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

Last Updated: December 16, 2025

Profile for Japan Patent: 2023065622


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Japan Patent: 2023065622

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
10,456,399 Feb 3, 2037 Taiho Oncology LONSURF tipiracil hydrochloride; trifluridine
10,960,004 Feb 3, 2037 Taiho Oncology LONSURF tipiracil hydrochloride; trifluridine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2023065622

Last updated: July 28, 2025


Introduction

Japan Patent JP2023065622 (hereinafter JP5622) relates to an innovative pharmaceutical invention filed under the Japanese patent system. This patent's primary importance lies in its novelty, inventive step, and commercial potential within the healthcare and pharmaceutical sectors. This report provides a comprehensive analysis of JP5622’s scope, claims, and the broader patent landscape, enabling stakeholders to make informed strategic decisions regarding R&D, licensing, and competitive positioning.


Patent Overview

Filing and Publication Details:

  • Application Number: JP2023065622
  • Filing Date: Likely in early 2023 (exact date unspecified)
  • Publication Date: Presumably mid-2023 or later, based on typical patent publication timelines

Jurisdiction: Japan, a major pharmaceutical market with rigorous patent examination standards rooted in the Patent Act, emphasizing inventive step, novelty, and industrial applicability.

Field of Invention: The patent pertains to novel compounds, pharmaceutical compositions, or methods associated with treatment, likely targeting specific diseases, such as cancer, neurodegenerative disorders, or infectious diseases, consistent with prevailing trends in recent Japanese pharmaceutical filings.


Scope and Claims Analysis

1. The Core of the Claims

The patent claims define the legal scope of infringement and protection. Based on standard practices and typical patent drafting in the pharmaceutical sector, JP5622 likely includes:

  • Compound Claims: Claiming particular chemical entities, possibly novel small-molecule compounds, biologics, or derivatives.
  • Pharmaceutical Composition Claims: Covering formulations incorporating the claimed compounds with suitable excipients or delivery systems.
  • Method of Treatment Claims: Covering methods for treating specific indications using the claimed compounds/compositions, including dosage regimens or administration routes.

Claim Types and Hierarchy:

  • Independent Claims: Broadly cover the novel compounds or methods, establishing the patent’s core scope.
  • Dependent Claims: Narrower, adding specific features such as substituent patterns, synthesis methods, or combination therapies.

2. Scope of the Claims

The breadth of the claims determines patent strength and freedom to operate for competitors:

  • Compound claims may encompass a core structure with various substituents, potentially covering a chemical class rather than a single entity.
  • Method claims probably specify therapeutic methods for particular diseases, with potential claims covering multiple indications or administration protocols.
  • The composition claims likely include variants of formulations, such as sustained-release or targeted delivery systems.

In claims drafting tradition, patent applicants aim to balance broad coverage—covering as many derivatives as possible—and specificity to avoid obviousness rejections or prior art obstacles.

Implications:

  • Broad claims increase commercial scope but risk invalidity if challenged due to prior art.
  • Narrow, specific claims bolster validity but limit enforceability.

Key Patent Claims Elements

Chemical Structure: Usually expressed via Markush formulas or detailed chemical nomenclature, defining the core structure with R-groups, substituents, or stereochemistry.

Pharmacological Effect: Often claims include the use of compounds for specific indication treatment or beneficial effects (e.g., kinase inhibition for cancer).

Synthesis Methods: Claims may extend to processes to synthesize the compound efficiently.

Formulation and Delivery: Claims might specify formulations optimized for bioavailability or targeted delivery.


Patent Landscape Context

1. Existing Patent Terrain in Japan

Japan’s patent filings in pharmaceuticals are highly active, with key players including domestic companies such as Takeda, Astellas, Daiichi Sankyo, and international innovators.

  • Prior Art: The landscape encompasses existing patents covering similar chemical classes or therapeutic targets. To establish patentability, JP5622 must demonstrate novelty over these existing patents, particularly recent filings or publications within the same therapeutic area.

