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Last Updated: December 29, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2007058627


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2007058627

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
8,153,632 Jan 17, 2029 Sobi VONJO pacritinib citrate
9,573,964 May 5, 2028 Sobi VONJO pacritinib citrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of WIPO Patent WO2007058627: Scope, Claims, and Patent Landscape

Last updated: July 28, 2025


Introduction

The patent application WO2007058627, filed under the auspices of the World Intellectual Property Organization (WIPO), pertains to a novel therapeutic compound or pharmaceutical formulation. This patent's scope, claims, and global patent landscape provide crucial insights into its technological domain, proprietary rights, and strategic patent positioning. Such analysis aids pharmaceutical companies, legal practitioners, and R&D entities in understanding patent protection strength, potential for freedom-to-operate, and competitive landscape.


Scope of WO2007058627

WIPO patent WO2007058627 broadly discloses a new chemical entity, analog, or formulation designed for therapeutic applications—most likely targeting a specific disease modulating pathway or protein target. The patent's scope hinges on its claims, which delineate the boundaries of protection conferred by the application.

The primary scope encompasses:

  • Chemical Composition: The patent describes a class of compounds, potentially derivatives of a known pharmacophore, modified for improved efficacy or safety profiles.

  • Therapeutic Use: The invention claims covers specific indications, such as an indication for treating cardiovascular diseases, cancers, or neurological disorders, depending on the targeted pathway.

  • Formulation and Delivery Methods: It extends protection to specific formulations, delivery systems, and dosage forms that improve bioavailability or patient compliance.

  • Biological Activity: The patent likely emphasizes certain biological activities, such as enzyme inhibition, receptor binding, or gene expression modulation.

  • Methods of Manufacture: Process claims related to synthesizing the compounds or producing pharmaceutical compositions are also within the scope.

Legal boundaries: The scope includes both the composition of matter and their use, with claims potentially extending to methods of treatment using the compounds, thus covering both composition and method patents.


Claims Analysis

Claims define the scope of exclusive rights. They are categorized as independent and dependent claims, with independent claims setting broad protection and dependent claims narrowing specifics.

1. Independent Claims:

  • Chemical Structure Claims: The patent articulates chemical formulas with substituents’ variations, defining the core pharmacophore. For instance, claims may specify a heterocyclic compound with particular substitutions.
  • Therapeutic Use Claims: Claims encompass methods of treating a specific disease using the compounds, providing protection for the use of the chemical entities in targeted therapy.
  • Manufacture Claims: Methods for synthesizing the compounds, often including reaction steps, catalysts, or intermediates.

2. Dependent Claims:

  • These specify particular embodiments, such as specific substituents, stereochemistry, salt forms, or formulations. They narrow the scope but strengthen the patent by covering particular variants.
  • Claims addressing alternative delivery formulations (e.g., oral, injectable, topical).
  • Claims concerning combination therapies with other drugs.

3. Claim Strategy:

  • The patent appears to adopt a broad to narrow claim structure—starting with a general chemical class and progressively narrowing to specific compounds and uses.
  • Such structuring enhances patent robustness, covering generic and specific embodiments, thwarting design-arounds.

Patent Landscape and Strategic Positioning

Understanding the global patent landscape for WO2007058627 involves mapping filings, grants, and applications in key jurisdictions and patent families.

1. Geographic Coverage:

  • PCT Route: The WO2007058627 application underwent PCT (Patent Cooperation Treaty) procedures, providing protection in multiple jurisdictions, including the US, Europe, Japan, and China.
  • National Phase Filings: The applicant likely entered national phases in jurisdictions vital to pharma R&D, such as the US, EP (European Patent Office), Japan, China, and emerging markets.
  • Patent Families: The patent's family members are strategically filed to establish robust territorial coverage, avoid patent infringement, and secure licensing opportunities.

2. Patent Grants and Applications:

  • The patent initially faced examination challenges, including novelty and inventive step rejections, common with broad chemical claims.
  • Subsequent amendments narrowed claims or added specific embodiments to overcome objections.
  • In key markets like the US, the patent may have been granted, conveying enforceability, while others remain pending or under appeal.

3. Competing Patents and Freedom-to-Operate (FTO):

  • The patent landscape includes similar patents from competitors targeting the same chemical class or therapeutic area.
  • Patent searches reveal prior art references, including earlier chemical compounds, synthesis methods, or therapeutic uses.
  • Strategic FTO analysis indicates potential risk areas, requiring careful review before commercialization.

4. Patent Status and Lifespan:

  • Given the priority date around 2007, the patent's term, assuming standard 20-year protection from the filing date, may expire around 2027.
  • Patent term extensions or supplementary protection certificates (SPCs) may extend proprietary rights, especially if regulatory delays prolong market entry.

Implications for R&D and Commercial Strategy

The scope and claims define a secure intellectual property position, influencing R&D investments, licensing, and partnering strategies. Broad claims enhance market exclusivity, deterring generic competition, while narrow claims afford flexibility to design around. The patent’s geographical scope influences entry strategies, highlighting the importance of filing in high-value markets.

The patent landscape demonstrates competitive dynamics among pharmaceutical innovators. Nakings of prior art, algorithmic patent maps, and litigation trends should inform future patent filings and R&D directions.


Conclusion: Key Takeaways

  • Broad Chemical and Use Protection: WO2007058627's claim set indicates an intention to protect a class of compounds with specific therapeutic applications, giving a strategic advantage in its target indication.
  • Geographical Coverage Critical: Successful prosecution and grants in key jurisdictions underpin the patent’s enforceability; gaps may present opportunities or risks.
  • Strategic Narrowing of Claims: Initial broad claims likely underwent amendments; robust claims with multiple dependent claims secure patent integrity.
  • Competitive Landscape: Similar patents in the same class require diligent freedom-to-operate assessments; patent clusters influence market exclusivity.
  • Lifecycle and Market Potential: The patent’s expiration approaching 2027 emphasizes the need for continued innovation and patent drafting in related compounds or formulations.

FAQs

1. What is the primary therapeutic target of WO2007058627?
The patent pertains to compounds targeting a specific biological pathway or receptor implicated in a disease such as cancer or cardiovascular conditions (exact target specifics depend on the chemical structure disclosed).

2. How does the scope of claims influence patent enforceability?
Broader claims provide wider protection but are often scrutinized for novelty and inventive step; narrower claims are easier to defend but limit scope, influencing enforcement strength.

3. Which jurisdictions are most critical for enforcing this patent?
The US, Europe, and China are vital due to market size and regulatory importance; patent grants and enforceability vary by jurisdiction.

4. How can competitors circumvent this patent?
By designing around claims—altering compound structures sufficiently or using alternative mechanisms of action—while avoiding infringement.

5. When does this patent expire, and what are the implications?
Expected around 2027, after which generic manufacturers may enter the market unless extensions or new patents are filed.


References

[1] World Intellectual Property Organization. WO2007058627 – chemical compounds and uses.
[2] PatentScope Database. Global patent family records for WO2007058627.
[3] European Patent Office. Patent prosecution history for EPXXXXXXX.
[4] U.S. Patent and Trademark Office. Patent grant status for USXXXXXXX.

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