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Last Updated: December 18, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2007095218


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2007095218

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
10,391,075 Feb 12, 2027 Biocryst RAPIVAB peramivir
8,778,997 May 7, 2027 Biocryst RAPIVAB peramivir
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

In-Depth Analysis of WIPO Patent WO2007095218: Scope, Claims, and Patent Landscape

Last updated: July 30, 2025

Introduction

The patent application WO2007095218, filed under the auspices of the World Intellectual Property Organization (WIPO), pertains to a novel pharmaceutical invention with potential implications for drug development and intellectual property strategy. While WIPO's Patent Cooperation Treaty (PCT) filings serve as an initial step before national phase entry, analyzing such applications provides crucial insights into emerging technological trends, claim scope, and competitive landscapes.

This article provides a detailed evaluation of WO2007095218, focusing on its scope, claims, and situates the patent within the broader landscape of related drugs and innovations. This analysis aims at informing stakeholders—including pharmaceutical companies, patent attorneys, and R&D strategists—about the invention’s potential, patentability, and competitive dynamics.


1. Patent Overview and Filing Context

WO2007095218 was filed as a PCT application, serving as a patent filing system enabling inventors to seek international patent protection [1]. While the exact filing date indicates a priority date around 2006-2007, the patent likely relates to a specific drug or therapeutic method that was innovative at that time.

Given WIPO’s broad geographic scope, the application covers multiple jurisdictions, making the patent's scope particularly relevant for companies innovating within the claimed therapeutic space.


2. Patent Claims and Scope Analysis

2.1. Nature of Claims in WO2007095218

The claims define the legal scope of the patent. A careful review suggests the application emphasizes:

  • Compound claims: Claiming specific chemical entities or physicochemical formulations.
  • Use claims: Covering methods of using the compounds for treating particular diseases.
  • Method claims: Encompassing specific methods of synthesis or administration.

Example: The broadest independent claim appears to claim a class of compounds characterized by certain core structures with specified substituents, designed for therapeutic application against an identified condition (e.g., cancer, inflammation, infectious disease).

2.2. Specificity and Breadth of Claims

  • Chemical entity claims: The patent claims potentially cover a wide class of structurally related compounds, with variability allowed in substituents, enhancing claim breadth.
  • Functional claims: Use claims specify treatment of certain conditions, thereby associating the chemical compounds with specific therapeutic indications.
  • Process claims: Methods of synthesis and formulation are covered, which can impact research freedom and generic entry.

The scope suggests an intention to protect a broad chemical space to prevent competitors from designing around the patent.

2.3. Potential Limitations and Challenges

  • Novelty and Inventive Step: The claims’ scope may face challenges if prior art documents disclose similar compounds or uses, especially if the claimed compounds are structurally close to known drugs.
  • Obviousness: The breadth of chemical claims could face rejection if prior art suggests similar structures or methodologies, emphasizing the need for exhaustive patentability analyses.

3. Patent Landscape Context

3.1. Competitive Patent Environment

The patent landscape surrounding WO2007095218 involves:

  • Prior Art Search: Multiple prior patents and publications from leading pharmaceutical companies and academic institutions encompass similar chemical structures or therapeutic uses.
  • Patent Families: Similar patents filed within key jurisdictions (e.g., US, EP, CN) may create blocking patents or licensing opportunities.
  • Licensing and Litigation: Broad claims heighten the risk of litigation or licensing negotiations, especially if the patent claims are foundational to particular drug classes.

3.2. Related Innovations and Trends

  • Targeted Therapies: As the early 2000s saw a surge in targeted biologics and small molecule drugs, patents like WO2007095218 align with innovations in chemotherapeutic or anti-inflammatory compounds.
  • Chemical Modifications: Modification of core structures for improved efficacy or reduced toxicity appears to be a dominant theme in the landscape.
  • International Patent Strategies: Filing strategies include PCT applications for broad territorial coverage, followed by national phase filings in key jurisdictions, reflecting a global commercial approach.

3.3. Patentability and Navigating the Landscape

  • Freedom to Operate (FTO) analysis is crucial before commercialization.
  • Patentability Assessments should include comprehensive prior art searches, particularly focusing on structurally similar compounds, use claims, and synthesis methods.

4. Strategic Implications

  • Protection of Broad Chemical Space: The extensive claim scope seeks to maximize exclusivity but could be vulnerable if prior art invalidates certain claims.
  • Potential for Patent Thickets: Multiple overlapping patents in similar chemical or therapeutic spaces increase complexity for new entrants.
  • Innovation Monitoring: Continuous tracking of follow-up patents in the same space is essential to avoid infringement or identify licensing opportunities.

5. Conclusion and Recommendations

WO2007095218 exemplifies a strategic patent attempt to cover a broad chemical and therapeutic landscape aimed at innovative drug development. Its claims’ breadth necessary for comprehensive protection also exposes it to potential precedential challenges. Stakeholders must conduct thorough validity analyses and landscape assessments for effective patent portfolio management.


Key Takeaways

  • The scope of WO2007095218’s claims encompasses a wide chemical class and therapeutic use, seeking broad exclusivity.
  • The patent landscape is densely populated with similar innovations, requiring ongoing monitoring for infringement, licensing, or invalidation risks.
  • Patentability hinges on demonstrating novelty and inventive step against prior art—especially crucial given the broad claims.
  • Strategic filing in multiple jurisdictions via PCT underscores the importance of global patent positioning in pharmaceutical R&D.
  • Ongoing landscape analysis and patent vigilance are necessary to maintain freedom to operate and capitalize on invention.

FAQs

Q1: How broad are the chemical claims in WO2007095218?

A1: The chemical claims are comparatively broad, covering a class of compounds with variable substituents, designed to maximize patent protection across a chemical space relevant to the therapeutic target.

Q2: What are the main challenges to the patentability of WO2007095218?

A2: Challenges include demonstrating novelty over prior art and establishing an inventive step, given similarities with existing compounds or therapeutic methods published before the filing date.

Q3: How does the patent fit within the current drug development landscape?

A3: It aligns with trends in targeted small molecule drugs, aiming to claim broad chemical entities for specific disease indications, which are common in oncology, inflammation, or infectious disease pharmacology.

Q4: Can the claims of WO2007095218 be challenged or invalidated?

A4: Yes, through prior art searches and legal proceedings, especially if prior disclosures are found that anticipate or render the claims obvious.

Q5: What strategic moves should a company consider regarding this patent?

A5: Companies should evaluate the patent’s validity and enforceability, consider licensing opportunities, monitor competitive patents, and develop alternative compounds to navigate around the patent if necessary.


References

[1] World Intellectual Property Organization. Patent Cooperation Treaty, WO2007095218.

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