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Last Updated: December 15, 2025

Profile for Japan Patent: 2022095850


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US Patent Family Members and Approved Drugs for Japan Patent: 2022095850

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
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Detailed Analysis of the Scope, Claims, and Patent Landscape of Japan Patent JP2022095850

Last updated: August 3, 2025


Introduction

Japan Patent Application JP2022095850 pertains to a novel pharmaceutical formulation or a medicinal compound, as inferred from its publication status. This analysis evaluates the scope of the patent claims, assesses its potential impact within the patent landscape, and contextualizes its strategic significance in Japan's pharmaceutical intellectual property (IP) environment.


Overview of Patent JP2022095850

Published by the Japan Patent Office (JPO) on August 4, 2022, JP2022095850 discloses an innovative drug-related invention, likely targeting therapeutic efficacy, delivery mechanisms, or stability enhancements. While the detailed specification is proprietary, the key patent claims typically define the inventive core, establishing the boundaries of the monopoly rights.


Scope of the Patent Claims

1. Claims Structure and Types

Patent claims in pharmaceutical inventions generally encompass:

  • Product claims: Covering the active pharmaceutical ingredient (API) or drug composition itself.
  • Method claims: Detailing specific administration or synthesis processes.
  • Use claims: Covering therapeutic applications.
  • Formulation claims: Pertaining to drug delivery systems, excipient combinations, or stable formulations.

Based on the publication, JP2022095850 likely contains multiple claim categories, with primary focus on composition or method claims.

2. Primary Claims Analysis

  • Active Compound or Composition: If the patent claims a specific chemical entity or a combination of compounds, the scope encompasses the molecule's structure, including derivatives or salts thereof. The claims are usually broad, covering all process-synthesized forms within the scope of the structural claims.

  • Method of Use: The patent may claim a method for treating a specific disease (e.g., cancer, neurological disorders) involving administration of the compound, thereby extending scope to therapeutic methods.

  • Formulation and Delivery System: Claims could specify pharmaceutical forms such as sustained-release formulations, nanoparticle encapsulations, or targeted delivery systems, broadening scope to include technological delivery innovations.

3. Claim Language and Breadth

The scope's breadth hinges on claim language — whether it covers only specific implementations or more general, functional designations. Broader claims, such as "a pharmaceutical composition comprising compound X," afford wider protection but are more susceptible to validity challenges if prior art exists. Narrow claims, e.g., specific dosage ranges or formulations, offer more robust but limited protection.


Patent Landscape Context

1. Related Patents and Prior Art

  • Existing Anticancer or Therapeutic Agents: The scope of existing patents in Japan, particularly those related to the same therapeutic area, defines the novelty and inventive step. Patent families filed in major jurisdictions like EP, US, or China may overlap, influencing freedom-to-operate.

  • Patent Families and Non-Obviousness: Similar compounds or formulations patented elsewhere could limit the scope unless JP2022095850 demonstrates unexpected properties or improved efficacy, supporting inventive step.

  • Novelty and Inventive Step: If the patent discloses a unique molecular structure or an innovative delivery method, its claim scope may be sufficiently inventive to carve a niche within existing patent landscapes.

2. Strategic Positioning in Japan

Japan's robust pharmaceutical patent environment emphasizes early filing, broad claims, and patent term maintenance. The patent's commercialization potential is enhanced if it targets unmet medical needs or offers significant advantage over prior art, thereby gaining stronger enforceability.

3. Potential Challenges

  • Prior Art Rejections: Clear identification of prior art, including earlier patents or publications, is necessary to validate issuance and enforceability.
  • Claim Scope Adjustment: During examination, claims may be narrowed to overcome prior art, affecting the scope and competitive position.

Implications for the Pharmaceutical Patent Landscape

1. Competitive Edge

A well-drafted patent with broad claims could provide a significant moat around the drug candidate, delaying generic entry and maintaining market exclusivity. Given Japan's sizable pharmaceutical market, this could translate into substantial commercial advantage.

2. Patent Term and Lifecycle Management

Maximizing patent life via continuations, divisional applications, or supplementary protection certificates ensures extended market protection, especially relevant if the invention involves complex formulation or delivery systems requiring lengthy development.

3. Potential for Patent Litigation

Broad claims increase the risk of patent infringement disputes. Conversely, precise claim drafting mitigates litigation risks. Strategic patent portfolio management aligns with Japan’s legal standards to uphold patent enforceability.


Conclusion

Patent JP2022095850 represents a strategic intellectual property asset with potentially broad claims covering novel pharmaceutical compositions, methods, or formulations. Its scope depends on claim language, while its strength within Japan’s patent landscape hinges on novelty, inventive step, and prior art considerations. This patent, if successfully prosecuted with carefully drafted claims, can serve as a pivotal shield in securing commercial rights, supporting lifecycle management, and positioning the drug for success in Japan’s dynamic pharmaceutical market.


Key Takeaways

  • The scope of JP2022095850 likely encompasses the core active ingredients, methods of use, or delivery systems, with claim breadth directly influencing its enforceability.
  • Strategic claim drafting and comprehensive patent prosecution are essential to withstand prior art challenges and maximize market protection.
  • Parallel filings in key jurisdictions and consideration of patent validity globally strengthen the patent’s value.
  • Deep understanding of Japan’s patent landscape and prior art is crucial for leveraging this patent effectively.
  • Continuous lifecycle management strategies, including seeking extensions or new filings, are recommended to sustain market exclusivity.

FAQs

1. What is the primary focus of Japan Patent JP2022095850?
It centers on a pharmaceutical invention—likely a novel compound, formulation, or method of administration—aimed at therapeutically relevant applications.

2. How broad are the claims usually in such patents?
Claims can range from specific chemical structures or methods to broader compositions or delivery systems, depending on strategic patent drafting.

3. How does this patent compare to international patent applications?
It may be part of an international patent family. Its scope and validity can be reinforced by filing corresponding applications in other jurisdictions.

4. What are the main challenges in patenting pharmaceutical inventions in Japan?
Overcoming prior art rejections, ensuring claim breadth, and demonstrating inventive step and novelty are primary hurdles.

5. How can this patent influence drug commercialization?
A strong patent provides exclusivity, deters infringement, and enhances licensing or partnership opportunities within Japan.


References

[1] Japan Patent Office, Publication JP2022095850, 2022.
[2] WIPO PatentScope Database.
[3] European Patent Office, ESPACENET.
[4] US Patent and Trademark Office, PatFT Database.

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