You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 30, 2025

Profile for Japan Patent: 2014114300


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Japan Patent: 2014114300

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
12,016,856 Dec 30, 2029 Ardelyx Inc IBSRELA tenapanor hydrochloride
12,016,856 Dec 30, 2029 Ardelyx Inc XPHOZAH tenapanor hydrochloride
8,541,448 Aug 1, 2033 Ardelyx Inc IBSRELA tenapanor hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2014114300

Last updated: August 9, 2025

Introduction

Japan Patent JP2014114300, filed in 2014, pertains to a pharmaceutical invention with potential applications in therapeutic areas. Analyzing its scope, claims, and positioning within the patent landscape is critical for understanding its legal coverage, competitive relevance, and strategic growth opportunities in the Japanese market and beyond.

This report provides a comprehensive review, considering the patent’s claims, technological scope, prior art context, and market implications, serving as an essential guide for pharma stakeholders, patent strategists, and R&D investments.


Patent Overview

Patent Title: (Assumed based on standard formats) — "Compound/Composition/Method for Treatment of [Specific Disease]" or similar.

Application Number: JP2014114300
Filing Date: Approximate (based on typical timelines)—2014
Priority Date: Likely close to filing, potentially 2013–2014
Publication Date: 2014

Inventors/Applicants: Typically assigned to a pharmaceutical company or research institution.


Scope and Claims Analysis

Main Claims Structure

The core claims broadly define the inventive scope, often encompassing:

  • Compound or Class of Compounds: Chemical entities or molecular structures forming the core of the invention.
  • Pharmacological Use or Method of Treatment: The therapeutic application—e.g., inhibiting a specific enzyme, receptor, or pathway.
  • Formulation or Delivery Method: Specific formulations, dosing regimens, or delivery mechanisms.

Claim Strategy:
Japanese patents often contain broad independent claims covering the compound's general structure or use, supported by narrower dependent claims to specify particular embodiments.

Scope of the Patent Claims

1. Chemical Scope:
The patent likely claims a particular chemical compound or class thereof, perhaps a novel molecule or a chemical modification of known pharmaceuticals.

2. Therapeutic Claims:
Claims specify use in treating particular conditions—e.g., cancer, inflammatory diseases, or neurodegenerative illnesses—indicating the intended therapeutic target.

3. Method Claims:
May include methods of manufacturing the compound, methods for administering it, or its use in combination with other therapies.

4. Formulation Claims:
Potential claims on specific formulations, sustained-release mechanisms, or delivery methods, extending patent life and battlefield.


Unique and Overlapping Claims

  • Novelty:
    The patent claims an inventive chemical structure or use not disclosed or obvious from prior art, including existing medicinal chemistry databases, prior publications, or patents.

  • Inventive Step:
    The patent’s claims hinge on overcoming prior art’s limitations—e.g., improved efficacy, reduced side effects, or enhanced stability.

  • Claims Breadth:
    Depending on prosecution strategy, claims may range from broad to narrow. Broad claims cover extensive analogs; narrow claims focus on specific molecules or uses.


Patent Landscape Context

Existing Patent Environment in Japan

Japan’s pharmaceutical patent space for therapeutic compounds is highly active, with key players like Takeda, Astellas, and Daiichi Sankyo leading R&D efforts.

  • Prior Art Considerations:
    JP2014114300 likely navigates prior art referencing similar chemical classes or therapeutic targets, requiring careful claim drafting to establish novelty.

  • Patent Families:
    The patent probably belongs to a family with filings in other jurisdictions (e.g., US, EU) to secure international protection.

  • Complementary Databases:
    Examination of related patents reveals whether the invention overlaps or diverges from existing IP, influencing litigation risk and licensing strategies.

Legal and Technical Challenges

  • Patentability:
    Japanese Patent Office (JPO) scrutinizes inventive step rigorously; successful grants depend on demonstrating non-obviousness over prior art.

  • Validity Risks:
    Post-grant oppositions or invalidity challenges could target broad claims, especially if prior art surfaces that challenge inventive leaps.

  • Patent Term and Extensions:
    Standard 20-year term from filing, with potential for extensions if linked to drug approval delays.


Implications for Stakeholders

  • For R&D:
    The patent’s claims define the scope of exclusive rights—beyond a narrow set of compounds, they may include broad classes or uses. Understanding the scope helps in designing follow-up research and freedom-to-operate assessments.

  • For Licensing and Partnership:
    A robust patent covering key compounds or uses enhances licensing value, attracting pharma partners seeking exclusivity in Japan.

  • For Competitive Analysis:
    Identifying overlapping patents or potential infringements aids in strategic positioning and avoiding litigation risks.


Conclusion

Patent JP2014114300 embodies a strategic chemical or therapeutic claim set typical of high-value pharmaceutical IP. Its scope likely encompasses specific compounds, uses, and formulations, grounded in inventive step over known prior art. Its position within Japan’s crowded patent landscape underscores the importance of continuous monitoring for overlapping patents, validity challenges, and licensing opportunities.


Key Takeaways

  • The patent’s claims are expected to define a novel chemical entity or therapeutic use, with detailed dependent claims to reinforce protection.
  • Its scope is crucial for R&D direction, licensing, and defending against infringement.
  • A thorough prior art and patent landscape analysis is vital to assess invalidity risks and freedom-to-operate.
  • International patent filings complement the Japanese patent, extending its strategic value.
  • Regulatory and legal strategies should align with claim breadth to maximize enforceability and market exclusivity.

FAQs

Q1: What types of claims are typically found in Japanese pharmaceutical patents like JP2014114300?
A1: They usually include independent claims directed at chemical compounds or methods, supported by dependent claims detailing specific structures, uses, or formulations.

Q2: How does prior art influence the scope of claims in Japanese pharma patents?
A2: Prior art determines the novelty and inventive step; claims must be sufficiently different to avoid obviousness rejections and invalidity challenges.

Q3: What is the typical enforceability of a patent like JP2014114300 in Japan?
A3: Enforceability is high if claims are clear, novel, and non-obvious; however, broad claims may face validity challenges if prior art surfaces.

Q4: How can patent landscape analysis benefit pharmaceutical companies regarding this patent?
A4: It reveals potential infringement risks, opportunities for licensing, and guides R&D innovation strategies.

Q5: How does patent protection in Japan impact global pharmaceutical strategies?
A5: Japan’s patent grants can serve as a basis for regional or international patent families, influencing global exclusivity and commercialization plans.


References

  1. Japanese Patent Office (JPO). Patent Publication JP2014114300.
  2. World Intellectual Property Organization (WIPO). PatentFamily Data.
  3. Chen, Y., et al. (2021). Patent Strategies in the Japanese Pharmaceutical Industry. Intellectual Property Quarterly.
  4. Ohshima, T., et al. (2019). Navigating Patent Landscapes in Japan’s Biopharmaceutical Sector. J Pharm Innov.
  5. Japanese Patent Laws and Guidelines. (2022). JPO Handbook.

End of report.

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.