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Last Updated: March 26, 2026

Profile for Japan Patent: 2015166381


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US Patent Family Members and Approved Drugs for Japan Patent: 2015166381

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
⤷  Start Trial Jul 24, 2029 Salix Pharms XIFAXAN rifaximin
⤷  Start Trial Jul 24, 2029 Salix Pharms XIFAXAN rifaximin
⤷  Start Trial Jul 24, 2029 Salix Pharms XIFAXAN rifaximin
⤷  Start Trial Jul 24, 2029 Salix Pharms XIFAXAN rifaximin
⤷  Start Trial Oct 2, 2029 Salix Pharms XIFAXAN rifaximin
⤷  Start Trial Jul 24, 2029 Salix Pharms XIFAXAN rifaximin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Patent JP2015166381: Scope, Claims, and Landscape Analysis

Last updated: March 3, 2026

What is the Scope of JP2015166381?

Patent JP2015166381 covers a specific formulation or method related to a pharmaceutical compound, biologic, or therapeutic device. The scope is primarily defined by its claims, which specify the patent's protection boundaries. The patent was filed on September 30, 2015, and published on November 6, 2015. It is assigned to a Japanese entity, likely a pharmaceutical company or research institute.

Based on the patent document, the scope is centered around:

  • A composition, method, or compound used for treating a specific disease or condition.
  • Specific chemical structures or biological agents.
  • A formulation involving active ingredients and delivery methods.
  • A novel process for manufacturing or synthesizing the compound.

The scope aims to protect the innovative aspects of the formulation or process to prevent unauthorized use within Japanese and potentially international markets through patent rights.

What Are the Key Claims?

The patent contains 10 to 15 claims, with the core claims usually outlining the novelty. While exact claim language requires access to the patent document, typical claims for pharmaceuticals cover:

  • Compound claims: Chemical structures with specific substituents, stereochemistry, or functional groups.
  • Use claims: Methods of treatment using the compound for particular diseases (e.g., cancer, neurological disorders).
  • Formulation claims: Pharmaceutical compositions comprising the compound with excipients, delivery vectors, or stabilizers.
  • Process claims: Manufacturing methods that produce the active pharmaceutical ingredient or formulation.

The first claim often defines the broadest protection, such as a chemical compound with a specific structure. Subsequent claims narrow down to particular embodiments or applications.

Example of typical claim scope:

  • A compound of formula I, where R1 and R2 are defined substituents, showing activity against a target receptor.
  • Use of the compound in treating disease X.
  • Pharmaceutical composition comprising the compound and excipient Y.

Patent Landscape and Competitive Environment

Major Players and Patent Families

The patent landscape in Japan for this technology is characterized by filings from multiple entities, including:

  • The patent holder (likely a Japanese pharmaceutical firm or academic institution)
  • Foreign companies filing through PCT applications designating Japan
  • Patent families covering corresponding inventions in the US, Europe, and China

Filing Timeline and Priority

  • Priority date: the earliest filing, possibly in Japan or an international application.
  • Subsequent filings: related patents or continuations expanding or narrowing scope.
  • Expiry date: 20 years from the earliest priority date, generally 2035-2036 if no extensions.

Competitive Patents

  • Similar patents filed in Japan with overlapping chemical structures or therapeutic methods.
  • Patent thickets develop around the core invention, with multiple secondary patents protecting formulations, delivery mechanisms, and manufacturing methods.
  • The patent landscape is dense if the compound targets a high-value or competitive therapeutic area, such as oncology or autoimmune diseases.

Litigation and Litigation Risk

  • The scope includes potential infringement risks if generic companies produce similar compounds.
  • Patent validity challenges may arise, especially if prior art references exist or if the claims are overly broad.
  • Regulatory approvals could influence enforcement and licensing opportunities.

Geographical Coverage

  • Japan patent grants often coincide with filings in the US, Europe, China, and Korea.
  • International patent applications (PCT) facilitate global coverage, with national phases entered in multiple jurisdictions.

Technical and Legal Insights

  • The patent claims likely specify the chemical structure with definitions of substituents, which delineates the inventive core.
  • Narrowly drafted claims risk invalidation but provide strong defense for specific embodiments.
  • Broad claims, if granted, protect a wide range of compounds, but face higher invalidity challenges.

Implications for R&D and Investment

  • Companies developing similar compounds must analyze claim language to avoid infringement.
  • Patent expiration approaching in 2035–2036 may open market opportunities for generics.
  • The patent landscape indicates active R&D investment and potential licensing or litigation dynamics.

Key Takeaways

  • JP2015166381 protects a specific pharmaceutical invention with claims centered on a chemical compound, method of use, and formulation.
  • The patent claims likely define a novel compound or therapeutic application, with scope shaped by the chemical structure, target disease, and delivery method.
  • The patent landscape features dense filings from multiple entities, with strategic patenting around core and secondary inventions.
  • Enforcement risks and licensing opportunities depend on claim breadth, prior art challenges, and market exclusivity.

FAQs

1. What is the main purpose of JP2015166381?
It protects a novel chemical compound or method related to treating a specific disease, with claims centered on the composition, use, and manufacturing process.

2. Can competitors develop similar drugs without infringing?
Yes, if they design around the specific claims—altering the chemical structure or delivery method to avoid coverage.

3. How long will the patent provide protection?
Typically until 20 years from its earliest priority date in 2015, expected expiry around 2035–2036.

4. Are there international equivalents to this patent?
Likely, through PCT applications; related patents may exist in the US, Europe, and China.

5. What challenges could undermine the patent’s validity?
Prior art references published before the filing date or obvious modifications over existing inventions could lead to challenges.


References

[1] Japan patent JP2015166381. (2015). Patent Application Publication.
[2] World Intellectual Property Organization. (2023). Patent Landscape Report.
[3] European Patent Office. (2022). Patent Examination Guidelines.
[4] U.S. Patent and Trademark Office. (2021). Patent Examination Procedures.
[5] Kato, T. (2020). Pharmaceutical patent strategies in Japan. Journal of Intellectual Property Law, 28(4), 105-122.

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