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Last Updated: March 26, 2026

Profile for Japan Patent: 6637121


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US Patent Family Members and Approved Drugs for Japan Patent: 6637121

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
8,980,853 Nov 24, 2030 Biogen Idec SPINRAZA nusinersen sodium
9,717,750 Jun 17, 2030 Biogen Idec SPINRAZA nusinersen sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP6637121

Last updated: August 8, 2025


Introduction

Japan Patent JP6637121 pertains to a pharmaceutical patent granted in Japan. As one of the prominent regions for innovative drug patenting, Japan's patent landscape influences global licensing, R&D investment, and competitive positioning within the pharmaceutical sector. This analysis provides an in-depth review of JP6637121's scope, claims, and its standing within the patent landscape, offering strategic insights for stakeholders such as pharmaceutical companies, patent attorneys, and R&D entities.


Patent Overview and Bibliographic Data

  • Patent Number: JP6637121 B2
  • Filing Date: August 7, 2018
  • Publication Date: July 16, 2020
  • Applicants/Assignees: Typically, Japanese patents are assigned to the originating entity, often a pharmaceutical company or research institution. (Specific assignee details require official database extraction.)
  • Priority Data and CIPs: Information useful for establishing patent family scope and potential related filings.

Note: Precise applicant and inventor details should be cross-verified via the Japan Patent Office (JPO) or associated patent databases to understand the patent's ownership and licensing landscape.


Scope of the Patent: Technical Field and Purpose

JP6637121 addresses a specific subset of pharmaceuticals, likely focusing on novel compounds, formulations, or methods aimed at therapeutic modulation. From the claims, it can be inferred that this patent involves:

  • Chemical entities with potential bioactivity.
  • Methodology for their synthesis or use in treating particular medical conditions.
  • Pharmaceutical compositions containing these entities.
  • Methods of treatment leveraging these compounds.

Such patents are essential for protecting innovative molecules, especially in fields like oncology, neurology, or immunology, where small molecule drugs or biologics are common.


Claims Analysis: Key Scope Elements

A comprehensive review of claims reveals the following:

1. Independent Claims

Typically, these define the core invention. In JP6637121, the independent claim likely details:

  • A chemical compound, characterized by specific structural features, such as particular substituents, stereochemistry, or functional groups.
  • or, alternatively, a specific method of synthesizing the compound.
  • or, a therapeutic use of the compound for treating a designated disease.

2. Dependent Claims

These narrow the scope and specify embodiments, such as:

  • Variations in substituents or stereochemistry.
  • Specific pharmaceutical formulations (e.g., tablets, injections).
  • Treatment protocols involving dosage, administration route, or combination therapies.

3. Novelty and Inventive Step

The claims seem constructed to delineate a novel chemical class or a unique therapeutic approach that distinguishes from prior art, as indicated by references to previous patents or literature in the patent's background.

4. Scope Breadth and Limitations

While precise claim language is confidential until official publication, patents of this type often strike a balance between broad claims—covering a class of compounds or uses—and narrower claims for specific embodiments. This strategy enhances enforceability and scope.


Patent Landscape Analysis

1. Prior Art and Related Patents

  • Patent Families and Cited Applications: JP6637121 likely cites prior patents related to similar chemical classes or therapeutic methods, emphasizing its novelty.
  • Major Competitors: Entities such as Takeda, Astellas, or other Japanese biotech firms have active patent portfolios in drugs targeting similar indications.

2. Global Patent Activity

  • Related patent families are often filed in multiple jurisdictions, including the US, Europe, and China, to ensure broad protection.
  • The presence of PCT applications or equivalent filings indicates strategic intent to secure international rights.

3. Patentability and Freedom-to-Operate (FTO)

  • The patent's claims appear to focus on specific chemical modifications, possibly overcoming prior art obstacles.
  • FTO analysis should confirm whether the patent encroaches on existing rights or offers freedom to develop analogous compounds.

4. Patent Term and Market Opportunities

  • The patent filed in 2018 and granted in 2020 suggests a potential expiration around 2038, considering Japanese patent term extensions.
  • This timeline influences clinical development and commercialization strategies.

Legal and Commercial Implications

  • Enforceability: As a B2 patent, JP6637121 benefits from substantive examination, strengthening its robustness.
  • Licensing Potential: The scope and claims position the patent as a significant exclusivity asset, suitable for licensing or partnering.
  • Infringement Risks: Broad claims covering specific chemical classes can lead to infringement suits, especially if the patented uses or compounds are adopted in generic development.

Strategic Considerations for Stakeholders

  • R&D Focus: Developing compounds that do not infringe on the specific claims of JP6637121 while targeting related indications.
  • Patent Filings: Filing subsequent patents that carve around the claims or extend the scope via new use or formulations.
  • Litigation and Defense: Monitoring competitor filings for potential legal challenges; preparing validity and infringement analyses.

Key Takeaways

  • Narrow vs. Broad Claims: JP6637121 combines specific chemical entities with potential therapeutic applications, providing a solid but targeted patent shield.
  • Strategic Patent Position: It occupies a valuable niche in the Japanese market, with potential for international patenting to support global development.
  • Expiry and Market Entry: Given patent term timelines, commercial strategies should align with the patent’s remaining enforceability window.
  • Innovation and Clear Claims: Precise claims bolster enforceability against infringers while enabling the patent holder to leverage exclusivity.

FAQs

1. What types of compounds does JP6637121 cover?
It covers specific chemical entities with defined structural features likely designed for therapeutic use, possibly within a particular disease class.

2. How does JP6637121 influence the competitive landscape?
It offers patent protection within Japan, restricting generic entries and providing exclusivity, thus shaping licensing and R&D strategies.

3. Is JP6637121 likely to be part of an international patent family?
Yes, similar inventions typically are filed internationally in key jurisdictions to secure broader rights.

4. Can other companies develop similar drugs around this patent?
Possibly, by designing compounds that avoid the patent claims' scope or pursuing different therapeutic pathways.

5. What should patent applicants consider to strengthen similar patents?
Focusing on clear, well-defined claims, including various embodiments, and citing relevant prior art during prosecution.


References

  1. Japan Patent Office (JPO). Patent database record for JP6637121.
  2. WIPO Patent Scope. International filings and family data.
  3. Patent attorneys' analysis based on claim structures and legal standards.

(Note: Ensure to verify specific claim language and applicant data from official JPO records for detailed legal evaluations.)


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