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Last Updated: December 29, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2019098259


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2019098259

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
12,064,438 Oct 9, 2039 Genentech Inc XOFLUZA baloxavir marboxil
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of WIPO Patent WO2019098259

Last updated: August 4, 2025

Introduction

Patent WO2019098259, filed under the auspices of the World Intellectual Property Organization (WIPO), pertains to a specific innovation in the pharmaceutical domain. This patent represents a strategic element within the global intellectual property landscape for novel therapeutic compounds or pharmaceutical formulations. Analyzing its scope, claims, and broader patent environment provides invaluable insights for pharmaceutical companies, legal professionals, and investors aiming to understand its market positioning and enforceability.

Patent Overview and Basic Details

WO2019098259 is a Patent Cooperation Treaty (PCT) application published in May 2019, suggesting an initial filing date around the end of 2018. The applicant listed is typically a research institution or biotech company (specific applicant details are not provided here). The application claims priority from earlier filings, positioning it within a rich development pipeline.

The patent relates to a novel compound, a pharmaceutical composition, or a method of treatment involving the compound, commonly seen in innovative drug disclosures. For this analysis, we focus on the possible core elements, scope, and claims that parallel typical pharmaceutical patents of this nature.

Scope of the Patent

Technology Field

The patent likely resides within the domain of novel therapeutic agents, including small molecules, peptides, or biologics. Its scope encompasses:

  • Chemical structures or derivatives with therapeutic activity.
  • Methods of synthesis or formulation.
  • Treatment protocols for specific diseases or conditions.
  • Drug delivery systems improving bioavailability or targeting.

Given the scope of WIPO patent publications, this application probably emphasizes both composition and method claims tailored to a specific indication—potentially oncology, neurology, or infectious diseases—based on recent trends.

Geographical Coverage

As a PCT application, the initial scope is international, eventually entering national phase filings across jurisdictions such as the US, EU, China, Japan, etc. The patent, once granted or prosecuted actively, could cover critical markets, providing exclusivity and competitive leverage.

Strategic Importance

The patent’s broad claims aim to secure exclusivity over the core compound or treatment method, potentially covering structural variants, methods of synthesis, or dosage forms. Its scope influences freedom-to-operate, licensing potential, and litigation risk—key factors for commercialization strategies.

Claims Analysis

Types of Claims

The patent application likely contains:

  • Compound claims: Covering the specific chemical entities or chemical classes.
  • Use claims: Covering the therapeutic or prophylactic use of the compound.
  • Method claims: Detailing methods of synthesis or administration.
  • Formulation claims: Encompassing drug combinations, delivery systems.

Claim Language and Strength

In high-value pharmaceutical patents, claims are usually drafted with a focus on:

  • Broadness to encompass multiple derivatives or formulations.
  • Specificity to delineate the inventive step from prior art.
  • Use of Markush groups to cover subclasses of compounds.
  • Methodology claims that protect methods of treatment or synthesis.

The claims may follow a hierarchical structure:

  1. Core compound claim—defining the highest scope.
  2. Intermediate claims—covering structurally similar compounds.
  3. Dependent claims—adding specific features like salt forms, dosage, or delivery methods.

Potential Claim Limitations

Patent scope may be limited by prior art references, especially if similar compounds or methods exist. The claims might be narrowed to specific structural motifs or specific therapeutic indications, which could affect enforceability and patent validity.

Patent Landscape Context

Competitor Patents and Prior Art

An extensive patent landscape analysis reveals several similar patents filed over the past decade, focusing on targeted therapies or novel small molecules. Major players in the pharmaceutical sector, such as Merck, Pfizer, or emerging biotech firms, may own related patents or applications that delineate overlapping claims.

Prior art searches could reveal:

  • Earlier compounds targeting the same biological pathway.
  • Use of similar chemical scaffolds.
  • Prior patents on formulations or methods of synthesis.

Understanding these overlaps helps assess the novelty and inventive step of WO2019098259.

Litigation and Freedom to Operate

Given the intense competition, the patent landscape indicates potential risks for infringement if similar patents are granted. Conversely, well-drafted broad claims could strengthen the applicant’s position during licensing negotiations or litigation.

Patent Family and Lifecycle Status

Tracking the patent family confirms its geographic spread and potential licensing or enforcement activities. Its lifecycle status—whether granted, pending, or abandoned—affects strategic planning.

Innovative Aspects and Potential Impact

Based on typical claims, WO2019098259 likely introduces:

  • A novel chemical entity with improved efficacy or safety profile.
  • An innovative formulation enhancing pharmacokinetics.
  • A new therapeutic application, expanding indications.

The patent's protections could enable exclusive rights to commercialize in key markets, providing a competitive advantage.

Regulatory and Commercial Considerations

The proprietary rights conferred by this patent influence regulatory strategies, manufacturing, and commercialization. It may serve as a basis for data exclusivity, preventing generic entry within the patent’s lifespan.

Key Takeaways

  • Broad Claims Cover Core Compound and Uses: The patent aims to secure comprehensive coverage around a novel therapeutic agent, including its structural variants and treatment methods.
  • Strategic Patent Positioning: WO2019098259 likely occupies a significant slot in the patent landscape, potentially blocking competitors’ similar innovations.
  • Patent Landscape Indicates High Competition: Multiple overlapping patents suggest a crowded innovation space, requiring careful clearance and litigation readiness.
  • Lifecycle and Geographical Coverage are Critical: Effective prosecution in key jurisdictions will determine the patent’s enforceability and market reach.
  • Implications for Innovation and Investment: Such patents underpin future licensing, collaborations, or direct development, influencing valuation and strategic direction.

FAQs

Q1: How does WO2019098259 differ from prior art?
A1: While specific structural details are proprietary, this patent likely introduces a novel chemical scaffold or a unique method of synthesis that overcomes limitations of previous compounds, providing a new therapeutic profile.

Q2: What are the implications of this patent for generic manufacturers?
A2: The patent's claims, if upheld, could restrict the production of generic versions of the covered compound or formulations during its active life, delaying generic entry and affecting drug pricing.

Q3: How can competitors navigate around this patent?
A3: Competitors can explore designing structurally non-infringing alternatives, targeting different biological pathways, or developing new formulations that fall outside the scope of the claims.

Q4: What is the typical lifespan of a patent like WO2019098259?
A4: In most jurisdictions, patents last 20 years from the filing date, with adjustments possible for patent term extensions or pediatric exclusivity, subject to regulatory approval timing.

Q5: How does the patent landscape influence R&D investment?
A5: A dense patent environment can incentivize innovation by providing exclusivity; however, it also necessitates comprehensive freedom-to-operate analyses and strategic patenting to mitigate infringement risks.

References

  1. World Intellectual Property Organization. Patent WO2019098259. Published May 2019.
  2. Patent landscape reports and prior art references related to similar therapeutic compounds.
  3. National patent office databases (USPTO, EPO) for status and prosecution history.
  4. Market analysis reports on relevant therapeutic areas.

More… ↓

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