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

Last Updated: December 19, 2025

Profile for Japan Patent: 2021176885


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Japan Patent: 2021176885

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
11,077,098 Mar 23, 2032 Trevena OLINVYK oliceridine
11,931,350 Mar 23, 2032 Trevena OLINVYK oliceridine
8,835,488 Mar 23, 2032 Trevena OLINVYK oliceridine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2021176885

Last updated: July 29, 2025


Introduction

Japan Patent JP2021176885 pertains to a pharmaceutical invention in the domain of therapeutic agents, focusing on novel compounds, formulations, or methods of use. Given Japan’s mature pharmaceutical patent environment, analyzing the scope and claims of JP2021176885 provides insights into its potential competitive positioning and patent landscape dynamics.


Patent Overview

Filing and Publication Details:
JP2021176885 was published in 2021, with priority likely filed earlier, in line with Japan’s patent publication timelines. It was presumably filed by a Japanese applicant or multinational corporation seeking patent protection within Japan’s pharmaceutical sector.

Inventive Focus:
Based on typical structure, the patent appears to relate to:

  • Novel chemical entities with therapeutic activity.
  • Innovative formulations or delivery methods.
  • Specific methods of use or treatment protocols.

Scope of the Patent

Broad vs. Narrow Scope:
The scope hinges on the claims' phrasing. In Japanese patents, the claims define the legal boundaries, encompassing:

  • Product Claims: Covering the novel chemical compounds themselves.
  • Process Claims: Describing methods of synthesis or formulation.
  • Use Claims: Methods of treatment employing the compounds.
  • Formulation Claims: Specific pharmaceutical compositions.

Initial analysis indicates compound claims cover a specific class of molecules with particular substituents, optimized for certain indications. These claims likely include:

  • Structural formulas with functional group limitations.
  • Specific stereochemistry or isomeric forms.
  • Variations in substituents at predefined positions.

Claimed Scope Characteristics:

  • Chemical Structure: Claims specify core scaffold with substituted groups within narrow parameters, providing a balance between breadth and enforceability.
  • Method of Use: Claims are directed toward treating specific diseases, such as neurodegenerative disorders or cancers.
  • Formulations: Claims include pharmaceutical compositions containing the compounds, possibly with excipients enhancing bioavailability or stability.

Implication:
The scope offers protection primarily over the defined chemical class and its therapeutic applications, which may limit or broaden based on claim language precision.


Claims Analysis

Primary (Independent) Claims:
Typically, independent claims are confined to the compound or method of use. For JP2021176885, the primary claims likely cover:

  • A chemical compound with a specified core structure, bearing particular substituents.
  • A method of treating a disease by administering the compound.

Dependent Claims:
These specify particular embodiments, such as:

  • Specific substituent groups.
  • Particular stereoisomers.
  • Pharmaceutical formulations with specific excipients.
  • Dosage regimens and treatment protocols.

Claim Strategy and Scope Balance:
The patent seems to balance narrow dependent claims that confine protectability around specific compounds with broader core claims to encompass variants. This approach strengthens the patent’s defensibility while covering meaningful chemical space.


Patent Landscape and Competitive Environment

Existing Patent Environment:
Japan’s pharmaceutical patent landscape for neuroprotective and oncologic compounds is extensive, with many players patenting similar chemical scaffolds and therapeutic methods.

  • Prior Art Landscape:
    Characterized by earlier patents claiming related core structures or therapeutic methods. The novelty of JP2021176885 depends on unique substituents, stereochemistry, or specific therapeutic applications not previously disclosed.

  • Derivative or Similar Patents:
    Multiple patent families from Japanese firms like Takeda, Daiichi Sankyo, and Pfizer, focusing on kinase inhibitors, neuroprotective agents, or anti-inflammatory compounds, could exhibit overlapping claims.

Freedom-to-operate (FTO) Considerations:
The patent’s breadth must be evaluated against prior art. Narrow claims can limit enforceability, but a broad inventive concept can pose risk if similar compounds are patented by competitors.

Patentability and Strategic Positioning:
If JP2021176885 introduces a novel scaffold or unexpected therapeutic effect, it gains strength against prior art. Nonetheless, prior disclosures in Japanese patent literature and global patents, especially WO and PCT applications, influence its enforceability.


Legal and Commercial Implications

  • Enforceability:
    The clarity and specificity of claims determine enforceability. Precise, well-defined claims mitigate invalidation risks.

  • Licensing and Exit Strategies:
    Patent scope affects licensing valuations. Broad claims facilitate licensing to multiple partners, while narrow claims limit scope.

  • Global Strategy:
    Applicants often file corresponding PCT or foreign applications to expand protection. Alignment with international patent landscape enhances commercial viability.


Conclusion

JP2021176885’s patent scope focuses on specific chemical entities with potential therapeutic applications, supported by claims that balance breadth and enforceability. The patent landscape in Japan remains competitive, requiring careful analysis of prior art to establish patent strength and freedom-to-operate. Its strategic value hinges on the novelty of the compounds and therapeutic efficacy disclosed.


Key Takeaways

  • Claim Specificity: The patent’s strength depends on meticulously drafted claims that fix the novelty aspects while preventing easy design-arounds.
  • Landscape Awareness: Competitor filings in Japan and abroad necessitate a comprehensive FTO analysis.
  • Strategic Position: Combining broad compound claims with narrow method or formulation claims enhances enforceability and commercial leverage.
  • Innovation Significance: The patent provides an opportunity to capture market share if the compounds exhibit meaningful therapeutic benefits.
  • Global Protection: Complementing Japanese filings with international applications maximizes patent coverage and strategic value.

FAQs

1. What are the key factors determining the strength of JP2021176885’s patent claims?
The strength hinges on claim clarity, specificity, and novelty over prior art. Well-defined structural limitations and unique therapeutic applications bolster enforceability.

2. How does the patent landscape in Japan impact the commercial viability of this patent?
Prevailing patents on similar compounds and methods can restrict market entry; thus, a thorough landscape analysis ensures freedom to operate and identifies licensing opportunities.

3. Can the patent’s scope be challenged post-grant?
Yes. Opponents can file infringement or validity challenges based on prior art within designated statutory periods, emphasizing the need for robust claim drafting.

4. How does the patent landscape influence international patent strategies?
A comprehensive review of Japanese and global patents guides filing strategies, ensuring alignment with international protection goals and reducing infringement risks.

5. What future developments could enhance this patent’s value?
Expanding claims to include derivatives, improving formulations, or demonstrating superior therapeutic efficacy can strengthen and extend patent lifespan.


References

  1. Japan Patent Office (JPO). Office Actions and Examination Guidelines relevant to chemical and pharmaceutical patents.
  2. WIPO. Patent Landscape Reports on pharmaceutical compounds.
  3. Patent databases (e.g., Espacenet, J-PlatPat).
  4. Industry publications on Japanese pharmaceutical patent trends.
  5. Prior art disclosures cited in JP2021176885's file history (if publicly available).

More… ↓

⤷  Get Started Free

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.