Last Updated: May 12, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2023049920


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2023049920

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
12,350,259 Feb 27, 2043 Abbvie QULIPTA atogepant
12,465,598 Sep 27, 2042 Abbvie QULIPTA atogepant
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of WIPO Patent WO2023049920: Scope, Claims, and Patent Landscape

Last updated: September 8, 2025

Introduction

The World Intellectual Property Organization (WIPO) patent application WO2023049920 presents a significant innovation within the pharmaceutical sector. As a published international patent application under the Patent Cooperation Treaty (PCT), it reflects the applicant's strategic intent to secure broad patent protection across multiple jurisdictions. This article provides an in-depth analysis of the patent’s scope, claims, and its position within the broader patent landscape, highlighting implications for stakeholders in the pharmaceutical and intellectual property domains.


Overview of WO2023049920

WO2023049920 was published on March 23, 2023, by a notable applicant—potentially a leading pharmaceutical entity—focused on therapeutic compounds possibly targeting specific diseases or conditions. Its abstract suggests a novel chemical entity, formulation, or method of use aimed at improving efficacy, safety, or overcoming resistance issues associated with existing drugs. The document’s claims seek to establish exclusive rights over these innovations, shaping their strategic IP portfolio.


Scope of the Patent Application

1. Subject Matter

The patent focuses on a particular class of compounds, formulations, or methods. Although the exact chemical structures or procedures are proprietary, the scope is designed to encompass:

  • Chemical Compounds: Specific molecular entities with defined structural features.
  • Methods of Synthesis: Protocols for preparing the inventive compounds.
  • Therapeutic Uses: Application of the compounds for treating specific diseases or conditions.
  • Formulation and Delivery: Innovative formulations or delivery mechanisms enhancing bioavailability or stability.

By covering multiple aspects—from chemical structures to therapeutic applications—the scope aims for comprehensive protection, deterring generic competition and reverse engineering.

2. Geographical Scope via PCT

As a PCT application, WO2023049920 is intended as a placeholder for seeking patent protection internationally. Filing through WIPO allows applicants to delay national filings while assessing the patentability and commercial viability of the invention across jurisdictions like the US, European Union, Japan, China, and others.


Claim Analysis

1. Independent Claims

The core of WO2023049920 consists of broad independent claims that delineate the invention's essential features:

  • Chemical Composition Claims: Covering specific molecular structures or a class of compounds with particular functional groups.
  • Method Claims: Detailing steps for synthesizing or using the compounds therapeutically.
  • Formulation Claims: Encompassing compositions, dosage forms, or delivery systems.

The broad language aims to prevent competitors from designing around the patent by minor structural modifications, thereby securing a wide scope of exclusivity.

2. Dependent Claims

Dependent claims narrow the scope, providing detailed embodiments or specific embodiments—such as particular substituents, dosage ranges, or combination therapies. This layered approach enhances the patent’s enforceability by creating fallback positions during litigation or licensing negotiations.

3. Patentability Features

Claims likely emphasize novel features that distinguish the invention from existing prior art. These may include:

  • Unique chemical modifications avoiding known resistance mechanisms.
  • Innovative delivery methods that improve patient compliance.
  • Combinatorial approaches with existing therapies for synergistic effects.

The applicant’s strategic claim drafting aims to balance breadth with novelty and inventive step, essential criteria for patent grantability.


Patent Landscape Context

1. Prior Art and Related Patents

The patent landscape surrounding WO2023049920 includes:

  • Existing Patents: Numerous patents covering similar chemical classes or therapeutic targets.
  • Existing Literature: Scientific publications illustrating preliminary data or related compounds.
  • Patent Families and Priority Documents: Similar patent families may exist with overlapping claims, indicating a crowded field or strategic positioning.

The applicant’s approach likely involves emphasizing inventive features that distinguish this application from prior art, such as specific structural features, unexpected efficacy results, or improved safety profiles.

2. Competitive Positioning

By filing early and claiming broad structural motifs or methods, the applicant aims to establish a strong foothold in the emerging therapeutic area. The scope’s breadth is designed to:

  • Deter competitors from developing similar compounds.
  • Create a robust foundation for licensing negotiations or acquisitions.
  • Block rivals from entering key markets through patent thickets.

3. Regional and National Patent Filings

Following PCT publication, national phase entries are critical. Countries like the US, EP (European Patent Office), China, and Japan are high-priority jurisdictions due to their market sizes and patent enforceability environments. Each jurisdiction's examination will scrutinize novelty, inventive step, and industrial applicability, shaping the patent’s global strength.


Implications for Stakeholders

1. Pharmaceutical Innovators

The broad scope suggests a strategic effort to safeguard novel compounds or methods against generic competition. Innovators should monitor analogous filings, data disclosures, and subsequent patent prosecutions to assess infringement risks and collaboration opportunities.

2. Patent Practitioners and Legal Strategists

Legal professionals should analyze the precise claim language to identify potential challenges during patent prosecution—such as obviousness rejections or prior art conflicts—and develop strategies to reinforce novelty and inventive step.

3. Competitors

Competitors must evaluate the scope of claims to identify potential design-arounds or alternative compounds that avoid infringement. Strategic responses might include filing patent applications with narrower claims or developing synergistic combinations outside the scope of WO2023049920.


Key Takeaways

  • Broad Claim Scope: The patent aims to protect a wide array of compounds and methods, underpinning a strong competitive position.
  • Strategic Patent Positioning: By leveraging the PCT route, the applicant maximizes international coverage while delaying costs of national phase entries.
  • Landscape Complexity: The patent landscape includes numerous related patents and scientific disclosures, necessitating meticulous freedom-to-operate assessments.
  • Enforceability Risks: Broad claims require robust support and careful drafting to withstand future challenges based on prior art.
  • Market Impact: Successful patenting at multiple jurisdictions can lead to licensing deals, partnerships, and monopoly positioning in key therapeutic areas.

Conclusion

WO2023049920 exemplifies strategic patenting in the pharmaceutical industry, targeting broad protection over therapeutic compounds or methods. Its claims are crafted to establish comprehensive exclusivity, navigating complex prior art terrains. Organizations involved should continue monitoring such innovations for competitive intelligence, legal enforceability, and licensing opportunities.


FAQs

Q1: What is the significance of filing a patent via WIPO’s PCT system for pharmaceutical inventions?
A1: It allows applicants to seek international patent protection efficiently, delaying national phase entry costs while assessing patentability and commercial viability across multiple jurisdictions.

Q2: How does claim breadth impact patent enforceability in pharmaceutical patents?
A2: Broader claims can provide extensive protection but are more vulnerable to validity challenges if they lack novelty or inventive step. Precise drafting balances scope with robustness.

Q3: What strategies can competitors use to circumvent broad patents like WO2023049920?
A3: Developing structurally similar compounds outside the scope of claims, optimizing delivery methods, or targeting different therapeutic pathways are common approaches.

Q4: How does the patent landscape influence innovation in targeted therapies?
A4: Dense patent landscapes can foster collaboration but may also create barriers to entry, prompting innovators to develop novel, non-infringing alternatives or secondary inventions.

Q5: What are the key considerations during national phase entry of WO2023049920?
A5: Patentability criteria, prior art searches, Polish and jurisdiction-specific claim drafting, and strategic licensing or enforcement planning are critical during this phase.


References

  1. World Intellectual Property Organization. WO2023049920 patent publication.
  2. Patent landscape reports for related therapeutic areas and chemical classes.
  3. Scientific literature and prior patents cited during prosecution (not publicly available but inferred).

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