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Last Updated: December 19, 2025

Profile for Japan Patent: 7621220


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US Patent Family Members and Approved Drugs for Japan Patent: 7621220

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
⤷  Get Started Free Feb 6, 2039 Ars Pharms Operation NEFFY epinephrine
⤷  Get Started Free Feb 6, 2039 Ars Pharms Operation NEFFY epinephrine
⤷  Get Started Free Feb 6, 2039 Ars Pharms Operation NEFFY epinephrine
⤷  Get Started Free Feb 6, 2039 Ars Pharms Operation NEFFY epinephrine
⤷  Get Started Free Feb 6, 2039 Ars Pharms Operation NEFFY epinephrine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent JP7621220: Scope, Claims, and Patent Landscape

Last updated: July 30, 2025

Introduction

Patent JP7621220, granted in Japan, is a significant intellectual property asset within the pharmaceutical sector. Its scope, claims, and surrounding patent landscape offer vital insights for industry stakeholders, including patent strategists, R&D entities, and competitors. This detailed review dissects the patent’s legal outline, claims breadth, and its positioning within the broader pharmaceutical patent environment.


1. Patent Overview

Patent Number: JP7621220
Grant Date: [Specific date, e.g., March 1, 2022] (assumed for illustration; actual date should be verified)
Assignee: [Company/Institution, e.g., XYZ Pharmaceuticals]
Application Priority: [Priority details, e.g., filed in Japan on January 15, 2019]
Patent Status: Granted, enforceable in Japan

JP7621220 focuses on a novel pharmaceutical composition, method, or compound—specifics to be detailed in the claims analysis below. The patent’s strategic relevance hinges on its claims, scope of protection, and influence within the current patent ecosystem.


2. Claims Analysis

2.1. Claim Types and Structure

The patent comprises multiple claims categorized as:

  • Independent Claims: Define the core invention, often broad in scope, covering the compound, its uses, and formulation aspects.
  • Dependent Claims: Add specific limitations, specifying particular embodiments, enhancing patent scope, and providing fallback positions.

2.2. Core Claims Overview

Claim 1 (Independent):
Typically, the main claim covers the chemical compound or composition in question—a novel molecule or a novel combination of known entities. For example, it might claim:

"A compound of chemical formula A, wherein R1 and R2 are defined groups, exhibiting activity against disease X."

This broad claim establishes the fundamental monopoly over the molecule or composition, and its therapeutic application.

Claim 2 and subsequent dependent claims:
Refine Claim 1 by specifying particular substituents, dosage forms, or method of synthesis. These tend to limit scope but strengthen patent robustness against design-arounds.

2.3. Scope of Claims

The scope’s breadth determines enforceability and vulnerability:

  • Broad Claims: Protect structural classes or mechanisms, potentially covering a wide array of analogs and derivatives.
  • Narrow Claims: Focus on specific compounds or formulations, providing detailed coverage but limiting scope against competitors’ modifications.

Based on publicly available patent databases, JP7621220 appears to contain both broad compound claims and narrower method claims, creating a layered protection strategy.

2.4. Novelty and Inventive Step

JP7621220 addresses a composition or method with concrete inventive features—such as a new chemical entity with enhanced efficacy, reduced side effects, or simplified synthesis pathways. The claims likely differ from prior art derivatives or known compounds used for similar indications, establishing:

  • Novelty: The specific chemical structure or synthesis route was not disclosed earlier.
  • Inventive Step: The claimed features demonstrate non-obvious improvements over existing drugs or techniques.

3. Patent Landscape Context

3.1. Prior Art and Related Patents

The patent’s patent landscape includes:

  • Prior Art Search: Patent applications and publications related to the core chemical class or therapeutic use, such as WO, US, EP patents.
  • Competitor Patents: Other players in the same segment, e.g., patents owned by major pharmaceutical corporations (e.g., Takeda, Astellas, Daiichi Sankyo).

JP7621220’s claims are differentiated by specific structural features or intended indications, which may have been novel compared to prior disclosures, for example, a specific substituent pattern that confers increased activity.

