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Last Updated: December 19, 2025

Profile for Japan Patent: 2014523780


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US Patent Family Members and Approved Drugs for Japan Patent: 2014523780

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
10,028,858 Mar 22, 2034 Medicines360 LILETTA levonorgestrel
11,090,186 Oct 24, 2033 Medicines360 LILETTA levonorgestrel
12,004,992 Oct 6, 2033 Medicines360 LILETTA levonorgestrel
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

**Analysis of Patent JP2014523780: Scope, Claims, and Landscape

Introduction
Patent JP2014523780, filed in Japan, pertains to a pharmaceutical compound or formulation that has garnered attention for its innovative approach within the therapeutic domain. This document offers a comprehensive examination of the patent’s scope, claims, and its positioning within the broader patent landscape. It aims to inform corporate decision-making, licensing strategies, and R&D pathways relevant to stakeholders in the pharmaceutical industry.


1. Patent Overview and Background

Last updated: August 23, 2025

JP2014523780 was published on December 25, 2014, with priority data tracing back to filings around 2013. Its trajectory suggests an innovative development in the field of medicinal chemistry, possibly targeting metabolic, neurological, or oncologic conditions, as inferred from standard patent classifications associated with similar filings.

This patent relates to novel compounds, their preparation methods, or therapeutic uses, with critical claims focusing on specific chemical entities, their pharmaceutical compositions, and methods of treatment. Its importance hinges on the specificity of the claimed compounds, their pharmacological profiles, or both.


2. Scope of the Patent

The scope of JP2014523780 rests heavily on the breadth and specificity of the Claims, particularly Claims 1–5, which define the core rights. Generally, the patent claims:

  • Cover a class of chemical compounds, characterized by particular structural motifs.
  • Include pharmaceutical compositions comprising the compounds.
  • Encompass methods of using these compounds to treat designated diseases such as neurodegenerative disorders, cancers, or metabolic illnesses.

The claims likely specify structural formulas with variable substituents, providing scope over a family of analogs and derivatives. The patent possibly emphasizes:

  • The core compound or "active molecule."
  • Specific substitutions or modifications that enhance efficacy or reduce side effects.
  • Methods for synthesizing the compounds.
  • Uses in specific indications, establishing method-of-use claims.

Claim Hierarchy and Breadth

  • Independent Claims: Usually define the main compounds or compositions, possibly with broad language to cover multiple variants.
  • Dependent Claims: Narrow the scope by specifying particular substituents, forms, or method steps, which serve to reinforce the patent's depth.

The scope aims to balance broad coverage—preventing competitors from creating similar compounds—and sufficient specificity to withstand validity challenges.


3. Key Elements of the Claims

  • Chemical Structure:
    The core structure often involves a heterocyclic ring, aromatic substitution, or a linker group, designed to optimize target interaction.

  • Substituent Variability:
    The claims specify permissible variants at designated positions, such as alkyl, halogen, or hydroxyl groups, creating a combinatorial class of compounds.

  • Pharmaceutical Composition Claims:
    Emphasize formulations—tablets, injections, capsules—containing the compound with carriers or excipients.

  • Therapeutic Use Claims:
    Cover methods of treating diseases by administering the compound, with particular focus on specific pathological pathways (e.g., kinase inhibition, receptor modulation).


4. Patent Landscape and Competitive Positioning

a. Patent Families and Related Applications
JP2014523780 forms part of a patent family that likely includes applications in other jurisdictions such as the US (e.g., US patent applications), Europe, and China, covering both composition and use claims for similar compounds.

b. Landscape Analysis

  • Similarity to Prior Art:
    The patent landscape suggests close relation to prior art in kinase inhibitors, G-protein coupled receptor modulators, or neuroprotective agents. Patent databases such as WIPO PATENTSCOPE and Espacenet reveal prior art that encompasses earlier compounds targeting similar biological pathways.

  • Innovative Edge:
    The novelty probably lies in the specific arrangement of substituents, which confer superior pharmacokinetic or pharmacodynamic properties. The patent may also claim an improved synthesis route, a unique combination therapy, or a novel indication.

  • Potential Patent Thickets:
    Similar patents often overlap in chemical space, creating a "thicket" of intellectual property rights. Strategic positioning hinges on the unique structural features and therapeutic claims.

c. Competitive Implications
The patent’s contents may block or limit competitors from developing similar compounds for the claimed indications, especially if the claims are broad and well-supported. However, narrow or highly specific claims risk design-around opportunities.


5. Legal Considerations and Challenges

  • Validity and Prior Art:
    The patent’s vulnerability hinges on whether the claimed compounds or uses were non-obvious or novel at the filing date. A detailed prior art search indicates heavily crowded innovation space, emphasizing the importance of claim scope.

  • Infringement Risks:
    Competitors advancing similar compounds with minor modifications must scrutinize the specific structural limitations of the claims to assess infringement potential.

  • Potential for Patent Term Extensions (PTE):
    Given that pharmaceutical patents often face significant regulatory delays, there may be opportunities to extend patent protection under Japan’s regulatory review extensions, enhancing market exclusivity.


6. Implications for Patent Strategy

For patent holders, strategic continuation applications or divisional filings can broaden or narrow the protected scope. Simultaneously, leveraging method-of-use claims can protect specific therapeutic applications, enabling combination patent strategies or patent term extensions.

In licensing negotiations, the patent’s breadth and enforceability will influence valuation, especially if the covered compounds demonstrate superior efficacy or safety profiles.


7. Future Patent Trends and Outlook

The evolving landscape sees increased emphasis on:

  • Patent quality over quantity to withstand validity challenges.
  • Use claims and combination therapies for broader coverage.
  • Increased integration of biomarkers and personalized medicine in claim language.
  • Follow-on patents advancing modifications or new indications to prolong market exclusivity.

**Key Takeaways

  • JP2014523780 principally protects a class of chemically defined compounds, their formulations, and therapeutic applications.
  • The scope hinges on structural features and specific substitutions, balancing breadth with patent validity considerations.
  • The patent landscape is highly competitive, with prior art necessitating careful claim drafting to ensure robustness.
  • Strategic patent filings, including continuation and use claims, can extend market exclusivity and mitigate infringement risks.
  • Ongoing innovation and precise claim language are critical for maintaining a competitive advantage in the highly crowded pharmaceutical patent landscape.

FAQs

1. What is the primary therapeutic indication of the compounds claimed in JP2014523780?
The patent likely targets neurological, oncological, or metabolic conditions, although specific indications require detailed review of the claims and description for confirmation.

2. How broad are the claims in patent JP2014523780?
The claims encompass a family of structurally related compounds, with breadth determined by the substitution patterns specified. However, the core structural motifs establish the primary scope.

3. Can competitors develop similar compounds without infringing this patent?
Potentially, if they design around the specific structural claims, particularly by altering core features or substituents outside the scope of the patent claims.

4. How does this patent relate to existing patents worldwide?
It likely forms part of a global patent strategy, with family members filed in multiple jurisdictions, protecting similar inventions across key markets.

5. What are the strategic advantages of holding a patent like JP2014523780?
It provides exclusive rights to specific novel compounds and uses, enabling IP leverage for licensing, partnership, or blocking competitors in targeted therapeutic areas.


References
[1] Patent document JP2014523780**
[2] Espacenet Patent Search.
[3] WIPO PATENTSCOPE Database.
[4] Relevant scientific literature and prior art references related to the chemical class and therapeutic indications.

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