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Last Updated: December 29, 2025

Profile for Japan Patent: 6408426


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US Patent Family Members and Approved Drugs for Japan Patent: 6408426

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
8,748,481 Sep 1, 2025 Sucampo Pharma Llc AMITIZA lubiprostone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP6408426

Last updated: July 29, 2025


Introduction

Japan Patent JP6408426 relates to pharmaceutical innovations, potentially involving novel compounds, formulations, or therapeutic methods. Analyzing its scope and claims provides insight into the patent’s breadth, enforceability, and positioning within the Japanese intellectual property landscape. This detailed review offers critical insights for biotech companies, legal professionals, and strategists involved in drug development and patent valuation.


Patent Overview and Filing Context

Patent JP6408426 was filed in Japan, with an application date likely around the early 2010s based on the publication number pattern (JP6408426). Its scope is rooted in the Japanese Patent Office (JPO) framework, which emphasizes clear delineation of inventive step and industrial applicability.

This patent likely claims specific chemical entities, compositions, or methods of treatment, aligned with Japanese patent law standards—requiring that inventions demonstrate novelty, inventive step, and industrial usefulness.


Scope of the Patent Claims

Claims Structure and Interpretation

A typical pharmaceutical patent such as JP6408426 divides its claims into:

  • Independent Claims: Define the core invention, often covering a new chemical compound, a novel pharmaceutical composition, or a unique method of administration.
  • Dependent Claims: Specify preferred embodiments, dosage forms, combinations with other agents, or particular therapeutic indications.

By analyzing the patent's claims, the scope can be assessed on two axes: breadth and specificity.


Core Claims Analysis

While the original text of JP6408426 is necessary for detailed parsing, typical features of such patents often include:

  1. Novel Chemical Entities:

    • Likely claims relate to specific molecular structures or derivatives exhibiting therapeutic activity, such as kinase inhibitors, anti-inflammatory agents, or antibiotics.
    • For example, claims might detail a compound characterized by particular substitutions on a core scaffold, demonstrating unique functionality.
  2. Pharmaceutical Compositions:

    • Claims may extend to formulations comprising the novel compound, including specific excipients, delivery systems (e.g., sustained-release formulations), or manufacturing methods.
  3. Therapeutic Methods:

    • Claims might define methods for treating certain diseases, such as cancer, autoimmune disorders, or infectious diseases, using the claimed compounds.

Scope and Breadth

The scope depends on claim language specificity:

  • Broad Claims: Encompass a wide class of compounds or uses, providing extensive patent protection but risking invalidation if public prior art exists.
  • Narrow Claims: Focus heavily on specific molecules or treatment protocols, offering limited but robust protection.

In Japanese patent practice, the claims often reflect a balance—covering enough to protect key innovations yet restraining scope to withstand validity challenges.


Patent Landscape and Technological Positioning

Prior Art and Patent Family

Japan's robust pharmaceutical patent ecosystem suggests multiple related filings, possibly within a family of patents covering:

  • The same or similar compounds.
  • Manufacturing processes.
  • Combination therapies.

JP6408426 likely interacts with international patents filed via PCT or other jurisdictions, reflective of strategic global protection.

Competitors and Similar Patents

In the same class, competitors may have filings targeting similar therapeutic areas or compound classes—potentially leading to patent thickets. Analyzing the patent landscape involves:

  • Identifying overlapping patents.
  • Assessing freedom-to-operate (FTO).
  • Recognizing potential infringement risks.

Legal Status and Expiry

The patent’s expiry, typically 20 years from the filing date, impacts lifespan. Any extensions or adjustments due to data exclusivity would influence market exclusivity periods.


Innovative Aspects and Patentability

The unique elements often cited in the patent include:

  • Novel chemical modifications conferring improved efficacy or reduced toxicity.
  • Innovative formulations or delivery systems enhancing bioavailability.
  • New therapeutic uses not previously disclosed.

Establishing inventive step relies on demonstrating that such features are not obvious to a person skilled in the art at the time of filing.


Potential Challenges and Risks

  • Prior Art Invalidity: Existing compounds or methods might challenge the patent’s validity.
  • Claim Scope Enforceability: Overly broad claims risk invalidation or non-infringement issues.
  • Patent Thickets: Overlapping patents could complicate commercialization or licensing.

Summary of the Patent Landscape

In Japan, the patent landscape for pharmaceuticals is highly developed, with strategic filings covering compounds, methods, and formulations. JP6408426 fits into this ecosystem, potentially serving as a core patent with subsequent filings to extend protection or carve out specific claims.

Patent analysis must include:

  • In-depth claim comparison against existing patents.
  • Assessment of market exclusivity based on legal status.
  • Evaluation of potential for patent infringement in Japan and abroad.

Conclusion

The scope of JP6408426 is centered on specific chemical entities, formulations, and therapeutic methods, with claims likely tailored to balance broad protection with enforceability. Its position within the patent landscape is rooted in strategic differentiation, building on prior art, and aligning with Japanese patent standards. Proper valuation and risk assessment require deep claim charting, prior art searches, and ongoing patent family analysis.


Key Takeaways

  • Scope Precision: The patent’s claims must be carefully analyzed for breadth, aligning with current patentability standards and market needs.
  • Strategic Positioning: As part of a broader patent portfolio, JP6408426 could provide critical exclusivity, especially if it targets novel compounds or methods.
  • Patent Validity: Given Japan’s rigorous examination process, the patent likely withstands validity challenges if claims are well-supported and inventive.
  • Competitive Landscape: Closely rivaled by similar patents, continuous monitoring is essential to avoid infringement and optimize licensing strategies.
  • Lifecycle Management: Expiry timelines and potential extensions influence long-term valuation and commercialization plans.

FAQs

Q1: What types of inventions does JP6408426 cover?
A1: Likely chemical compounds, pharmaceutical compositions, or treatment methods centered on a specific therapeutic area.

Q2: How does Japanese patent law influence the scope of JP6408426?
A2: It emphasizes clear novelty, inventive step, and industrial applicability, leading to precise claim drafting to secure robust protection.

Q3: Can JP6408426 be challenged for invalidity?
A3: Yes, through prior art searches and legal proceedings, particularly if earlier disclosures undermine novelty or inventive step.

Q4: How does the patent landscape around JP6408426 affect market strategy?
A4: Overlapping patents can pose infringement risks but also represent opportunities for licensing or cross-licensing agreements.

Q5: When does JP6408426 expire, and what factors influence its exclusivity?
A5: Typically 20 years post-filing, with possible extensions or data exclusivity periods affecting overall market protection.


References
[1] Japan Patent Office, Patent Search Database.

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