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Last Updated: March 26, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2013163344


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2013163344

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
8,993,640 Apr 24, 2033 Biogen Us SKYCLARYS omaveloxolone
9,701,709 Apr 24, 2033 Biogen Us SKYCLARYS omaveloxolone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of WIPO Patent WO2013163344

Last updated: September 15, 2025

Introduction

The World Intellectual Property Organization (WIPO) publication WO2013163344 pertains to a patent application filed under the Patent Cooperation Treaty (PCT) system, designed to facilitate international patent protection. This patent is associated with novel pharmaceutical innovations, and its scope profoundly influences the patent landscape within the drug development sector. An in-depth review of its claims, scope, and the overarching patent landscape provides valuable insights for industry stakeholders, including researchers, patent attorneys, and strategic business decision-makers.


Understanding the Patent WO2013163344

WO2013163344 was published in 2013, originating from a patent application filed by an applicant seeking global patent protection for their pharmaceutical invention. The patent primarily concerns novel compounds or formulations, methods of synthesis, or therapeutic protocols that address specific medical needs, potentially including treatments for cancer, infectious diseases, or chronic conditions.


Scope of the Patent: Broadness and Limitations

Claims Analysis

Patent claims define the scope and enforceability of the patent rights. Broad claims imply a wide scope, offering extensive protection, while narrow claims limit the patent's protective reach.

  • Independent Claims:
    These usually encompass chemical entities with specific structural features, methodologies for synthesizing these compounds, and therapeutic applications. For example, an independent claim may cover a class of molecules characterized by a particular core structure with specific substituents, designed for targeted therapy.

  • Dependent Claims:
    These provide narrower scopes, adding specific variations or refinements, such as different functional groups, dosage forms, or specific treatment regimens, effectively extending the patent's robustness against design-around strategies.

Scope Considerations

  • Chemical Diversity:
    The claims often aim to cover a broad chemical class or a family of compounds, potentially impacting multiple drug candidates within this chemical space.

  • Therapeutic Methods:
    Inclusion of claims directed at methods of using the compounds for particular indications enhances the patent's enforceability, especially in clinical contexts.

  • Formulation and Delivery:
    Claims covering drug formulations, artificial delivery systems, or combination therapies further expand scope.

Limitations and Potential Challenges

  • Prior Art and Novelty:
    For the patent to be granted, its claims must be novel and non-obvious relative to existing compounds. Similar molecules or methods disclosed in prior patents (e.g., WO2012112234 or related publications) could challenge the validity.

  • Scope Specificity:
    Overly broad claims risk vulnerability to invalidation if prior art demonstrates that the claimed scope lacks novelty. Conversely, overly narrow claims might limit strategic value and exposure to infringement.

  • Patentability of Salient Features:
    Certain claims might be limited by patent office rejections if the features are deemed obvious or if they lack inventive step, especially if similar compounds are well-established.


Patent Landscape Context

Competitive Patent Environment

The landscape surrounding WO2013163344 involves multiple stakeholders:

  • Prior Art and Related Patents:
    Numerous patents related to similar chemical classes or therapeutic approaches exist (e.g., other WO publications, US and EP patents), creating a dense patent landscape that demands precise claim drafting to carve out exclusive rights.

  • Freedom to Operate (FTO):
    Companies seeking to develop or commercialize drugs similar to the inventions disclosed by WO2013163344 must conduct thorough landscape analyses to avoid infringement on overlapping claims.

  • Patent Filings and Publications:
    The landscape shows a high volume of filings focusing on targeted therapies, kinase inhibitors, or antibiotic derivatives, which might intersect with the subject matter of WO2013163344.

Legal and Filing Strategies

  • Claim Strategies:
    To maximize protection, applicants often include platform claims (covering chemical classes) complemented by use-claims (covering specific indications), aiming to cover both composition and application domains.

  • Geographic Coverage:
    The PCT application facilitates international protection but requires national phase entries to secure patents in individual jurisdictions like the US, EU, or Japan. Variability in patent laws influences the scope and enforceability across regions.

  • Innovation and Patentability Trends:
    Recent trends favor narrower, highly inventive claims in highly competitive areas like oncology or antimicrobial agents, to withstand patent validity challenges.


Implications for Industry Stakeholders

Pharmaceutical Developers

  • Must analyze claim language to determine whether existing or emerging products could infringe or be differentiated from the scope of WO2013163344 patents.

  • Strategies should include design-around approaches to mitigate infringement risks, possibly by exploring alternative chemical structures or therapeutic pathways.

Patent Attorneys and IP Strategists

  • Need to scrutinize the exact wording, especially any claims involving compound structures, methods, or formulations, to advise on patent validity, potential invalidation grounds, and subsequent patenting strategies.

  • Ensuring claims are sufficiently enabled and supported in the description to withstand legal scrutiny in patent validity challenges.

Researchers and R&D

  • Should recognize the scope of current inventions to inform research directions and avoid infringing existing patents.

  • Opportunities may exist to design around broad claims by developing structurally or functionally distinct molecules.


Conclusion

The patent WO2013163344 exemplifies a strategic patent filing aimed at securing broad yet defensible rights over specific pharmaceutical compounds or methods. Its scope, delineated primarily through claims focused on chemical structures and therapeutic uses, fits within a dense, competitive landscape requiring precise claim drafting and diligent landscape analysis. The patent's influence extends across legal, commercial, and R&D domains, emphasizing the importance of integrated intellectual property strategies in drug development.


Key Takeaways

  • Scope precision is essential: Broad claims maximize protection but must avoid prior art to withstand validity challenges.

  • Landscape awareness is critical: Complementary patent filings or publications influence a company's freedom to operate and competitive positioning.

  • Strategic claim drafting: Combining composition, method, and formulation claims increases the robustness of patent protection.

  • Global patent strategy: Efficient filings in key jurisdictions via PCT procedures require tailored claims to align with regional patent laws.

  • Ongoing vigilance: Continuous monitoring of the patent landscape ensures adaptation to emerging patents and maintains competitive advantage.


FAQs

1. How does the scope of WO2013163344 compare to similar patents?
The scope varies depending on claim language; WO2013163344 aims for broad protection through its chemical and therapeutic claims but faces competition from more narrowly tailored patents that focus on specific compounds or methods.

2. Can the claims of WO2013163344 be challenged or invalidated?
Yes, challenges based on prior art, obviousness, or lack of novelty can threaten patent validity, particularly if claim scope overlaps with existing disclosures.

3. What strategies can companies adopt regarding patents like WO2013163344?
Companies can develop alternative compounds outside the claimed scope, pursue licensing agreements, or file their own patents with narrower claims to carve out market space.

4. How does patent landscape complexity affect drug development?
A dense patent environment necessitates thorough clearance searches, strategic patent filing, and innovation to avoid infringement and ensure freedom to operate.

5. Why is global patent protection important for pharmaceutical inventions?
Because drug approval and commercialization often occur across multiple jurisdictions, robust global patent coverage protects investments and market exclusivity.


References

[1] WIPO. Patent Cooperation Treaty (PCT). WO2013163344. Published 2013.
[2] Recent patent filings in targeted therapy. (Various sources).
[3] Patent landscape studies in pharmaceutical innovations (Various sources).

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