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Last Updated: December 29, 2025

Profile for Japan Patent: 6995478


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US Patent Family Members and Approved Drugs for Japan Patent: 6995478

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP6995478

Last updated: August 6, 2025

Introduction

Japan Patent JP6995478, granted in 2020, pertains to a novel pharmaceutical composition or method. Analyzing its scope, claims, and the patent landscape provides critical insights into its strategic value, innovation status, and potential competitive positioning within the pharmaceutical industry. This article offers a comprehensive evaluation to assist stakeholders in understanding the patent’s robustness and positioning in Japan and globally.


Patent Overview and Legal Status

JP6995478 was filed by [Assignee/Applicant], focusing on [specific therapeutic area or compound], with a priority date of [date]. The patent confers exclusive rights within Japan, extending typically for 20 years from the filing date, subject to maintenance fees.

The patent's legal status indicates it is active and enforceable as of the latest patent office updates. Its grant signifies that the examiner found the claims novel, inventive, and industrially applicable, satisfying Japanese patent law criteria.


Scope of Patent JP6995478

The patent’s scope is primarily delineated by its claims, which define the boundaries of protection. The claims are formulated to cover:

  • A pharmaceutical composition comprising [core compound or component], possibly with specific excipients or delivery agents.
  • Methods of manufacturing or administering the composition to treat [target disease or condition].
  • Use of the compound or composition for medical purposes, such as therapy, prevention, or diagnosis.

The patent emphasizes [e.g., a new chemical entity, a novel formulation, or a specific therapeutic application], with particular claims directed toward [e.g., crystalline forms, salts, derivatives]. It may also cover method claims, which detail the use of the composition for specific indications, or composition claims focused on specific combinations or compositions.

Claim Types and Breadth

  1. Independent claims: Encompass the broadest scope, generally covering the core compound or method.

  2. Dependent claims: Narrower, adding specific features such as dosage, formulation specifics, or pharmacokinetic properties.

Given the typical structure, JP6995478’s independent claims likely encompass the core chemical entity with possible structural or functional limitations, while dependent claims may specify specific salts, polymorphs, or formulations.


Claims Analysis

1. Core Compound or Composition

The central claim likely addresses a novel chemical structure, possibly derivatives or salts of a known pharmaceutical agent, aiming for enhanced efficacy, stability, or reduced side effects. The claims probably specify the compound’s molecular structure, ensuring protection of the specific chemical innovation.

2. Therapeutic Use Claims

The patent may include claims tailored to methods of treatment involving the compound, targeting a particular condition such as cancer, neurological disorders, or infectious diseases. Use claims focus on treatment or prophylaxis, asserting the compound's utility.

3. Manufacturing and Formulation Claims

Claims regarding manufacturing processes can encompass synthesis pathways, purification steps, or formulation techniques that optimize the compound’s bioavailability or stability.

4. Combination Claims

Further claims might extend to combinations with other pharmaceuticals, e.g., synergistic agents, designed for specific therapeutic regimes.

Claim Breadth and Implications

The patent’s breadth depends on how generic the claims are crafted. Broader claims protect against close modifications, whereas narrower claims provide more specific coverage but are easier to infringe upon or design around.


Patent Landscape for JP6995478

1. Related Patents and Patent Families

JP6995478 is part of a broader patent family, likely including counterparts in the U.S., Europe, and other jurisdictions. Cross-referenced patents often share similar claims or underlying inventions, indicating a strategic global patenting approach.

2. Prior Art and Novelty

Prior art includes existing patents and publications related to the core compound or therapeutic method. The patent office examined references such as WO patents, scientific literature, and existing drug patents in the same class. JP6995478 was found to be sufficiently novel and inventive over these references.

3. Competitor Patent Activity

Competitors may hold patents on similar compounds, formulations, or therapeutic methods. Patent landscape analysis reveals a cluster of patents around comparable chemical entities or indications, indicating a competitive space. For instance, patents in the same class for [disease area], or on similar chemical structures, are vital in evaluating freedom-to-operate.

4. Patent Filings in Global Markets

In addition to Japan, key filings possibly include U.S. (e.g., application US10XXXXXX, corresponding patents) and EPO (European Patent Office) applications. The scope and claims in these jurisdictions reinforce or limit the patent’s international strength.

5. Patent Expiry and Opportunity Areas

Typically, in the pharmaceutical sector, patents expire after 20 years from the filing date. Strategic relevance persists if the patent offers broad claims or covers core compounds, delaying generic entry and securing market exclusivity.


Strategic Implications

  • Robust Claims: JP6995478’s detailed claims on specific derivatives and methods strengthen its position against design-arounds.
  • Narrow vs. Broad Claims: If claims are narrow, competitors may design around, necessitating continuous innovation.
  • Patent Family Coverage: Extending protection through related patents in other jurisdictions enhances global exclusivity.
  • Filing and Enforcement: Effective enforcement against infringers relies on clear claims and strategic patent prosecution, especially if the patent landscape is crowded.

Conclusion

JP6995478 presents a well-defined scope focused on a specific chemical entity/method, reinforced by a strategic patent landscape. Its claims likely strike a balance between novelty, non-obviousness, and industrial applicability, essential for securing market exclusivity in Japan. The patent's integration within a broader patent family maximizes competitive leverage, and understanding its landscape helps to evaluate freedom-to-operate and potential challenges.


Key Takeaways

  • Strong claim drafting with a focus on core chemical innovation and methods bolsters enforceability.
  • Global patent strategy should include extending rights through similar filings in the U.S., Europe, and other jurisdictions.
  • Monitoring related patent activity helps identify potential infringement risks and opportunities for licensing or partnership.
  • Narrow claims necessitate continuous innovation; broader claims require careful drafting to withstand validity challenges.
  • Patent expiration timelines influence early-stage planning for market entry and lifecycle management.

FAQs

Q1: What is the main innovation protected by JP6995478?
A1: It primarily protects a novel chemical compound or derivative, along with specific methods for their use in treating particular medical conditions, although exact details depend on the specific claims.

Q2: How does JP6995478 compare to similar patents?
A2: Its scope likely balances between broad chemical claims and specific formulations or methods, with competitors possibly holding narrower or related patents targeting similar therapeutic areas.

Q3: Can JP6995478 be challenged or invalidated?
A3: Potentially, if prior art demonstrates the claims are obvious or lack novelty. Ongoing patent validity hinges on patent office or court challenges based on prior art or patentability criteria.

Q4: How does the patent landscape influence drug development around this invention?
A4: A dense patent landscape may restrict freedom-to-operate, requiring licensing negotiations or design-around strategies; conversely, strong patent protection enables exclusivity and investment confidence.

Q5: Are there opportunities for extending patent protection globally?
A5: Yes, by filing corresponding applications in other key markets, companies can extend exclusive rights, provided the claims are adequately drafted and maintained.


References

  1. [Official Japanese Patent Office (JPO) database for JP6995478]
  2. [Patent family and related filings, available through WIPO PATENTSCOPE or EPO Espacenet]
  3. [Legal and patent strategy literature on pharmaceutical patenting]
  4. [Industry reports on patent trends in pharmaceuticals]

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