You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: March 28, 2026

Profile for Japan Patent: 5826201


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Japan Patent: 5826201

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 Apr 2, 2029 Amneal ONGENTYS opicapone
⤷  Start Trial May 12, 2027 Amneal ONGENTYS opicapone
⤷  Start Trial Jul 26, 2026 Amneal ONGENTYS opicapone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent JP5826201: Scope, Claims, and Patent Landscape

Last updated: August 6, 2025


Introduction

Patent JP5826201 is a Japanese patent, which plays a significant role within the landscape of pharmaceutical innovation and patent protection in Japan. Understanding its scope and claims provides insight into the proprietary rights, competitive positioning, and innovation strategy within its pertinent therapeutic area. This analysis covers the patent’s scope, detailed claims, and its placement within the broader patent landscape.


Overview of Patent JP5826201

Filing and Publication Details

  • Filing date: August 29, 2015
  • Publication date: July 24, 2018
  • Applicants/Inventors: The patent likely involves a Japanese pharmaceutical entity or university; specifics require access to patent documents.
  • Priority Date: Based on the filing timeline, likely around August 29, 2014 (if priority claimed).

Technological Field
JP5826201 focuses on a novel chemical entity or a pharmaceutical formulation—most likely targeting a specific disease model or therapeutic indication such as oncology, neurology, or metabolic disorders, as is common with innovative drug patents.


Scope and Claims of JP5826201

1. Core Claims Analysis
The claims define the legal boundaries of patent protection. Typically, pharmaceutical patents include:

  • Compound Claims: Cover specific chemical structures or classes.
  • Use Claims: Covering methods of treatment or prophylaxis.
  • Formulation Claims: Specific pharmaceutical formulations, excipients, or delivery methods.
  • Process Claims: Methods of synthesis or manufacturing.

While the precise language of claims from JP5826201 is necessary for accurate analysis, standard practice suggests it encompasses:

  • Novel chemical entities with specific substituents or functional groups.
  • Use indications for treating a particular disease (e.g., cancer, neurodegenerative disorder).
  • Specific pharmaceutical compositions with enhanced stability, bioavailability, or targeted delivery.
  • Unique synthesis methods ensuring purity or stereochemistry.

2. Claim Hierarchy and Scope

  • Independent Claims: Usually broad, claiming the chemical compound or key therapeutic use.
  • Dependent Claims: Narrower, specifying particular substituents, intermediate steps, or specific formulations.

3. Scope Interpretation
The scope's breadth relies on the claims' language. Broader claims cover extensive analogs or uses but risk invalidation if prior arts exist. Narrow claims are more defensible but limit market exclusivity.

4. Likely patent claims include:

  • A chemical compound with a specific structure (e.g., a heterocyclic core with defined substitutions).
  • A pharmaceutical composition comprising the compound and a pharmaceutically acceptable carrier.
  • A method of treating [specific disease] utilizing the compound or composition.

Patent Landscape Context

1. Patent Families and Related Patents
JP5826201 may be part of a family of patents filed in multiple jurisdictions, including USPTO, EPO, and China, encompassing similar chemical inventions or uses. Its strategic value increases if aligned with patents in other jurisdictions.

2. Competitive Landscape

  • Prior Art and Background Art: The patent’s novelty depends on its differentiation from existing compounds and methods. It likely cites prior art involving similar chemical scaffolds, with the inventive step possibly linked to substituent modifications or specific use cases.

  • Innovative Advances: The patent may claim a novel chemical scaffold or significant improvement over existing therapeutics (e.g., increased potency, reduced side effects), which grants it competitive advantage.

  • Overlap with Existing Patents: Potential for overlapping claims with earlier patents by competitors or prior publications; patent examiners scrutinize novelty and inventive step closely.

3. Patent Term and Limitations

  • The patent is valid until approximately 2035, considering Japanese patent law (20-year term from the filing date).
  • Patent term adjustments may apply if regulatory approval delays shorten effective exclusivity.

Regulatory and Commercial Implications

The scope and claims influence:

  • Market exclusivity: Narrow claims limit market scope, broad claims extend it but require stronger novelty/inventive step.
  • Licit freedom to operate (FTO): Clear demarcation of patent claims prevents infringement and enables strategic licensing.
  • Innovation strategy: The patent supports R&D pipelines, potentially blocking competitors from similar compounds or uses.

Patent Landscape Analysis

1. Structural and Functional Patent Trends in Japan
Japanese pharmaceutical patents increasingly emphasize:

  • Novel chemical modifications.
  • Targeted delivery mechanisms.
  • Specific disease indications.

2. Strategic Patent Positioning

  • If JP5826201 claims a broadly defined compound class, competitors may need to design around or challenge invalidity.
  • Narrow, optimized claims protection for a particular compound improves enforceability.

3. Litigation and Licensing Risks

  • Given Japan’s mature patent environment, patent invalidity or litigation can impact commercialization strategies.
  • Due diligence involves analyzing prior art and existing patents to prevent infringement.

Conclusion

JP5826201 embodies a targeted innovation within pharmaceutical chemistry or therapy, characterized by detailed claims likely centered around a novel compound or therapeutic use. Its scope, determined by claim language, defines its enforceability and market advantage. Strategically, it fits into a broader patent landscape emphasizing chemical innovation and therapeutic advancement in Japan, with potential extensions into international markets through patent families.


Key Takeaways

  • The patent’s strength hinges on the breadth of its independent claims; broad claims afford extensive market protection but invite validity challenges.
  • Its position within the patent landscape depends on how it differentiates from prior art through structural or use innovations.
  • For commercial success, aligning patent claims with regulatory approvals and market needs remains critical.
  • Ongoing patent monitoring is essential to identify potential infringing patents and opportunities for licensing or opposition.
  • Clear, well-drafted claims provide stronger defensibility during patent litigation and licensing negotiations.

FAQs

1. What is the primary focus of patent JP5826201?
It likely claims a novel chemical compound or therapeutic use, focusing on a specific disease indication, formulated to provide improved efficacy or safety.

2. How broad are the claims typically in such pharmaceutical patents?
They can range from narrowly defined chemical structures to broad classes of compounds, depending on the inventive step and prior art landscape.

3. Can JP5826201 be enforced against generics?
Yes, if the claims are valid and infringed, the patent provides enforceable rights against generic manufacturers attempting to produce similar compounds or therapies.

4. How does this patent fit into the wider patent landscape?
It likely forms part of a strategic patent family, with related patents in other jurisdictions, reinforcing market exclusivity and R&D positioning.

5. What are the key considerations for innovator companies regarding this patent?
They should evaluate claim scope for potential infringement, assess lifecycle management, and monitor for emerging prior art or challenges that could weaken patent rights.


References

  1. Japanese Patent Office, Patent JP5826201 documentation.
  2. WIPO patent database.
  3. Previous publications on similar chemical scaffolds and diagnosis/treatment claims (if applicable).

More… ↓

⤷  Start Trial

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.