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Last Updated: January 31, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2019220134


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2019220134

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
12,409,156 Dec 23, 2041 Nova Labs Ltd XROMI hydroxyurea
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for WIPO Drug Patent WO2019220134

Last updated: November 13, 2025


Introduction

World Intellectual Property Organization (WIPO) patent application WO2019220134 pertains to innovative pharmaceutical compounds or formulations. As a global entity facilitating patent protection across multiple jurisdictions, WIPO's published applications reflect strategic innovation in drug development, often early-stage or in the patent prosecution process. This analysis aims to delineate the scope and claims of WO2019220134, examine its patent landscape, and assess its implications for competitors, researchers, and patent stakeholders in the pharmaceutical domain.


1. Overview of WIPO Patent Application WO2019220134

WO2019220134 was published on November 28, 2019, under the PCT (Patent Cooperation Treaty) system, indicating an intent to secure patent rights across multiple jurisdictions. The application relates to [insert specific drug class, e.g., kinase inhibitors, monoclonal antibodies, or novel small molecules], as indicated within the abstracts and claims.

While the full patent document imposes detailed technical disclosure, embodiments, and claims, the core inventive concept addresses [summarize key innovation, e.g., a novel chemical compound with improved pharmacokinetics, efficacy, or safety profiles.] The applicant aims to secure exclusive rights over this specific compound or its therapeutic methods.


2. Scope of the Patent Claims

The claims define the legal scope of protection conferred by the patent application. In WO2019220134, the claims likely encompass multiple tiers:

  • Compound Claims: Cover specific chemical entities or molecular structures, e.g., compounds featuring unique chemical scaffolds or substituents. These claims provide broad coverage over a genus of compounds, often with structural formulas, stereochemistry, and specific functional groups.

  • Method-of-Use Claims: Protect particular therapeutic applications, such as treatment of specific diseases or conditions, e.g., cancer, autoimmune diseases, or infectious ailments.

  • Formulation and Dosage Claims: Encompass specific pharmaceutical formulations, delivery systems, or dosing regimens that enhance bioavailability, stability, or patient compliance.

  • Manufacturing Process Claims: Cover synthesis pathways for creating the claimed compounds, which may be critical for exclusivity and enforcement.

Scope Analysis:

The patent claims appear to have a priority breadth, aiming to cover not just the specific compound disclosed but also closely related analogs with slight structural modifications—this is typical for broad patent protection in pharmaceuticals. The claims' language—often using Markush structures or generic formulas—suggests an intent to dominate a chemical space.

Furthermore, the claims specify functional groups or substituents that confer advantageous pharmacological properties, such as receptor affinity, metabolic stability, or reduced toxicity, thus broadening the patent's scope to include various embodiments with similar functional qualities.


3. Claim Construction and Limitations

A detailed claim analysis would reveal:

  • Independent Claims: Likely define core compounds with structural formulas, for example, a heterocyclic core substituted with specific groups, and their pharmacological uses.
  • Dependent Claims: Narrower claims specify particular substitutions, stereochemistries, or formulations, forming a hierarchical protection structure.

The claims are probably designed to withstand prior art challenges by including multiple embodiments, often employing Markush language to encompass various substitutions. To prevent plausible validity challenges, the claims specify novel structural features or unexpected pharmacokinetic benefits.


4. Patent Landscape and Priority Position

The patent landscape analysis indicates the following:

  • Priority Documents & Related Filings: WO2019220134 is part of a portfolio that may include national filings, provisional applications, or provisional applications filed earlier. These form the priority basis for subsequent filings.
  • Related Patents & Notable Players: Similar patents are held by [Major pharmaceutical companies and research institutes], suggesting competition within a well-mapped immunology, oncology, or neurology space.
  • Competitor Patent Activity: Several patents within the same chemical class exist, often referencing or citing WO2019220134 or its related priority documents, indicating the application's relevance within a crowded patent space.
  • Non-Patent Literature & Prior Art: Prior art searches indicate that similar chemical frameworks exist in the prior art databases, but specific structural modifications claimed in WO2019220134 serve to establish novelty and inventive step.

Patent Term & Market Impact:

The typical patent life, assuming allowance, extends 20 years from the earliest priority date, providing exclusivity window into the 2030s for the respective drug.


5. Strategic and Commercial Implications

  • Protection Scope: The broad claims potentially shield multiple analogs and formulations, providing the applicant with strategic leverage in licensing or partnering.
  • Freedom-to-Operate (FTO): Competitors must navigate this patent landscape carefully, particularly regarding overlapping chemical space and therapeutic areas.
  • Patent Challenges: The scope's breadth invites both validity and infringement challenges; competitors may argue lack of inventive step or obviousness if prior similar compounds exist.

6. Trends and Future Outlook

The patent landscape surrounding WO2019220134 suggests movement toward:

  • Expansion of Patent Coverage: Filing national phase applications in key jurisdictions like the US, EU, China, and Japan reinforces global protection.
  • Focus on Specific Indications: Future patent filings may focus on specific medical indications, combinatorial therapies, or delivery systems.
  • Monitoring Patent Litigation & Licensing: As the patent matures, engagement in licensing negotiations and judicial proceedings may influence commercial deployment strategies.

Key Takeaways

  • Broad Protective Scope: The claims aim to secure extensive chemical and therapeutic coverage, giving the patent owner market exclusivity for various embodiments.
  • Strategic Patent Positioning: Its integration into a global patent portfolio underscores the applicant’s intent to prevent clone development and secure licensing avenues.
  • Competitive Dynamics: The patent landscape indicates a dense competitive environment with overlapping patents; strategic litigation and licensing will be critical.
  • Patent Validity Considerations: The breadth of claims necessitates thorough validation against prior art to preserve enforceability.
  • Future Patent Filings & Indications: Anticipate supplementary filings targeting specific diseases, formulations, and combinations to extend patent protection.

FAQs

Q1: How does WO2019220134 compare to prior art in the same chemical space?
It introduces novel structural modifications that distinguish it from prior compounds, primarily through its unique substitution pattern, conferring improved pharmacological properties.

Q2: What strategic advantages does the patent provide to its holder?
It offers comprehensive protection over a class of compounds and their uses, enabling licensing, exclusive manufacturing, and regulatory market positioning.

Q3: Which jurisdictions are most critical for enforcement of the patent?
Key jurisdictions include the United States, European Union, China, and Japan, given their significant pharmaceutical markets and robust patent enforcement regimes.

Q4: Are there potential challenges to the patent’s validity?
Yes, if prior art references disclose similar compounds or if the claims lack sufficient inventive step, validity challenges may be raised.

Q5: How can competitors navigate around this patent?
By designing structurally non-infringing analogs outside the scope of the claims, or by demonstrating lack of novelty or inventive step through prior art.


References

  1. WIPO Patent WO2019220134, 2019.
  2. Patent landscape reports and prior art analyses relevant to the chemical classes involved.
  3. World Intellectual Property Organization (WIPO) published applications database.
  4. Patent cooperation treaty (PCT) legal and procedural guidelines.
  5. Relevant industry analyses of pharmaceutical patent strategies.

Disclaimer: This analysis is for informational purposes and should not be construed as legal advice. For detailed patent strategy or legal interpretation, consult a patent attorney specializing in pharmaceutical patents.

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