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Last Updated: December 16, 2025

Profile for Japan Patent: 2017515863


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US Patent Family Members and Approved Drugs for Japan Patent: 2017515863

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
11,827,646 Jan 25, 2036 Genentech Inc EVRYSDI risdiplam
9,969,754 May 11, 2035 Genentech Inc EVRYSDI risdiplam
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2017515863

Last updated: August 15, 2025


Introduction

Japan Patent JP2017515863, filed by [Applicant Name], represents a strategic patent in the pharmaceutical landscape. This patent targets specific innovations in [brief description of the technical field, e.g., novel drug formulations, therapeutic methods, or chemical compounds], offering insights into its scope, claims, and positioning within the larger patent landscape. Analyzing its scope and claims is essential for understanding its strength, breadth, and potential for market or licensing leverage.


Patent Overview

JP2017515863 was filed on [filing date] and published on [publication date] under the Japanese Patent Office (JPO). It encompasses [summary: for example, "a new class of compounds for treating neurological disorders," or "a novel delivery mechanism enhancing bioavailability"]. The patent’s priority claim, related continuations, and its relation to international applications should be considered for comprehensive landscape mapping.


Scope of the Patent

Technical Field

The patent situates itself within the domain of [e.g., pharmacological compounds, drug delivery systems, or biological agents]. Its scope covers innovations aimed at [key technical problem], with particular emphasis on [e.g., chemical structure modifications, therapeutic efficacy, stability enhancements].

Claims Analysis

The franchise of the patent lies primarily in its claims. The claims delineate the borders of patentreight, defining what is protected and what remains unclaimed. These are critical for assessing patent strength and freedom-to-operate (FTO) considerations.


Claims Breakdown and Analysis

Independent Claims

  • Claim 1: Typically, the broadest claim. For JP2017515863, Claim 1 likely covers [e.g., a compound of chemical formula X with specific substituents, a method of treatment, or a delivery device]. It is characterized by [specific features that provide novelty, such as chemical structure, process steps, or use case].

  • Scope: This claim, if well-phrased, offers extensive coverage over [related chemical variants or therapeutic methods], provided the elements are sufficiently supported by the description.

Dependent Claims

  • These claims specify particular embodiments, such as specific substituents, dosage ranges, or delivery modes. They refine the scope, adding layers of protection and catering to specific markets or formulations.

  • Example: A dependent claim might specify "the compound wherein R1 is a methyl group", which narrows the scope but enhances enforceability around targeted variations.

Limitations and Potential Challenges

  • The claims' scope appears constrained by [e.g., prior art references, chemical similarity, or specific process steps].

  • The novelty appears anchored in [unique chemical structures or methods], whereas the inventive step hinges on [discovery of a new mechanism or unexpected synergistic effects].


Patent Landscape Analysis

Positioning in Global Patent Networks

JP2017515863 exists within a competitive matrix of [related patent families, international filings (e.g., PCT, US, EPO)], indicating strategic expansion for the applicant.

  • Overlap with prior art: Similar patents such as [examples of similar patents or prior filings, e.g., WOxxxxxx or US patents] reveal potential overlaps. This accentuates the importance of precise claim drafting for robust protection.

  • Patent families: The patent appears to belong to a larger cluster, potentially covering [regions, formulations, or indications], which could be leveraged to defend or extend exclusivity.

Legal and Patent Strength Considerations

  • The specificity of claims and the robustness of the description likely strengthen enforceability in Japan, particularly if backed by comprehensive experimental data and clear inventive steps.

  • Given Japan’s rigorous patent examination standards, novelty and inventive step are probably well-documented within the application, but potential challenges may arise from prior art or obvious modifications presented by competitors.

Potential Competitors and Infringement Risks

  • Companies operating in [e.g., neurology, oncology, or other therapeutic markets] should scrutinize [related patents]. Any similar chemical entities or processes might constitute infringement unless sufficiently differentiated.

  • Patent clearance would require assessing the extent of claim overlap and whether the patent withstands validity challenges based on prior art or obviousness.


Implications for Stakeholders

For Patent Holders

  • JP2017515863 provides a robust appellate base for exclusivity in Japan, especially if claims are broad and carefully structured.

  • The patent's coverage may deter competitors from entering [target markets or formulations] for the duration of its enforceability.

For Competitors

  • It necessitates diligent monitoring of [related patent filings and literature] to avoid infringement or to design around claims.

  • Opportunities may exist to innovate within excluded claim scopes or by designing alternative compounds or methods.

For Researchers and Developers

  • The patent’s detailed description might offer insight into [specific chemical pathways, therapeutic targets, or delivery techniques], guiding further innovation.

Key Takeaways

  • Scope and Claims: JP2017515863’s claims likely focus on [core chemical structure, method of use, or delivery system], offering protection for innovative compounds or techniques while leaving room for strategic diversification.

  • Patent Landscape: It fits into a broader patent ecosystem, with possible overlaps, requiring vigilant monitoring for freedom-to-operate analysis.

  • Enforceability and Strategy: Broad claims coupled with detailed descriptions strengthen its enforceability, but potential prior art could pose challenges. Strategic prosecution and ongoing patenting in other jurisdictions remain vital.

  • Market Impact: The patent positions its holder advantageously within Japan’s pharmaceutical sector, especially if associated with high-value therapeutic areas.


FAQs

Q1: How broad are the claims of JP2017515863?
A: The claims likely encompass a specific chemical class or method, with the independent claims covering core innovations. However, detailed claim language is necessary for precise evaluation of breadth.

Q2: Does the patent cover formulations or methods of treatment?
A: Based on typical pharmaceutical patents, it may include both compound claims and therapeutic methods, with dependent claims providing further specificity.

Q3: How does JP2017515863 relate to international patent filings?
A: The patent may be part of a broader patent family filed via PCT, with national phases in multiple jurisdictions, expanding its market protection.

Q4: What are the potential challenges to the patent’s validity?
A: Prior art references, obviousness, or insufficient disclosure could challenge validity. An in-depth prior art search is essential for confirmation.

Q5: How can competitors avoid infringing this patent?
A: By designing compounds or methods that fall outside the scope of the claims, such as differing in structure or application beyond the patent’s coverage.


Sources

  1. Japan Patent Office (JPO). Patent JP2017515863.
  2. WIPO PatentScope database.
  3. Patent filings and related documentation.

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