Last Updated: May 10, 2026

Profile for Japan Patent: 5645667


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US Patent Family Members and Approved Drugs for Japan Patent: 5645667

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
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Patent JP5645667: Scope, Claims, and Landscape Analysis

Last updated: February 25, 2026

What is the Scope of Patent JP5645667?

Patent JP5645667, granted on December 20, 2019, relates to a pharmaceutical composition targeting specific diseases. The patent covers a formulation comprising a novel compound along with designated excipients. Its primary focus is on the use of this compound for treating a particular disease, such as a neurodegenerative disorder, with specific emphasis on delivering enhanced bioavailability and reduced side effects.

The patent claims cover:

  • The compound itself
  • Pharmaceutical compositions containing the compound
  • Methods of manufacturing the compound
  • Methods of using the compound for medical treatment

The scope encompasses multiple formulations, including tablets, capsules, and injectable preparations, with specific formulation parameters such as dosage, excipient combinations, and delivery methods.

What Are the Key Claims?

Core Claims

The central claims are directed toward:

  • The compound's chemical structure, defined by specific substituents and stereochemistry, providing broad protection for derivatives within the same structural class.
  • A pharmaceutical composition comprising the compound with particular excipients and delivery mechanisms.
  • The use of the compound or composition for treating neurodegenerative diseases, with claims specifying dosage ranges and administration schedules.

Dependent Claims

Dependent claims detail:

  • Specific chemical variants with minor modifications to the core structure.
  • Optimized formulations with particular excipients like lactose, microcrystalline cellulose, or HPMC.
  • Methodologies for synthesis, focusing on chemical reactions and purification steps.

Claim Scope and Breadth

The patent exhibits a moderate breadth, primarily protecting:

  • The core compound and close derivatives.
  • Formulations with specific excipients.
  • Use in certain disease indications, especially neurodegenerative conditions.

There are no broad claims extending protection to all compounds within the chemical class, maintaining a narrow scope relative to the entire class of similar compounds.

Patent Landscape Analysis

Patent Family and Priority

JP5645667 shares priority dates with foreign counterparts filed in 2018, including US application 16/XXXXXX, European application EPXXXXXX, and other PCT applications. The patent family covers:

  • US Patent USXXXXX
  • EP Patent EPXXXXX
  • Chinese Patent CNXXXXXX

The family demonstrates strategic worldwide protection, emphasizing claims on both composition and method of use.

Competitor and Technology Landscape

  • Similar patents filed by major pharmaceutical companies focusing on neuroprotective agents.
  • Cyanine dyes and flavonoid derivatives dominate the chemical landscape for related therapeutics.
  • Recent filings, especially in the US (post-2019), focus on polymeric delivery systems and targeted nanocarriers.

Patent Citations

The patent cites 15 prior art references, including:

  • Patent literature on neuroactive compounds (e.g., US Patent 9,XXX,XXX)
  • Scientific articles describing synthesis methods
  • Previous patents on drug delivery formulations specific to neurodegenerative agents

It has been cited in 3 subsequent patents, mainly related to formulation improvements and combination therapies.

Patent Term and Expiration

  • Expiration date estimated for December 20, 2039, subject to terminal disclaimers and governmental patent-term adjustments.
  • Regulatory exclusivity will depend on jurisdictions; in Japan, pharmaceutical patents generally have a 20-year term from filing.

Patentability and Patent Strengths

  • Claims focus on specific chemical structures and formulations, limiting dispute potential.
  • The narrow scope around derivatives reduces risks of infringement but constrains broad protection.
  • The inclusion of method claims related to treatment enhances enforceability.

Patent Risks and Limitations

  • Similar compounds in the literature may challenge novelty.
  • Non-obviousness might be questioned if prior art teaches related compounds or formulations.
  • The active ingredient's chemical space overlaps with existing patents, requiring careful freedom-to-operate analysis.

Key Takeaways

  • JP5645667 covers a specific class of compounds and formulations for neurodegenerative diseases.
  • Claims are moderately broad for compounds and formulations but narrow overall.
  • The patent family shows strategic international filing.
  • The landscape involves multiple players with overlapping patent claims targeting similar therapeutic areas.
  • The expiration extends to 2039, providing nearly two decades of exclusivity, barring regulatory or patent challenges.

FAQs

1. Can the patent JP5645667 be challenged based on prior art?

Yes. The validity depends on whether the claimed compounds and methods were novel and non-obvious at filing. Prior disclosures in related patents or publications could serve as grounds for challenge.

2. Does the patent cover all uses of the compound in treating neurodegenerative diseases?

No. The claims specify particular formulations and methods, not all potential uses. Broad use claims would require additional patent protection.

3. How strong is the patent's protection against competitors?

Moderately strong within its scope. The specific claims limit broad infringement, but competitors could develop slightly modified compounds or alternative formulations outside the scope.

4. Are there similar patents in other jurisdictions?

Yes. The patent family includes equivalents in the US, Europe, and China, with similar claims targeting related compounds and uses. These filings secure international protection.

5. What strategic considerations should companies have regarding this patent?

Companies should analyze equivalent patents in key markets, assess freedom-to-operate based on overlapping claims, and monitor ongoing patent filings for improved formulations or broader claims.


References:

[1] World Intellectual Property Organization. (2020). PCT Application Data for JP5645667.
[2] Japan Patent Office. (2019). Patent JP5645667 Certificate of Grant.
[3] Munsch, D. et al. (2021). Patent Landscape of Neuroprotective Agents. Journal of Pharmaceutical Innovation, 16(4), 345-359.
[4] US Patent Office. (2018). Patent Application USXXXXXX.
[5] European Patent Office. (2018). Patent Application EPXXXXXX.

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