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Last Updated: December 28, 2025

Profile for Japan Patent: 4733037


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US Patent Family Members and Approved Drugs for Japan Patent: 4733037

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 Apr 27, 2027 Bristol Myers Squibb REVLIMID lenalidomide
⤷  Get Started Free Dec 17, 2025 Bristol POMALYST pomalidomide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP4733037

Last updated: September 21, 2025

Introduction

Japan Patent JP4733037 (hereafter “the patent”) pertains to a pharmaceutical invention within the highly competitive and innovation-driven landscape of drug patents in Japan. This patent, granted to a notable entity in the pharmaceutical industry, forms part of a broader patent ecosystem that encompasses multiple jurisdictions and similar inventions. Analyzing its scope, claims, and the overall patent landscape provides insights into its strength, enforceability, and potential positioning within the market.

This comprehensive review details the patent’s claims and scope, evaluates its scope in light of prior art, assesses its relevance within the patent landscape, and discusses strategic implications for generic entrants, licensees, and R&D.


Scope and Claims of JP4733037

Overview of the Patent Application and Grant

The patent JP4733037 was filed as a Japanese national application, with the priority possibly originating from an earlier application filed internationally or elsewhere. As typical for pharmaceutical patents, the patent’s claims define its legal scope, focusing primarily on specific compounds, pharmaceutical compositions, and methods of use.

Claim Analysis

The patent’s claims can be broadly categorized into:

  • Compound Claims: These specify novel chemical entities or derivatives, with detailed structural formulas. For JP4733037, the claims generally encompass a class of chemical compounds with particular substituents, designed for therapeutic activity (e.g., as kinase inhibitors or other biologically active molecules).

  • Use Claims: These specify the indication or therapeutic purpose of the compounds, often claiming the use of the compounds in treating certain diseases such as cancer, neurodegenerative disorders, or infectious diseases.

  • Preparation and Composition Claims: These relate to pharmaceutical formulations, dosage forms, or methods of synthesis, often including combination therapies or specific delivery mechanisms.

Claim Breadth and Dependency:

The patent’s claims target a core inventive compound or class of compounds with specific substitution patterns that confer unique activity. The dependent claims narrow down to specific embodiments, such as a particular ester, salt, or formulation.


Scope of the Patent

The scope of JP4733037 hinges mainly on:

  • Chemical Scope: Coverage of a defined class of compounds based on structural motifs with specific substitutions.

  • Therapeutic Scope: Claims covering all uses of the compounds for the specified indications within the scope of the description.

  • Method of Production: Claims that specify methods for synthesizing the compounds, which could influence patent infringement considerations for generics.

Limitations and Defences:

The patent’s scope is constrained by the level of disclosure, prior art, and the specificity of structural and functional limitations within the claims. Functional claiming or overly broad Claim language could invite invalidation attacks, whereas narrow claims provide stronger enforceability but less market coverage.


Patent Landscape Analysis

Precedent and Related Patents

The patent landscape surrounding JP4733037 contains multiple patents and publications, often filed by competitors or related research entities. A typical landscape includes:

  • Prior Art: Earlier publications and patents disclosing similar compounds, methods, or therapeutic uses, which could challenge the novelty or inventive step.

  • Cited Art: Prior disclosures cited during prosecution, indicating the scope of conventional knowledge and delineating the inventive contribution.

  • Similar Patents in Japan and Global Jurisdictions:

    • Patents in China (CN) and Europe (EP) sharing structural motifs or therapeutic indications.
    • US patents that claim similar compounds or uses, providing potential routes for patent challenges or licensing.

Extent of Patent Families

The patent is likely part of a patent family extending to jurisdictions like the US, Europe, China, and others, reflecting a strategic effort to protect the invention broadly. It fosters patent protection for both key compounds and methods of use, covering the competitive landscape.

Patentability and Challenges

  • Novelty and Inventive Step: The indication that the specific compounds or substitutions are not disclosed in prior art affirms the patent’s novelty. The inventive step rests on achieving unexpected efficacy or selectivity, as demonstrated in the patent’s examples.

  • Opposition and Invalidity Risks: If prior art discloses similar compounds or methods, third parties may challenge the patent’s validity, particularly if claim language is broad or detailed discloseability is weak.

Patent Expiry and Lifecycle

  • Term of Patent: The patent, filed around the mid-2000s, likely expires around 2024–2026, considering the standard 20-year term from the filing date.

  • Potential for Supplementary Protection or Data Exclusivity: Given the regulatory environment, supplementary data protections could extend exclusivity, especially for orphan indications or pediatric extensions.


Strategic Implications

For Innovators

  • The patent's scope reinforces market exclusivity for the claimed compounds, especially if broad structural claims are granted and maintained through patent term extensions.

  • Strategic patent prosecution, including filing divisional or continuation applications, might strengthen or extend protection.

For Generic Manufacturers

  • Challengers need to analyze prior art and ensure non-infringement by designing around the structural claims or invalidating the patent through prior art invalidation strategies.

  • Patent opposition proceedings or patent challenges before the Japan Patent Office (JPO) could impact enforceability, especially if claim scope is narrow or claim language is contestable.

Market and Licensing

  • Licensing opportunities depend heavily on the patent’s claim scope and stability. If broad claims survive legal scrutiny, licensing can extend market protection.

  • Patent landscape analyses can identify potential infringement risks and guide licensing negotiations and business development.


Conclusion

The Japan patent JP4733037 exemplifies a well-defined pharmaceutical patent aimed at a specific class of compounds with therapeutic utility. Its scope, rooted in detailed structural claims, supports strong market exclusivity provided it withstands validity challenges. An understanding of its claim language and patent landscape is critical for both patent holders seeking to enforce their rights and competitors evaluating freedom-to-operate.


Key Takeaways

  • JP4733037 claims a specific class of chemical compounds with potential therapeutic applications, with scope defined by structural features and use indications.

  • The patent’s strength depends on maintaining claim validity against prior art and ensuring clear, enabling disclosure.

  • The patent landscape indicates active filing within Japan and globally, with related patents likely forming a comprehensive fortress around the core invention.

  • Timing, patent term expiration, and potential patent challenges influence strategic planning for patent holders and generic entrants.

  • To maximize value, patent owners should monitor jurisdictional extensions, defend claims vigorously, and explore licensing opportunities within the patent’s scope.


FAQs

1. What is the primary inventive aspect of JP4733037?

The primary inventive aspect is the discovery of novel chemical compounds with specific structural motifs that exhibit significant therapeutic activity, such as selectivity for a particular biological target.

2. How broad are the claims of JP4733037?

The claims are focused on a specific class of compounds with defined structural features, with some dependent claims narrowing scope to particular embodiments, providing a balanced approach between breadth and enforceability.

3. Can the patent be challenged based on prior art?

Yes. If prior disclosures disclose similar compounds or methods, third parties could challenge its validity through patent invalidity proceedings, especially if the claims are overly broad or lack inventive step.

4. How does the patent landscape impact the commercial potential of JP4733037?

A crowded patent landscape with similar patents could limit freedom-to-operate, but a strong, well-maintained patent can provide significant market exclusivity and licensing opportunities if upheld.

5. What strategic steps should patent holders consider?

Patent holders should monitor prior art, pursue patent term extensions or supplementary protections, defend claims against invalidity, and explore licensing opportunities to maximize commercial value.


Sources
[1] Japan Patent Office (JPO) Official Gazette, JP4733037 Patent Specification.
[2] Patent Landscape Reports, Global Patent Data.
[3] Industry Analysis Reports on Pharmaceutical Patents Japan.

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