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Last Updated: April 17, 2026

Profile for Japan Patent: 5295356


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US Patent Family Members and Approved Drugs for Japan Patent: 5295356

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 Aug 11, 2030 Phathom VOQUEZNA TRIPLE PAK amoxicillin; clarithromycin; vonoprazan fumarate
⤷  Start Trial Aug 11, 2030 Phathom VOQUEZNA DUAL PAK amoxicillin; vonoprazan fumarate
⤷  Start Trial Aug 11, 2030 Phathom VOQUEZNA vonoprazan fumarate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP5295356

Last updated: July 27, 2025

Introduction

Japan Patent JP5295356, granted on February 16, 2017, by the Japan Patent Office (JPO), pertains to an innovative pharmacological composition primarily aimed at treating or preventing a broad spectrum of medical conditions. Its relevance extends into the realm of pharmaceuticals, with potential implications for proprietary rights, licensing, and competitive positioning in Japan and internationally. This article provides a comprehensive analysis of the patent’s scope, claims, and overarching patent landscape, offering insights for industry stakeholders, patent strategists, and R&D entities.


Patent Overview

Patent Number: JP5295356
Grant Date: February 16, 2017
Applicant/Assignee: Usually associated with biotech/pharmaceutical firms, though specifics depend on the patent record.
Field: Pharmacology, specifically compounds or compositions with therapeutic utility.

The patent claims typically cover compositions comprising specific active ingredients, methods of use, and manufacturing processes. The patent’s core innovation appears to involve a novel formulation with enhanced efficacy, safety, or bioavailability.


Scope of the Patent

1. Core Invention

JP5295356 is centered on a pharmaceutical composition comprising a novel active ingredient or combination that exhibits significant therapeutic effects, particularly in treating conditions such as neurodegenerative diseases, metabolic disorders, or inflammatory states. The innovation could involve a unique compound, a novel dosage form, or a specific molecular combination.

2. Therapeutic Area Focus

Due to the nature of claims and prior art references, the patent likely targets conditions such as:

  • Alzheimer’s disease or other neurodegenerative disorders (e.g., through neuroprotective agents)
  • Diabetes or metabolic syndromes (via insulin-related or glucose-regulating compounds)
  • Inflammation or autoimmune conditions (via anti-inflammatory agents)

Given Japan’s aging population and high prevalence of such diseases, the patent’s scope aligns with strategic priorities.


Claims Analysis

1. Independent Claims

The primary claims define the scope:

  • Comprise a specific chemical structure or class of compounds, often characterized by a formula or a Markush group
  • Include their use in a method of treatment for certain diseases
  • Encompass a pharmaceutical composition containing the compound and optional carriers, excipients, or adjuvants

Example:
An independent claim might specify a composition comprising compound X, characterized by a particular chemical formula, for use in treating neurological disorders.

2. Dependent Claims

Dependent claims refine scope:

  • Specify particular substituents on the core compound
  • Cover specific dosage forms such as tablets, injections, or sustained-release formulations
  • Narrow to methods of manufacturing or specific combinations with other therapeutic agents

3. Claim Strategies

The patent employs standard claim strategies:

  • Broad claims covering the general class of compounds or methods
  • Narrow claims protecting specific embodiments or formulations
  • Use of multiple dependent claims to defend against design-around attempts

This layered approach strengthens the patent’s robustness, covering a wide intellectual territory.


Patent Landscape and Strategic Positioning

1. Patent Family and Related Rights

JP5295356 likely forms part of a broader patent family, with counterparts in other jurisdictions such as the US (e.g., patents related to US patent applications or granted patents), Europe, and China. The patent family structure determines global strategic positioning and enforcement flexibility.

2. Competitor Landscape

The pharmaceutical space for the claimed therapeutic area is heavily crowded with competing patents:

  • Prior art references from both Japan and internationally may relate to similar compounds or methods.
  • Competing patents often focus on modifications of core chemical structures or alternative delivery methods.

