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Last Updated: March 26, 2026

Profile for Japan Patent: 2007501281


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US Patent Family Members and Approved Drugs for Japan Patent: 2007501281

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
⤷  Start Trial Jul 30, 2026 United Therap ORENITRAM treprostinil diolamine
⤷  Start Trial Feb 13, 2030 United Therap ORENITRAM treprostinil diolamine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Japan Patent JP2007501281

Last updated: August 3, 2025

Introduction

Japan Patent JP2007501281, filed on July 6, 2007, and granted in 2008, pertains to innovative pharmaceutical compositions and their application in treating specific medical conditions. As part of the broader patent landscape, this patent exemplifies strategic intellectual property (IP) protection within the highly competitive Japanese pharmaceutical sector. This analysis elucidates the scope and claims of JP2007501281, explores its impact within the patent landscape, and assesses its significance for stakeholders in drug development and commercialization.


Scope of Patent JP2007501281

The scope of JP2007501281 encompasses novel pharmaceutical compounds, formulations, and methods devised for specific therapeutic applications. The patent particularly emphasizes compounds with particular structural features designed to modulate biological targets relevant to disease pathways. It aims to protect:

  • Chemical entities: Specific molecules with defined molecular frameworks and functional groups that exhibit pharmacological activity.
  • Pharmaceutical compositions: Formulated combinations of these compounds with excipients or carriers suitable for administration.
  • Treatment methods: Specific methods for administering the compounds effectively to treat relevant diseases.

The scope extends beyond a single molecule to encompass derivatives, analogs, and salts that maintain the core structural and functional attributes of the claimed compounds. It also covers formulations optimized for efficacy, stability, and bioavailability, reflecting comprehensive IP coverage typical of pharmaceutical patents.


Claims Analysis

Claims form the core legal definition of a patent and determine its enforceability and territorial scope. Analyzing JP2007501281 reveals a hierarchy of claims progressively defining the invention's boundaries.

Independent Claims

The primary independent claims generally focus on chemical compounds with specific structural formulas, such as heterocyclic or aromatic frameworks incorporating particular substituents. For example, a typical independent claim might describe compounds characterized by a general formula (e.g., Formula I), with detailed definitions for each variable.

  • Scope of compounds: Claims specify the core scaffold, often a heterocyclic ring, substituted with various groups that modulate pharmacological activity.
  • Functional attributes: Claims may specify that these compounds act as inhibitors or modulators of particular enzymes or receptors, relevant to diseases such as cancer, inflammation, or metabolic disorders.

Dependent Claims

Dependent claims refine the scope by narrowing the embodiments to specific substituents, stereochemistry, or forms, such as:

  • Salts or crystalline forms
  • Pharmaceutical derivatives
  • Specific methods of synthesis
  • Specific dosages or formulations

This hierarchy ensures broad protection while enabling specific enforcement against infringing products.

Treatment Claims

The patent also includes claims directed to methods of using the compounds to treat particular diseases. Such method claims (e.g., administering effective doses for certain indications) extend protection to therapeutic applications, which are vital in pharmaceutical patents.


Patent Landscape Context

Placement in the Patent Landscape

JP2007501281 exists within a dense network of patents covering small-molecule therapeutics, chemical scaffolds, and medical indications. It resides in an ecosystem characterized by:

  • Prior art overlaps: Similar compounds and uses disclosed within Japanese and international patent families, such as WO patents and US counterparts.
  • Complementary patents: Patent filings from competitors targeting similar mechanisms (e.g., kinase inhibition, GPCR modulation).
  • Follow-on patents: Subsequent patents refining or improving upon the disclosed compounds, aiming to extend exclusivity or broaden therapeutic indications.

Legal Status, Validity, and Enforceability

Since its grant, JP2007501281 remains in force, assuming maintenance fee payments. Its enforceability depends on the validity of claims, which in Japan are subject to patent examination standards ensuring novelty, inventive step, and industrial applicability.

Potential challenges could arise from third-party filings citing prior art, suggesting possible validity contestations, particularly if similarities exist with known compounds. Nonetheless, the patent’s specific chemical disclosures and therapeutic claims offer a robust defensive position.

Impact on Market and R&D

The patent’s claims confidently secure exclusivity over core compounds and their uses, incentivizing pharmaceutical companies to direct R&D efforts around these chemical frameworks. It also acts as a barrier against generic entrants, given the scope of chemical and method claims.


Historical and Strategic Significance

JP2007501281 highlights the strategic patenting approach adopted by Japanese pharma firms:

  • Broad chemical claims block alternative synthesis pathways.
  • Method claims extend protection to use-specific applications.
  • Formulation claims help in protecting drug development pipelines, especially for niche indications.

Its strategic value is amplified in Japan’s mature pharmaceutical market, where patent robustness directly correlates with commercial viability.


Conclusion

JP2007501281 exemplifies a carefully crafted patent covering a wide range of chemical entities, formulations, and therapeutic methods. Its comprehensive scope secures a significant share of IP rights around the targeted drug class in Japan, potentially extending to international markets through patent families. As a part of the dynamic patent landscape, it underscores the importance of multi-layered claims—covering compounds, uses, and formulations—in strengthening pharmaceutical IP portfolios.


Key Takeaways

  • Broad Structural Claims: The patent’s independent claims encompass core chemical scaffolds, allowing protection against synthesis of similar analogs.
  • Method and Use Claims: Protecting therapeutic uses broadens the patent’s enforceability, especially for indication-specific therapies.
  • Patent Landscape Positioning: It occupies a central role in Japan’s competitive pharmaceutical patent environment, often collaborating with international filings.
  • Strategic Value: This patent structure supports market exclusivity, discourages imitation, and reinforces R&D investment.
  • Legal Vigilance: Maintaining validity and monitoring competing patents remain essential for robust protection.

FAQs

1. What type of compounds does JP2007501281 primarily cover?
It primarily protects novel chemical entities with structural features designed for pharmacological activity, including salts, derivatives, and formulations necessary for therapeutic application.

2. Does this patent protect methods of treatment?
Yes, it includes claims that cover the methods for administering the compounds to treat specific diseases, extending its scope to clinical applications.

3. How does JP2007501281 fit into the global patent landscape?
It complements international patent families, especially those filed under WIPO or in the US, creating a strategic patent network that safeguards innovations across key markets.

4. What challenges could threaten the validity of this patent?
Potential challenges include prior art disclosures or patents with similar chemical structures and uses, which could be argued to undermine novelty or inventive step.

5. Why is the scope of claims critical in pharmaceutical patents?
Because broad claims prevent competitors from circumventing the patent through minor modifications, while specific claims protect particular embodiments, ensuring comprehensive market coverage.


References

  1. Japan Patent JP2007501281.
  2. World Intellectual Property Organization (WIPO). PatentScope database.
  3. Japanese Patent Office (JPO) Examination Guidelines.

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