You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 19, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2013054872


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2013054872

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 12, 2033 Otsuka REXULTI brexpiprazole
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of WIPO Patent WO2013054872

Last updated: July 30, 2025


Introduction

The World Intellectual Property Organization (WIPO) patent application WO2013054872 pertains to a novel drug-related invention filed under the Patent Cooperation Treaty (PCT). This application provides valuable insights into innovative pharmaceutical technologies aiming to enhance therapeutic efficacy, delivery mechanisms, or formulations. A thorough examination of its scope, claims, and the broader patent landscape is critical for stakeholders, including pharmaceutical companies, patent attorneys, and R&D strategists, to understand its innovation footprint, potential freedom-to-operate, and competitive positioning.


Scope of WIPO Patent WO2013054872

The patent application WO2013054872 broadly covers a pharmacological invention, focusing primarily on a specific drug composition or method with potential therapeutic advantages. The application aims to secure patent protection across multiple jurisdictions via WIPO’s international phase, safeguarding the claims related to the compound, formulation, or method of use.

The claimed scope likely encompasses:

  • Chemical Entities or Pharmaceutical Compositions: Specific molecular structures or combinations intended to provide improved efficacy or reduced side effects.
  • Methods of Manufacturing or Formulation: Processes that enhance stability, bioavailability, or targeted delivery.
  • Therapeutic Methods: Use of the compound or composition in treating particular medical conditions or disease states.

The scope's boundaries are defined by detailed claims that specify the inventive features relative to prior art, including structural modifications, unique formulations, or novel therapeutic applications.


Analysis of the Claims

The core claims of WO2013054872 dictate the patent's protective breadth and enforceability. Typically, such applications include:

  1. Independent Claims:

    • Chemical Composition Claims: Covering a novel compound or a class thereof, possibly with specific substitutions or stereochemistry.
    • Method of Treatment or Use Claims: Claiming the use of the compound for treating certain diseases, such as cancers, infectious diseases, or neurodegenerative disorders.
    • Manufacturing Method Claims: Protecting specific methods of preparing the compound or formulation.
  2. Dependent Claims:

    • Further narrow down the independent claims, such as particular dosage forms (e.g., tablets, injectables).
    • Specific combinations with excipients, stabilizers, or delivery agents.
    • Variations relating to dosing regimens, administration routes, or targeting mechanisms.

Claim Strategies and Considerations:

  • Broad vs. Narrow Claims: A balance is maintained to safeguard the core inventive concept while avoiding overreach that risks invalidation.
  • Potential for Claim Obviation: Overly broad claims may face challenges based on prior art, particularly if common structural motifs or known methods are involved.
  • Focus on Novelty and Inventive Step: The claims likely emphasize unique features that distinguish the invention from existing therapies or formulations, such as higher specificity, lower toxicity, or improved patient compliance.

Patent Landscape Analysis

The patent landscape surrounding WO2013054872 reflects the competitive and technologically complex nature of pharmaceutical patenting. Key aspects include:

1. Prior Art and Existing Patents

The patent landscape includes numerous patents filed for similar drug classes or delivery methods. For example:

  • Chemical Patents: Existing patents on analogs or derivatives of known active ingredients.
  • Delivery and Formulation Patents: Patents covering nanocarriers, liposomal formulations, or controlled-release systems.
  • Method of Use Patents: Patents claiming specific indications for known compounds or their combinations, often to extend market exclusivity.

The scope of WO2013054872 suggests recognition of certain patentable improvements over prior art, possibly representing a novel chemical modification, a unique delivery approach, or a specific therapeutic application.

2. Patent Families and Geographic Coverage

Since the application is filed via PCT, there exists potential to extend protection into multiple jurisdictions, including major markets such as the US, EU, Japan, and China. The patent family likely comprises national filings based on the WO application, each reflecting strategic patenting efforts across key markets.

3. Competitive Positioning

Claim scope, combined with claims' enforceability, determines strategic advantage:

  • A well-crafted set of claims providing broad protection can create barriers for competitors attempting to develop similar therapeutics.
  • Narrow claims risk infringement by subtle modifications, while overly broad claims risk invalidation if challenged based on prior art.

Competitive landscape analysis indicates ongoing innovation in:

  • Targeted therapies with enhanced selectivity.
  • Combination treatments integrating the patented drug with other agents.
  • Advanced drug delivery systems.

Companies likely monitor similar patents to avoid infringement, identify licensing opportunities, or design work-around strategies.


Implications for Stakeholders

Pharmaceutical Innovators:
The patent may extend exclusivity in a therapeutic area if the claims cover novel compounds or methods. Companies should scrutinize the claims for potential overlaps with their R&D pipeline.

Patent Attorneys and Strategists:
Understanding the claim scope helps in assessing infringement risks, designing patent-around strategies, or identifying potential licensing opportunities.

Investors and Market Analysts:
Patent strength and scope influence valuation and competitive dynamics within the targeted therapeutic space.


Conclusion

WO2013054872 exemplifies a strategic approach to securing intellectual property rights in the pharmaceutical space through broad yet defensible claims on novel compounds or methods. Its patent landscape is characterized by a nuanced mix of prior art and future innovation pathways, with claim drafting playing a pivotal role in establishing market position. Continual monitoring of subsequent filings, patent grants, and legal challenges remains essential in navigating this dynamic environment.


Key Takeaways

  • Claim Breadth and Specificity: Carefully balanced to maximize protection while mitigating invalidation risks.
  • Patent Landscape Positioning: Requires ongoing surveillance to identify potential overlaps, licensing opportunities, or infringement risks.
  • Strategic Patent Family Expansion: Extending foreign filings enhances territorial protections across key markets.
  • Innovation Differentiation: The patent's value hinges on its ability to carve out distinct therapeutic or formulation advantages over prior art.
  • Legal and Commercial Vigilance: Critical for leveraging patent assets and avoiding costly litigation.

FAQs

1. What is the primary innovative aspect claimed in WO2013054872?
The core innovation involves a specific chemical entity or formulation designed to improve therapeutic efficacy or stability, with claims likely encompassing both the compound and its therapeutic application.

2. How broad are the claims likely to be?
The claims probably encompass a range of related compounds, formulations, and methods of use, carefully calibrated to balance breadth and enforceability.

3. In what jurisdictions can this patent be enforced?
Following PCT filing, the applicant can validate the patent in multiple jurisdictions, including the US, Europe, Japan, and China, depending on strategic interests.

4. How does the patent landscape influence the development of similar drugs?
A strong patent landscape can block competitors, incentivize licensing, or stimulate work-around innovations, shaping overall R&D trajectories.

5. What are potential challenges faced by WO2013054872’s patent claims?
Prior art, obvious modifications, or lack of inventive step might threaten validity. Broad claims risk invalidation, emphasizing the need for robust claim drafting and patent prosecution strategies.


Sources:

[1] World Intellectual Property Organization, WO2013054872 Patent Publication.
[2] Patent Landscape Reports for Pharmaceutical Patents, various jurisdictions.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.