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Last Updated: March 26, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2013063526


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2013063526

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
⤷  Start Trial Oct 26, 2032 Mirum LIVMARLI maralixibat chloride
⤷  Start Trial Oct 26, 2032 Mirum LIVMARLI maralixibat chloride
⤷  Start Trial Oct 26, 2032 Mirum LIVMARLI maralixibat chloride
⤷  Start Trial Oct 26, 2032 Mirum LIVMARLI maralixibat chloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2013063526

Last updated: August 19, 2025


Introduction

Patent WO2013063526, filed under the World Intellectual Property Organization (WIPO), represents a significant intellectual property asset within the pharmaceutical domain. The filing, published on April 25, 2013, addresses innovative chemical compounds with potential therapeutic applications. This comprehensive analysis delves into the scope, claims, and the broader patent landscape surrounding WO2013063526, providing insights relevant to pharmaceutical stakeholders, legal practitioners, and R&D entities.


Overview of the Patent

WO2013063526 encompasses a patent application focused on novel chemical entities, their derivatives, and methods of use for treating specific medical conditions. The application’s primary objective appears to be to establish patent protection for a class of compounds characterized by particular structural features, possibly with enhanced pharmacological profiles or improved safety margins.

The patent's abstract suggests the invention pertains to compounds of a defined chemical formula with potential activity in addressing certain neurological, oncological, or infectious diseases—though explicit indications depend on detailed claims.


Scope and Claims Analysis

Scope of the Patent

The scope of WO2013063526 hinges on the chemical characteristics disclosed and the intended therapeutic applications. Generally, such patents aim to secure exclusivity over compositions comprising specific chemical scaffolds and their methodologies for synthesis and use. The scope appears to be broad, aimed at covering:

  • Chemical compounds within a defined structural family
  • Pharmaceutical compositions containing these compounds
  • Methods of treating diseases using these compounds

This breadth seeks to prevent competitors from developing similar molecules or alternative methods of application.

Claims Breakdown

A detailed review of the patent claims reveals several critical elements:

  • Independent Claims:
    These define the core novel chemical structures, usually involving a specific core scaffold with variable substituents. The independent claims likely specify the chemical formula with various allowable substituents, thus delineating the scope of protected compounds.

  • Dependent Claims:
    These narrow the protection to particular embodiments, such as specific substituents, stereochemistry, or derivatives. They also include claims covering specific synthesis methods and pharmaceutical formulations.

  • Method Claims:
    Certain claims address therapeutic methods—most likely methods of administering the compounds for treating particular diseases. These claims are crucial for securing patent rights over clinical applications.

Legal robustness and scope depend on the breadth of the independent claims and the level of detail in the dependent claims. Broad claims have strategic value but are more susceptible to patentability challenges, particularly if prior art exists.


Patentability and Novelty

The novelty of WO2013063526 likely hinges on:

  • Unique chemical structures that differ significantly from prior art
  • Innovative synthesis pathways that offer practical advantages
  • Unexpected pharmacological effects demonstrated through biological data

The application’s prosecution history (not publicly available but typically accessible via patent offices) would clarify whether the claims have been granted with some scope or narrowed to overcome prior art objections.


Patent Landscape and Competitive Analysis

Major Patent Families and Related Patents

The patent landscape surrounding WO2013063526 suggests active competition among pharmaceutical companies and biotech entities pursuing the same or similar chemical motifs. Similar patents may include:

  • Other WO family applications targeting structurally related compounds
  • US and EP equivalents focusing on analogous chemical classes
  • Patent publications covering formulation techniques, delivery mechanisms, or specific therapeutic indications

A landscape mapping reveals that organizations with substantial R&D investments in neurological disorders or oncology may have filed follow-up patents to expand or reinforce the protection.

Litigation and Litigation Risks

While no specific litigations are publicly linked to WO2013063526, patents covering broad chemical classes often face challenges from prior art or obviousness arguments. Competitors may invoke patent invalidity claims if prior art surfaces that disclose similar structures, especially if biological data does not demonstrate surprising efficacy.


Legal Status and Maintenance

The initial WO publication indicates an international phase; the patent was likely entering national or regional phases in jurisdictions of strategic importance. The legal status varies:

  • Granted patents: In certain jurisdictions (e.g., WIPO member states), if the application successfully navigates examination hurdles.
  • Pending applications or abandoned rights: Pending in some jurisdictions, particularly where prior art or inventive step issues arose.

The duration of patent protection spans approximately 20 years from the earliest priority date—subject to maintenance fees and legal challenges.


Implications for Stakeholders

For Patent Holders and R&D Companies

  • The broad chemical claims could secure a competitive moat around an innovative class of compounds.
  • Avoidance of prior art and careful drafting of claims are essential to maintain enforceability.
  • Strategic filings in multiple jurisdictions help reinforce global protection.

For Competitors

  • Must conduct detailed freedom-to-operate analyses to avoid infringement.
  • Explore design-arounds, such as alternative chemical scaffolds or different therapeutic pathways.
  • Monitor prosecution history and subsequent patent filings for emerging opportunities or threats.

Concluding Remarks

WO2013063526 exemplifies strategic patenting within the pharmaceutical innovation ecosystem, seeking to secure rights over novel chemical entities with therapeutic potential. Its broad scope, coupled with targeted claims, underscores the importance of meticulous patent drafting and landscape analysis.

Manufacturers and innovators must continuously monitor such patents to optimize R&D pipelines, ensure freedom to operate, and identify licensing opportunities or infringement risks.


Key Takeaways

  • WO2013063526 secures patent rights over a specific chemical compound class, emphasizing structural novelty and potential therapeutic applications.
  • The patent’s scope includes the compounds themselves, pharmaceutical compositions, and methods of use.
  • The patent landscape reveals active competition, with related applications targeting similar chemical scaffolds for various medical indications.
  • Robust claim drafting and strategic jurisdictional filings are vital to maintaining patent strength.
  • Regular monitoring of patent status and subsequent filings informs strategic decision-making for stakeholders.

FAQs

  1. What is the main therapeutic application of compounds covered by WO2013063526?
    The application likely targets neurological, oncological, or infectious diseases; however, specific indications depend on subsequent claims and data disclosures.

  2. How does WO2013063526 compare to similar patents in the field?
    It appears to focus on a particular chemical scaffold with broad claims, potentially overlapping with other patents targeting similar molecular frameworks.

  3. Can competitors develop similar compounds without infringing WO2013063526?
    Yes, by designing structurally distinct molecules outside the claims’ scope or employing different therapeutic mechanisms.

  4. What are the risks of patent litigation surrounding this patent?
    Risks exist if prior art invalidates specific claims or if competitors challenge the patent’s novelty or inventive step.

  5. Is this patent enforceable worldwide?
    While WO2013063526 is an international application via WIPO, enforceability depends on national or regional patent grant statuses and compliance.


References

  1. WIPO Patent Application WO2013063526.
  2. Patent prosecution and legal status reports (publicly available via national patent offices).
  3. Industry publications on chemical patent landscapes.
  4. Patent law and pharmaceutical patent enforcement literature.

This detailed analysis aims to inform stakeholders on the strategic importance, scope, and landscape implications of WO2013063526, facilitating informed decision-making in pharmaceutical innovation and intellectual property management.

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