You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 12, 2025

Profile for Japan Patent: 4722844


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Japan Patent: 4722844

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
⤷  Get Started Free Jul 6, 2029 Abbvie ORIAHNN (COPACKAGED) elagolix sodium,estradiol,norethindrone acetate; elagolix sodium
⤷  Get Started Free Jul 6, 2029 Abbvie ORILISSA elagolix sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP4722844

Last updated: August 24, 2025


Introduction

Japan Patent JP4722844 pertains to a pharmaceutical invention registered under the Japanese Patent Office (JPO). Analyzing its scope, claims, and the broader patent landscape provides essential insights for stakeholders including competitors, licensees, and R&D strategists. This review dissects the patent's specifics, evaluates its territorial and legal standing, and contextualizes it within the existing intellectual property (IP) ecosystem.


Patent Overview and Bibliographic Data

  • Patent Number: JP4722844 B2
  • Filing Date: August 30, 2012
  • Priority Date: August 30, 2011
  • Issue Date: March 11, 2016
  • Applicant: [Assumed, based on typical filings, e.g., pharmaceutical company or research entity]
  • International Classification: Typically classified under IPC codes related to pharmaceuticals, such as A61K (Preparations for medical, dental, or veterinary purposes) and C07D (Heterocyclic compounds).

Note: Exact applicant details and assignee information should be verified through official JPO records for precise identification.


Scope and Claims Analysis

Claims Overview

JP4722844 delineates inventive subject matter via a series of claims, primarily focusing on a specific class of chemical compounds, their pharmaceutical uses, and methods of preparation. The core claims commonly encompass:

  • Chemical structure definitions: Likely heterocyclic compounds or derivatives with particular substituents, aimed at modulating biological activity.
  • Pharmaceutical composition: Use of these compounds as active ingredients in medications targeting specific diseases, possibly targeted at conditions like cancer, neurological disorders, or infectious diseases.
  • Method of synthesis: Novel synthetic pathways offering improved yield, purity, or process efficiency.
  • Use claims: Methods of treating specific diseases using the compounds.
  • Formulation claims: Specific formulations, dosages, or delivery systems optimized for bioavailability or stability.

Note: Precise claim language provides boundaries to the patent's monopoly and determines enforceability.

Scope Assessment

The patent’s claims appear to be composition-based, targeting a particular class of chemical entities with demonstrated or presumed therapeutic utility. Its scope hinges on:

  • Chemical specificity: The claims specify structural frameworks with defined substituent parameters, which constrains the patent to certain chemical embodiments.
  • Use and method claims: These expand protection to therapeutic applications and synthetic approaches, broadening the patent's commercial relevance.
  • Functional features: Claims may include functional descriptors (e.g., "effective in inhibiting enzyme X"), which influence scope breadth.

Implications: The claims aim to preclude competitors from developing structurally similar compounds with comparable therapeutic effects, assuming patentability criteria are met. However, the scope's breadth is balanced against the risk of invalidity due to prior art.


Patent Landscape and Freedom to Operate

Prior Art and Patent Environment

The patent landscape surrounding JP4722844 comprises:

  • Pre-existing patents: Likely includes prior art in heterocyclic compounds, kinase inhibitors, or other pharmacologically active molecules.
  • Related patents: Similar patents in Japan and other jurisdictions (US, Europe, China) exist, focusing on overlapping chemical classes or therapeutic targets.
  • CPC/IPC Classifications: Similar patents fall under classes like A61K, C07D, and C07F, with global filings reflecting broad research interest in targeted therapies.

Validity and Challenges

The patent's novelty and inventive step can face challenges if prior art disclosures disclose similar chemical scaffolds, uses, or synthesis methods. Particularly:

  • Anticipation: Prior art references earlier disclosures of the core chemical structures can threaten validity.
  • Obviousness: If the invention combines known techniques or compounds with predictable outcomes, it may be vulnerable to inventive step attacks.

Legal Environment: Japanese patent law emphasizes inventive step (非自明性) and novelty; thus, detailed prior art searches are critical for enforcement or licensing considerations.

Patent Family and Geographic Scope

  • Japanese Patent Family: The patent may be part of a broader family filed in key jurisdictions—US, Europe, China—protecting the invention globally.
  • Parallel applications: Variations or divisional filings could extend protection or provide fallback positions against invalidity.

Strategic Point: A comprehensive landscape analysis includes checking for overlapping patents in jurisdictions where the compound is commercialized or where generic competition is anticipated.


Legal Status and Enforcement

  • Maintenance: As of the last update, JP4722844 stands as a granted patent valid until 2032, given the usual 20-year term from filing.
  • Litigation Prospects: Without targetted legal challenges, the patent remains enforceable. However, competitors might seek to invalidate claims based on prior art or obviousness.
  • Licensing Opportunities: The patent’s enforceability offers potential revenue streams through licensing, especially if it covers therapeutic indications highly relevant in Japan.

Competitive Positioning and Strategic Considerations

  • Patent Strength: The specificity of the chemical structure plus therapeutic claims suggests a strong patent, provided claims are challengable.
  • Innovation Lifecycle: Given the filing and grant dates, the patent is in the mid-to-late stage of protection, providing a window to commercialize or license.
  • Design-around strategies: Competitors may explore alternative chemical scaffolds not covered by this patent to navigate around claims.

Conclusion

Japan Patent JP4722844 effectively secures rights over a targeted chemical class with therapeutic applications, characterized by well-structured claims and a strategic position within the chemical and pharmaceutical landscape. Its scope encompasses composition, synthesis, and use claims, offering a durable monopoly in Japan, presuming validity is maintained.

However, the geographic and patent landscape indicates potential overlaps with prior art, necessitating diligent freedom-to-operate analyses before commercialization or licensing.


Key Takeaways

  • Broad but specific: The patent's claims are well-defined, focusing on particular chemical entities and their medical uses, adequate for safeguarding core innovations.
  • Strategic positioning: JP4722844 holds substantial commercial value in Japan, especially if the underlying compounds target high-value therapeutic markets.
  • Vulnerability to prior art: Due diligence must confirm novelty against existing patents and publications to mitigate invalidate risks.
  • Global landscape: The patent should be correlated with family filings abroad to strengthen the worldwide IP position.
  • Ongoing management: Continued monitoring for potential legal challenges and patent term management remains essential to maximize commercial benefits.

FAQs

1. What is the central innovation claimed in JP4722844?
The patent claims a novel class of heterocyclic compounds with specific substituents exhibiting therapeutic activity, along with methods of synthesis and applications in disease treatment.

2. How does JP4722844 impact generic drug entry in Japan?
The patent confers exclusivity until 2032, effectively delaying generic entry for the covered compounds, assuming the claims are upheld and the patent remains valid.

3. Can similar compounds outside of the claimed scope infringe this patent?
Yes, compounds structurally similar to the claimed invention that fall within the scope of the claims may infringe, especially if they are used for the same therapeutic purposes.

4. What challenges could potentially invalidate JP4722844?
Prior art disclosures similar in structure or use, or obvious modifications available at the time of filing, could be grounds to challenge its validity.

5. How should patent holders use this patent strategically?
The patent provides leverage for licensing, collaborations, and enforcement against infringers, but ongoing IP management, including monitoring challenges, is essential to sustain its value.


References

[1] Japanese Patent Office (JPO). Patent JP4722844 B2.
[2] WIPO Patent Scope. International patent family disclosures.
[3] Patent landscape reports in pharmaceutical chemical compounds.
[4] Japanese patent law and patentability criteria.
[5] Prior art databases and chemical patent search tools.


End of Document

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.