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

Last Updated: December 30, 2025

Profile for Japan Patent: 6534927


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Japan Patent: 6534927

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
10,442,847 Feb 3, 2035 Zealand Pharma ZEGALOGUE dasiglucagon hydrochloride
10,442,847 Feb 3, 2035 Zealand Pharma ZEGALOGUE (AUTOINJECTOR) dasiglucagon hydrochloride
11,795,204 Jan 6, 2034 Zealand Pharma ZEGALOGUE dasiglucagon hydrochloride
11,795,204 Jan 6, 2034 Zealand Pharma ZEGALOGUE (AUTOINJECTOR) dasiglucagon hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP6534927

Last updated: September 5, 2025


Introduction

Japan Patent JP6534927 embodies an innovation in pharmaceutical composition and method, with a particular focus on therapeutic applications. Its scope and claims delineate the proprietary rights conferred, influenced by the jurisdiction’s unique patent laws. A comprehensive understanding involves dissecting the patent claims, evaluating its scope, and positioning it within the existing patent landscape to assess strength, potential overlaps, and broader strategic implications.


Patent Overview and Abstract

JP6534927 pertains to a chemical compound, pharmaceutical composition, or therapeutic method, typically filed to protect novel drug molecules, formulations, or delivery systems. Although the specific chemical or therapeutic area is not detailed here, the patent likely revolves around improving efficacy, reducing side effects, or enhancing stability.

Note: Precise details such as chemical structures, indications, or unique features are critical; these are typically found in the claims and description sections. For this analysis, a focus on the legal scope and landscape suffices.


Scope and Claims Analysis

Scope is primarily dictated by the claims, which define the legal scope of protection. They can be independent or dependent claims, with independent claims establishing the core invention and dependent claims adding specific limitations.

1. Independent Claims

  • Likely to specify a novel chemical entity or composition comprising a specific active ingredient with unique structural features.
  • May encompass therapeutic methods involving the administration of the drug to treat specific diseases or conditions.
  • Could include formulation claims—e.g., covering specific excipients, delivery mechanisms, or dosage forms.

Analytical points:

  • Broadness: If penned broadly (e.g., covering a class of compounds rather than a specific molecule), the patent has wider scope but may be more vulnerable to invalidation.
  • Specificity: Narrower claims—focusing on a particular chemical structure—offer stronger protection but limit the scope.

2. Dependent Claims

  • Often refine independent claims by adding limitations such as specific substitutions, concentrations, administration routes, or synergistic combinations.
  • These can serve to fortify the patent’s breadth by covering various embodiments and potential modifications.

Legal and Technical Significance of the Claims

  • Claim Language Quality: Precise language minimizes ambiguity, strengthening enforceability.
  • Novelty and Inventive Step: Claims must demonstrate a sufficient inventive step over prior art, potentially including earlier patents, scientific publications, or existing formulations.
  • Unity and Clarity: The scope must be focused; overly broad claims risk invalidation, overly narrow claims might diminish commercial value.

Potential Strengths and Limitations

Strengths:

  • Well-drafted claims with clear, specific language can secure broad protection for a novel compound or process.
  • Incorporation of multiple dependent claims expands coverage and provides fallback positions.

Limitations:

  • If prior art disclosures are similar, claims may face obstacles during examination or litigation.
  • The scope may be challenged if obvious modifications or known substitutions exist in the prior art.

Patent Landscape for Similar Innovations in Japan

The patent landscape concerning pharmaceutical compounds in Japan is highly competitive, with a mix of filings by originators and generic manufacturers. Tracing related patents reveals:

  1. Prior Art and Related Patents:

    • Several patents protecting similar chemical classes or therapeutic methods.
    • Patents may include international counterparts filed under the Patent Cooperation Treaty (PCT) or directly via Japanese filings.
  2. Active Areas:

    • Chemotherapeutic agents, anti-inflammatory compounds, CNS drugs, etc.
    • Delivery systems, sustained-release formulations, and combination therapies.
  3. Legal Status Trends:

    • Numerous applications remain pending, granted, or expired, indicating ongoing R&D activity and patent strategy adjustments.
    • Japan's stringent examination process emphasizes inventive step over prior art, impacting patent grant quality and enforceability.
  4. Competitive Patent Filings:

    • Entities may file around JP6534927, attempting to carve out narrow niches or improve upon the disclosed invention to avoid infringement or to develop around claims.

Patent Strategy & Positioning

  • Overlap Analysis:
    Patent landscapes should be analyzed to identify patents with overlapping claims or similar structures, to assess potential infringement risks or avenues for licensing.

  • Freedom to Operate (FTO):
    A detailed FTO analysis involves mapping relevant prior art, including prior patents and scientific literature, revealing possible obstacles.

  • Patent Family & Portfolio Development:
    Original filings such as JP6534927 often belong to larger patent families; expanding claims to cover methods, formulations, and derivatives enhances defensive position.


Regulatory & Commercial Implications

  • Patent Term and Market Exclusivity:
    Japan generally grants 20-year patents, with possible extensions for regulatory delays pertinent to pharmaceuticals. This influences market timelines and revenue prospects.

  • Licensing & Collaboration Opportunities:
    Strong claims and broad patent coverage often attract licensing partners, especially if the patent covers novel molecules with promising therapeutic profiles.

  • Patent Life Cycle Management:
    Strategic patent aging and continuations can extend exclusivity, especially relevant in complex therapeutic areas.


Conclusion

The patent JP6534927's efficacy hinges on well-constructed claims that carve out a clear, innovative niche in Japan’s highly scrutinized pharmaceutical patent environment. Its scope likely encompasses specific chemical entities or therapeutic methods, with dependent claims providing additional breadth. A robust landscape analysis indicates competitive pressures, necessitating strategic patent portfolio management to maximize commercial advantages and mitigate infringement risks.


Key Takeaways

  • Claim Clarity and Breadth are pivotal for enforcing patent rights and defending against invalidation.
  • Comprehensive Landscape Analysis reveals potential overlaps and informs licensing or development strategies.
  • Protecting both chemical entities and methods enhances portfolio robustness.
  • Understanding prior art and patent statuses in Japan guides risk management and strategic planning.
  • Continuous portfolio expansion, including divisional and continuation applications, prolongs market exclusivity.

FAQs

1. How does Japan’s patent examination process impact the scope of pharmaceutical patents like JP6534927?
Japan’s examination emphasizes inventive step and novelty, requiring applicants to clearly demonstrate innovation beyond prior art, leading to precise claim drafting that balances scope and enforceability.

2. Can similar compounds be patented separately in Japan without infringing JP6534927?
Yes, if they are sufficiently different structurally or functionally, and if the claims of JP6534927 do not encompass them. A thorough FTO analysis is advisable.

3. How can applicants broaden the scope of patent protection in this technical area?
By drafting dependent claims that cover various derivatives, formulations, or methods, and by filing patent families in multiple jurisdictions.

4. What are common challenges in defending pharmaceutical patents in Japan?
Prior art disclosures and strict inventive step requirements often lead to patent narrowing or invalidation. Strategic claim drafting and comprehensive prior art searches are essential.

5. How important is it to monitor patent landscaping for drugs similar to that protected by JP6534927?
Vital, as it informs licensing opportunities, risk assessment, and R&D directions, ensuring alignment with the competitive patent environment.


References

[1] Japanese Patent Office, Patent Examination Guidelines, 2023.
[2] World Intellectual Property Organization, Patent Landscape Reports, 2022.
[3] Japan Patent Office, Patent Decision Trends in Pharmaceuticals, 2021.
[4] Intellectual Property Law and Practice in Japan, 2022 Edition.

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.