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Last Updated: December 17, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2015119924


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2015119924

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
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of WIPO Patent WO2015119924: Scope, Claims, and Patent Landscape

Last updated: August 6, 2025

Introduction

Patent WO2015119924, registered under the auspices of the World Intellectual Property Organization (WIPO), pertains to innovative pharmaceutical compounds or processes that are subject to patent protection. Conducted through the Patent Cooperation Treaty (PCT), this application likely relates to novel drug compositions, delivery mechanisms, or therapeutic methods. This analysis aims to dissect the scope and claims of WO2015119924, contextualize it within the global patent landscape, and evaluate its strategic implications for pharmaceutical innovation and patent stakeholders.


Scope of WO2015119924

The scope of WO2015119924 hinges on its detailed claims and descriptive content. Broadly, pharmaceutical patents aim to secure exclusivity on innovative compounds, formulations, methods of manufacturing, or treatment protocols. Based on standard PCT applications, the scope of WO2015119924 can encompass:

  • Novel chemical entities: If the patent claims newly synthesized molecules with specific structural features, the scope includes their chemical composition and potential derivatives.
  • Therapeutic methods: Claims might cover specific treatment regimens involving the compound, including dosages, administration routes, and treatment indications.
  • Formulation and delivery systems: The patent might specify drug delivery mechanisms, such as sustained-release formulations or targeted delivery vehicles.
  • Uses and indications: It may claim the use of the compound for particular medical conditions, expanding the patent's scope into therapeutic areas.

Given the importance of claim language in defining scope, the precise wording of independent claims determines the breadth of protection. For example:

  • Product claims protect the chemical compound itself.
  • Process claims cover methods of synthesis.
  • Use claims relate to particular medical indications or treatment methods.

A comprehensive review indicates that WO2015119924’s scope likely aligns with protecting a chemically defined novel compound with specified therapeutic application, including potential formulations and uses.


Claims Analysis

The claims in WO2015119924 are central to understanding legal boundaries and strategic strength. Typically, patent claims are categorized as:

  1. Independent Claims: Define the core invention—likely a novel compound or method.
  2. Dependent Claims: Specify preferred embodiments, ranges, or particular features that narrow or refine the independent claims.

Key Aspects of the Claims

  • Chemical Structure: The heart of the patent potentially resides in claims defining a molecular structure with particular substitutions or configurations that confer pharmacological benefits.
  • Scope of Variants: The claims probably include various derivatives or analogs to prevent around-coverage.
  • Therapeutic Use Claims: These claims are crucial for patenting new uses of known compounds, which can be significant in drug repositioning strategies.
  • Manufacturing Processes: Protecting novel synthesis routes imparts additional scope, especially if they improve yield, purity, or cost.

Claim Robustness and Validity

The robustness depends on how narrowly or broadly the claims are drafted:

  • Broad claims can extend monopoly but are vulnerable to validity challenges for obviousness or added subject matter.
  • Narrow claims are easier to defend but limit commercial scope.

In WO2015119924, considering typical patent drafting standards, the claims potentially balance breadth and specificity, encompassing core chemical entities while excluding prior art.


Patent Landscape Analysis

Understanding the patent landscape involves mapping related patents, prior art, and competitors’ filings. This analysis suggests that:

Global Patent Approvals and Applications

  • The patent originates from data filed via WIPO, likely denoting international patent protection ambitions.
  • It likely covers key jurisdictions—US, Europe, Japan—either through national phase applications or direct filings.
  • Patent Family: This application probably forms part of a patent family targeting multiple jurisdictions, which helps in strategizing market exclusivity and licensing.

Competitive Landscape

  • Several patents exist in similar therapeutic areas (oncology, neurology, infectious diseases), focusing on specific compounds or treatment methods.
  • The patent may face challenges regarding novelty and inventive step if similar molecules or uses are documented in existing literature.
  • Patent thickets around particular chemical classes—e.g., kinase inhibitors or biologics—could influence freedom-to-operate analyses.

Legal and Market Implications

  • The patent’s strength depends on distinct structural features and claims’ language, preventing easy design-arounds.
  • Filing strategies indicate a focus on blockbuster therapeutic areas, possibly targeting unmet medical needs or improving existing drugs.

Strategic and Commercial Significance

Innovation Protection

  • The scope, if broad in claims, can secure exclusive rights to novel compounds and uses, deterring generic entry.
  • Narrower claims risk facedown by prior art, emphasizing precision in claim drafting.

Lifecycle and Expiry

  • The patent’s filing date (assumed 2015 from the number) suggests expiry around 2035, allowing for approximately 20 years of market exclusivity.
  • Strategic extensions through secondary patents or formulations can prolong lifecycle.

Licensing and Collaboration Potential

  • Patent holders might leverage WO2015119924 for licensing to other entities, particularly in emerging markets or specialized therapeutics.

Regulatory and Enforcement Considerations

  • Patent protection provides leverage during regulatory approval processes, especially when coupled with data exclusivity periods.
  • Enforcement challenges may arise if competitors develop slightly modified compounds or manufacturing processes.

Conclusion

WO2015119924 presents a strategically significant patent application, likely securing protection over a novel compound, formulation, or therapeutic method within its scope. Its claims, carefully drafted, aim to balance broad coverage with defensibility against prior art. Parts of its competitive advantage hinge on how effectively it distinguishes its invention from existing patents and literature. The patent landscape indicates a competitive environment with multiple filings and potential for patent thickets, emphasizing the importance of comprehensive IP strategies.


Key Takeaways

  • Precise claim drafting is critical: Broad claims ensure extensive protection but must withstand validity challenges.
  • Patent scope influences market exclusivity: Protecting not only the chemical entity but also therapeutic uses and formulations can maximize commercial valuation.
  • Global patent strategies require family filings: Securing rights across jurisdictions amplifies enforcement and market reach.
  • Competitive landscape complexity necessitates vigilance: Continuous monitoring of related patents is vital to avoid infringement and carve out new innovation niches.
  • Patents are essential assets in strategic positioning: They underpin licensing, investments, and negotiations in the pharmaceutical industry.

FAQs

1. What types of claims are predominant in WO2015119924?
The patent most likely includes product claims to the chemical entity, process claims for synthesis routes, and use claims for specific therapeutic applications.

2. Can the scope of this patent prevent competitors from developing similar drugs?
Yes, if claims are broad and well-drafted, they can prevent competitors from manufacturing or selling similar compounds or methods within the patent’s jurisdiction until expiry.

3. How does WO2015119924 compare to existing patents?
Its novelty and inventive step depend on the uniqueness of the chemical structure, synthesis process, or therapeutic use compared to prior art.

4. What are the risks of patent infringement for related drugs?
If competitors develop structurally similar compounds not covered by the claims or used alternative routes, they might circumvent the patent, though enforcement remains challenging.

5. How can patent holders extend the commercial life of WO2015119924?
Through secondary patents on formulations, combination therapies, or novel uses, and by strategic patent prosecution and maintenance.


Sources:
[1] WIPO Patent Cooperation Treaty full text of WO2015119924 (assumed).
[2] Patent law best practices and standards.
[3] Global patent landscape analyses for pharmaceutical compounds.

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