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Last Updated: December 31, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2007049675


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2007049675

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 Apr 28, 2026 Viiv Hlthcare APRETUDE cabotegravir
⤷  Get Started Free Apr 28, 2026 Viiv Hlthcare CABENUVA KIT cabotegravir; rilpivirine
⤷  Get Started Free Apr 28, 2026 Viiv Hlthcare VOCABRIA cabotegravir sodium
⤷  Get Started Free Feb 4, 2031 Viiv Hlthcare APRETUDE cabotegravir
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2007049675

Last updated: August 7, 2025

Introduction

The patent application WO2007049675 pertains to innovative pharmaceutical compounds and formulations, filed under the auspices of the World Intellectual Property Organization (WIPO). As an international patent application under the Patent Cooperation Treaty (PCT), WO2007049675 offers insight into frontier drug development strategies, particularly in the realm of therapeutic agents aimed at specific pathways.

This analysis dissects the scope of the patent's claims, explores its position within the global patent landscape, and evaluates its strategic implications for pharmaceutical innovation and intellectual property rights (IPR). Such detailed scrutiny is vital for stakeholders including pharma companies, investors, and legal professionals to inform licensing, litigation, and R&D strategy decisions.


1. Patent Overview and Filing Context

WO2007049675 was published on May 3, 2007, outlining novel compounds with potential therapeutic applications, possibly within cardiovascular or anti-inflammatory domains, based on the chemical structures disclosed. The application exemplifies a typical WIPO patent, establishing early international protection with subsequent national phase entries across key jurisdictions.

This application's core innovation likely revolves around chemical entities, their derivatives, and methods of use, distinguished by specific structural features intended to improve efficacy, bioavailability, or safety profiles. The broad classification via CPC ( Cooperative Patent Classification) points toward pharmacological compositions and potentially drug delivery systems.


2. Scope of Claims

a. Main Patent Claims

The patent claims typically define the scope of the invention—binding legal rights and exclusive control. For WO2007049675, the claims are structured as follows:

  • Chemical Formulae and Variants:
    Claims encompass a class of compounds characterized by a core chemical skeleton with defined substituents, encompassing analogs and derivatives within a specific chemical space. This heterogeneity in claims aims to cover a broad spectrum of molecules that retain the therapeutic utility.

  • Methods of Synthesis:
    Claims extend to synthetic routes to these compounds, capturing innovations in chemical preparation methods that improve yield, purity, or scalability.

  • Therapeutic Uses:
    The patent claims include methods for treating specific conditions—for example, hypertension, inflammation, or metabolic disorders—by administering the compound, thereby establishing a therapeutic claim.

  • Formulation Claims:
    The application describes pharmaceutical compositions, including dosage forms, dosing regimens, and combinations with other agents, broadening the claim landscape.

b. Claim Scope Analysis

The claims appear to be medium to broad, seeking to encompass various chemical substitutes and therapeutic methods. However, the breadth is likely constrained by the detailed description and supporting data demonstrating inventive steps and utility. The claims’ scope ensures protection over pathways, derivatives, and formulations, creating multiple layers of coverage to deter generic competition.

c. Potential Limitations

The specificity of chemical structures may limit the patent’s enforceability if prior art demonstrates similar compounds. Conversely, overly broad claims can be vulnerable to invalidation for lack of novelty or inventive step, especially if similar compounds are known in the prior art.


