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Last Updated: December 29, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2015119919


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2015119919

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 Jan 30, 2035 Abbvie QULIPTA atogepant
⤷  Get Started Free Jan 30, 2035 Abbvie UBRELVY ubrogepant
⤷  Get Started Free Dec 22, 2041 Abbvie UBRELVY ubrogepant
⤷  Get Started Free Dec 22, 2041 Abbvie UBRELVY ubrogepant
⤷  Get Started Free Jan 30, 2035 Abbvie UBRELVY ubrogepant
⤷  Get Started Free Dec 22, 2041 Abbvie UBRELVY ubrogepant
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of WIPO Patent WO2015119919: Scope, Claims, and Patent Landscape

Last updated: August 8, 2025

Introduction

Patent WO2015119919, filed under the auspices of the World Intellectual Property Organization (WIPO), represents a notable entry in the field of pharmaceutical innovation. The patent application focuses on novel drug compositions, methods of synthesis, and therapeutic applications, reflective of advancements in medicinal chemistry and drug delivery systems. This analysis dissects the scope, claims, and broader patent landscape associated with WO2015119919, offering insights into its strategic significance within the global pharmaceutical patent environment.

Scope of Patent WO2015119919

Legal and Technical Boundaries

The scope of WO2015119919 encompasses the invention of specific chemical compounds, formulations, and methods linked to therapeutic efficacy. It delineates the boundaries of the intellectual property (IP), defining what aspects are protected and what are in the public domain. The patent predominantly covers:

  • Novel Chemical Entities: The patent claims novel compounds with defined structural features, potentially exhibiting enhanced bioavailability, stability, or specificity.
  • Pharmaceutical Compositions: It extends protection to pharmaceutical formulations incorporating the claimed compounds, including dosage forms such as tablets, capsules, or injectables.
  • Methods of Use: It encompasses methods of treating specific diseases or conditions using the novel compounds or compositions.

Geographical and Jurisdictional Scope

While WIPO applications are international by design, they do not inherently grant patent rights but serve as a basis for national phase entries. The scope, therefore, depends on subsequent filings in jurisdictions such as the US, EU, China, etc., where claims are examined and granted. The initial PCT application ensures broad patentability prospects across major markets.

Claims Analysis

Claim Hierarchy and Structure

The patent comprises independent and dependent claims. The independent claims define the broadest scope, usually covering:

  • A class of compounds characterized by specific chemical frameworks.
  • Pharmaceutical compositions comprising these compounds.
  • Therapeutic methods utilizing these compounds for particular indications.

Dependent claims narrow the scope, adding specific features such as:

  • Particular substitutions on the core chemical structure.
  • Specific salt, ester, or derivative forms.
  • Composition ratios, excipient combinations, or delivery methods.

Core Claims

The core claims focus on:

  • Chemical Structure: Claiming the innovation of a particular chemical scaffold, possibly a derivative of known pharmacophores, optimized for improved activity.
  • Therapeutic Indication: The inventions target diseases such as cancer, autoimmune conditions, or infectious diseases—reflecting a strategic focus on high-impact health areas.
  • Method of Synthesis: Claims may also cover efficient synthetic routes, facilitating commercialization and manufacturing.

Claim Breadth and Potential Challenges

The breadth of the claims suggests an attempt to secure broad IP coverage, which could extend to multiple compounds within a designated chemical class. However, broad claims face potential validity challenges during examination, such as:

  • Novelty: Demonstrated by prior art references, including earlier patents or publications.
  • Inventive Step: Established through showing unexpected advantages over existing solutions.
  • Sufficiency of Disclosure: The application must sufficiently enable others skilled in the art to reproduce the invention.

The patent’s enforceability and scope hinge on how narrowly or broadly its claims are drafted and how effectively the applicant can defend them against prior art challenges.

