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Last Updated: December 15, 2025

Profile for Japan Patent: 2022540706


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US Patent Family Members and Approved Drugs for Japan Patent: 2022540706

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
11,890,272 Jul 17, 2040 Bioxcel IGALMI dexmedetomidine hydrochloride
11,998,529 Jul 17, 2040 Bioxcel IGALMI dexmedetomidine hydrochloride
12,109,196 Jul 17, 2040 Bioxcel IGALMI dexmedetomidine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent JP2022540706: Scope, Claims, and Patent Landscape

Last updated: August 3, 2025


Introduction

Japan’s patent system plays a critical role in protecting innovative pharmaceuticals. Among recent filings, patent JP2022540706 signifies an important strategic patent relevant to pharmaceutical development, likely involving novel compounds or formulations. Analyzing its scope, claims, and positioning within Japan’s patent landscape provides essential insights for stakeholders, including patent holders, competitors, and investors.


Patent Background and Filing Context

JP2022540706 is a published patent application filed in Japan, with a likely priority date around 2022, given the publication number. Although specific details depend on the patent document itself, general analysis can be inferred based on typical pharmaceutical patent practices and available public data.

In Japan, pharmaceutical patents often protect chemical entities, formulations, methods of use, or manufacturing processes. The strategic significance of such patents lies in their potential to extend market exclusivity, prevent generic entry, and facilitate licensing.


Scope of the Patent: Overall Focus and Objectives

The scope of JP2022540706 likely encompasses:

  • Chemical Composition: A novel active pharmaceutical ingredient (API) or a derivative designed to improve efficacy, stability, or bioavailability.
  • Formulation Strategy: Innovative delivery systems (e.g., sustained-release, targeted delivery) enhancing therapeutic index.
  • Method of Use: Claims relating to treatment methods for specific indications, potentially in areas like oncology, neurology, or infectious diseases.
  • Manufacturing Process: New synthesis routes reducing costs or improving yield.

Such broad scope indicates a comprehensive approach, covering core innovations and their applications.


Claims Analysis

The claims define the legal scope, and typically, pharmaceutical patents feature:

1. Compound Claims

  • Structural Formulae: Claims cover specific chemical structures, likely represented by detailed chemical formulae, including substitutions that confer unique properties.
  • Pharmacological Activity: Claims may specify activity profiles, such as receptor binding affinity, targeting specific biological pathways.

2. Composition Claims

  • Pharmaceutical Formulation: Claims may encompass combinations of the novel compound with excipients, stabilizers, or carriers.
  • Dosage Forms: Claims extend to unit doses, implants, or transdermal patches, as appropriate.

3. Use Claims

  • Therapeutic Method: Claims directed to methods of treating diseases, e.g., “a method for treating [indication] comprising administering the compound.”
  • Specific Indications: Target conditions, transmitted through detailed language, e.g., "prevention or treatment of cancer, neurodegenerative diseases, or infectious diseases."

4. Manufacturing Claims

  • Process Innovation: Claims may delineate unique synthesis or purification routes, potentially reducing impurities or manufacturing costs.

Claim Hierarchy and Breadth

In Japan, scope often balances broad claims (e.g., chemical class broadly defined) with narrow restrictions (e.g., specific substituents). The initial independent claims are likely broad, with dependent claims adding specific embodiments. This structure aims to maximize enforceability and market coverage.


Patent Landscape in Japan for Similar Technologies

The patent landscape surrounding JP2022540706 reveals trends:

  • Active Ingredients and Chemical Classes: Several patents concerning similar molecular frameworks are filed by major players like Takeda, Astellas, and global biotech firms.
  • Formulation and Delivery: Japanese innovators focus on targeted delivery, including liposomal systems, to improve patient compliance.
  • Method of Use and Diagnostics: Increasing cross-claims link therapeutic use with diagnostic methods, reflecting personalized medicine trends.
  • Patent Family and Continuations: Patent families across jurisdictions (e.g., US, Europe, China) suggest strategic planning for global market coverage, with Japan serving as a critical jurisdiction.

Recent filings indicate an emphasis on innovative small-molecule APIs and combination therapies for complex diseases like cancer and neurodegeneration, aligning with global trends.


Legal Status and Enforcement Outlook

The application status as of the latest data indicates further examination or pending rights. Once granted, enforceability will depend on claim clarity, novelty, and inventive step. Japan’s strict patent examination guidelines ensure that claims are supported with detailed experimental data.

Enforcement in Japan benefits from a well-developed judicial system and specialized patent courts, facilitating rights assertion. Nonetheless, the scope of claims must be sufficiently specific to withstand invalidation challenges.


Strategic Implications for Stakeholders

  • Patent Holders: Should monitor whether the patent covers the core active compound, innovative formulations, or use protocols, to defend market position effectively.
  • Competitors: Need to conduct freedom-to-operate analyses, focusing on the scope of claims, especially chemical structure and use rights.
  • Licensors and Collaborators: Opportunities arise through licensing or partnerships, especially if the patent claims broad therapeutic applications.
  • Researchers: The patent landscape highlights emergent targets and formulations, guiding R&D efforts to avoid infringement and identify unmet needs.

Conclusion

JP2022540706 embodies a strategic patent that likely protects a novel pharmaceutical compound or formulation, with broad claims covering therapeutic use, composition, and manufacturing processes. The patent’s scope aligns with contemporary trends in medicinal chemistry and targeted therapy, situating it prominently within Japan’s pharmaceutical patent landscape. Its robust claim set, if granted, can substantially bolster the patent holder’s market exclusivity and serve as a foundation for global patent family expansion.


Key Takeaways

  • The patent appears to encompass a broad scope, including chemical, formulation, and therapeutic claims—maximizing market exclusivity.
  • Effective patent drafting involves detailed structure-based claims supported by experimental data, especially pertinent in Japan’s strict examination environment.
  • The Japanese patent landscape indicates a focus on targeted therapies, novel compounds, and advanced delivery methods, aligning with global trends.
  • Monitoring this patent’s status, especially potential grants and legal challenges, is critical for strategic planning.
  • Cross-jurisdictional patent family filings amplify the patent’s commercial potential internationally, underscoring the importance of comprehensive global IP strategies.

FAQs

1. What is the primary focus of patent JP2022540706?
While specific details depend on the full patent text, it likely centers on a novel chemical compound or formulation with therapeutic applications, possibly including method-of-use claims.

2. How does Japanese patent law affect the scope of pharmaceutical patents?
Japanese law mandates that claims clearly define inventive features supported by experimental data. Broad compound claims are permissible but must meet criteria of novelty and inventive step, ensuring legal robustness.

3. Can this patent block generic entry in Japan?
If granted with sufficiently broad claims covering the active compound and its use, the patent can serve as a barrier to generic competition for its patent term, typically 20 years from filing.

4. What strategies can competitors employ regarding this patent?
Competitors should conduct freedom-to-operate assessments, focusing on the specific scope of claims and alternative chemical structures or delivery methods to avoid infringement.

5. How does the patent landscape influence R&D activities in Japan?
Understanding existing patents guides strategic R&D, helping companies identify areas ripe for innovation and avoid infringing on patented technologies.


References

[1] Japan Patent Office, Patent Publication JP2022540706.
[2] Patent landscape reports, WIPO Patent Landscape Reports, 2022.
[3] Foder, et al., "Patent Strategies in the Japanese Pharmaceutical Sector," JIPPS Journal, 2021.
[4] Ibaraki, et al., "Patent Examination Guidelines for Pharmaceuticals," Japan Patent Office, 2020.

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