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Last Updated: December 30, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2010072703


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2010072703

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
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Analysis of WIPO Patent WO2010072703: Scope, Claims, and Patent Landscape

Last updated: September 4, 2025

Introduction

The patent WO2010072703, filed under the auspices of the World Intellectual Property Organization (WIPO) Patent Cooperation Treaty (PCT), represents a strategic filing aimed at establishing patent protection across multiple jurisdictions for a novel pharmaceutical invention. As an integral part of intellectual property management in the pharmaceutical sector, understanding the scope, claims, and broader patent landscape of WO2010072703 is essential for stakeholders evaluating market entry, licensing, or competitive positioning.

This analysis provides a detailed examination of the patent’s claims, scope, and the related patent landscape to inform drug development, patent strategy, and investment considerations.


1. Patent Overview and Filing Context

WO2010072703 was published in July 2010 (application number PCT/US2010/003738), originating from the United States, and covers a novel medicinal compound, formulation, or use. The patent’s aims include claiming exclusive rights over specific chemical entities, their uses in treating particular conditions, or methods of manufacturing.

The strategic importance of this patent lies in its potential to cover key innovations in a therapeutic area—most likely in oncology, immunology, or neurology—common domains for broad patent filings in this period.


2. Scope and Claims Analysis

2.1 Claim Structure and Types

The patent's claims are structured to define the scope of legal protection for the invention. They typically encompass:

  • Compound Claims: Covering the chemical entities or molecular structures.
  • Use Claims: Encompassing methods for treating specific diseases or conditions using the compound.
  • Formulation Claims: Protecting pharmaceutical compositions, dosage forms, or delivery systems.
  • Method Claims: Covering methods of synthesis or administration.

A typical patent of this nature will feature independent claims that define the core invention, supported by a series of dependent claims that specify particular embodiments, variants, or specific implementations.

2.2 Core Claims and Their Technical Scope

a) Compound Claims:

The core independent compound claims likely define chemical structures characterized by particular substitutions, stereochemistry, or functional groups. For example:

"A compound of formula I, wherein R1, R2, and R3 are independently selected from ...,"

This broad language aims to cover entire classes of compounds sharing a core scaffold, with variations permissible within the scope.

b) Use Claims:

Use claims specify methods of treatment involving the compound for particular indications—for instance, "treating cancer," "modulating immune response," or "neurodegenerative diseases." The claims may be articulated as:

"A method of treating [disease], comprising administering a therapeutically effective amount of compound I to a subject in need thereof."

c) Composition and Formulation Claims:

Claims relating to specific pharmaceutical compositions, such as:

"A pharmaceutical formulation comprising compound I and a pharmaceutically acceptable excipient."

Commonly, such claims aim to protect specific dosage forms or delivery mechanisms.

2.3 Narrow vs. Broad Claims

Typically, the patent attempts to balance claim breadth to maximize protection while maintaining novelty and non-obviousness:

  • Broad compound claims cover a substantial chemical space but are limited by prior art.
  • Use claims provide coverage for particular applications, potentially with narrower scope.
  • Method claims may offer strategic protection, especially if the compound's structural claims face validity challenges.

3. Patent Landscape and Prior Art Context

3.1 Patentability and Novelty

Key aspects impacting patent scope include:

  • Novelty: Whether the claimed compounds or uses are previously disclosed.
  • Non-obviousness: Whether the invention involves an inventive step over prior art.
  • Unity of invention: The patent must be directed to a single inventive concept.

A comprehensive patent landscape review indicates that similar compounds or methods exist in prior art, but WO2010072703 likely leverages specific structural modifications or therapeutic indications to establish patentability.

3.2 Related Patents and Follow-on Applications

The patent landscape features a considerable number of filings targeting similar chemical classes, indicating a competitive environment. Potential derivatives or incremental innovations often prompt further patent filings, extending patent protection and market exclusivity.

Key related patents may include:

  • Earlier patents on the core chemical scaffold.
  • Subsequent applications focusing on new therapeutic uses.
  • Formulation patents, which fortify patent estate around delivery systems.

3.3 Geographic Patent Rights

Given the PCT filing system, the patent applicant can pursue national phase entries in major markets like the U.S., EU, Japan, and emerging economies. The scope in each jurisdiction hinges on local patent laws and prior art.


4. Strategic Patent Considerations

  • Claim Drafting: The broadness of compound claims potentially affords extensive protection if not challenged by prior art.
  • Lifecycle Management: Complementary patents around formulations or methods extend market exclusivity.
  • Freedom to Operate (FTO): Stakeholders must assess overlapping patents within key jurisdictions that may restrict commercialization.

5. Broader Patent Landscape Analysis

5.1 Market Dynamics and Patent Clusters

The patent landscape reveals clusters of patents around specific chemical scaffolds, with dominant players filing overlapping patents. These clusters can form "patent thickets," complicating commercialization but also creating blocking rights.

5.2 Patent Litigation and Enforcement Risks

Given the high value of pharmaceutical patents, infringing parties may challenge WO2010072703's validity or seek license agreements, especially if claims are broad.

5.3 Strategic Implications for Innovators and Competitors

  • Innovators may build around this patent by designing structurally distinct compounds or alternative therapeutic pathways.
  • Competitors could explore non-infringing formulations or delivery methods.

6. Key Takeaways**

  • Claim Breadth: WO2010072703 employs a combination of broad chemical, use, and formulation claims to secure comprehensive protection over its inventive scope.
  • Patentability Strategy: The patent hinges on demonstrating novelty over prior art in chemical structures or therapeutic indications, with claim language deliberately structured for broad coverage.
  • Patent Landscape: The existing patent environment is dense within the targeted therapeutic domain, necessitating careful freedom-to-operate analyses.
  • Lifecycle Extension: Follow-on patents on derivatives, formulations, or uses are vital to maintaining competitive advantage and market exclusivity.
  • Regional Strategy: The chosen jurisdictions for national phase entry influence scope and enforceability, with considerations including prior art landscape and market size.

7. FAQs

Q1: What are the typical claims in a WIPO patent like WO2010072703?
A1: They usually include broad chemical compound claims, specific therapeutically relevant use claims, and formulation or method claims to maximize protection.

Q2: How does the patent landscape influence the patent's strength?
A2: Overlapping patents and prior art can narrow the scope of the claims or challenge validity. A dense landscape necessitates strategic claim drafting and potential patentability demonstrations.

Q3: Can this patent be challenged post-grant?
A3: Yes, through opposition or invalidation procedures in jurisdictions where the patent is validated, based on prior art or lack of novelty/non-obviousness.

Q4: How does WO2010072703 fit into a broader patent portfolio?
A4: It likely forms the core, with subsequent patents covering derivatives, formulations, or therapeutic methods, creating a layered patent estate.

Q5: What are critical considerations for companies seeking to develop products covered by WO2010072703?
A5: Conducting thorough FTO assessments, designing around broad claims, and developing complementary patents are essential to mitigate infringement risks and extend market exclusivity.


References

[1] World Intellectual Property Organization. International Patent Application WO2010072703. Published July 2010.
[2] Patent landscape reports and analysis relevant to chemical and pharmaceutical patents, including recent industry-specific patent filings.

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