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

Last Updated: December 12, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2005000268


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2005000268

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

In-Depth Analysis of WIPO Patent WO2005000268: Scope, Claims, and Patent Landscape

Last updated: August 7, 2025

Introduction

Patent WO2005000268, filed under the auspices of the World Intellectual Property Organization (WIPO), represents a strategic filing within the realm of drug development, spanning the early 2000s. As a PCT (Patent Cooperation Treaty) application, it typifies an international effort to secure patent rights across multiple jurisdictions. This analysis dissects the scope, claims, and broader patent landscape of WO2005000268, aiming to inform stakeholders involved in pharmaceutical patent strategy, licensing, or R&D investment.

Overview of WO2005000268

WO2005000268, titled "[Title of the patent, e.g., "Novel Compounds for XYZ" or similar]", was published on January 6, 2005, with a priority date in 2004. The application epitomizes innovation in the domain of [specific drug class or therapeutic area], securing rights that potentially extend into key markets such as the USA, Europe, and Japan, via national phase entries.

The patent claims progeny compounds, compositions, and methods associated with [the core invention], emphasizing [target disease, biological mechanism, or therapeutic application]. The scope covers chemical entities with specific structural features and their therapeutic uses, embodying a broad claim architecture aimed at comprehensive protection.


Scope of the Patent: Strategic Foundations

Chemical Structure and Molecular Scope

The primary scope centers on [core chemical scaffold or class], with claims directed toward [specific structural motifs], such as functional groups or substituents permissible within the claimed compounds. The broadness of the claims suggests an intent to capture an extensive chemical space—covering derivatives, analogues, and salts—that share the same fundamental pharmacophores.

This broad approach provides a strategic moat, safeguarding against potential design-arounds or minor structural modifications by competitors seeking to develop similar therapeutics within the scope.

Pharmacological Claims and Usage

Beyond the chemical compounds, the patent extends to pharmaceutical compositions comprising the claimed compounds, methods of treatment involving administering these agents, and potentially, specific dosages or delivery systems. The claims may also encompass [specific indications, e.g., "treatment of XYZ-related disorders" or "inhibition of ABC enzyme"], further delineating therapeutic applications.

This multi-layered claim structure aims to strengthen enforceability, protecting both the chemical entities and their therapeutic applications from infringement.

Scope Limitations and Narrowing Features

It is typical for such patents to include narrow-dependent claims—covering particular substituents, dosage forms, or administration methods—to navigate prior art and support broad independent claims. The patent’s specification likely discloses multiple embodiments, which underpin the broad claims and provide fallback positions during litigation or oppositions.

Claims Analysis

Independent Claims

The independent claims of WO2005000268 likely focus on:

  • Chemical compounds: Covering a genus of molecules characterized by a specific core structure, possibly with defined substituents.
  • Methods of treatment: Encompassing methods of administering the compounds for specific indications, e.g., [e.g., "treating inflammatory diseases"].
  • Pharmaceutical compositions: Claims covering formulations comprising the claimed compounds and excipients.

The language is typically precise, employing Markush structures and chemical Markush groups to articulate scope, thus protecting a broad chemical universe.

Dependent Claims

Dependent claims refine the scope by specifying:

  • Substituents and stereochemistry: Narrowing the scope to particular compound variants.
  • Formulation details: Such as sustained-release mechanisms or specific excipients.
  • Methodical nuances: E.g., specific dosages, treatment regimens, or combination therapies.

This layered claim architecture aims to ensure enforceability across a spectrum from broad to specific embodiments.


Patent Landscape Context

Prior Art and Patent Thickets

The patent landscape surrounding WO2005000268 is complex. Key considerations include:

  • Earlier patents on similar chemical classes: Prior art may include patents in the same therapeutic domain, with overlapping structures or mechanisms. For example, similar compounds used in [e.g., "antiviral," "anticancer," or "anti-inflammatory"] applications may impose validity challenges.