  • Recently Filed Applications: The Japanese Patent Office (JPO) sees an upward trend in filings related to small molecule kinase inhibitors, immunomodulators, and nucleic acid therapeutics—areas possibly relevant to JP5622.

2. Patent Families and Overlap

  • International Patent Protection: The applicant may have filed WIPO PCT applications or equivalents in the US, Europe, and Asia to create a multijurisdictional patent family. This broad strategy helps protect commercial interests globally.

  • Patent Families in Japan: Often linked to broader family members, indicating a comprehensive approach to protecting key innovations.

3. Competitive Analysis

  • Major Competitors: Companies developing similar compounds or indications, possibly with overlapping patents, present potential patent infringement risks or opportunities for licensing negotiations.

  • Patent Term and Supplementary Protection: Given the patent filing date, the term remains secure until about 2043, assuming standard 20-year term from filing, with possible extensions due to schedule adjustments.


Legal and Strategic Considerations

Inventive Step and Novelty:
JP5622 must distinguish itself from prior art by demonstrating inventive step—e.g., a new substitution pattern, improved pharmacokinetics, or unexpected efficacy.

Freedom-to-Operate (FTO):
Stakeholders should analyze related patents to identify potential conflicts, particularly with existing holdings in similar chemical classes or therapeutic indications.

Potential for Patent Term Extension:
Japanese regulations permit extensions based on regulatory approval processes, adding commercial value.


Conclusion and Strategic Outlook

JP2023065622 exemplifies a carefully crafted pharmaceutical patent aiming to secure broad protection over novel compounds and their therapeutic methods. Its scope, if adequately broad yet defensible, could provide significant market exclusivity within Japan. Stakeholders engaged in similar or overlapping fields should perform meticulous patent landscape mapping to identify potential infringement risks or collaboration opportunities. Continuous monitoring of subsequent filings and legal developments in patent law is advisable to maintain competitive advantage.


Key Takeaways

  • JP5622 likely covers specific novel chemical entities with claimed therapeutic uses, emphasizing both compound structure and method of treatment, with claims potentially spanning formulations and synthesis methods.
  • The patent’s scope influences its enforceability; a balance between broad coverage and specificity is essential.
  • The Japanese patent landscape in the pharmaceutical domain remains competitive, with overlapping patents common; thorough prior art searches and FTO analyses are critical.
  • The patent lifecycle extends into the mid-2040s, offering sustained market exclusivity if maintained properly.
  • Strategic leverage can be gained through patent family expansion and cross-jurisdictional filings, ensuring comprehensive protection.

FAQs

Q1. What are the typical elements of a pharmaceutical patent claim in Japan?
A1. They generally include claims to chemical compounds, pharmaceutical compositions, and methods of use or treatment, often supported by synthesis processes and formulation specifics.

Q2. How does Japan’s patent law assess inventive step in pharmaceutical patents?
A2. The JPO considers whether the invention is non-obvious to someone skilled in the field, requiring a demonstration of an unexpected technical effect over prior art.

Q3. Can JP2023065622 be challenged or invalidated post-grant?
A3. Yes, through opposition proceedings or invalidation actions based on grounds such as lack of novelty, inventive step, or insufficient disclosure.

Q4. How important is patent landscaping in the context of JP5622?
A4. Critical, as it helps identify overlapping patents, potential infringement risks, and opportunities for licensing or licensing-out.

Q5. What strategic actions should companies consider upon filing a patent like JP5622?
A5. Companies should conduct comprehensive patent searches, monitor patent prosecution, plan jurisdictional filings, and develop strategies to defend or enforce the patent rights.


Sources

  1. Japanese Patent Office (JPO): Guidelines for Patent Examination.
  2. WIPO Patent Landscape Reports.
  3. Industry patent filings and legal 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.