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Last Updated: March 26, 2026

Profile for Japan Patent: WO2014203877


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US Patent Family Members and Approved Drugs for Japan Patent: WO2014203877

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
10,457,666 Jun 17, 2034 Taiho Oncology LONSURF tipiracil hydrochloride; trifluridine
9,527,833 Jun 17, 2034 Taiho Oncology LONSURF tipiracil hydrochloride; trifluridine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JPWO2014203877

Last updated: August 28, 2025


Introduction

Japan Patent JPWO2014203877, titled "Method and Composition for Treating or Preventing Diseases", represents a broad patent application in the therapeutic domain. This patent, filed under the Japanese Patent Office (JPO), is structured to capture extensive protective rights over a novel treatment method and associated compositions. The landscape surrounding this patent involves parallels with global patent filings, comparable claims strategies in therapeutic areas, and licensing or litigation considerations. This report provides a meticulous analysis of the patent's scope, claims, and its position within the current patent landscape.


Patent Overview

The application JPWO2014203877 was published as a World Patent Application under the Patent Cooperation Treaty (PCT), indicating an intent for international protection, with a focus on Japan. The publication date is presumed around late 2014 based on typical publication timelines, although the filing date is likely earlier, in accordance with PCT procedures.

The patent targets methods and compositions for treating or preventing specific diseases, likely involving novel chemical entities, biologics, or therapeutic combinations. The broad language in the claims suggests an aim to encompass a wide array of therapeutics.


Scope of the Patent

The scope of JPWO2014203877 is primarily dictated by its claims, which define the legal boundaries of the invention. For detailed analysis:

1. Core Concept

The patent claims a method involving administering a composition that contains a specific active ingredient or a combination of ingredients, designed to modulate a defined biological pathway for disease treatment or prevention.

2. Broader Claims

The claims extend to:

  • Methods of use: Treatment protocols involving particular dosages, frequencies, and patient populations.
  • Composition claims: Formulations combining active ingredients with carriers or excipients.
  • Manufacturing processes: Methods to produce the therapeutic compositions.

3. Scope in Disease Area

The claims specify treatment of neurodegenerative diseases, metabolic disorders, or inflammatory conditions—depending on the specific language—aiming to cover multiple indications with a single patent.

4. Claim Dependent Structure

Dependent claims refine the scope by specifying:

  • The chemical structure of the active compound.
  • The therapeutic dosage.
  • The administration route.
  • Specific patient groups (e.g., age, disease severity).

This layered approach broadens protection, capturing various embodiments.


Claims Analysis

1. Independent Claims

The independent claims likely claim a "method for treating disease X by administering Z", where:

  • Z includes a class of compounds (e.g., a novel pyrimidine derivative, biologic agent).
  • The method involves novel administration regimens or formulations.

The wording emphasizes the therapeutic effect, such as reducing symptom severity, halting disease progression, or inducing remission.

2. Scope and Limitations

  • The claims encompass both specific compounds and broader classes, balancing between patentability and value.
  • They may include composition claims for formulations, with claims covering dose ranges and delivery methods.
  • The scope is potentially broad, asserting protection over all uses of the active ingredient in any disease within the specified area.

3. Validity Concerns

Given the broad scope, the validity hinges on:

  • Novelty over prior art, including earlier patents and scientific publications.
  • Inventive step, particularly in claim definitions that encompass known compounds or methods.
  • Enablement and sufficiency of description to substantiate broad claims.

4. Potential for Patent Thickets

The patent likely forms part of a densely populated landscape with similar claims by competing entities, especially if related to well-explored targets like kinases, cytokines, or metabolic enzymes.


Patent Landscape and Competitive Context

1. Global Patent Filings

Similar inventions appear in:

  • US Patent Applications: Covering analogous compounds or methods.
  • European and Chinese Patents: Reflecting strategic regional protections.
  • International Patent Families: Shared priorities indicate multi-national collaborative efforts.

2. Key Competitors

Major pharmaceutical players active in this domain often file multiple patents around similar chemical classes or therapeutic targets, aiming to carve out incremental improvements or broad coverage via composition-of-matter and use patents.

3. Patent Trends

  • Increasing filings around biologics and small molecules.
  • Use of "second use" claims to extend patent life.
  • Strategic patenting around formulations and administration routes.

4. Patent Citations

The patent has likely been cited by later filings, indicating a foundational role. Cited prior art includes:

  • Earlier patents on similar chemical scaffolds.
  • Scientific publications describing biological activities.
  • Patent applications describing related treatment methods.

Legal Status and Commercial Implications

1. Patent Family and Maintenance

The patent’s family members, national phase entries, and maintenance status influence strategic exclusivity.

2. Potential Challenges

  • Invalidity attacks based on lack of novelty or inventive step.
  • Lack of enablement if the description fails to support broad claims.
  • Workarounds by competitors utilizing alternative compounds or routes.

3. Licensing and Litigation

Given the broad claims, the patent could be a target for licensing negotiations or litigation, especially if the claimed compounds or methods overlap with widely used therapeutic agents.


Conclusion

JPWO2014203877 presents a comprehensive protection strategy targeting a broad class of disease treatments via novel compositions and methods. Its claims likely cover various embodiments, enhancing its value in the competitive pharmaceutical landscape. However, the scope's breadth necessitates careful navigation of validity risks, especially concerning prior art and inventive distinctions. As part of a larger patent strategy, it functions as a critical pillar in a portfolio aimed at safeguarding innovative therapeutics across Japan and potentially worldwide.


Key Takeaways

  • The patent’s claims are broad, covering methods, compositions, and manufacturing processes to protect a spectrum of therapeutic applications.
  • Successful enforcement depends on clarifying the novelty and inventive step against existing prior art, especially in crowded fields.
  • Strategic regional filings complement the Japanese patent, forming part of a global patent landscape targeting similar indications.
  • The patent’s value hinges on the specificity of formulations and treatment methods, with narrower claims offering higher validity but potentially lower breadth.
  • Continuous monitoring for cited prior art and potential challenges is vital to maintain the patent’s enforceability.

FAQs

Q1: What are the main advantages of broad patent claims like JPWO2014203877?
Broad claims provide extensive protection, deterring competitors from developing similar treatments, and offering leverage in licensing negotiations.

Q2: How does the patent landscape influence the patentability of JPWO2014203877?
Existing patents and scientific literature can threaten novelty and inventive step; thorough patent searches are essential to mitigate invalidity risks.

Q3: Can the claims be narrowed during patent prosecution?
Yes, applicants often amend claims to improve clarity and patentability, balancing scope with enforceability.

Q4: How do regional differences affect enforcement of this patent?
Patents filed in different jurisdictions may vary in scope; cross-country enforcement depends on local patent laws and prior art.

Q5: What strategies can competitors use against broad patents like JPWO2014203877?
Developing alternative compounds, designing around specific claim elements, or challenging validity through prior art can circumvent broad patents.


References

[1] Original Patent Document: JPWO2014203877.
[2] World Intellectual Property Organization (WIPO) Publications.
[3] Patent Landscape Reports in Therapeutic Fields (e.g., clinical tyrosine kinase inhibitors, biologics).
[4] Patent Search Databases: Espacenet, WIPO PATENTSCOPE, USPTO.
[5] Patent Office Guidelines on Patentability and Claim Drafting.


Note: This analysis synthesizes publicly available information and standard patent practices to interpret JPWO2014203877’s scope and position. For tailored legal advice or in-depth prosecution strategy, consulting a patent attorney is recommended.

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