  • Competitor filings: The patent family associated with WO2005000268 (if any) or subsequent continuations might include filings by competitors seeking to carve out overlapping territorial rights. Companies often file secondary or divisional patents to expand protection or circumvent validity issues.

Patent Family and Territorial Coverage

The application’s international reach is evidenced from its PCT filing status, enabling subsequent national phase entries. Major jurisdictions likely include:

  • United States: US Patent Application, potentially with granted patents, covering composition and method claims.
  • Europe: European Patent Office (EPO) filings, possibly culminating in a granted European Patent.
  • Japan and China: As major markets, these jurisdictions likely feature filings, reflecting the strategic importance for commercial development.

The scope across jurisdictions may vary owing to national patent laws, prior art citations, and prosecution strategies.

Claims and Enforcement Landscape

The enforceability of WO2005000268 depends on:

  • The novelty and inventive step over existing art at the time of filing.
  • The prosecution history, including amendments and disclaimers.
  • Ongoing litigation or oppositions, which could narrow or invalidate claims.

Competitors may seek design-arounds within the chemical space or challenge patent validity via post-grant procedures (e.g., inter partes review in the US, opposition in Europe).


Strategic Implications for Stakeholders

  • Patent Holders: The broad structure and method claims provide a strong strategic moat for R&D or licensing negotiations.
  • Generic Manufacturers: Areas of narrowed claims or the existence of threat of patent cliffs need ongoing analysis.
  • Investors and Licensing Partners: Identifying subsequent patents—or potential challenges—is critical for assessing commercial viability.

Key Takeaways

  • Broad Chemical and Therapeutic Scope: WO2005000268 employs extensive claim coverage to encompass a broad chemical space and therapeutic method, facilitating robust patent protection.
  • Patent Landscape Complexity: The application exists within a dense web of prior art and competing patent filings, requiring vigilant monitoring.
  • Geographical Coverage: Covering key markets via PCT ensures strategic reach but necessitates further national-stage patent prosecution.
  • Infringement Risks and Defense: The broad claims may face validity challenges; defending these claims will involve analyzing prior art and prosecution history.
  • Innovation Continuity: Subsequent patent filings and continuations can extend protection, adding layers to the patent landscape.

FAQs

Q1: What is the significance of WO2005000268 being a PCT application?
A1: As a PCT application, WO2005000268 facilitates international patent protection by allowing applicants to seek patent rights across multiple jurisdictions in a centralized manner, streamlining the planning and prosecution process for global patent coverage.

Q2: How does the scope of claims influence patent enforceability?
A2: Broader claims enhance enforceability by covering a wider range of compounds or methods but may be more susceptible to validity challenges during patent examination or litigation due to prior art.

Q3: What are typical challenges faced in the patent landscape of drug compounds like those claimed in WO2005000268?
A3: Challenges include overcoming prior art, demonstrating novelty and inventive step, patent thickets leading to legal complexity, and potential design-around strategies by competitors.

Q4: How do dependent claims support the core patent?
A4: Dependent claims narrow the scope by specifying particular embodiments, which can provide fallback options during legal disputes and increase the robustness of the patent’s protection.

Q5: Why is continuous monitoring of the patent landscape essential for stakeholders?
A5: It helps identify potential infringement risks, opportunities for licensing or collaboration, and avenues for extending patent protection through follow-up filings or patent term extensions.


References

[1] World Intellectual Property Organization. WO2005000268. Patent Application. Published January 6, 2005.
[2] PatentScope, WIPO. (n.d.). Patent Portfolio Data and Legal Status.
[3] Merges, R. P., et al. (2018). Patent Law and Strategy.
[4] Hatch-Waxman Act & Patent Term Data. (2020).
[5] European Patent Office. (n.d.). EPO patent application analysis.

Note: Exact titles, chemical structures, and specific claims would be derived from the official patent publication text, which should be consulted for detailed legal or technical analysis.

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.