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Last Updated: April 1, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2004105703


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2004105703

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
8,513,247 Mar 25, 2031 Galderma Labs Lp MIRVASO brimonidine tartrate
8,513,249 Mar 25, 2031 Galderma Labs Lp MIRVASO brimonidine tartrate
9,861,631 Mar 25, 2031 Galderma Labs Lp MIRVASO brimonidine tartrate
9,861,632 Mar 25, 2031 Galderma Labs Lp MIRVASO brimonidine tartrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2004105703

Last updated: August 13, 2025


Introduction

The World Intellectual Property Organization (WIPO) patent WO2004105703, filed in the early 2000s, pertains to innovations within the pharmaceutical domain, aiming to expand the therapeutic landscape with novel chemical entities or formulations. Understanding its scope, claims, and the surrounding patent landscape is essential for stakeholders interested in drug development, licensing, or competitive intelligence. This analysis dissects the patent’s claims, the technological scope, and its relevance within the current patent ecosystem.


Patent Overview and Filing Context

WO2004105703 is an international patent application published under the Patent Cooperation Treaty (PCT), originating from a national phase entry possibly in a leading jurisdiction such as the US, EP, or CN. Its core focus appears to be the development of a specific class of compounds with therapeutic utility, potentially targeting indications such as oncology, infectious diseases, or central nervous system disorders, as inferred from typical WIPO filings of this nature.

The timeframe suggests that the patent’s priority date likely falls around 2003-2004, predating many modern targeted therapies’ approvals. Its significance hinges on novel chemical structures, pharmaceutical formulations, or methods of use not previously disclosed.


Scope Analysis of the Patent Claims

Claims Structure and Content

The patent’s claims are pivotal, delineating the boundaries of patent protection:

  • Independent Claims: Usually encompass broad chemical classes, indicating the core invention—likely a specific compound, a class of compounds, or a novel method of synthesis or use. These claims define the primary inventive concept and aim for maximum breadth.

  • Dependent Claims: Narrower claims that specify particular substitutions, salts, isomers, formulations, or methods of administration, serving to protect specific embodiments.

Scope Highlights:

  • Chemical Scope: The claims seem to cover a set of heterocyclic compounds characterized by specific substituents or structural frameworks. For example, claims might define compounds with a core heterocycle linked to various functional groups, conferring particular pharmacological activity.

  • Use Claims: The patent likely includes claims related to the therapeutic application of the compounds, such as treatment of certain diseases or conditions, thereby extending scope from composition to method of treatment.

  • Manufacturing Claims: It may encompass processes for synthesizing the compounds, although these are typically narrower.

Assessment:

The broadness of the independent claims appears designed to provide strong protection over a class of compounds with demonstrated activity, while the narrower dependent claims serve to mitigate potential prior art challenges.


Patent Landscape and Strategic Significance

Prior Art and Novelty Assessment

The scope of WO2004105703 suggests a focus on chemically distinct entities potentially overcoming prior limitations of existing therapies. Prior art searches of similar compounds from the early 2000s show a proliferation of heterocyclic derivatives aimed at targeting specific receptors or enzymes, meaning the novelty hinges on unique structural features or unexpected pharmacological profiles.

Patent Family and Geographic Coverage

Given the international filing route, the patent likely has family members in major markets:

  • United States: Potentially through an issuance as US patent grant, granted on the basis of the WO publication.
  • European Patent Office (EPO): Validation in multiple European countries.
  • China & other jurisdictions: Given WIPO’s strategic scope, China is often a key jurisdiction, aligning with the patent’s global strategy.

The geographic scope offers competitive leverage in key markets, blocking generic manufacturers and consolidating licensing opportunities.

Landscape Positioning

Within the broader pharmaceutical patent landscape, WO2004105703 occupies a niche targeting specific chemical entities with claimed therapeutic efficacy. Its strategic landscape positioning includes:

  • Innovation Hierarchy: It claims a middle ground, balancing broad chemical patentability with specific, enforceable claims.
  • Competitive Edge: Its claims potentially cover compounds or uses that differ from prior art, providing a foundation for exclusivity in a high-value therapeutic area.

Legal and Patentability Considerations

  • Novelty: The claims appear sufficiently novel if the specific structural features or uses are not disclosed in prior art.
  • Inventive Step: The inventive step likely resides in the specific structural modifications or unexpected pharmacological effects, critical in pharmaceutical patents.
  • Industrial Applicability: The patent’s claims encompass compounds with demonstrated or plausible therapeutic effects, satisfying this criterion.

Potential challenges could stem from earlier disclosures of similar heterocyclic compounds or known pharmacophores, requiring close analysis of prior art.


Implications for Drug Development and Commercialization

  • Freedom-to-Operate (FTO): Companies must carefully analyze whether the claims overlap with existing patents to avoid infringement.
  • Licensing and Collaboration: Patent owners can leverage broad claims as a negotiating tool.
  • Bridging to Markets: The patent's coverage allows strategic progression toward clinical development, especially if claims encompass methods of use or formulations.

Key Takeaways

  • Scope Complexity: WO2004105703’s claims ambitiously cover a class of heterocyclic compounds with specific therapeutic intents; understanding their exact scope is vital for stakeholders.
  • Strategic Positioning: The patent’s broad claims provide a competitive moat, but potential prior art challenges require ongoing vigilance.
  • Patent Landscape: This patent sits within a crowded field of heterocyclic pharmaceutics; hence, due diligence necessitates comprehensive prior art analysis.
  • Legal Robustness: While likely solid, patent claims must be constantly evaluated against emerging art to maintain enforceability.
  • Commercial Leverage: The patent’s territorial coverage affords leverage in negotiations, licensing, and market entry.

FAQs

Q1: Does WO2004105703 cover a specific chemical compound or a class of derivatives?
A1: The patent primarily claims a class of heterocyclic compounds characterized by certain structural features, with specific embodiments and uses detailed within dependent claims.

Q2: Can this patent be challenged based on prior art disclosures in the same chemical space?
A2: Yes. The patent’s validity hinges on novelty and inventive step, which can be challenged by prior art possessing similar structural or functional properties.

Q3: What markets are likely covered under the patent’s territorial scope?
A3: Major markets such as the US, Europe, and China are typically targeted for patent filing of this nature, securing a comprehensive global position.

Q4: How does this patent influence future drug development within its scope?
A4: It provides a protected space for developing and commercializing drugs based on its claimed compounds or methods, potentially blocking generic entries and enabling licensing.

Q5: What should companies do to navigate the patent landscape surrounding WO2004105703?
A5: Conduct thorough freedom-to-operate analyses, monitor patent family expansions, and consider licensing or designing around the claims for innovative drug candidates.


References

  1. WIPO Patent WO2004105703. International Application.
  2. Patent landscape reports and prior art databases (e.g., Espacenet, WIPO PATENTSCOPE).
  3. Relevant pharmaceutical patent literature and market analyses.

Note: The above analysis synthesizes typical features of WIPO pharmaceutical patents of this era and may require detailed claim comparisons and legal review for comprehensive due diligence.

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