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

Last Updated: December 15, 2025

Profile for Japan Patent: 5552700


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Japan Patent: 5552700

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 Oct 16, 2028 Pierre HEMANGEOL propranolol hydrochloride
⤷  Get Started Free Oct 16, 2028 Pierre HEMANGEOL propranolol hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Japan Patent JP5552700: Scope, Claims, and Patent Landscape

Last updated: August 23, 2025

Introduction

Japan Patent JP5552700 pertains to a pharmaceutical invention whose scope and claims define its innovative coverage, while its positioning within the patent landscape influences the competitive landscape and potential licensing opportunities. This analysis delves into the patent's claims, their scope, and broader landscape implications, offering insights for pharmaceutical companies, patent strategists, and legal professionals.

Patent Overview

JP5552700 was filed by a Japanese applicant, with publication date in accordance with Japan Patent Office (JPO) standards. The patent generally relates to a specific compound, formulation, or method relevant to a therapeutic area, potentially involving novel chemical entities, drug delivery mechanisms, or therapeutic methods. Precise classification and the patent's priority filings influence its territorial scope and potential patent life.

Exact details of the patent's title, assignee, filing date, and application number are essential to contextualize its legal strength and validity, although these are not provided explicitly here. Given its scope, the patent likely addresses a medicinal compound or approach in a specific disease indication, possibly within oncological, neurological, or metabolic areas.


Scope and Claims Analysis

Scope and claims define the legal boundaries of patent exclusivity. They determine what is protected and influence infringement risk assessments and licensing strategies. Analyzing JP5552700 involves examining:

Independent Claims

Independent claims serve as the broadest legal coverage, outlining the core inventive concept. These claims generally specify the compound's chemical structure, mechanism of action, formulation, or method of use.

Typical characteristics include:

  • Chemical Structure Claims: If the patent involves a novel chemical entity, claims specify the molecular formula, substructures, or specific functional groups conferring activity.

  • Method of Use Claims: Claims may cover administering the compound for particular diseases, dosing regimens, or treatment methods.

  • Formulation Claims: Aspects like enhanced stability, bioavailability, or specific delivery techniques.

Implications:
Broad independent claims protect core innovations but are often challenged during examination or potential litigation for clarity or novelty issues. Narrower claims, aligned with specific structures or uses, enhance validity but may limit enforceability.

Dependent Claims

Dependent claims add limitations, such as specific substituents, dosages, or formulations, narrowing the scope and strengthening the patent's defensibility against close variants.

Legal Strategy:
A balanced set of claims ensures broad coverage while maintaining enforceable specificity.


Claim Scope Specifics

  • Chemical Entities:
    It appears the patent covers a compound that exhibits specific biological activity, possibly targeting a certain receptor or enzyme. Novel substituents or stereochemistry may be claimed to distinguish it from prior art.

  • Therapeutic Application:
    Claims might include methods for treating particular conditions, e.g., neurological disorders, implying an inventive step in a specific use case.

  • Formulations and Delivery:
    Innovations in nanoparticle encapsulation, sustained release, or targeted delivery are common claim features, potentially extending patent life and market exclusivity.

Patent Claims Validity & Limitations:
The scope is contingent on prior art, especially prior publications or patents disclosing similar compounds or methods. The patent's claims must demonstrate novelty, inventive step, and industrial applicability under JPO standards.


Patent Landscape Context

Understanding the patent landscape involves evaluating:

Previous Patents and Prior Art

  • Chemical Families: Similar compounds or derivatives disclosed in prior art impact claim scope. If JP5552700’s compounds share core features with earlier patents, the scope may be restricted or subject to invalidation.

  • Use Claims: Prior art might disclose the use of similar compounds for different indications, which can be a limiting factor if the claim’s specific therapeutic area is not novel.

Competitor Patent Activity

  • Patents Filed by Major Industry Players:
    Comparing with filings from companies like Takeda, Astellas, or global pharmaceutical giants reveals whether JP5552700 is part of a broader patent cluster in the same therapeutic field.

  • Patent Families:
    Cross-jurisdiction equivalents extend protection globally; the presence of similar patents indicates a strategic patent landscape.

Legal Status & Maintenance

  • Validation status, renewal payments, and expiry dates influence the patent's strength. If JP5552700 remains active and well-maintained, it signals ongoing strategic value.

Potential Challenges

  • Opposition or Invalidity Proceedings:
    Articulations of prior art differences or lack of inventive step can threaten patent enforceability.

  • Design-around Strategies:
    Competitors may develop structural modifications or alternative use methods to circumvent the patent, leading to an active innovation race.


Implications for Stakeholders

  • For Patent Holders:
    The scope determines market exclusivity, licensing potential, and enforcement avenues. Ensuring claims are sufficiently broad yet defensible enhances commercial value.

  • For Competitors:
    Analyzing the patent's scope guides the development of novel compounds or uses that avoid infringement, often focusing on structural differences, alternative delivery methods, or different therapeutic indications.

  • For Legal Professionals:
    Evaluating validity and infringement risks requires assessing claim language against prior art and real-world practice.

  • For R&D Strategists:
    Patent landscape insights inform innovation pipelines, licensing negotiations, and market entry timing.


Conclusion

JP5552700 encapsulates a targeted innovation within Japan's pharmaceutical patent sphere, with its scope heavily reliant on the precise language of its claims. Its value depends on novelty over prior art, strategic claim drafting, and ongoing patent maintenance. The expansive landscape around it underscores the competitive nature of pharmaceutical patenting, demanding diligent monitoring and strategic patent management.


Key Takeaways

  • Patent scope hinges on the breadth of independent claims, with broad claims offering market exclusivity but higher scrutiny.
  • The patent landscape's richness influences enforceability, licensing, and innovation direction.
  • Careful claim drafting and thorough prior art searches are essential to optimize patent longevity.
  • Active patent maintenance and monitoring are vital to uphold patent rights effectively.
  • Strategic insights from patent claims and landscape analysis enable informed decision-making in R&D, licensing, and legal proceedings.

FAQs

Q1: How can competitors challenge the validity of JP5552700?
A1: They can file prior art references or argue lack of inventive step during opposition or litigation proceedings, focusing on similar compounds or methods disclosed earlier.

Q2: Can the scope of claims in JP5552700 be expanded post-grant?
A2: Generally, claims cannot be broadened after grant but can be narrowed or supplemented through amendments during examination or opposition, subject to legal constraints.

Q3: How does this patent compare to international patents in the same field?
A3: Examination of equivalent filings in jurisdictions like the US (e.g., through PAIR or Patent Center), Europe, or China reveals whether the invention is protected globally or primarily in Japan.

Q4: What are the key factors influencing the strength of the patent’s claims?
A4: Novelty, inventive step, clear claim language, and compliance with patentability requirements under Japanese law determine strength.

Q5: How does patent landscape analysis support strategic patenting?
A5: It identifies gaps, overlapping rights, and potential infringement risks, guiding filing strategies and R&D focus.


References:

  1. Japan Patent Office (JPO). Patent Examination Guidelines.
  2. WIPO. Patent Landscape Reports.
  3. Industry Patent Databases: PatCase, Asian Patent Databases.

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.