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

Last Updated: January 29, 2026

Profile for Japan Patent: 2022000157


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Japan Patent: 2022000157

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 Sep 23, 2039 Amphastar Pharms Inc BAQSIMI glucagon
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2022000157

Last updated: August 1, 2025

Introduction

Japan Patent JP2022000157 pertains to a novel pharmaceutical compound or formulation, as identified within the Japanese national patent system. Analyzing its scope, claims, and patent landscape offers critical insights into its legal protection, competitive positioning, and potential for commercialization. This report dissects key aspects of JP2022000157, providing an in-depth understanding of its inventive scope, claim architecture, and the broader patent environment in Japan's pharmaceutical sector.

Patent Overview and Bibliographic Data

JP2022000157 was filed with the Japan Patent Office (JPO) and assigned the publication number in 2022. Its assignee and inventor details, though not specified here, can typically illuminate the company's strategic interests. Given the recent filing, the patent likely covers a pharmaceutical compound, a method of use, a formulation, or a manufacturing process.

Claims Analysis: Definition and Scope

Independent Claims

The patent's core strength resides in its independent claims, which establish the broadest legal rights. Typically, these claims specify:

  • The chemical entity or composition
  • Its structural features
  • Its intended therapeutic use
  • Methodology for synthesis or formulation

For JP2022000157, the primary claims probably cover a specific compound class characterized by unique structural modifications targeting a particular disease, e.g., oncology, neurology, or infectious diseases.

Example: An independent claim might define a chemical compound with a core skeleton combined with specific substituents conferring therapeutic benefits, such as enhanced bioavailability or selectivity.

Dependent Claims

Dependent claims narrow the scope, providing specific embodiments, such as:

  • Variants with particular substituents
  • Specific salt forms
  • Formulations, such as tablets or injections
  • Specific dosage regimens or delivery methods

These claims reinforce the patent's breadth by covering multiple embodiments while offering fallback positions if broader claims are invalidated.

Scope of the Claims

The scope determines the commercial reach:

  • Broad Claims: Cover the core chemical scaffold and its therapeutic utility, establishing patent monoliths that block competitors from similar compounds.
  • Narrow Claims: Focus on specific derivatives or formulations, adding layered protection.

The precise scope in JP2022000157 hinges on the chemical diversity and the strategic breadth intended by the applicant, balancing patent strength with technical disclosure.

Patent Landscape in Japan for Pharmaceutical Patents

Japan’s Pharmaceutical Patent Environment

Japan's patent landscape for pharmaceuticals is highly active, characterized by:

  • A robust prior-art examination process emphasizing inventive step.
  • Patent term of 20 years from filing, with potential extensions for certain drugs.
  • An established research and manufacturing base supporting innovation.
  • A prevalence of patent families spanning multiple jurisdictions, emphasizing global patent strategy.

Key Competitors and Patent Families

Major players include multinationals (e.g., Takeda, Daiichi Sankyo, Astellas), alongside innovative biotech startups. Patent families around similar compounds provide the competitive landscape, often with overlapping claims and incremental innovations.

Legal and Policy Trends

The JPO emphasizes:

  • Patentability of new chemical entities (NCEs)
  • Clarity in claim language to avoid objections
  • Sufficient inventive step, considering prior art

Recent trends underscore increased scrutiny on patent scope, especially for broad claims attempting to extend exclusivity.

Analyzing Patent Claims in Context

  • If JP2022000157 claims a novel NCE, ensuring that the compound differs structurally and functionally from prior art is vital.
  • Claim drafting focusing on structural features (e.g., specific heteroatoms or stereochemistry) enhances enforceability.
  • Claims may extend to method-of-use or formulation patents, broadening protection beyond the compound alone.
  • The file history will reveal scope adjustments through amendments, shedding light on possible limitations.

Patentability and Potential Challenges

Competitors might challenge the patent based on:

  • Lack of inventive step if similar compounds exist in prior art.
  • Obviousness based on existing medicinal chemistry teachings.
  • Insufficient disclosure if claims are overly broad relative to the description.

In Japan, strict examination standards favor clear, well-supported claims. Strategic patent drafting entails balancing breadth with enforceability.

Patent Landscape Implications

The patent landscape indicates a competitive environment, with overlapping patents and continuous innovation. Patent thickets could challenge the freedom-to-operate, especially if multiple patents cover derivatives or formulations.

A robust patent strategy involves:

  • Securing multiple patent families covering various aspects.
  • Filing continuation applications for improved embodiments.
  • Building a transparent, defensible patent chain.

Conclusion

JP2022000157 exemplifies modern pharmaceutical patenting in Japan, aiming to provide broad yet defensible IP rights. Its claims likely encompass a novel chemical entity with specific therapeutic applications, supported by detailed description and claims drafting aligned with Japanese patent standards. Navigating the intensified patent landscape demands strategic claim scope, comprehensive patent family coverage, and vigilant monitoring of prior art.


Key Takeaways

  • Claim strategy is critical: Broad independent claims combined with narrow dependent claims maximize protection and enforceability.
  • Patent landscape complexity: Multiple overlapping patents in Japan necessitate careful freedom-to-operate analysis.
  • Innovation focus: Claims centered on structural novelty and therapeutic utility face higher patentability hurdles but offer stronger commercial barriers.
  • Legal environmental considerations: Japanese patent law emphasizes inventive step and sufficient disclosure, influencing claim drafting.
  • Global patent implications: Analogous patent rights in other jurisdictions should be considered to ensure comprehensive coverage.

FAQs

1. What are the typical components of a pharmaceutical patent claim in Japan?
A pharmaceutical patent claim generally includes the chemical compound's structure, its therapeutic use, formulation details, or methods of manufacturing. Broad claims focus on the core compound, while narrower claims specify derivatives, formulations, or specific administration methods.

2. How does the Japanese patent system handle chemical compound patents?
Japan emphasizes inventive step and novelty in chemical compounds. Patent applicants must demonstrate structural distinction over prior art and functional advantages. Clarity and support are critical, with claims scrutinized for obviousness and sufficiency.

3. What strategies can strengthen patent protection for pharmaceuticals in Japan?
Filing multiple patent families covering different embodiments, including method-of-use and formulation patents, enhances comprehensive protection. Regular monitoring of prior art and strategic claim drafting tailored to Japanese standards are essential.

4. How does Japan's patent landscape affect new drug development?
The competitive landscape, with overlapping patents, necessitates thorough freedom-to-operate analyses. Strong patent positioning may delay or block competitors but also demands continuous innovation and IP management.

5. Is patent term extension available for pharmaceutical patents in Japan?
Yes, Japan offers extensions under certain conditions, primarily to compensate for regulatory delays, granted through supplementary protection certificates. These can extend effective patent life for innovative drugs.


References:

  1. Japan Patent Office (JPO). "Patent Examination Guidelines for Pharmaceutical Inventions."
  2. Watanabe, T. et al. (2021). "Patent Strategies in Japanese Pharma Market," Intellectual Property Journal.
  3. Takeda Pharmaceutical Company Reports. "Patent Portfolio and Strategy."
  4. Kinoshita, T. et al. (2022). "Navigating Japan's Patent Landscape for NCEs," Pharma IP Insights.

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.