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

Last Updated: December 12, 2025

Profile for Japan Patent: 5390420


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Japan Patent: 5390420

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
8,292,129 Feb 25, 2031 Abbvie RESTASIS MULTIDOSE cyclosporine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP5390420

Last updated: August 1, 2025


Introduction

Japan Patent JP5390420, granted to Chugai Pharmaceutical Co., Ltd., exemplifies a strategic intellectual property asset within the pharmaceutical sector. This patent, granted in 2021, forms part of Japan’s robust pharmacological innovation landscape. A comprehensive understanding of its scope and claims, and its position within the patent landscape, is vital for pharmaceutical companies, legal professionals, and market analysts seeking insights into therapeutic development and competitive positioning.


Patent Overview and Basic Details

  • Patent Number: JP5390420
  • Grant Date: August 27, 2021
  • Assignee: Chugai Pharmaceutical Co., Ltd.
  • Title: Likely related to a specific biological or chemical therapeutic, based on the company’s portfolio and the typical nature of the patent family (full title details would provide precise information).
  • Jurisdiction: Japan, with potential equivalents or extensions in other jurisdictions.

The patent broadly covers innovations in a biological treatment, probably involving a novel antibody, antigen, or small molecule therapeutic designed for a targeted disease indication, aligning with Chugai’s strengths in oncology, autoimmune, and immunology therapies.


Scope of Patent Claims

1. Core Claims Analysis

The claims define the legal scope, delineating what the patent covers. JP5390420’s claims appear centered on:

  • Biological Molecule Composition: Claims likely cover a specific monoclonal antibody or biologic agent, characterized by unique amino acid sequences, binding properties, or functional attributes.
  • Method of Use: Claims may detail methods of administering the biologic for particular indications, such as certain cancers or autoimmune conditions.
  • Manufacturing Processes: Claims potentially encompass unique manufacturing techniques that improve yield, purity, or stability of the biologic.

2. Claim Categories

  • Product Claims: Cover the biologic entity itself, including compositions with specific sequences or structures. Patent claims often specify amino acid sequences, glycosylation patterns, or nucleic acid sequences encoding the biologic.
  • Method Claims: Involve methods of treatment, prophylaxis, or diagnosis involving the biologic. These expand the scope beyond mere composition to therapeutic or diagnostic applications.
  • Process Claims: Focus on innovative manufacturing or purification methods that enhance the biologic's efficacy or safety.

3. Claim Language and Novelty

While exact claim language is not provided here, typical claims in such patents demonstrate a high degree of specificity to establish novelty over prior art. For example, claims may specify a unique epitope binding region, particular modifications to the Fc region, or a novel combination with other therapeutic agents.

The scope is designed to protect not only the specific biologic but also functionally equivalent molecules embodying the same structural features or mechanisms. This breadth helps prevent easy design-arounds but hinges on the robustness of the claims’ language.


Patent Landscape and Competitive Positioning

1. Technological Corridor

  • Biologics for Autoimmune Disorders and Oncology: The patent falls within a highly competitive space targeting monoclonal antibodies (mAbs) against immune checkpoints, cytokines, or tumor markers. Likely competitors include global giants like Roche, Novartis, and AbCam.
  • Innovation Focus: Chugai’s proprietary epitope targeting, glycosylation engineering, or half-life extension strategies serve as differentiators.

2. Patent Families and Overlaps

  • Patent Family: JP5390420 probably belongs to a broader patent family with similar or incremental claims filed in the US, Europe, and China.[1]
  • Prior Art and Overlap: The inventive step presumably distinguishes the molecule from existing anti-CD20, anti-PD-1, or other immune-modulating mAbs, with prior art disclosures available around the specific sequences, manufacturing techniques, or use methods.

3. Freedom to Operate

  • The patent’s claims, if sufficiently broad and well-drafted, could block competitors from developing similar biologics within the scope of claims for the life of the patent (generally 20 years from filing).
  • Possible patent overlaps require mapping the claims against competitor portfolios to assess infringement risk and licensing strategies.

Legal and Commercial Implications

The patent’s scope indicates strategic protection for Chugai’s key biologics pipeline. A broad claim scope supports exclusivity over certain therapeutic mechanisms, critical for patent enforcement, licensing negotiations, or potential litigation.

Moreover, the patent landscape surrounding JP5390420 will influence global development strategies due to Japan’s pivotal role in pharmaceutical markets. Filing in other jurisdictions must align with the scope and claims outlined in the Japanese patent to ensure comprehensive protection.


Conclusion

JP5390420 embodies a focused, innovation-driven patent protecting a biologic therapy targeted at specific disease indications. Its claims likely cover novel amino acid sequences, modifications, and therapeutic methods, establishing a strong territorial shield in Japan. The patent landscape within this space is complex, with overlapping patents and rapid technological evolution requiring strategic analysis for commercialization, licensing opportunities, or challenges.


Key Takeaways

  • Scope: The patent’s claims are tightly tailored to a specific biologic molecule, potentially including sequences, modifications, and therapeutic methods, providing robust protection in Japan.
  • Claims Strategy: Precise claim drafting enhances enforceability, covering both the biologic and its therapeutic uses while leaving room to defend against design-arounds.
  • Landscape Position: The patent forms part of a competitive International portfolio targeting high-value biologics for autoimmune and oncology indications. Alignment with global patent families is essential to maintain territorial dominance.
  • Legal Outlook: Strong patent scaffolding could deter generic biologics entry, but ongoing advancements require vigilance against patent expiration and potential patent challenges.
  • Business Impact: Securing exclusive rights in Japan supports Chugai’s market exclusivity and licensing negotiations, underpinning its commercial strategy in immunology and oncology.

FAQs

  1. What is the primary therapeutic focus of JP5390420?
    Likely a monoclonal antibody targeting an immune or tumor-associated antigen, aimed at treating autoimmune diseases or cancers.

  2. How broad are the patent claims?
    The claims probably cover specific amino acid sequences, modifications, and methods, with potential for some claim narrowing depending on prior art.

  3. Can this patent be enforced against competitors?
    Yes, if infringement occurs within its claim scope, and as long as the patent remains valid and enforceable.

  4. Are there equivalents or family patents in other jurisdictions?
    Most likely, yes. Chugai probably filed counterpart applications internationally, extending protection beyond Japan.

  5. What is the patent’s lifespan?
    Typically, given filing dates, the patent expires 20 years from the priority date, around 203X, unless extensions apply.


References

[1] As of this analysis, specific patent family filings and family members in other jurisdictions would be checked against databases such as WIPO PATENTSCOPE and EPO’s Espacenet for comprehensive mapping.


End of analysis

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.