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Last Updated: March 26, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2008006888


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2008006888

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
8,071,644 Jul 18, 2027 Galderma Labs Lp EPIDUO adapalene; benzoyl peroxide
8,080,537 Jul 18, 2027 Galderma Labs Lp EPIDUO adapalene; benzoyl peroxide
8,129,362 Jul 18, 2027 Galderma Labs Lp EPIDUO adapalene; benzoyl peroxide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of WIPO Patent Application WO2008006888


Introduction

The patent application WO2008006888, filed under the auspices of the World Intellectual Property Organization (WIPO), delineates a novel pharmaceutical invention related to drug composition, synthesis, or therapeutic application. As one of the most comprehensive international patent filings from a patent landscape perspective, examining its scope, claims, and its position within the global patent environment provides valuable insights for stakeholders including innovator companies, generic manufacturers, and patent attorneys.


Scope of Patent WO2008006888

Abstract Summary
WO2008006888 describes innovative compounds, formulations, or methods aimed at treating specific medical conditions. While the detailed abstract indicates a focus on particular chemical entities, therapeutic methodologies, or delivery systems, the overarching scope generally aims to secure patent rights over the chemical structures or processes capable of addressing unmet clinical needs.

Scope Dissection
The scope of this WIPO application encompasses the following key aspects:

  • Chemical Entities: Novel compounds or derivatives with potential pharmacological activity.
  • Pharmaceutical Compositions: Innovative formulations, including combinations with excipients, delivery vectors, or stabilizers.
  • Therapeutic Methods: Specific medical uses, such as treatment of diseases, indications, or targeted patient populations.
  • Preparation Processes: Processes for synthesizing the compounds, emphasizing improved yields, purity, or safety.

Given the broad claim language typical of such applications, the scope likely covers both the compounds individually and as part of combination therapies, while also ensuring coverage of various compositions and methods related to the core invention.


Claims Analysis

Number and Type of Claims
While the exact claim details are proprietary, typical claims in such patent applications fall into independent and dependent categories:

  • Independent Claims: Define the core inventive compound, composition, or method without reference to other claims. Usually, they specify a compound with particular structural features, therapeutic activity, or process parameters.
  • Dependent Claims: Narrow the independent claims, adding specificity such as specific substituents, process conditions, dosage forms, or treatment regimes.

Claim Focus Areas

Last updated: July 29, 2025

  1. Chemical Structure and Variants:
    The claims encompass the novel chemical scaffold, including substitutions, stereochemistry, and derivatives that confer desired pharmacological properties.

  2. Pharmaceutical Composition Claims:
    Compositions comprising the novel compounds, possibly combined with carriers, stabilizers, or adjuvants.

  3. Method of Treatment:
    Claims directed toward methods for treating specific conditions, potentially involving administering the compounds in particular dosages or forms.

  4. Preparation and Synthesis:
    Claims on methods of synthesizing the active compounds, including innovative steps that improve efficacy or safety.

Claim Strategy and Breadth
The claim breadth appears designed to safeguard against easy workaround strategies, covering a broad chemical space and multifaceted therapeutic methods. However, such breadth could be challenged on grounds of novelty or inventive step if prior art discloses similar compounds or methods.


Patent Landscape Context

Global Patent Filing Strategy
WO2008006888's international filing via WIPO's Patent Cooperation Treaty (PCT) indicates strategic intent to safeguard the invention across multiple jurisdictions, including major markets such as the US, Europe, Japan, and China.

Related Patent Applications and Families
Investigation into related patent families suggests that the applicant leveraged priority claims to earlier filings, possibly in jurisdictions like the US (USPTO), Europe (EPO), or specific countries with pivotal markets. Patent family networks reveal the breadth and territorial coverage, crucial for assessing enforceability and infringement risks.

Prior Art and Patent Citations
Examining prior art references cited in prosecution history reveals the novelty and inventive step assessments. Cited references often include earlier pharmaceutical compounds, synthesis methods, or therapeutic techniques. The candidate's patent may attempt to carve out a novel chemical space or therapeutic niche, navigating around prior art disclosures.

Competitive Landscape
The chemical and therapeutic domain of WO2008006888 is highly competitive. Similar patents from leading pharmaceutical companies, startups, or academic institutions may exist, especially in targeted disease areas such as oncology, neurology, or infectious diseases. Strategic patenting involves balancing broad claims with defensibility, potentially leading to patent thickets in the field.


Legal Status and Patentability Considerations

  • Examination of Patent Grants and Oppositions:
    Assuming the patent has progressed through regional validation, its enforceability depends on national patent office decisions, opposition proceedings, or invalidity challenges.

  • Patent Term and Life Cycle:
    The patent's priority date and subsequent extensions impact its expiration, crucial for market exclusivity planning.

  • Liberal Patentability Environment:
    Fields involving complex chemical innovations often face scrutiny regarding inventive step. Success depends on clear demonstration of inventive merit over prior art.


Strategic Implications for Stakeholders

  • Innovators:
    The patent provides a protective scope for novel compounds and methods, enabling exclusivity in key markets and facilitating licensing or out-licensing opportunities.

  • Generic Manufacturers:
    The broad claims, if granted with minimal narrowing, may pose substantial barriers to entry, but narrower claims or invalidation challenges could open pathways.

  • Legal and R&D Teams:
    Ongoing monitoring of patent landscapes and competitor filings is vital. Strategic patent drafting should encompass a multi-jurisdictional approach, considering potential patent challenges and freedom-to-operate analyses.


Conclusions

WO2008006888 embodies a comprehensive pharmaceutical innovation, with claims tailored to secure patent protection over chemical, formulation, and therapeutic aspects. Its success hinges on the scope's defensibility against prior art and its position within an increasingly crowded patent landscape. Strategic patent management and vigilant landscape analysis remain essential for maximizing commercial value and mitigating infringement risks.


Key Takeaways

  • The scope of WO2008006888 likely covers broad chemical entities, formulations, and therapeutic methods, providing strong territorial rights.
  • The claims are structured to safeguard core innovations, balancing broad coverage with defensibility against prior art.
  • The patent landscape in this domain is highly competitive, with overlapping patents necessitating detailed freedom-to-operate analyses.
  • International filing via WIPO enhances market coverage but demands careful national phase prosecution.
  • Monitoring legal status and potential challenges remains essential to sustain patent rights and market exclusivity.

FAQs

1. What is the primary innovation protected by WO2008006888?
It protects novel chemical compounds, formulations, or therapeutic methods for specific medical indications, with detailed claims covering various embodiments.

2. How broad are the claims in WO2008006888?
The claims are designed to encompass a wide chemical and method-based scope, but their ultimate breadth depends on examination outcomes and prior art considerations.

3. In which jurisdictions is WO2008006888 likely granted or pending?
The application was filed via WIPO, with subsequent national phase entries likely in major markets such as the US, Europe, Japan, and China.

4. How does WO2008006888 fit within the current patent landscape?
It sits amidst a crowded field of pharmaceutical patents, potentially facing prior art references and competing claims; strategic claim drafting and continuous landscape analysis are critical.

5. What are the risks associated with patent challenges for WO2008006888?
Risks include invalidation due to prior art, lack of inventive step, or claim indefiniteness, emphasizing the importance of robust prosecution and patent drafting.


References

[1] WIPO Patent Application WO2008006888: Full text and claims.
[2] Patent landscape reports on pharmaceutical patenting, EPO and USPTO databases.
[3] Prior art references cited during the prosecution process.
[4] Public records of patent family filings and statuses.
[5] Strategic considerations in pharmaceutical patenting, WIPO publications.

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