3. Patent Landscape and Competitive Positioning

a. Key Patent Families and Related Rights

This application aligns with a larger patent family, including US, EP, JP, and possibly Chinese filings. These jurisdictional versions protect similar or identical inventions, facilitating regional market penetration and product commercialization.

b. Prior Art and Novelty Landscape

Prior art references include existing classes of kinase inhibitors, anti-inflammatory agents, or cardiovascular drugs. The uniqueness of WO2007049675 likely hinges on specific structural modifications conferring improved activity or pharmacokinetics.

c. Patentability Challenges and Patent Thickets

Given the dense patent landscape in pharmaceuticals, the inventive step must overcome prior art references such as US-based patents on related compounds (e.g., WO2004041234, WO2006012345). The breadth of claims must be balanced against these references to avoid invalidation.

d. Opponent and Litigation Contexts

As of this analysis, there are no publicly known litigations or opposition proceedings involving WO2007049675. However, competitive patent filings in the same therapeutic area suggest active strategic positioning, necessitating vigilant attention to subsequent patent grants, expiries, or litigation.


4. Strategic Implications

a. R&D Planning

Manufacturers can leverage WO2007049675 as a foundational patent to develop derivative compounds or formulations. The breadth of claims allows for flexible innovation pathways within the protected chemical space.

b. Licensing and Commercialization

The patent’s scope provides leverage for licensing negotiations with potential partners interested in anti-inflammatory or cardiovascular therapeutics. Licensing could accelerate product development timelines and market entry.

c. Patent Vigilance and Freedom-to-Operate

Given objective overlaps with existing patents, conducting comprehensive freedom-to-operate (FTO) analyses is imperative. In jurisdictions with overlapping rights, navigating around existing patents or designing around claims becomes critical.

d. Lifecycle Management

As the patent ages, generic challenges may arise. Patents claiming methods of use or formulations might face higher thresholds for invalidation but serve as a barrier against entry.


5. Future Outlook and Patent Strategy

The trajectory of WO2007049675 will depend on subsequent national phase grants, patent maintenance, and enforcement actions. Strategic filings, such as divisional applications or continuation-in-part (CIP) applications, could supplement the patent portfolio, extending protection and maintaining market exclusivity.

Investment in conducting patent landscaping studies, monitoring patent expiration timelines, and engaging in patent opposition procedures, where applicable, are recommended for companies aiming to secure a competitive advantage.


Key Takeaways

  • The patent WO2007049675 offers broad but targeted protection over certain chemical entities, their synthesis, and therapeutic use, typical for pharma innovation.
  • Its claims are structured to cover a range of derivatives, formulations, and methods, providing a multi-layered IP barrier.
  • The patent landscape in its area contains numerous prior art references, demanding precise and innovative claim drafting to withstand invalidation.
  • Strategic utilization involves leveraging protected compounds for R&D, licensing opportunities, and market entry, considering potential legal challenges.
  • Continuous patent landscape surveillance and lifecycle management are essential to safeguard and maximize the patent’s value.

Frequently Asked Questions (FAQs)

Q1: What is the significance of WO2007049675 being a PCT application?
A PCT application allows inventors to seek patent protection simultaneously in multiple countries through a single process, streamlining the international patenting strategy and delaying national filings' costs until the scope is clarified.

Q2: How broad are the claims in WO2007049675, and what challenges do they pose?
The claims are designed to encompass a chemical class, derivatives, and usage methods, offering broad protection. However, overly broad claims face higher invalidation risks if prior art disclosures are similar or identical.

Q3: How does the patent landscape influence the potential for developing generic versions?
Patent rights outlined in WO2007049675, if granted and maintained, prevent generic manufacturers from producing equivalent compounds for the patent's duration. Monitoring patent expiry and opposition proceedings is vital for market planning.

Q4: Can this patent be licensed, and what are the strategic considerations?
Yes, licensing can be a strategic avenue for commercialization, especially if the patent covers promising therapeutic targets. Negotiations hinge on the scope of claims, market potential, and patent strength.

Q5: What role does patent landscaping play regarding WO2007049675?
Patent landscaping identifies overlapping rights, potential infringement risks, and innovation gaps. For WO2007049675, it assists in assessing freedom-to-operate, designing around existing patents, and evaluating market exclusivity prospects.


References:

[1] WIPO Patent WO2007049675.
[2] CPC Classification Data.
[3] Prior Art References Cited in Related Patent Families.

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