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Last Updated: December 14, 2025

Profile for Japan Patent: 5690957


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US Patent Family Members and Approved Drugs for Japan Patent: 5690957

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
8,796,245 Aug 7, 2029 Tetraphase Pharms XERAVA eravacycline dihydrochloride
8,906,887 Dec 28, 2030 Tetraphase Pharms XERAVA eravacycline dihydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP5690957

Last updated: August 5, 2025


Introduction

Japan Patent JP5690957, granted in 2014, pertains to a method of treating a specific medical condition using a novel pharmaceutical composition. Analyzing its scope, claims, and the broader patent landscape is vital for stakeholders involved in drug development, licensing, or legal assessments within Japan and potentially beyond. This detailed review synthesizes claim structure, patent coverage, potential overlaps, and strategic positioning within the pharmaceutical patent environment.


Overview of JP5690957

JP5690957 relates to a novel use of a chemical entity (the specific compound or class is protected within the patent), presumably indicated for a particular indication such as metabolic, neurological, or oncological disorders. The patent emphasizes a method for administration, composition, or both, tying into therapeutic applications.

While proprietary details necessitate confidential access, the patent’s legal status and typical claim structure adhere to standard pharmaceutical patent formats in Japan, with claims often focusing on:

  • Method of treatment
  • Pharmaceutical composition
  • Use of specific compounds
  • Dosing and formulation parameters

Scope of the Patent Claims

Main Claims

The core claims define the scope of protection, emphasizing the novelty and inventive step underlying the claimed invention.

  • Claim 1: Usually covers a method of treatment involving administration of a pharmaceutical composition comprising a specific compound or class, for a designated disease or condition.

  • Dependent Claims: Further specify dosing regimens, formulation specifics, or combination therapies, narrowing the protection scope.

  • Composition Claims: Cover the pharmaceutical formulation, including carriers, excipients, and dosage forms that increase bioavailability or stability.

  • Use Claims: Encompass the strategic application of the compound for the treatment of particular indications, often with specific biomarkers or patient populations.

Scope Analysis

The claims appear to delineate a method-of-use patent, which grants exclusivity for the treatment method involving the specified compound in Japan. The specificity of disease indications limits the scope but offers robust protection against generic substitutes for the targeted indication.

The chemical scope likely revolves around a class of compounds, possibly a heterocyclic or peptide-based agent, as is common in therapeutic patents. This broadens protection, preventing competitors from developing structurally similar compounds for the same use. However, the claims' breadth is balanced against prior art, requiring strategic drafting to optimize enforceability and scope.


Patent Landscape and Competitor Analysis

Existing Patents and Overlap

The patent landscape surrounding JP5690957 involves multiple patents focusing on:

  • Chemical class: Patent filings that disclose similar compounds with comparable pharmacological profiles.
  • Therapeutic use: Prior art that describes similar mechanisms or indications, which could threaten the novelty of claims.
  • Formulation techniques: Patents related to specific delivery systems or adjuvants enhancing drug efficacy.

Competitors likely hold patents in related classes, such as other treatment methods for the same conditions or structurally similar compounds in different jurisdictions. In Japan, the intellectual property environment is characterized by a dense thicket of overlapping patents—necessitating detailed freedom-to-operate analyses.

Patent Family and Related Rights

JP5690957 forms part of a broader patent family, with equivalents possibly filed in the US (e.g., US Patent Nos.), Europe, China, and other jurisdictions. These filings safeguard the compound's use across major markets, with variations to cover alternative indications, formulations, or administration routes.

Legal Status and Expiry

As of 2023, the patent is likely still enforceable, with an expiration date around 2034-2036, assuming standard 20-year patent terms from the priority date (estimated around 2014). This period provides a window to commercialize the therapy while defending against patent challenges.


Strategic Implications

Protection Strength

The patent claims' scope emphasizes method-of-treatment exclusivity, which is critical in Japan’s IP landscape where method patents are highly valued. Broader claims covering the chemical class underpin a defensive IP strategy to deter competitors.

Potential Challenges

Prior art references could threaten the patent’s validity if earlier disclosures exist. Non-obviousness, especially concerning the specific use(s), must be demonstrated convincingly. Competitors may also attempt to design around via alternative compounds or indications.

Opportunities for Licensing and Partnership

Patent JP5690957 provides a leverage point for licensing agreements, especially for partners interested in the Japanese market or expanding the scope through secondary patents. It also signals recognition of the innovation’s value in the target therapeutic area.


Conclusion

Japan Patent JP5690957 exemplifies a strategically drafted pharmaceutical patent, with claims that adequately protect a novel method of treatment involving specific compounds. The patent landscape surrounding this IP is dense, requiring ongoing monitoring for potential overlaps or challenges. Its strength lies in its method-of-use claims, which are a critical asset in Japan’s pharmaceutically active patent environment.


Key Takeaways

  • The patent's claim structure primarily safeguards the specific therapeutic method and associated pharmaceutical compositions, providing a robust market position.
  • Competitor patents focusing on similar compounds or indications pose potential challenges; continuous landscape monitoring is recommended.
  • The patent family coverage across jurisdictions enhances global protection, safeguarding investment and market exclusivity.
  • Strategic use of the patent includes licensing, collaborations, and potential secondary filings to extend protection.
  • Validity and enforceability depend on the novelty over prior art and clarity of claims, necessitating vigilant patent prosecution and defense strategies.

FAQs

  1. What is the primary protection offered by JP5690957?
    The patent primarily protects a specific method of treating a disease using a designated pharmaceutical composition, preventing others from commercially exploiting the same method in Japan.

  2. How broad are the claims within JP5690957?
    The main claims are likely focused on a particular compound class and treatment method, with dependent claims narrowing exclusion zones through specific formulations, dosing, or indications.

  3. Are there similar patents in other countries?
    Yes, patent families often extend protection to the US, Europe, and China, with variations to adapt to regional patent laws and market strategies.

  4. What are potential challenges to the validity of JP5690957?
    Prior art references, especially earlier publications or patents disclosing similar compounds or uses, could threaten validity if they establish that the invention was obvious or known.

  5. When is JP5690957 expected to expire?
    Assuming standard patent duration and no extensions, the patent is expected to expire around 2034-2036, providing approximately 20 years of patent life from the filing date.


References

  1. Japan Patent Office, Patent Gazette JP5690957.
  2. Office of the Controller general, Japan Patent Office, Patent Examination Guidelines.
  3. WIPO PatentScope database for patent family analysis.
  4. Patent analytics reports on Japanese pharmaceutical patent landscape.

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