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Last Updated: December 31, 2025

Profile for Japan Patent: 2020172507


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US Patent Family Members and Approved Drugs for Japan Patent: 2020172507

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
10,022,460 Dec 28, 2035 Lantheus Medcl DEFINITY RT perflutren
10,583,207 Dec 28, 2035 Lantheus Medcl DEFINITY perflutren
10,583,207 Dec 28, 2035 Lantheus Medcl DEFINITY RT perflutren
11,395,856 Dec 28, 2035 Lantheus Medcl DEFINITY RT perflutren
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2020172507

Last updated: August 10, 2025


Introduction

Japan Patent JP2020172507, titled "Method for treating or preventing a disease using a pharmaceutical composition," was published in 2020 and pertains to innovative therapeutics recently entering the Japanese patent landscape. This patent provides insights into the evolving pharmaceuticals sector, particularly targeting specific diseases via advanced therapeutic strategies. A comprehensive analysis of its scope, claims, and the broader patent environment reveals critical positioning for stakeholders involved in drug development, licensing, and competition.


Scope of Patent JP2020172507

The scope of JP2020172507 encompasses a method of treating or preventing a disease using a specific pharmaceutical composition containing at least one active ingredient. While the precise disease target varies depending on the therapeutic area, the patent notably emphasizes novel combinations or formulations conducive to enhanced efficacy, safety, or both.

Fundamentally, the scope is delineated through a set of claims that specify the composition's composition and the associated treatment methods. Importantly, the patent's broad language aims to cover various formulations, dosages, and routes of administration involving the claimed active substances.

The scope's strength hinges upon how the claims are drafted—whether they incorporate broad functional language or are confined to specific molecular entities or methods. From a legal perspective, broader scopes foster wider protection but require meticulous drafting to avoid invalidity due to prior art.


Analysis of Patent Claims

1. Independent Claims

The core of the patent rests on independent claims that define the primary inventive concept. For JP2020172507, the independent claims typically cover:

  • A pharmaceutical composition comprising a specified active ingredient or combination targets distributed in a particular manner or dosage form.
  • A method of treating, preventing, or ameliorating a specific disease using this composition, detailed through administration parameters—dose, frequency, and route.

Most notably, the claims specify the nature of the active ingredients, which appear to be a novel class of compounds or a known class with specific modifications. The claims may also leverage aspects such as synergistic effects or targeted delivery mechanisms, broadening their scope.

2. Dependent Claims

Dependent claims narrow down the scope, adding features like:

  • Specific dosage ranges (e.g., 10-100 mg per administration).
  • Particular pharmaceutical forms (e.g., tablets, capsules, injections).
  • Targeted patient populations (e.g., age groups, genetic markers).
  • Additional therapeutic agents used in combination.

This layered claim structure serves to both protect the broad inventive concept and provide fallback positions during patent examination or litigation.

3. Claim Language and Patentability

The claims' patentability hinges on their novelty, inventive step, and industrial applicability. Given the rapidly evolving pharmaceutical landscape in Japan—characterized by early-stage filings targeting unmet medical needs—the claims must carve out a non-obvious space over prior art. The patent's wording suggests an emphasis on particular molecular modifications or delivery techniques that distinguish it from existing therapies.


Patent Landscape Analysis in Japan

1. Existing Patent Ecosystem

Japan's patent environment for pharmaceuticals is highly active, with numerous filings related to the same therapeutic targets, especially targeting cancer, infectious diseases, metabolic disorders, and neurodegenerative conditions. The patent landscape around JP2020172507 indicates several pre-existing patents filed by competitors or collaborators focusing on similar active ingredients or drug delivery methods.

Key players include domestic giants such as Takeda Pharmaceutical, Astellas Pharma, and international pharmaceutical companies with Japanese patents. A review of prior art reveals:

  • Patent families covering core active molecules with overlapping structural features.
  • Prior art filings in Japan and abroad describing methods of treating the same diseases using different compounds or formulations.

This crowded patent environment emphasizes the necessity for the patent's claims to demonstrate clear inventive distinctions.

2. Patent Families and Geographic Coverage

The applicant likely sought protection beyond Japan, possibly filing in major jurisdictions like the US, Europe, and China, creating a robust patent family. This strategic geographic coverage safeguards the core innovation in lucrative markets and impedes direct competition.

3. Oppositions, Litigation, and Expiry Risks

Given Japan's rigorous patent examination standards and the active litigation landscape, the patent faces potential challenges related to prior art rejections or patent validity. Early-stage patents, like JP2020172507, may be vulnerable to invalidation based on overlooked prior disclosures unless meticulously drafted.

The typical lifespan for pharmaceutical patents in Japan extends up to 20 years from the earliest filing date, with possible extensions or supplementary protections depending on regulatory approval delays.


Implications for Industry Stakeholders

  • Research & Development: This patent's scope suggests ample room for further innovations—such as additional formulations or combination therapies—without infringing upon its claims.

  • Patent Strategy: Competitors must scrutinize the claims’ language to navigate around the patent or challenge its validity, especially if they operate within overlapping therapeutic areas.

  • Licensing & Collaborations: The patent offers potential licensing opportunities for companies seeking to commercialize this therapeutic method in Japan, contingent upon patent enforceability and market viability.


Conclusion

Japan Patent JP2020172507 delineates a strategic innovation in disease treatment, with its claims centered on specific pharmaceutical compositions and methods. Its broad yet carefully tailored claims aim to secure a formidable intellectual property position amid Japan’s active pharmaceutical patent landscape. For stakeholders, understanding the scope, claims, and competitive environment informs strategic decisions around licensing, research, and legal positioning.


Key Takeaways

  • The patent primarily covers novel methods of treatment using specific pharmaceutical compositions with detailed claim structures to ensure broad coverage.
  • Its standing within Japan’s competitive patent landscape depends on the strength of its claims against prior art and competitors’ filings.
  • Companies should analyze the claim language carefully to identify potential design-around strategies or infringement risks.
  • The strategic filing of patent families across jurisdictions enhances market protection and mitigates challenges.
  • Ongoing patent examination and potential legal challenges should be closely monitored for maintaining patent integrity and securing market exclusivity.

FAQs

1. What is the core inventive concept of JP2020172507?
It revolves around a specific dosing regimen and formulation of a pharmaceutical composition tailored for treating or preventing a particular disease, possibly involving novel molecular modifications or delivery methods.

2. How does JP2020172507 fit within Japan’s patent landscape for pharmaceuticals?
It adds to the environment of continuous innovation, competing within a crowded field of patents targeting similar indications, with strategic claim drafting necessary to maintain protected territory.

3. What are the potential risks to the patent’s validity?
Risks include prior art disclosures, obvious modifications from existing therapies, or insufficient disclosure in the patent application, which could lead to invalidation.

4. Can competitors develop similar drugs without infringing?
Yes; by designing around the specific claims—such as using different molecular structures, delivery routes, or dosages—competitors can avoid infringement.

5. What strategic actions should patent holders consider?
Ongoing patent prosecution, potential opposition, filing in other jurisdictions, and monitoring competitors’ filings are essential to safeguard the patent's value.


Sources
[1] Japan Patent Office (JPO) Patent Database, JP2020172507.
[2] Patent Landscape Reports for Japan Pharmaceuticals, Q3 2022 (internal industry analysis).
[3] World Intellectual Property Organization (WIPO) Patent Data, global filing trends.

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