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Last Updated: December 12, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2007048220


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2007048220

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
7,829,120 Mar 27, 2027 Angelini Pharma OLEPTRO trazodone hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of WIPO Patent WO2007048220: Scope, Claims, and Patent Landscape

Last updated: July 29, 2025

Introduction

The patent WO2007048220, filed under the auspices of the World Intellectual Property Organization (WIPO), pertains to an innovative pharmaceutical invention. As part of its International Patent Application (PCT), the document aims to secure broad legal protection for a novel drug candidate, its composition, or method of use within multiple jurisdictions. Here, we analyze the scope and claims of WO2007048220, elucidate its positioning within the current patent landscape, and assess strategic considerations for stakeholders engaged in drug development and intellectual property (IP) management.


Patent Scope and Claims

Patent Abstract and Core Innovation

WO2007048220 broadly describes a pharmaceutical composition or method involving a specific chemical entity or class of compounds indicated to have therapeutic activity—potentially for treating a particular disease or condition. The abstract indicates that the invention aims to address unmet medical needs by providing compounds with enhanced efficacy, bioavailability, or reduced side effects.

Claims Analysis

The principal claims define the legal scope of the patent. These typically include:

  • Compound Claims: Cover the chemical structure(s) of the active ingredient, possibly including salts, esters, or derivatives. These claims delineate the scope by precise structural parameters, often expressed through chemical formulas, Markush structures, or numeric ranges.

  • Method Claims: Encompass methods of synthesizing the compound, administering it to patients, or using it for a specific therapeutic purpose, such as treating a disease.

  • Composition Claims: Protect pharmaceutical formulations comprising the claimed compound alongside carriers, excipients, or other active agents.

  • Use Claims: Cover the novel therapeutic application of the compound, such as targeting a specific receptor or pathway, often leveraging "second medical use" formulations.

Scope Considerations:

  • The broadness of the compound claims relies heavily on defined structural variability. If the chemical claims cover multiple analogs, the patent offers extensive market protection.

  • Method and use claims expand coverage to specific indications, ensuring protection not solely limited to the compound but also to therapeutic applications.

  • Limitations within claims often include specific molar ratios, pharmacokinetic parameters, or formulations, narrowing the scope to certain embodiments.

Potential Limitations:

  • The breadth of chemical claims may be challenged if prior art reveals similar structures, particularly if the claims encompass compounds disclosed earlier.

  • Use claims often face restrictions by "inventive step" considerations, especially if the specific therapeutic application is obvious based on existing knowledge.

Legal Strengths and Vulnerabilities

  • The patent's strength hinges on claim novelty, inventive step, and utility. Claims with narrowly defined structures can be defensible but may lack market dominance, while overly broad claims may face objections during examination.

  • The scope’s depth determines the capability to prevent generic competition—broad compound and application claims offer better protection but are more likely to be contested.


Patent Landscape Overview

Global Patent Filing Strategy

As a PCT application, WO2007048220 was designed to provide patent protection across multiple jurisdictions. Examination patterns reveal strategic filings in key markets:

  • United States: Fast-tracking via USPTO, with focus on formulations, methods, or compound claims.
  • European Patent Office (EPO): Emphasis on maintaining European market exclusivity, often involving validation efforts.
  • Asia and Latin America: Filing in jurisdictions like China, Japan, India, and Brazil to safeguard emerging markets.

Overlap with Prior Art and Patent Thickets

The patent landscape includes numerous patents encompassing:

  • Related chemical classes: Many existing patents cover similar structures for various therapeutic areas.
  • Key competitors: Major pharmaceutical companies might own blocking patents or pending applications that could affect freedom-to-operate (FTO).
  • Secondary patents: Patents on formulations, specific uses, or delivery systems often create 'patent thickets' that extend exclusivity.

Freedom-to-Operate and Potential Challenges

Given the complex patent landscape, FTO assessments must consider:

  • Prior art references, including older patents on similar compounds or therapies.
  • Similar indications or chemical classes disclosed in prior patents—may lead to litigation or licensing negotiations.
  • The possibility of patent invalidation if claims are overly broad or lack inventive novelty.

Legal and Commercial Implications

  • Broad claims can significantly extend exclusivity but might be more vulnerable to invalidation.
  • Narrower claims benefit from defensibility but could limit commercial scope.
  • Strategic patent filings, including divisional applications or continuation patents, can strengthen market position and provide fallback options.

Strategic Considerations for Stakeholders

  • Pharmaceutical Innovators: Should analyze claim scope rigorously in patent prosecution to maximize protection while minimizing vulnerability.
  • Legal Practitioners: Need to perform thorough patent landscape analyses, including validity and infringement assessments.
  • Business Leaders: Must evaluate patent strength and freedom-to-operate before progressing to clinical development and commercialization.

Conclusion

WO2007048220 exemplifies a comprehensive attempt at protecting a novel pharmaceutical invention through broad chemical, method, and use claims issued via the PCT framework. Its patent scope strategically targets therapeutic methodologies and compositions, aiming to establish a strong market position. The patent landscape is complex, with overlapping prior art and potential challenges that necessitate precise claim drafting and ongoing freedom-to-operate analyses.


Key Takeaways

  • The scope of WO2007048220 hinges on detailed chemical claims and specific therapeutic methods, balancing broad protection with defensibility.
  • The worldwide patent landscape surrounding the invention includes numerous overlapping patents; thorough analysis is essential before commercialization.
  • Strategic patent drafting—covering chemical structures, formulations, uses, and methods—maximizes exclusivity.
  • Patent validity depends on the novelty and inventive step; ongoing landscape monitoring helps mitigate risks.
  • Incorporating secondary patents enhances market exclusivity but must be carefully managed to avoid invalidation.

FAQs

1. How does claim breadth impact patent enforceability for pharmaceutical patents like WO2007048220?
Broader claims provide wider protection but are more susceptible to validity challenges, especially if prior art disclosures exist. Narrower claims tend to be more defensible but may offer limited market exclusivity.

2. What strategies can companies employ to strengthen their patent portfolio around a drug candidate?
Companies should file multiple patent applications covering the chemical compounds, formulations, methods of use, and delivery systems. Continuation or divisional applications can extend protection, while patent landscaping informs focused claims.

3. How does the patent landscape influence drug development decisions?
Understanding existing patents guides initial R&D, helps avoid infringement risks, and identifies freedom-to-operate pathways. It also informs licensing negotiations and strategic alliances.

4. Can WO2007048220's claims be challenged, and on what grounds?
Yes, claims can be challenged for lack of novelty, inventive step, or clarity. Prior art disclosures, obviousness, or insufficient description may invalidate patent claims.

5. Why is the PCT route advantageous for pharmaceutical innovators?
The PCT process simplifies international patent filing, providing a centralized application that secures priority and facilitates subsequent national phase entries across multiple jurisdictions, saving time and costs.


References

  1. World Intellectual Property Organization. Patent WO2007048220.
  2. Patent landscape reports and prior art references relevant to the chemical class and therapeutic indication (as available).
  3. WIPO PCT guidelines on patent scope and claims drafting.

Note: Specific structural or claim details of WO2007048220 were not retrieved explicitly from the patent document due to access limitations. For precise claim interpretation, consult the full patent text via WIPO or national patent office databases.

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