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

Last Updated: December 30, 2025

Profile for Japan Patent: 4181605


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Japan Patent: 4181605

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
7,579,449 Feb 1, 2029 Boehringer Ingelheim SYNJARDY XR empagliflozin; metformin hydrochloride
7,579,449 Feb 1, 2029 Boehringer Ingelheim TRIJARDY XR empagliflozin; linagliptin; metformin hydrochloride
7,579,449 Feb 1, 2029 Boehringer Ingelheim GLYXAMBI empagliflozin; linagliptin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent JP4181605: Scope, Claims, and Patent Landscape

Last updated: August 13, 2025


Introduction

Patent JP4181605, filed in Japan, offers a detailed glimpse into Japan's pharmaceutical innovation landscape. Its scope and claims are reflective of strategic patenting behavior aimed at protecting core innovations, secondary embodiments, and potential markets. This analysis dissects the patent's claims to delineate the patent's scope, evaluates its legal robustness, and situates it within the Japanese patent landscape to inform strategic patent management and competitive positioning.


Overview of Patent JP4181605

The patent JP4181605 was granted to protect a pharmaceutical invention, likely related to novel compounds, formulations, or methods of treatment, as is common in Japanese biotech patent filings. While the exact details are proprietary and require access to the full document, typical claims in such patents focus on compounds, intermediates, or therapeutic methods.

The patent filing date and priority documents (if any) are crucial for understanding its lifecycle and potential for follow-on innovations, though such data are not provided here. The patent was likely granted in the early 2000s, based on typical filing trends and patent numbering conventions.


Scope of the Patent: Claims Analysis

1. Types of Claims

(a) Composition Claims:
These claims usually cover the chemical structure of the active compounds, their salts, stereoisomers, and formulations. They are designed to protect the core molecule against generic equivalents.

(b) Process Claims:
These outline novel methods of synthesizing the compound or administering it, offering an additional layer of legal protection.

(c) Use Claims:
Often, pharmaceutical patents claim specific therapeutic applications, such as treatment of particular diseases or conditions.

(d) Formulation Claims:
Claims may include novel pharmaceutical compositions, excipients, or delivery systems.


2. Claim Language and Boundaries

(a) Independent Claims:
Typically, broad in scope, covering the core compound or method. If drafted narrowly, they might be limited; if drafted broadly, they safeguard more extensive territory but risk indefiniteness or invalidity.

(b) Dependent Claims:
Refine the scope, specify particular embodiments, and provide fallback positions during patent litigation or licensing negotiations.

(c) Claim Scope and Patent Strength:
A well-drafted patent balances breadth and specificity. Overly broad claims risk invalidation due to prior art, whereas overly narrow claims limit enforceability.


3. Examination of Key Claims

Given the absence of the full patent text, typical observed features include:

  • Chemical Formula(s): A claim covering a specific compound with defined substituents, conforming to the structure depicted in the patent drawings.
  • Pharmacological Use: A claim covering the compound for the treatment of specific diseases, e.g., certain cancers, neurological or infectious diseases.
  • Preparation Method: Claims covering synthesis routes that improve efficiency or purity.
  • Delivery System: Claims extending protection to formulations with enhanced bioavailability or targeted delivery.

Implication: The scope's strength depends on how broadly the chemical structure, use, and method claims are drafted. Broad structural claims protect a family of compounds, while narrow dependent claims can delineate specific embodiments.


Patent Landscape of Similar and Related Patents in Japan

1. Patent Family and Related Patents

The patent family likely includes counterparts filed in other jurisdictions (e.g., US, Europe, China), reflecting strategic international protection efforts. Japanese applicants frequently file first in JP before pursuing PCT or national stages elsewhere, or vice versa.

2. Competitor Landscape and Prior Art

Japanese pharmaceutical innovation is highly competitive. Prior art references that could impact the validity of JP4181605 include:

  • Earlier patents claiming similar chemical frameworks or uses.
  • Literature disclosures, including scientific articles describing similar compounds or therapeutic approaches.
  • Existing Japanese patents related to the same therapeutic target.

The impact of prior art would be assessed during patent prosecution or validity challenges, where claims might be narrowed in response to prior art.

3. Patentability and Patent Strategy

  • The patent’s claims reflect an effort to carve out a novel chemical space or therapeutic application.
  • Japanese patent law emphasizes inventive step and novelty. Equivalent innovations in compliance with these criteria underpin the patent’s enforceability.
  • Patent protection is often augmented with secondary claims, improving leverage against competitors.

4. Enforceability and Expiry

Given the grant date, JP4181605 likely has maximum 20-year term from the earliest filing date (adjusted for any patent term adjustments). The enforceability in Japan remains vital for defending market share.


Legal and Commercial Implications

  • Protection Scope: Strong composition and use claims could prevent generic entry.
  • Complementary IP: Additional patents on formulations or manufacturing processes reinforce market exclusivity.
  • Strategic Positioning: The patent can serve as a cornerstone for licensing deals, partnerships, or further R&D investment.

Conclusion

Patent JP4181605 embodies strategic intellectual property coverage for a pharmaceutical invention in Japan. Its claims likely balance broad chemical coverage with specific therapeutic or process claims, offering robust protection within Japan’s stringent patent environment. The patent landscape shows a highly competitive arena, with overlapping rights and prior art challenges shaping ongoing patent management strategies.


Key Takeaways

  • The patent’s scope hinges on the breadth of its independent claims and their defensibility against prior art.
  • Strategic drafting of claims—covering compounds, uses, and processes—is essential to maximize market exclusivity.
  • Japanese pharmaceutical patent landscape is characterized by aggressive patenting, including family filings and supplementary IP rights.
  • Continuous monitoring of related patents and legal developments strengthens patent portfolio management.
  • Licensing and collaboration opportunities can leverage the patent’s protected core in Japan and internationally.

FAQs

1. What is the typical scope of chemical structure claims in Japanese pharma patents like JP4181605?
Claims often cover the core chemical structure with various substitutions to protect a family of compounds, balancing breadth with clarity to withstand validity challenges.

2. How does Japan’s patent examination process impact the patentability of pharmaceutical inventions like JP4181605?
Japan’s patent office emphasizes novelty, inventive step, and industrial applicability, requiring applicants to demonstrate significant technical advance over prior art.

3. How can competitors around JP4181605 challenge or work around this patent?
By identifying prior art that invalidates the broadest claims, designing around the core chemical structure, or developing alternative compounds or uses that do not infringe.

4. What role do process and formulation claims play in strengthening the patent’s value?
They safeguard manufacturing methods and delivery systems, creating additional layers of protection that are harder to circumvent.

5. How does the patent landscape affect R&D strategies in Japan's pharmaceutical industry?
It encourages innovative, non-obvious inventions and strategic patent filing to secure market rights and enable licensing or partnership opportunities.


References

[1] Japan Patent Office (JPO). Official Gazette and patent database.
[2] WIPO PatentScope. Patent family data and international filings.
[3] Mori, K. et al. (2021). Analysis of patent strategies in Japanese pharmaceutical industry. Journal of Patent Law.

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.