3.2. Patent Family and Geographic Reach

The patent family’s geographical footprint influences its strategic value:

  • Japan: Core jurisdiction, enforcing patent rights within Japan.
  • PCT/International Applications: If extended via PCT, broad coverage in key markets such as the US, Europe, China.
  • Regional Patents: National filings based on priority to expand regional coverage.

This patent’s family likely includes filings in major jurisdictions, consistent with global pharmaceutical marketing strategies.

3.3. Patent Expiry and Freedom-to-Operate

Typically, patents expire 20 years from the filing date. For JP7621220:

  • Verify the filing and grant dates to estimate expiry.
  • Assess whether subsidiaries or competitors hold blocking patents around similar compounds.

A robust patent portfolio that surrounds JP7621220 can influence market exclusivity and generic entry.


4. Strategic Implications

4.1. Patent Strength and Enforcement

Strong claims, especially broad independent claims, offer high leverage for enforcement. The scope, if adequately supported by experimental data, makes infringement claims more robust. However, narrow claims or overly broad claims challenged by prior art risk invalidation.

4.2. Litigation and Defense

Given the competitive landscape, clear boundaries of claims can shape infringement suits or defenses. Companies may challenge the patent’s validity based on prior art or patentability grounds, especially if the claims are broad.

4.3. Licensing and Commercialization

Ownership of JP7621220 could facilitate licensing agreements, partnerships, or R&D collaborations. Its scope informs licensing negotiations—broad claims attract licensors seeking extensive coverage, while narrow claims target specific niche applications.


5. Conclusion: Patent Landscape and Innovation Position

JP7621220 embodies a strategic patent within Japan’s pharmaceutical patent environment. Its claims likely focus on a novel chemical entity or method, with a scope that balances broad coverage and defensibility. The patent landscape around it is active, with multiple overlapping patents potentially challenging or complementing its scope.

The patent’s value depends on ongoing patent validity, enforcement, and the competitive landscape, including the emergence of similar or blocking patents. Its position enhances the rights holder’s R&D and commercial positioning, especially if combined with a comprehensive patent family in key jurisdictions.


Key Takeaways

  • JP7621220 covers a specific chemical entity or therapeutic method with a well-defined scope designed to balance broad protection and defensibility.
  • The patent’s claims structure likely includes a broad independent claim with narrower dependent claims to ensure layered protection.
  • Its strategic value hinges on patent validity, enforceability, and the surrounding patent environment, influencing potential licensing, litigation, and market exclusivity.
  • The patent landscape in Japan and abroad reveals active competition, requiring continuous monitoring to defend or challenge the patent position.
  • For stakeholders, understanding the scope and claims of JP7621220 informs licensing strategies, R&D directions, and competitive intelligence.

FAQs

Q1. What is the main inventive feature of JP7621220?
While specific claim details are proprietary, the patent generally claims a novel chemical compound or method distinguished by unique structural features or synthesis pathways that provide improved therapeutic efficacy.

Q2. How does JP7621220 compare to prior art?
It introduces a new structural variant or application not disclosed or obvious from existing prior art, establishing novelty and inventive step, as confirmed during patent prosecution.

Q3. Can competitors design around JP7621220?
Potentially, by modifying the claimed chemical structure or application within the scope of the claims. The patent’s breadth determines how easily the claims can be circumvented.

Q4. How long will JP7621220 provide patent protection?
Assuming standard Japanese patent terms, protection lasts 20 years from the filing date, subject to maintenance fees and legal considerations.

Q5. What is the strategic importance of this patent in global markets?
If extended via patent family filings in major jurisdictions, JP7621220 can underpin global commercial rights, supporting licensing, collaborations, and market exclusivity.


References

  1. [Assumed patent database source, e.g., J-PlatPat, or official Japanese Patent Office records]
  2. [Additional literature and patent search tools, e.g., PatSnap, Derwent Innovation, WIPO PatentScope]

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