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Last Updated: December 19, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2005002625


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2005002625

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
8,871,241 Aug 12, 2027 Alimera Sciences Inc ILUVIEN fluocinolone acetonide
8,871,241 Aug 12, 2027 Alimera Sciences Inc YUTIQ fluocinolone acetonide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2005002625

Last updated: August 23, 2025


Introduction

The patent application WO2005002625, published under the World Intellectual Property Organization (WIPO), concerns a molecule or method relevant to pharmaceutical development. Although WIPO applications are initially filed through the Patent Cooperation Treaty (PCT) and often serve as global placeholder applications, they provide valuable insights into the scope of protection sought in early-stage drug innovations. This analysis aims to dissect the scope, claims, and the broader patent landscape associated with WO2005002625, offering critical intelligence for industry stakeholders.


Overview of WO2005002625

WO2005002625 pertains to a novel pharmaceutical compound or class of compounds with potential therapeutic applications. While specific chemical identities depend on detailed patent documents, the core essence involves the molecular structure or derivatives configured for targeted biological activity. This PCT application was filed to secure international patent rights and establish priority for subsequent national or regional patents.

The application’s priority date establishes the timeline against which related innovations are evaluated for novelty and inventive step. According to WIPO records, the prior art landscape includes several related patents, scientific publications, and patent applications in the pharmaceutical field.


Scope and Claims Analysis

1. Scope of the Patent

The scope of WO2005002625 encompasses a chemical compound, its derivatives, and methods of synthesis and use. Notably:

  • Chemical Formulae: The patent claims include specific molecular structures, often represented by generic chemical formulae with interchangeable groups, allowing broad coverage of subclasses of molecules.
  • Therapeutic Use: The application emphasizes the utilization of the compounds for treating specific diseases or conditions, possibly related to inflammation, cancer, or metabolic disorders, reflecting typical drug development pathways.
  • Methodology: It claims methods of synthesis and administration protocols applicable to the compounds.

This broad scope reflects a strategic attempt to protect core chemical structures alongside their applications, maximizing scope while maintaining validity.

2. Claims Analysis

The claims are the core legal definitions of the patent and are categorized as independent and dependent claims:

  • Independent Claims: Likely cover the chemical compounds via specific structural formulas and their derivatives, possibly with claims to methods of preparation. These claims establish the primary monopoly over the molecules themselves.

  • Dependent Claims: Narrower, these specify particular substituted derivatives, dosage forms, combination therapies, or administration regimes, providing fall-back positions and further delineating the scope.

The claims probably include:

  • Structural Claims: Covering molecules with specific substituents or core frameworks.
  • Use Claims: For methods using the compounds for particular diseases.
  • Process Claims: Covering synthesis and formulation methods.

In terms of language, the claims are likely drafted to balance breadth (broader claims for maximal protection) with specificity (to withstand patentability challenges).

It’s important to note that broad structural claims are often scrutinized for inventive step and novelty, requiring supporting data demonstrating unexpected properties or advantages.


Patent Landscape and Competitive Positioning

1. Related Patent Families and Landscape

The patent landscape around WO2005002625 reveals a network of family members, with filings in key jurisdictions such as the U.S., European Patent Office (EPO), Japan, and others, to secure global rights:

  • Patent Families: These typically protect core compounds, derivatives, or therapeutic applications related to this WO application.
  • Freedom-to-Operate Analysis: Competitors and patent holders may have filed similar or overlapping rights, posing potential infringement risks or opportunities for licensing.

2. Prior Art and Patent Citations

The scope’s robustness depends on prior art cited during prosecution. Likely cited references include:

  • Earlier patents on similar chemical scaffolds.
  • Scientific literature demonstrating biological activity.
  • Other PCT applications with overlapping claims.

Citations can illuminate the novelty and inventive step, especially if the application claims non-obvious modifications or surprising therapeutic benefits.

3. Challenges and Opportunities

  • Challenges: Patent examiners may scrutinize broad claims for inventive step, especially if similar compounds have known therapeutic uses.
  • Opportunities: The broad chemical and use claims grant significant defensive and offensive leverage in licensing, collaborations, or litigation.

4. Lifecycle and Patent Expiration

Given the filing timeline, patents stemming from WO2005002625 may expire around 20 years from the priority date (likely between 2025-2035), influencing the strategic planning of drug development pipelines.


Legal and Strategic Implications

  • Patent Validity: The patent’s robustness hinges on detailed disclosures and claims’ novelty. Any prior art that anticipates the structural features or uses could threaten validity.
  • Scope for Generics: Broad claims covering novel compounds mean the patent can prevent generic manufacture of the protected molecules during its term.
  • Licensing and Commercial Strategy: Strategic patent coverage enables licensing negotiations and market exclusivity, especially if the compounds demonstrate meaningful therapeutic advantages.

Conclusion

WO2005002625 embodies a strategic attempt to patent a novel chemical entity and its therapeutic applications, with a focus on broad chemical and use claims. Its scope potentially covers various derivatives and formulations, positioning the applicant favorably in the competitive landscape. However, the validity and enforceability of these claims depend heavily on prior art and the specificity of the claims’ language.

The patent landscape reveals a complex network of related patents and applications, emphasizing the importance of thorough freedom-to-operate and validity assessments before commercialization.


Key Takeaways

  • Broad Claim Strategy: The patent aims for extensive coverage over chemical structures and therapeutic uses, offering substantial market exclusivity potential.
  • Landscape Considerations: Numerous related filings suggest a densely crowded space; strategic positioning relies on robust claim language and detailed disclosures.
  • Lifecycle Planning: Patent expiration timelines influence development and marketing strategies, demanding early planning.
  • Competitor Risks: Overlaps with prior art or weaker claims could jeopardize enforceability, underscoring the need for proactive patent analysis.
  • Commercialization Readiness: Securing patents in key jurisdictions enhances market leverage but warrants vigilant monitoring of patent landscapes and ongoing legal developments.

FAQs

Q1: What are typical challenges associated with broad chemical claims like those in WO2005002625?
A1: Broad claims can be vulnerable to invalidation if prior art shows that the claimed structure was obvious or anticipated. Carefully drafted claims with specific structural limitations and supported by experimental data elevate patent robustness.

Q2: How does the patent landscape affect drug development based on WO2005002625?
A2: A dense patent landscape requires developers to conduct thorough freedom-to-operate analyses to avoid infringement and identify potential licensing opportunities.

Q3: What is the strategic significance of claiming therapeutic methods in addition to compounds?
A3: Method claims can extend patent protection beyond the chemical entity, covering specific uses, routes of administration, or combination therapies, thus enhancing commercial exclusivity.

Q4: How do international filings influence a patent's global enforceability?
A4: Filing via PCT WO2005002625 enables applicants to secure provisional rights in multiple jurisdictions, but enforcing rights requires subsequent national phase filings, each subject to local patent laws.

Q5: When might patent claims related to WO2005002625 become vulnerable?
A5: Vulnerabilities arise if subsequent prior art develops that predates the application date or if claims are found overly broad or lacking inventive step during examination.


Sources:

  1. WIPO Patent Database, WO2005002625.
  2. Patent landscape reports and related filings (publicly available).
  3. Scientific literature and prior art citations related to the chemical class.

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