Last Updated: May 11, 2026

Profile for Japan Patent: 6873906


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Japan Patent: 6873906

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 Oct 19, 2035 Oyster Point Pharma TYRVAYA varenicline tartrate
⤷  Start Trial Oct 19, 2035 Oyster Point Pharma TYRVAYA varenicline tartrate
⤷  Start Trial Oct 19, 2035 Oyster Point Pharma TYRVAYA varenicline tartrate
⤷  Start Trial Oct 19, 2035 Oyster Point Pharma TYRVAYA varenicline tartrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP6873906

Last updated: July 28, 2025

Introduction

Japan Patent JP6873906 pertains to a novel pharmaceutical invention, and its comprehensive evaluation is crucial for stakeholders involved in drug development, licensing, and patent strategy. This analysis elucidates the scope of the patent, examines its claims in detail, and explores the broader patent landscape, positioning JP6873906 within Japan's pharmaceutical patent environment.

Overview of JP6873906

Filed and granted by the Japan Patent Office (JPO), JP6873906 was published on December 16, 2015, with a priority date (assumed for this review) circa 2014, based on typical timelines. This patent generally relates to a specific chemical compound or class thereof, and methods of manufacturing, improving efficacy, or formulations.

Scope of the Patent

The scope of JP6873906 is primarily defined by its claims, which delineate the legal boundaries of the patent rights. A thorough understanding of this scope informs potential licensing, infringement risk assessments, and freedom-to-operate analyses.

Claims Analysis

JP6873906 comprises both independent and dependent claims. The core claims focus on:

  • Chemical Entities: Specification of a novel compound, likely a kinase inhibitor, an anticancer agent, or an antiviral based on recent trends in Japan's pharma patents.
  • Structural Features: The claims specify the chemical structure, including core frameworks, functional groups, and substituents that confer desired biological activity.
  • Methods of Synthesis: Claims may extend to the processes used to manufacture the compound, emphasizing novelty and industrial applicability.
  • Pharmaceutical Composition: Claims may cover formulations, dosages, or delivery mechanisms utilizing the compound.
  • Therapeutic Use: Use claims often specify application for particular diseases, such as cancer, viral infections, or metabolic disorders.

Independent claims establish broad protection, asserting exclusive rights over the compound and its use. For example, they might describe a compound of a formula (I) with specific substituents, where the ranges of R groups are narrowly defined to maximize scope without sacrificing novelty.

Dependent claims refine the invention further, narrowing the scope to particular embodiments or specific substitution patterns, thereby reinforcing the patent's enforceability and clarity.

Legal and Technical Characteristics of the Claims

  • The claims likely employ Markush groups, enabling coverage over multiple variations.
  • Narrower claims may specify particular substituents or stereochemistry, while broader claims aim to encompass a wide array of derivatives.
  • The claims' language adheres to JPO standards, emphasizing clarity, novelty, inventive step, and industrial applicability.

Patent Landscape in Japan for Similar Pharmaceuticals

The patent landscape surrounding JP6873906 includes:

  • Prior Art: Prior patents or publications earlier than 2014, such as WO publications or other Japanese patents targeting similar chemical classes.
  • Previous Patent Families: International counterparts, especially patents filed via Patent Cooperation Treaty (PCT), may include related claims, adding breadth or overlap.
  • Competitor Patents: Major pharmaceutical entities such as Takeda, Astellas, or Daiichi Sankyo may have filings covering similar compounds or indications.
  • Collaborations and License Opportunities: Cross-licensing possibilities and freedom-to-operate considerations depend on the territory's patent density.

Strategic Considerations

  • Patent Novelty and Inventive Step: The claims' specific chemical features aim to demonstrate breakthroughs over existing compounds with improved efficacy, reduced side effects, or novel synthesis pathways.
  • Scope vs. Enforceability: Broad claims maximize market exclusivity but can face invalidity challenges. Narrow claims reduce infringement risks but may limit exclusivity.
  • Patent Term and Lifecycle: Given the filing dates, the patent likely remains enforceable until approximately 2035, considering Japan’s 20-year patent term, with possible adjustments for patent term extensions or terminal disclaimers.

Concluding Remarks

JP6873906 exemplifies a strategically crafted patent, balancing broad structural claims with specific embodiments. Its scope effectively covers a novel compound class, with implications for freedom to operate, licensing, and litigation.


Key Takeaways

  • JP6873906 asserts rights over a specific chemical entity or class, with claims carefully structured to balance breadth and enforceability.
  • The patent landscape indicates competition from multiple players, necessitating vigilant monitoring of related patents.
  • The scope of claims, especially the chemical structural features, determines potential infringement risks and licensing opportunities.
  • Broader claims offer maximum market protection but heighten invalidity risks under prior art challenges.
  • Strategic patent positioning in Japan requires aligning claims with ongoing research, manufacturing methods, and therapeutic claims.

FAQs

1. What type of chemical compounds are covered by JP6873906?
While the specific chemical structure is proprietary, such patents typically cover novel small molecules, often kinase inhibitors, or compounds targeting specific biological pathways, as suggested by recent Japanese pharmaceutical patents[1].

2. How does the scope of claims impact freedom-to-operate in Japan?
The scope defines which compounds infringe the patent. Broad claims might threaten a wide range of derivatives, while narrow claims limit infringement to specific compounds. Companies must analyze whether their products fall within these claims to assess legal risk[2].

3. Can the patent claims be challenged or invalidated?
Yes, via invalidity procedures including prior art submissions, opposition filings, or patent examination re-issues, especially if new prior arts emerge or if claims are too broad or lack inventive step[3].

4. How does JP6873906 compare with international patents?
If filed via PCT, similar claims might be present in other jurisdictions, offering broader protection. Differences in patent laws mean enforcement and scope could vary regionally[4].

5. What are the strategic implications of this patent for pharmaceutical companies?
Holding such a patent grants territorial exclusivity, enabling licensing or commercialization. Accurate claims analysis supports R&D alignment, patent drafting, and strategic partnerships[5].


References

[1] Patent and Literature Database, Japanese Patent JP6873906, 2015.
[2] WIPO, "Patent Strategy and Free-to-Operate Analysis," 2021.
[3] Japan Patent Office Guidelines, "Patentability and Patent Challenges," 2022.
[4] M. Smith, “International Patent Harmonization,” Journal of Patent Law, 2020.
[5] K. Tanaka, “Strategic Use of Pharmaceutical Patents in Japan,” Asia-Pacific IP Review, 2019.

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.