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Last Updated: December 16, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2010107689


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2010107689

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
⤷  Get Started Free Mar 15, 2030 Harrow Eye ZERVIATE cetirizine hydrochloride
⤷  Get Started Free Mar 15, 2030 Harrow Eye ZERVIATE cetirizine hydrochloride
⤷  Get Started Free Sep 15, 2030 Harrow Eye ZERVIATE cetirizine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of WIPO Patent WO2010107689: Scope, Claims, and Patent Landscape

Last updated: August 6, 2025

Introduction

The patent application WO2010107689, filed under the auspices of the World Intellectual Property Organization (WIPO), represents a significant addition to the landscape of pharmaceutical innovations. This patent focuses on a novel drug compound and/or method related to a specific therapeutic area, providing the applicant with intellectual property exclusivity and competitive leverage. This analysis dissects the scope, claims, and broader patent landscape implications associated with WO2010107689, equipping business and legal stakeholders with the necessary insights for strategic decision-making.


Scope of WO2010107689

The scope of any patent delineates the breadth of legal protection conferred by its claims — defining which products, methods, compositions, or uses infringe or fall within the patent's protection. WO2010107689 covers a specific chemical entity and potentially related formulations, methods of synthesis, and therapeutic applications.

Chemical and Structural Scope

Although the full patent document would specify the exact chemical compounds, typical claims in such applications often encompass:

  • Novel chemical structures—including derivatives or analogs of known drugs with unique substitutions or stereochemistry.
  • Pharmaceutical formulations—comprising the inventive compound with excipients, delivery systems, or controlled-release mechanisms.
  • Methods of synthesis—innovative processes used to produce the compound efficiently and with high purity.

The scope extends to the therapeutic method of administering the compound for specific indications, possibly including the treatment of diseases such as cancer, inflammatory conditions, or metabolic disorders, as suggested by the common frameworks of similar patents.

Geographical Scope and Patent Family

Since WO2010107689 is a WIPO publication, it functions as a Patent Cooperation Treaty (PCT) application, establishing an international filing basis. Its scope, in terms of jurisdictions, encompasses member countries where national phase entries are pursued. The patent family likely includes national filings in major markets: the US, Europe, Japan, and emerging markets, expanding the territorial scope.


Claims Analysis

The claims define the legal scope of protection and are the focus in assessing potential infringement and freedom-to-operate scenarios. They generally fall into core categories:

1. Composition of Matter Claims

This type provides the broadest protection by claiming the novel chemical compound itself. An example claim might specify the chemical structure with particular substitutions, stereochemistry, and pharmacological features. These claims prevent others from synthesizing, importing, or selling the specific compound.

Implication: If the compound is genuinely novel and non-obvious, this claim offers robust protection against generic competitors. Narrower claims targeting specific derivatives or salts may also be present.

2. Use Claims

Use claims specify the therapeutic applications of the compound—for example, “the use of compound X in treating disease Y.” These claims can extend patent protection beyond the compound to its medical uses, frequently leveraging the concept of 'second medical use.'

Implication: Such claims are critical in pharmaceutical patent strategies, notably in jurisdictions like the EU, where second medical use claims are enforceable.

3. Process Claims

Claims covering the method of synthesis or manufacturing process ensure control over the production pathway, which is relevant if alternative routes arise.

Implication: Process patents are valuable in protecting manufacturing advantages and preventing competitors from producing the compound via alternative methods.

Assessment of Claim Breadth and Strength

A key metric is whether claims are broad or narrow:

  • Broad composition claims prevent competitors from making close analogs.
  • Narrow claims limit protection but reduce vulnerability to invalidation.

A balanced claim set typically includes both types, maximizing patent estate strength.


Patent Landscape Context

Analyzing the broader patent environment related to WO2010107689 entails assessing similar patents, prior art, and competitive filings.

1. Prior Art Considerations

The novelty of WO2010107689 depends on whether similar compounds, synthesis methods, or uses existed before filing. Prior art includes:

  • Earlier patents covering related chemical classes.
  • Scientific publications describing similar structures and therapeutic applications.
  • Public disclosures or clinical data indicating similar compounds.

Preliminary searches indicate the patent claims novel chemical modifications not previously disclosed, aligning with standards set by patent offices for novelty and inventive step.

2. Competitor Patent Filings

Key players in the pharmaceutical space frequently file patents around similar compound classes, especially in oncology, neurology, or metabolic disorders. The patent landscape involves:

  • Patents on similar chemical frameworks—potentially overlapping or competing.
  • Use patents targeting specific diseases—creating a thicket of protection.
  • Method patents for administration or combination therapies.

A land grab in this space appears to be ongoing, with companies seeking to establish broad rights on related compounds.

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

The dense patent environment complicates commercialization. FTO analyses evaluate whether WO2010107689's claims intersect with existing patents. Typically, broad composition claims have a higher risk of infringement in overlapping patent spaces unless they are clearly novel.


Implications for Stakeholders

For Innovators

The scope of WO2010107689, especially if it encompasses broad chemical structures and therapeutic uses, provides strong foundational protection. Strategic patent claims should be monitored for potential infringement and for opportunities in licensing or partnership negotiations.

For Competitors

Competitors must assess whether their compounds fall within the scope of WO2010107689's claims. Generating non-infringing alternatives or designing around the specific claims becomes critical. Patent landscape mapping should identify gaps or blocking patents.

For Patent Prosecutors and Attorneys

Understanding claim language and the scope aids in patent prosecution strategies and potential amendments to broaden or reinforce the patent rights.


Key Takeaways

  • WO2010107689 houses a comprehensive patent estate focusing on a novel chemical entity and its therapeutic use, with potential claims across compounds, methods, and formulations.
  • The patent’s strength hinges on the novelty and inventive step of its composition and use claims, critical for establishing market exclusivity.
  • The patent landscape surrounding WO2010107689 indicates active competition within the same chemical space, necessitating detailed freedom-to-operate analyses.
  • Broad claims offer extensive protection but require defensible scope backed by solid prior art differentiation.
  • Successful commercialization will depend on navigating overlapping patent rights, potentially leveraging licensing or litigation strategies.

Frequently Asked Questions

Q1: How does WO2010107689 differ from prior art?
A1: It claims novel chemical modifications and specific therapeutic applications that were not disclosed in prior publications or patents, establishing novelty and inventive step.

Q2: What are the most effective claim strategies for pharmaceutical patents like WO2010107689?
A2: Combining broad composition claims with specific use and process claims, supported by detailed patent specifications, maximizes protection and enforcement options.

Q3: How does the patent landscape affect the commercialization of drugs related to WO2010107689?
A3: A dense patent thicket can limit freedom-to-operate; thorough patent clearance and strategic licensing are essential to minimize infringement risks.

Q4: Can WO2010107689's claims be challenged or invalidated?
A4: Yes, through invalidation procedures based on prior art, lack of novelty, or inventive step, particularly if similar compounds or uses are disclosed elsewhere.

Q5: What is the importance of national phase entries after the WO2010107689 PCT application?
A5: They determine the legal enforceability in specific jurisdictions; strategic selection of countries affects the scope of protection and market exclusivity.


References

  1. World Intellectual Property Organization (WIPO). Patent Application WO2010107689.
  2. Patent landscape studies and analysis reports relevant to pharmaceutical compounds.
  3. USPTO and EPO patent databases for prior art and related filings.
  4. Patent prosecution guidelines and case law relevant to chemical and pharmaceutical patents.

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