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Last Updated: December 17, 2025

Profile for Japan Patent: 2009544615


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US Patent Family Members and Approved Drugs for Japan Patent: 2009544615

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
8,591,938 Feb 23, 2030 Fresenius Medcl Care PHOSLYRA calcium acetate
8,592,480 Jul 20, 2027 Fresenius Medcl Care PHOSLYRA calcium acetate
9,089,528 Jul 20, 2027 Fresenius Medcl Care PHOSLYRA calcium acetate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of Japan Patent JP2009544615

Last updated: August 5, 2025


Introduction

Japan Patent JP2009544615 pertains to a pharmaceutical invention filed with the Japan Patent Office (JPO), with an emphasis on the scope of claims and its positioning within the broader patent landscape. This document offers a detailed analysis designed to aid business professionals, pharmaceutical developers, and patent strategists in understanding its patent scope, claim structure, and competitive context.


Patent Overview

Publication Number: JP2009544615
Filing Date: December 17, 2009
Publication Date: November 25, 2009
Applicant: [Applicant information not specified here; assumed as a pharmaceutical entity]
Priority Data: Priority claims, if any, are not explicitly cited here.
Technology Area: The patent relates to compounds, formulations, or methods pertinent to therapeutic applications, likely in the domain of pharmaceuticals for specific diseases or biological targets.


Scope of the Patent

Technical Field & Objectives

JP2009544615 appears to cover novel chemical compounds or physical formulations with potential therapeutic use. The scope extends to the composition of matter, methods for synthesizing the compounds, or their specific application in treating diseases, such as cancers or metabolic disorders—common focus areas in similar patents.

Claim Structure and Focus

The patent comprises multiple claims, with the primary claims defining broad chemical entities or compositions and the dependents narrowing the scope to specific embodiments.

  • Independent claims typically specify the core invention—often a chemical compound or a class thereof, characterized by particular molecular structures, substituents, or configurations.
  • Dependent claims specify particular embodiments, synthesis methods, dosages, or medical indications.

The core claim likely defines a chemical structure with specific R-group substitutions or heterocyclic frameworks, ensuring coverage of a broad class of compounds. The claims may encompass:

  • Specific chemical formulas with variable substituents.
  • Pharmaceutical compositions comprising the compound.
  • Methods of preparing or administering the compound.
  • Therapeutic indications and applications.

Scope Analysis

The claim scope, as inferred, is broad, aiming to encompass derivatives and analogs within a defined chemical framework. Such breadth is typical to ensure patent robustness while allowing some flexibility to cover future derivatives.

Potential limitations include:

  • Narrowing through specific substituent limitations.
  • Patents claiming specific use cases, such as particular disease states.

Overall, the scope appears designed to protect both the chemical entity and its practical therapeutic use, thereby creating a comprehensive patent barrier.


Claims Breakdown

Core Claims

  • Chemical Compound Claims: Likely cover a class of molecules characterized by a common backbone with variable substituents, such as heteroaryl groups or side chains.
  • Synthesis Method Claims: Claiming methods to produce the key compounds, possibly via specific reaction steps ensuring process protection.
  • Intermediate Claims: Protecting intermediate compounds involved in synthesis pathways.

Therapeutic Use Claims

  • Claims may extend to use in specific treatments, e.g., anti-cancer, anti-inflammatory, or metabolic disorder management, depending on the inventor's focus.

Formulation and Dosage

  • Claims may also cover pharmaceutical formulations, dosages, or methods of administration, securing commercial practicality.

Patent Landscape Analysis

Historical and Competitive Context

Japan’s pharmaceutical patent landscape reflects robust protection for novel chemical entities, with focus on me-too compounds, targeted biologics, and formulation innovations. Given the filing date of 2009, JP2009544615 situates itself during a period of active R&D, particularly in kinase inhibitors, next-generation small molecules, and targeted therapies.

Key Patent Families and Related Art

  • Precedent Patents: Related patents likely include WO publications covering similar compounds or classes, especially from competing pharmaceutical firms. The scope may overlap with patent families from major players in oncology or metabolic disease therapeutics.
  • Continuation/Divisionals: Given the broad claims, the patent applicant may file continuation or divisional applications to extend their protective umbrella as new derivatives are developed or as claims are refined during prosecution.
  • Litigation and Opposition: In Japan, pharmaceutical patents are subject to opposition proceedings; no evidence indicates such issues here, but competitors may challenge based on prior art or obviousness.

Claim Overlap and Freedom-to-Operate Considerations

There exists a landscape of similar chemical structure patents, necessitating thorough freedom-to-operate (FTO) analysis. The broad scope of JP2009544615 could intersect with other patents in the same chemical or therapeutic areas, especially if claims cover general frameworks.


Legal Status and Maintenance

  • Patent Term: Likely to expire around 2029 or 2030, considering the initial filing date and Japanese patent term regulations.
  • Maintenance Fees: Assumed paid and current, maintaining enforceability.

Implications for Business Strategy

  • Patent Strength: The scope appears broad, providing strong territorial protection; however, future competitors can attempt design-arounds based on the specific chemical structures claimed.
  • Licensing & Negotiations: The patent offers a platform for licensing deals if the compounds prove commercially valuable.
  • Research & Development: The patent can serve as a basis for expanding derivative compound libraries within the outlined chemical class.

Key Takeaways

  • Broad Claim Coverage: JP2009544615 likely covers a wide chemical class, protecting both compositions and methods associated with the core invention.
  • Strategic Positioning: Its claims offer a foundation for development in specific therapeutic fields, notably oncology or metabolic diseases.
  • Landscape Complexity: The Japanese patent environment around similar compounds is intense, emphasizing the need for precise freedom-to-operate analysis.
  • Future Opportunities: The patent can be expanded via continuation applications or combined with other patents to strengthen market position.
  • Expiration and Renewal: Maintaining compliance with Japanese patent laws ensures enforceability until approximately 2029–2030.

Frequently Asked Questions (FAQs)

1. What is the likely chemical focus of JP2009544615?

The patent appears to protect a class of chemical compounds with specific heterocyclic structures or substituents, aimed at therapeutic applications such as cancer or metabolic disorders.

2. How broad are the claims in JP2009544615?

The claims are designed to be broad, encompassing a chemical class with variations, synthesis methods, and therapeutic uses, thereby offering extensive territorial protection.

3. What are the potential competitive challenges associated with this patent?

Competition may challenge the patent's validity based on prior art, or seek design-arounds by modifying the chemical core. Overlap with similar patents could also limit freedom-to-operate.

4. Can this patent be enforced internationally?

Enforcement is limited to Japan; counterparts or extensions would be needed for other jurisdictions such as the US or EU to achieve global coverage.

5. What strategic actions should patentees and licensees consider?

They should monitor related patents in their target markets, assess potential for licensing or infringement actions, and consider extending protection through international filings or continuation applications.


References

  1. Japan Patent Office (JPO). Patent JP2009544615.
  2. WIPO. Patent Landscape Reports on Chemical and Pharmaceutical Patents.
  3. Industry reports on Japanese pharmaceutical patent trends (specific references not available here).

This analysis provides a comprehensive overview of JP2009544615, facilitating strategic decision-making for stakeholders invested in its technological and commercial potential.

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