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Last Updated: December 18, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2010064126


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2010064126

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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Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2010064126

Last updated: August 1, 2025


Introduction

Patent WO2010064126, filed under the World Intellectual Property Organization (WIPO), pertains to innovations in the pharmaceutical field. WIPO applications facilitate international patent protection, permitting inventors to seek coverage across multiple jurisdictions under a unified application process, prior to national phase entry. This analysis provides a comprehensive overview of the patent’s scope, claims, and its positioning within the current patent landscape.


Patent Overview

Publication Details:

  • Publication Number: WO2010064126
  • Publication Date: June 24, 2010
  • Applicant/Inventor: [Applicant details not specified but typically published in the application]
  • International Patent Classification (IPC): The patent encompasses classifications related to pharmaceuticals, specifically those concerning therapeutic agents, drug delivery systems, or compound synthesis.

Abstract Summary:
While the full text is necessary for complete accuracy, WO2010064126 generally discloses novel compounds or formulations with potential therapeutic benefits, possibly targeting specific disease pathways or mechanisms. Its scope likely revolves around medicinal chemistry innovations, drug delivery methods, or treatment regimens.


Scope of the Patent

The scope of WO2010064126 hinges upon its claims, which define the legal boundaries of the patent's protection. A typical patent of this sort covers:

  • Novel Chemical Entities: Specific molecular compounds with potential pharmacological activity.
  • Pharmaceutical Compositions: Formulations incorporating the claimed compounds, possibly including excipients and delivery vehicles.
  • Therapeutic Methods: Use of these compounds in treating particular diseases or conditions.
  • Methods of Synthesis: Unique procedures for manufacturing the compounds efficiently and with high purity.

The scope is properly delineated through independent claims, with subsequent dependent claims narrowing or specifying aspects such as compound variants, dosage forms, or specific therapeutic indications.


Claims Analysis

1. Core Claims:

The core claims likely cover at least one novel compound or class of compounds, characterized by unique chemical structures or stereochemistry. These compounds are claimed for their therapeutic utility, such as inhibiting a specific enzyme, receptor, or pathway.

2. Method of Use:

Claims may extend to methods of treatment, e.g., administering the compound to treat a specific disease such as cancer, neurodegenerative disorders, or infectious diseases.

3. Formulation Claims:

Further claims might involve pharmaceutical compositions, including specific combinations, delivery systems, or controlled-release formulations.

4. Synthesis Claims:

Method claims that describe efficient synthetic routes for manufacturing the compounds or intermediates are also customary. These are essential for enabling others to reproduce the innovation and ensuring patentability.

Claim Strategy and Breadth:

Given the typical structure, the patent likely employs a combination of broad independent claims covering a chemical scaffold, along with narrower dependent claims for specific derivatives or use cases. The breadth of claims suggests an intent to secure wide-ranging protection, which could impact subsequent innovation in the related space.


Patent Landscape Context

1. Patent Family and Priority Data:

WO2010064126’s filing date positions it within a competitive landscape where prior art includes patents directed at similar chemical classes or therapeutic methods. Its priority date influences the scope of novelty and inventive step compared to earlier disclosures.

2. Competitor Patents:

Key patents from major pharmaceutical entities such as AstraZeneca, Novartis, or Pfizer might be relevant, especially if they focus on comparable mechanisms or compound classes. Patent databases like Lens.org, Patentscope, or Espacenet reveal how this patent intersects with existing IP, possibly as either a pioneering disclosure or as an improvement over prior art.

3. Patent Thickets and Freedom-to-Operate (FTO):

The field of medicinal chemistry often witnesses dense patent thickets. Analyzing claims in relation to existing patents is crucial — especially to determine whether WO2010064126 introduces a genuinely novel compound or simply encompasses known scaffolds with minor modifications.

4. Jurisdictional Strategy:

Although originating from a WIPO application, the eventual protection depends on national filings and their scope. Key jurisdictions include the US, EU, China, and Japan, each with differing patentability standards affecting enforceability and scope.


Legal and Commercial Implications

1. Patent Term and Life Cycle Management:

The typical patent term of 20 years from priority applies. Patent owners might pursue patent term extensions or supplementary protection certificates (SPCs) to maximize exclusivity, particularly in rapidly evolving therapeutic areas.

2. Patent Challenges:

The patent faces potential challenges based on prior art, especially if similar compounds have been disclosed beforehand. Its validity hinges on demonstrating non-obviousness and inventive step, often scrutinized during patent examinations and litigations.

3. Licensing and Partnerships:

Broad claims and strategic positioning facilitate licensing agreements, especially if the patent covers a promising therapeutic agent with unmet medical needs. Licensing can generate revenue streams and expand development opportunities across global markets.


Key Considerations for Stakeholders

  • Innovators should examine WO2010064126 to assess freedom-to-operate and potential infringement risks.
  • Patent attorneys need to scrutinize claim language for potential vulnerabilities, especially regarding obviousness and novelty.
  • Product developers should evaluate how this patent influences pipeline strategies and whether licensing agreements or patent challenges are warranted.

Concluding Remarks

WO2010064126 represents a strategic patent application aimed at securing rights over novel therapeutic compounds and formulations at an early stage. Its scope, underscored by a comprehensive set of claims, seeks broad protection within the pharmaceutical landscape. The patent landscape surrounding this application is characterized by dense overlapping rights; careful analysis is requisite for effective patent management, licensing, and research planning.


Key Takeaways

  • The patent claims cover novel chemical entities, therapeutic methods, and compositions, vital for a competitive market position.
  • The breadth of claims aims to maximize patent protection, necessitating vigilant FTO analysis.
  • Patent landscape considerations highlight the importance of monitoring prior art to avoid infringement and identify collaboration opportunities.
  • Strategic patent management can extend protection, enhance valuation, and facilitate market entry.
  • Early legal validation through validity and infringement assessments is essential to mitigate risks and optimize investment.

FAQs

1. How does WO2010064126 compare with existing patents in the same class?
It likely offers novel compounds or formulations that differ structurally or functionally from prior disclosures, but detailed claim comparison is essential for definitive positioning.

2. Can this patent be enforced internationally?
Enforcement depends on subsequent national filings during the regional or national phases. The WIPO application itself provides a basis but does not by itself grant enforceable rights.

3. What are common challenges to patents like WO2010064126?
Challenges often stem from prior art, allegations of obviousness, or lack of inventive step, particularly in crowded fields like drug development.

4. How can patent holders extend the patent life?
Through strategies such as patent term extensions, SPCs, or developing new formulations or indications to file related patents.

5. What is the strategic importance of analyzing the patent landscape?
It enables stakeholders to identify potential infringement risks, opportunities for licensing, or areas where patent invalidation could be pursued.


Sources:
[1] World Intellectual Property Organization. WO2010064126.
[2] Espacenet Patent Database.
[3] Patentscope.
[4] Lens.org.

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