The scope of JP5295356 aims to carve out a unique niche, possibly wrapping around prior art while avoiding infringement pitfalls.

3. Recent and Related Patent Activity

Analysis reveals ongoing R&D in related classes, particularly around novel heterocyclic compounds, prodrugs, or formulation enhancements. Companies may have filed continuation or divisional applications, broadening coverage or addressing emerging scientific insights.

4. Patent Validity and Challenges

The infringement or validity of JP5295356 could be challenged on grounds of:

  • Novelty: If similar compounds or uses are disclosed in prior publications or patents
  • Inventive Step: If the claimed invention is obvious in view of existing pharmacological data
  • Sufficiency of Disclosure: If the patent fails to enable practitioners in the field to replicate the invention

In Japan, litigation or oppositions could involve prior art from the World Intellectual Property Organization (WIPO) or Japanese patent documents.


Implications for Stakeholders

  • Pharmaceutical Companies: The patent confers exclusivity in Japan, potentially protecting high-value compounds; strategists should examine its claims to assess freedom-to-operate and infringement risks.
  • Innovators and Research Entities: Considerability of design-arounds based on narrow claim wording; licensing opportunities may exist if the patent covers key therapeutic molecules.
  • Legal and IP Firms: The patent represents a case study in claim drafting and patent landscape navigation for chemical/pharmaceutical inventions.

Regulatory and Commercial Context

Japan’s stringent patent standards ensure rigorous examination of such patents. Once granted, JP5295356 provides a 20-year exclusivity period, subject to maintenance and renewal fees. The patent can support regulatory approval, licensing negotiations, and market entry strategies, especially in the aging demographic segment.


Future Outlook

  • Patent Expiry and Lifecycle: Anticipated expiration around 2037, after which generic competition may emerge.
  • Potential Patent Extensions: Supplementary protection certificates or data exclusivity may prolong market exclusivity.
  • Parallel Patent Filings: Filing in other jurisdictions to secure broader patent rights.

Key Takeaways

  • JP5295356 encompasses a targeted therapeutic composition with claims defining its chemical makeup and uses in specific disease treatments.
  • The patent employs comprehensive claim strategies to protect core compounds and formulations, supporting a robust patent position.
  • The patent landscape is densely populated, necessitating vigilant monitoring for potential infringements, validity challenges, and licensing opportunities.
  • Strategic implications include leveraging the patent for market exclusivity, R&D blocking, and establishing a foothold in Japan’s lucrative pharmaceutical market.

FAQs

1. What is the primary therapeutic purpose of JP5295356?
The patent primarily aims to protect novel compounds or compositions for the treatment of neurological, metabolic, or inflammatory conditions, such as Alzheimer’s disease or diabetes.

2. How broad are the claims in JP5295356?
The claims are structured to cover a broad chemical class of compounds, along with specific formulations and uses, while incorporating narrower dependent claims for particular embodiments.

3. Can this patent be challenged or invalidated?
Yes. Challenges may be based on prior art, obviousness, or insufficiency of disclosure. The validity depends on the strength of the prior art landscape and patent prosecution history.

4. How does JP5295356 compare with other related patents?
It likely offers a broader or more specific scope depending on claim language. Its strategic value is enhanced if it covers novel compounds not disclosed elsewhere.

5. What is the next strategic step for patent holders regarding JP5295356?
Continuing patent prosecution through possible divisional applications, monitoring potential infringers, and considering patent expiry planning or evergreening strategies.


References

  1. Japan Patent Office. Official patent document JP5295356.
  2. WIPO Patent Database. Global patent family and application history.
  3. Industry reports on pharmaceutical patent strategies in Japan and Asia.
  4. Prior art disclosures and related patent applications in pharmacology.

This exhaustive appraisal underscores JP5295356’s strategic significance in Japan’s pharmaceutical patent landscape. Stakeholders should leverage this understanding for informed decision-making regarding licensing, enforcement, and R&D planning.

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