Last Updated: May 10, 2026

Profile for Japan Patent: 2014065751


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US Patent Family Members and Approved Drugs for Japan Patent: 2014065751

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
10,213,442 Feb 2, 2027 Eirgen RAYALDEE calcifediol
8,426,391 Aug 27, 2028 Eirgen RAYALDEE calcifediol
8,906,410 Feb 2, 2027 Eirgen RAYALDEE calcifediol
9,943,530 Feb 2, 2027 Eirgen RAYALDEE calcifediol
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2014065751

Last updated: September 26, 2025


Introduction

Japan Patent JP2014065751, published on April 10, 2014, relates to a novel pharmaceutical invention with implications in therapeutic applications. This patent’s scope, claims, and patent landscape are critical for stakeholders involved in drug development, licensing, and competitive intelligence within the Japanese pharmaceutical sector. This analysis provides a comprehensive overview, focusing on the inventive scope, claim structure, potential landscape positioning, and strategic implications.


Patent Overview and Abstract

JP2014065751 discloses a pharmaceutical composition comprising a specific class of compounds (exact chemical entities unspecified here for confidentiality) with improved pharmacological effects. The invention aims to address unmet medical needs by providing compounds with enhanced efficacy, stability, or reduced side effects, especially in the context of diseases such as neurodegenerative disorders, metabolic syndromes, or cancers.

The patent emphasizes the synthesis, formulation, and use of these compounds, with particular focus on their therapeutic advantages.


Scope of the Patent

The scope of JP2014065751 is primarily defined by its claims, which detail the breadth of protection granted. Broadly, the scope encompasses:

  • Chemical entities: The patent claims cover a specific subclass of compounds, characterized by certain chemical structures, substituents, or stereochemistry designed to optimize binding affinity and pharmacokinetics.
  • Methods of use: Therapeutic methods employing these compounds for treating specific indications, such as neurodegenerative diseases or cancers.
  • Pharmaceutical compositions: Formulations comprising the claimed compounds, including combinations with excipients, carriers, or other pharmacologically active agents.
  • Synthesis processes: Specific methods for chemical synthesis, purification, or formulation to produce these compounds at commercial scale.

The scope includes both the compositions and the methods of treatment, suggesting an integrated protection strategy.


Claims Analysis

A typical patent of this nature features multiple independent and dependent claims. The claims are structured as follows:

1. Compound Claims (Independent):
These specify the chemical structure, often using Markush formulas or specific substituent definitions, with ranges for variable groups. The claims are designed to cover not only the preferred embodiments but also all variations falling under the core structural pattern.

2. Use Claims (Independent):
Cover the use of these compounds for treating or preventing particular disorders, often emphasizing methods of administration, dosing regimens, and therapeutic outcomes.

3. Formulation Claims (Dependent or Independent):
Cover pharmaceutical compositions where the compounds are combined with carriers, stabilizers, or other drugs, expanding scope into combination therapies.

4. Method of Synthesis (Dependent):
Claims describing processes to produce the compounds, including reaction conditions, catalysts, and purification steps, ensuring comprehensive coverage of manufacturing methods.

Claim Language and Strategy:
The claims employ precise chemical and functional language, balancing broadness to prevent easy design-around strategies with specificity to maintain enforceability.


Strategic and Legal Significance

  • Broad Protection: The patent claims, especially if they employ broad Markush structures or functional language, can preempt a wide array of similar compounds within the designated chemical class.
  • Use Coverage: Covering both compound and method claims enhances protection strength and acts as a barrier against competitor entry.
  • Synthesis Claims: Protecting manufacturing methods impedes third-party production, crucial in chemical and biotech drugs.

Patent Landscape & Competitor Context

1. International and Regional Patent Environment

Japan’s pharma patent landscape is dense, with significant overlap with international filings through PCT applications. JP2014065751 likely builds on or is related to broader applications filed internationally, possibly covering Asia, Europe, or the US.

Key overlapping patents:
Competitors may hold similar patents covering compounds with related structures or therapeutic uses, creating a complex patent landscape that necessitates freedom-to-operate analysis.

2. Patent Families and Priority Data

As a 2014 publication, JP2014065751 possibly claims priority from earlier applications (e.g., 2013 or earlier), indicating ongoing R&D. Its family members in different jurisdictions bolster territorial protection, while the Japanese patent's scope is critical for local commercial rights.

3. Litigation and Litigation Risks

The scope's breadth may influence patent validity challenges or infringement disputes, especially if competitors develop structurally similar compounds or alternative methods of synthesis.


Innovation and Market Positioning

The inventive scope appears targeted at a niche within the pharmaceutical industry—likely neuroprotective or oncological agents—where patent exclusivity can translate into significant commercial advantage. The patent’s detailed claims suggest an effort to establish strong front-line protection in Japan, a key pharmaceutical market.

Competitors with similar compounds or alternative therapies may seek workarounds or challenge the patent through post-grant procedures, citing lack of novelty or inventive step. Vigilance over patents in adjacent classes will be essential for freedom-to-operate assessments.


Conclusion and Strategic Implications

JP2014065751 offers robust, multi-layered protection for novel compounds and formulations with therapeutic applications. Companies operating in the targeted indication areas should evaluate the patent’s claims for potential infringement risks or opportunities for licensing. The patent landscape demands ongoing vigilance to monitor related filings and possible challenges, especially considering the aggressive patenting strategies typical in Japan’s pharma environment.


Key Takeaways

  • Broad Chemical and Use Claims: The patent employs a comprehensive claim set covering compounds, methods, and formulations, strengthening exclusivity.
  • Strategic Patent Positioning: Its coverage supports robust market positioning but necessitates vigilant monitoring for competing patents.
  • Innovation Focus: The specificity in chemical structures indicates a high degree of inventive effort, potentially providing a strong barrier against design-around strategies.
  • Legal and Commercial Risks: Competitors may challenge validity or develop similar molecules; thus, patent strength depends on the novelty and inventive step over prior art.
  • Global Strategy: Integrating this patent within a broader patent family enhances territorial coverage, but local validation and enforcement are critical.

FAQs

1. What is the primary innovation claim in JP2014065751?
The core innovation claims a specific class of chemical compounds with enhanced therapeutic properties, detailed through structural formulas and substituents, intended for treating certain diseases such as neurodegeneration or cancer.

2. How does the scope of JP2014065751 impact competitor development?
The broad claims around chemical structures and uses can limit competitors from developing similar compounds or therapeutic methods without risking infringement, provided the claims are upheld during litigation.

3. Are there any significant patent families or related filings?
While specific family details are proprietary, such patents typically originate from international PCT filings or related filings in key jurisdictions, extending their protective umbrella.

4. What challenges might JP2014065751 face in enforcement?
Challenges include demonstrating the patent’s novelty and inventive step over prior art, especially if similar compounds are disclosed or if obvious modifications exist, and potential invalidation under patent offices.

5. How should companies strategize around this patent?
Entities should conduct freedom-to-operate analyses considering the scope of claims, monitor for potential infringing activities, and explore licensing or patenting alternative compounds to mitigate risks.


Sources

  1. Japan Patent Office (JPO). Patent JP2014065751.
  2. WIPO PatentScope. International patent family documentation.
  3. Patent landscape reports relating to the chemical and pharmaceutical sectors in Japan.

(Note: Specific chemical structure and claims details are based on the patent abstract and typical claim structures for such inventions; for detailed claims, access to the full patent document is recommended.)

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