Patent Landscape and Strategic Context

Global Patent Trends in Pharmaceuticals

The patent landscape surrounding WO2015119919 indicates a trajectory consistent with competitive innovation in pharmaceuticals:

  • Prior Art and Related Patents: Multiple patents exist covering similar chemical scaffolds, drug delivery mechanisms, and therapeutic indications. Notably, the landscape includes filings from major pharmaceutical firms and biotechs focusing on targeted therapies and personalized medicine.
  • Patent Clusters: The application aligns with clusters of patents targeting similar molecular classes, hinting at a crowded patent space requiring strategic navigation.
  • Cross-Reference to Existing IP: The patent references prior art for validity, including earlier WO publications and national patents, pointing to incremental or breakthrough innovation.

Jurisdictional Considerations

Post-WIPO application, key national or regional filings often include:

  • United States (USPTO): Known for vigorous patent examination, with significant emphasis on patent claims clarity and inventive step.
  • European Patent Office (EPO): Focused on inventive activity and added value over prior art, with restrictions related to inventive step.
  • China National Patent Office: Rapid patent prosecution and a growing pharmaceutical patent portfolio, especially in biologics and chemical entities.

Potential for Patent Thickets or Litigation

Given its broad claims, WO2015119919 could serve as a foundation for patent thickets—dense webs of overlapping patents—potentially leading to infringement litigation or licensing negotiations. This is especially relevant for compounds under development or commercialization.

Licensing and Commercialization Strategies

Ownership of this patent could provide leverage in licensing negotiations with generic manufacturers or research collaborations. Its strategic positioning in the patent landscape influences competitive dynamics and market entry timing.

Implications for Stakeholders

  • Innovators: Patents like WO2015119919 underscore the importance of detailed claims drafting and broad patent strategies to safeguard novel drug candidates.
  • Investors: The breadth and scope of the patent influence valuation, competitive advantage, and risk assessment.
  • Regulators: Understanding the patent’s scope is vital to predicting patent expiry and generic entry timelines.
  • Legal Practitioners: The landscape offers opportunities for patent oppositions, validations, and infringement analyses.

Key Takeaways

  • WO2015119919’s patent protection revolves around a novel class of chemical compounds and their therapeutic applications, with claims carefully structured to balance breadth and defensibility.
  • The scope extends across chemical structure, formulations, and usage methods, but potential challenges from prior art necessitate strategic claim drafting and prosecution.
  • Its position within a competitive patent landscape indicates a focus on high-value therapeutic areas, emphasizing the importance of patent strength for market exclusivity.
  • Broader patent strategies involve navigating multiple jurisdictions, considering potential patent thickets, and leveraging licensing opportunities.
  • Effective utilization of this patent demands continuous monitoring of related filings, patent litigation trends, and evolving regulatory landscapes.

FAQs

Q1: What is the primary innovation claimed in WO2015119919?
A: The patent claims a novel chemical scaffold with specific structural features designed for enhanced therapeutic efficacy in targeted disease treatments.

Q2: In which therapeutic areas does WO2015119919 mainly apply?
A: The claims primarily focus on diseases such as cancer, autoimmune disorders, or infectious diseases, depending on the specific compounds and methods disclosed.

Q3: How does WO2015119919 compare to existing patents in the same field?
A: It aims to provide broader or more optimized chemical entities than prior art, potentially offering improved bioactivity or pharmacokinetics, but must navigate patentability criteria amidst existing IP.

Q4: What are the key considerations when filing subsequent national patents based on this WO application?
A: Ensuring that claims are sufficiently narrow to overcome prior art, while maintaining broad enough protection to prevent easy design-arounds, is critical.

Q5: Can WO2015119919 be challenged or invalidated?
A: Yes; potential challenges include prior art invalidation, lack of inventive step, or insufficient disclosure, especially if the claims are too broad.

References

  1. [WIPO Patent Application WO2015119919], World Intellectual Property Organization, 2015.
  2. Patent landscape analyses and proceedings related to chemical and pharmaceutical patents (public patent databases).
  3. Industry reports on patent strategies within the pharmaceutical sector.

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