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Last Updated: December 19, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2012120338


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2012120338

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
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Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2012120338

Last updated: August 3, 2025


Introduction

Patent application WO2012120338, published under the auspices of the World Intellectual Property Organization (WIPO), pertains to a novel pharmaceutical invention with potential implications in drug development and commercialization. This patent's scope, claims, and broader patent landscape are critical for stakeholders seeking to understand patent protection, freedom-to-operate, and competitive positioning within the therapeutic class involved.


Patent Overview and Publication Details

WO2012120338 was published on September 13, 2012, under the Patent Cooperation Treaty (PCT), indicating a strategic move to secure international patent rights across multiple jurisdictions. The application focuses on a specific chemical entity or therapeutic method designed for treating a particular disease or condition, with detailed disclosures of chemical structures, synthesis methods, and usage indications.

The applicant or assignee’s identity is essential for understanding strategic patenting, though that information would require further investigatory disclosures. Nonetheless, the patent's geographical coverage likely encompasses key markets such as the US, EP (European Patent Office), and other major jurisdictions, emphasizing its potential global reach.


Scope of the Patent

Core Objective:

The patent claims revolve around novel chemical compounds or formulations that exhibit therapeutic efficacy against specific diseases. The scope primarily encompasses:

  • Chemical compositions: Specific molecules or derivatives with defined structural features.
  • Methods of use: Therapeutic applications of said compounds, including dosage and administration regimes.
  • Synthesis techniques: Methods to produce the compounds efficiently and reproducibly.
  • Pharmaceutical formulations: Specific formulations enhancing stability, bioavailability, or targeted delivery.

Claim Types:

  1. Independent Claims: These define the broadest scope, typically covering the core chemical compounds or the primary therapeutic methods.
  2. Dependent Claims: Narrower claims, specifying particular substituents, isomers, formulations, or use cases.

Example Hypotheses on Scope:

  • If the patent revolves around a new small-molecule inhibitor for kinase pathways, the claims likely cover the chemical core and analogs, alongside their method of administration.
  • Claims could extend to drug combinations if synergistic effects are claimed.
  • The scope may specify particular therapeutic indications, such as oncology, neurodegenerative diseases, or infectious diseases.

Limitations and Potential Scope Constraints:

  • The claims’ breadth may be limited to specific chemical classes or structural motifs, potentially leaving room for similar compounds outside the scope.
  • Emphasizing method claims over compound claims often limits patent life if patentability hinges on novelty over prior art.

Claims Analysis

While the exact language of the claims requires review of the patent document, typical analysis involves examining:

  • Novelty and Inventive Step: The claims must clearly distinguish the chemistry or method from prior art, such as existing drugs or known synthetic routes.
  • Claim Breadth: Broader claims offer wider protection but face higher scrutiny regarding inventive step.
  • Focus on Therapeutic Benefit: Claims may specify specific disease conditions, pump-priming the patent’s commercial utility.

Common Claim Structures in Pharmaceutical Patents:

  • Compound Claims: Cover a core molecule or genera of molecules with specific substituents.
  • Use Claims: Covering the use of the compound for particular medical indications.
  • Formulation Claims: Concerned with delivery mechanisms and pharmaceutical compositions.
  • Method Claims: Encompassing processes of synthesis or treatment protocols.

Potential Claim Vulnerabilities:

  • Overly broad claims may be challenged or invalidated if prior art exists.
  • Narrow claims enhance defensibility but restrict commercial scope.

Patent Landscape and Competitive Environment

Comparative Patent Analysis:

  • Identifying similar patents is critical for understanding infringement risks and freedom-to-operate (FTO). Similar chemical entities, delivery methods, or therapeutic indications may be protected by competing patents.
  • Leading pharmaceutical companies or biotech firms may possess patents that overlap or intersect, particularly if they focus on the same target pathways.

Patent Citations and Prior Art:

  • Patent WO2012120338 likely cites prior art in the fields of medicinal chemistry, pharmacology, or compound synthesis, establishing its novelty.
  • Competitors may have filed patents covering related compounds or methods, requiring detailed landscape mapping.

Generic and Biosimilar Challenges:

  • The patent's strength significantly influences market exclusivity. If the claims are narrow or face prior art challenges, generic entrants could threaten exclusivity post-patent expiry.
  • Secondary patents or patent thickets may extend protection but can be subject to legal contestation.

jurisdictions and Patent Family:

  • The patent’s territorial family indicates where protection is sought. US and European equivalents are common, but patents in emerging markets like Asia could present additional licensing or infringement risks.
  • Filing strategies suggest the patent owner’s long-term view of market potential in diverse geographies.

Legal Status and Enforcement

  • Pending, granted, or contested status impacts commercialization strategies.
  • Patent expiry dates, potential challenges, and opposition proceedings influence the competitive timeline.
  • Enforcement depends on the patent’s validity, territorial coverage, and the presence of infringing products.

Implications for Industry Stakeholders

  • Pharmaceutical Companies: Should evaluate the patent’s claims to ensure no infringement exists in their R&D pipeline.
  • Patent Holders: Must monitor competitive filings and enforce rights where infringement occurs.
  • Investors: Need to understand blanketing or gaps in the patent landscape to evaluate market exclusivity and potential licensing opportunities.
  • Regulatory and Commercial Teams: Should align patent strategies with clinical development and commercialization plans.

Key Takeaways

  • Strategic Broadness: WO2012120338 likely claims a combination of novel chemical entities and therapeutic methods with substantial scope, making it a valuable asset if upheld in litigation.
  • Patent Landscape Complexity: The intersection with existing patents necessitates comprehensive freedom-to-operate assessments before product development.
  • Continued Innovation: As patent claims evolve, secondary patents or improvements may extend competitive advantage, but legal robustness is vital.
  • Global Considerations: Patent protection must be tailored for major markets, with attention to jurisdiction-specific legal standards and prior art complexities.
  • Legal Vulnerability and Defense: Broad initial claims might be susceptible to invalidation, underscoring the importance of detailed prosecution histories and narrow claim enforcement.

FAQs

1. What is the primary therapeutic target of the compounds described in WO2012120338?
The patent primarily focuses on molecules targeting specific biological pathways relevant to a disease condition, such as kinase inhibition in oncology. Precise targets are detailed in the full patent description.

2. How broad are the claims in WO2012120338, and what impact does this have?
The claims likely cover core chemical compounds and their therapeutic applications, with the breadth influencing potential infringement risk and licensing opportunities.

3. How does the patent landscape influence the commercial viability of the invention?
A crowded patent landscape with overlapping claims from competitors or existing patents can limit market entry, requiring strategic licensing or design-around efforts.

4. Can secondary patents extend the protection beyond this patent’s expiry?
Yes. Innovator companies often file additional patents covering improvements, formulations, or methods, which can prolong exclusivity.

5. What steps should be taken to ensure freedom-to-operate concerning WO2012120338?
Conduct comprehensive patent searches and legal analyses to identify overlapping claims, assess potential infringement risks, and develop design-around strategies if necessary.


References

  1. World Intellectual Property Organization. Patent Cooperation Treaty (PCT). WO2012120338.
  2. WIPO Patent Database. [Accessed January 2023].

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