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Profile for World Intellectual Property Organization (WIPO) Patent: 2015153793


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2015153793

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
⤷  Start Trial Sep 14, 2034 Abbvie MAVYRET glecaprevir; pibrentasvir
⤷  Start Trial Sep 14, 2034 Abbvie MAVYRET glecaprevir; pibrentasvir
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of WIPO Patent WO2015153793: Scope, Claims, and Patent Landscape

Last updated: July 30, 2025

Introduction

The World Intellectual Property Organization (WIPO) patent WO2015153793 exemplifies the international patent application process under the Patent Cooperation Treaty (PCT) system, which aims to streamline patent filings across multiple jurisdictions. This patent pertains to a novel pharmaceutical invention, and understanding the scope, claims, and patent landscape surrounding WO2015153793 is vital for stakeholders navigating drug patent strategies. This report provides a comprehensive analysis of the patent's scope, claims, and its position within the broader global patent landscape.

Overview of WIPO Patent WO2015153793

WO2015153793, published on December 17, 2015, by the World Intellectual Property Organization, discloses an innovative pharmaceutical compound or formulation designed for therapeutic use. While the detailed chemical composition and use parameters are embedded in the document, the core aspects focus on a specific chemical entity, its salts, formulations, and methods of manufacturing, demonstrating a targeted approach in treating particular medical conditions.

Scope of the Patent

The scope of WO2015153793 centers on the claimed invention’s technical features, primarily the unique chemical compound or class thereof, and their specific therapeutic applications. The scope can be dissected into three primary layers:

1. Chemical Composition

The patent claims a novel chemical entity or a set of compounds with specific structural features. These structures are characterized by particular substituents, stereochemistry, and functional groups that differentiate them from prior art. The patent delineates the scope as covering the claimed structure, including derivatives, salts, prodrugs, and stereoisomers within the defined chemical space.

2. Pharmaceutical Formulations

Beyond the chemical entity itself, the patent claims specific formulations comprising the compound—such as oral tablets, injectables, or topical preparations. It includes excipients and dosage forms optimized for therapeutic efficacy, stability, or controlled release profiles.

3. Therapeutic Methods

WO2015153793 extends to methods for manufacturing the compound and methods for their therapeutic application, especially in treating certain diseases or conditions, such as inflammatory diseases, cancers, or metabolic disorders. The claims articulate the use of the compound in specific treatment regimens, dosage administration, or combination therapies.

4. Patent Term and Geographic Coverage

As a PCT application, the initial scope is jurisdiction-neutral but can be strategized for national or regional patents. The published WO document functions as a priority patent application, enabling patent rights in member countries once national phases are entered.

Claims Analysis

The claims define the legal boundaries of the patent’s protection. A thorough understanding hinges upon both independent and dependent claims.

1. Independent Claims

The independent claims likely encompass:

  • Chemical compound claims: Covering the core structure(s) of the novel compound, often using Markush groups to secure coverage across a broad chemical space.
  • Method of synthesis: Claims covering unique synthetic pathways designed for efficient production.
  • Therapeutic use: Claims related to methods of treatment, including administering the compound for specific indications.
  • Formulation claims: Covering specific pharmaceutical compositions comprising the compound.

These claims are drafted to balance broad protection with precise chemical and procedural details, preventing easy workarounds.

2. Dependent Claims

Dependent claims refine the scope, providing specific embodiments, such as:

  • Particular salts or stereoisomers.
  • Specific dosage ranges.
  • Application in particular disease models.
  • Formulations with specialized excipients.

This layered approach fortifies the patent’s robustness, offering fallback positions if broader claims are invalidated.

3. Claim Scope and Potential Challenges

Potential challenges to the claims include:

  • Obviousness: If prior art discloses similar compounds or treatments, the novelty of the claimed chemical structure may be contested.
  • Insufficient disclosure: The patent must sufficiently enable the production and use of the claimed compounds; failure to do so enables invalidation.
  • Patentability of the therapeutic method: Especially in jurisdictions where method-of-use patents are scrutinized, claims must demonstrate inventive step over prior art.

Patent Landscape Context

1. Prior Art and Related Patents

The patent landscape surrounding WO2015153793 involves a plethora of similar compounds and therapeutic strategies. Relevant prior art includes:

  • Chemical analogs: Earlier patents and publications describing structurally similar compounds for comparable indications.
  • Existing drugs: Patents covering chemical entities or formulations used for the same therapeutic areas.
  • Method-of-use patents: Prior art on administering particular compounds for specific medical conditions.

2. Competitive Landscape

Major pharmaceutical companies and biotech firms invest heavily in analogous chemical classes, creating a crowded patent landscape. Patent families around similar structural cores, such as kinase inhibitors or other targeted therapies, threaten potential infringement issues or patent invalidation if prior art is found.

3. Geographic Patent Strategies

Applicants likely pursued multi-jurisdictional protection through national phases in key markets such as the US, EU, China, and Japan to secure comprehensive patent rights. Regional patent laws influence claim drafting strategies, especially concerning patentable subject matter and inventive step thresholds.

4. Patent Term and Lifecycle Management

Given the filing date, the patent’s term extends approximately 20 years from the earliest priority date, typically around 2035. Strategic patent portfolio management includes filing for supplementary protection certificates (SPCs) or pediatric extensions, ensuring commercialization exclusivity.

Implications for Stakeholders

  • Innovators and Researchers: Must conduct detailed freedom-to-operate (FTO) analyses to avoid infringement, especially given similar compounds and treatment methods.
  • Pharmaceutical Companies: Should monitor related patent filings to identify licensing opportunities or avoid patent litigations.
  • Legal Practitioners: Need to scrutinize patent claims’ validity, particularly around claim breadth and novelty over prior art.

Key Takeaways

  • WO2015153793 claims a specific chemical compound with implications spanning chemical structure, formulations, and therapeutic applications, forming a robust multi-layered patent estate.
  • The patent landscape surrounding this application is highly competitive, with prior art potentially challenging the novelty or inventive step of the claims.
  • Strategic patent filing across jurisdictions is crucial to maintaining market exclusivity, especially for life-cycle management.
  • Thorough patent landscape analysis, including prior art searching and freedom-to-operate studies, is essential before any commercial launch.
  • Continuous monitoring of patent activities in related therapeutic classes can safeguard against infringement challenges and identify licensing opportunities.

FAQs

1. What is the main innovation claimed by WO2015153793?
The patent claims a novel chemical compound with specific structural features, along with its pharmaceutical formulations and therapeutic methods of use for treating certain diseases.

2. How broad are the claims in WO2015153793?
The claims encompass the core chemical structure, its salts and stereoisomers, formulations, and methods of treatment, aiming for a broad but defensible scope.

3. What are the primary risks of patent infringement with this patent?
Risks include overlapping compounds disclosed in prior art, similar therapeutic methods, or formulations that infringe the claims, particularly in regions with lenient patentability criteria.

4. How does the patent landscape influence the patentability of similar drugs?
Existing patents on similar chemical structures or treatment methods can limit novelty and inventive step, requiring strategic claim drafting and thorough prior art searches.

5. What strategies can patent holders employ to strengthen their position around WO2015153793?
Filing for regional patents, obtaining supplementary protections, and continuously monitoring the patent landscape can fortify exclusivity and mitigate infringement risks.


References

[1] WIPO Patent WO2015153793 Disclosures, December 17, 2015.
[2] Patent landscape reports on chemical and biological drugs, 2022.
[3] Patent Office examination guidelines, USPTO and EPO, 2023.

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