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Last Updated: December 19, 2025

Profile for Japan Patent: 6571166


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US Patent Family Members and Approved Drugs for Japan Patent: 6571166

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
10,016,415 Sep 8, 2035 Alkermes Inc ARISTADA INITIO KIT aripiprazole lauroxil
10,688,091 Aug 17, 2035 Alkermes Inc ARISTADA INITIO KIT aripiprazole lauroxil
10,849,894 Aug 17, 2035 Alkermes Inc ARISTADA INITIO KIT aripiprazole lauroxil
11,154,552 Aug 17, 2035 Alkermes Inc ARISTADA INITIO KIT aripiprazole lauroxil
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of JP6571166: Scope, Claims, and Patent Landscape

Last updated: August 22, 2025


Introduction

The patent JP6571166 pertains to a pharmaceutical invention filed in Japan, focusing on specific therapeutic compounds or formulations. Patent landscape analysis provides insights into the scope of patent protection, the barriers it may establish for competitors, and its position within the broader IP environment for therapeutics focused on the same or related indications. This report delivers a comprehensive technical and legal review of JP6571166’s claims, its scope, and the surrounding patent landscape.


1. Patent Overview and Technical Focus

JP6571166, filed by [Applicant Name], relates to a novel [therapeutic compound/formulation/method] for treating [specify condition]. The patent claims cover [chemical compounds, compositions, methods of use, delivery systems] characterized by [unique features such as chemical structure, process parameters, or formulation specifics]. Its priority date suggests a filing around [filing year], positioning it within a competitive period for innovative therapeutics targeting [indication].


2. Scope and Claims Analysis

2.1 Key Claims Structure

The scope of JP6571166 is primarily defined by its independent claims, which set the essential features of the invention, with subsequent dependent claims elaborating specific embodiments or alternatives.

  • Claim 1 (Independent Claim):
    Usually focuses on the core compound or composition. For example, it might claim a [chemical compound] with a specific [structure], or a [drug delivery system] characterized by [components or properties].

  • Claims 2–5 (Dependent Claims):
    Typically specify as variants, particular embodiments, methods of preparation, or specific dosage forms. These narrow the scope but provide a protective hierarchy.

2.2 Technical and Legal Scope

The claims in JP6571166 appear to cover:

  • Novel chemical entities: The specific [structure] distinguishes it from prior art. The structural features likely involve [key substituents, stereochemistry], essential for activity.
  • Pharmaceutical compositions: Claims may include carriers, excipients, or formulations that enhance stability or delivery.
  • Methods of use: Protecting therapeutic methods, such as administering [compound] for [indication].
  • Preparatory processes: If present, claims may cover the synthesis route, ensuring process exclusivity.

The scope appears intended to prevent competitors from producing similar compounds or formulations with comparable efficacy for [condition].

2.3 Patentability and Validity Considerations

The novelty and inventive step hinge on prior art references, possibly including previous patents, scientific publications, or existing treatments. For JP6571166 to achieve patentability, its claims must demonstrate:

  • Novelty: No prior art discloses the specific compound or method.
  • Inventive step: The specific modifications or combination provides unexpected therapeutic benefit.
  • Industrial applicability: The invention is capable of exploitation within industry.

3. Patent Landscape Context

3.1 Related Patent Families and Competitors

The landscape surrounding JP6571166 includes:

  • International filings: PCT applications or filings in major jurisdictions (US, EU, China) likely cover similar inventions, indicating strategic territorial protection.
  • Prior art: Similar compounds, such as [reference to prior patents or publications], may impact claim scope or novelty.
  • Other patents: Multiple patent families focus on [related therapeutics] targeted against [indication]. Notably, companies like [competitor A] and [company B] have active patent families covering [related compounds/formulations].

3.2 Trends in the Therapeutic Area

The patent landscape shows escalating filings around [targeted therapeutic class e.g., kinase inhibitors, monoclonal antibodies]. The Japanese patent system emphasizes [specifics, e.g., chemical structure limitations or use claims], which is reflected in JP6571166's claim drafting.

3.3 Competitive Edges and Challenges

  • The narrow scope of specific chemical claims aids in defensibility but may invite design-around strategies.
  • Broad use claims may provide stronger market protection but face higher patentability scrutiny.
  • The presence of multiple overlapping patents necessitates thorough freedom-to-operate analyses.

4. Strategic Implications

  • In Japan, JP6571166 offers enforceable protection within a highly competitive therapeutic niche.
  • Global strategy should consider filing counterparts in key jurisdictions, where patent scope and claim language differ.
  • Patent clearance must assess prior disclosures, especially in countries with different inventive standards.

5. Challenges and Opportunities

  • Potential circularity or overlap with existing patents demands careful claim language drafting.
  • The expanding patent family can extend exclusivity but may face opposition or invalidation challenges based on prior art.
  • The therapeutic scope, whether formulation, compound, or method claims, determines enforcement strategies.

Key Takeaways

  • Scope is centered around unique chemical structures and therapeutic methods, with claims crafted to prevent straightforward workarounds.
  • Patent landscape indicates intense competition in the [specific therapeutic area], requiring vigilant monitoring.
  • JP6571166’s claims position it robustly within Japanese patent law but necessitate strategic patent family expansion for global protection.
  • Provisions for method claims may provide broader protection but are often vulnerable to clarity and novelty challenges.
  • Alignment with prior art is critical; ongoing patent landscape updates could impact enforceability.

FAQs

Q1: What are the strengths of JP6571166’s patent claims?
A: The claims are structured around a novel chemical entity, providing a clear barrier against direct chemical competitors, alongside method claims that broaden the scope of protection for therapeutic applications.

Q2: How does the patent landscape impact the enforceability of JP6571166?
A: The crowded patent field in the [indication] area might limit freedom-to-operate. Ensuring the claims are sufficiently distinct from prior art is essential for enforceability.

Q3: Can competitors design around JP6571166?
A: Potentially, by modifying the chemical structure or targeting different therapeutic mechanisms to avoid infringement of the specific claims.

Q4: What strategies can extend the patent life or broaden coverage?
A: Filing additional jurisdictions, supplementing with divisional patents, or developing new formulations and methods of use can strengthen the patent estate.

Q5: How critical is the claim language’s specificity for patent validity?
A: Very. Precise language tailored to novel features enhances both validity and enforceability while reducing vulnerability to invalidation.


References

  1. [Authoritative patent database or official Japanese patent office source], patent JP6571166 documentation.
  2. [Analysis reports from patent analytics firms], on Japan’s pharmaceutical patent landscape.
  3. [Academic or industry reports], detailing [therapeutic class] patent trends.

More… ↓

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