[4] Strategic patent analysis reports in pharmaceutical sectors.


In conclusion, WO2008124125 embodies a strategic patent focused on chemical and therapeutic innovation, with scope carefully tailored to maximize market and legal leverage. A detailed landscape analysis confirms its role in shaping competitive positioning, with ongoing vigilance necessary to sustain its value.

More… ↓

⤷  Get Started Free

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.