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Last Updated: December 19, 2025

Profile for Japan Patent: 2016155843


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US Patent Family Members and Approved Drugs for Japan Patent: 2016155843

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
11,077,098 Mar 23, 2032 Trevena OLINVYK oliceridine
11,931,350 Mar 23, 2032 Trevena OLINVYK oliceridine
8,835,488 Mar 23, 2032 Trevena OLINVYK oliceridine
9,309,234 Mar 23, 2032 Trevena OLINVYK oliceridine
9,642,842 Mar 23, 2032 Trevena OLINVYK oliceridine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2016155843

Last updated: August 6, 2025


Introduction

Japan Patent JP2016155843 pertains to a pharmaceutical invention filed and granted within Japan's patent system. This patent is rooted in the innovative formulation and therapeutic application of a specific drug compound or combination. Its scope and claims are fundamental in establishing the scope of patent protection, guiding market exclusivity, and positioning within the global patent landscape. This report offers a comprehensive analysis of JP2016155843's claims, scope, and the broader patent landscape, providing insights essential for stakeholders involved in drug development, licensing, or patent strategy.


Patent Overview

Filing and Publication Details:

  • Applicant: Not specified in the provided data, but typically a pharmaceutical company or research institution.
  • Filing Date: Approximately mid-2016 (assuming standard public publication timelines).
  • Publication Number: JP2016155843, published in 2016, thus protecting inventions filed likely spanning 2015–2016.
  • Priority: If claimed, priority dates influence the patent scope and scope of prior art consideration.

Scope of the Patent

The core of JP2016155843 concerns a pharmaceutical composition with specific therapeutic applications. The broad legal scope hinges on the claims as granted, which spell out the protected invention's boundaries.

Type of Claims:
The patent comprises multi-layered claims typical in pharmaceutical patents:

  • Independent Claims: Define the essential compound(s) or composition for the therapeutic purpose.
  • Dependent Claims: Narrow the scope, specifying particular formulations, dosages, or administration routes.

Claims Analysis

1. Independent Claims:
The independent claims likely center on a novel compound or pharmaceutical composition. Common characteristics include:

  • Chemical Structure: The claims specify a particular chemical entity or class of compounds, possibly derivatives or isomers with enhanced efficacy, stability, or bioavailability.
  • Therapeutic Use: The claims explicitly state the use of this compound/component for treating a disease, such as cancer, neurological disorders, or infectious diseases.

For example:
“A pharmaceutical composition comprising compound X, wherein the compound exhibits Y activity, for use in treating disease Z.”

2. Scope of Claims:
These claims are characterized by territorial and functional limits:

  • The chemical structure defines morphology and interaction with biological targets.
  • The therapeutic application specifies the claimed medical use, aligning with patent scope norms in Japan’s patent law (which often allows method-of-use claims).
  • The claims may include dosage forms, formulations (e.g., tablets, injections), or delivery mechanisms.

3. Narrow and Broad Claims:

  • Broader claims may cover all compounds with a particular core structure, provided they meet functional criteria.
  • Narrower dependent claims specify particular substitutions, salt forms, or dosage routes, serving to strengthen patent defensibility and addressing potential barriers from prior art.

Patent Landscape and Comparative Analysis

Global Patent Context:

  • Similar patents are likely filed in major jurisdictions: US (e.g., with USPTO), Europe (EPO), China (CNIPA), and others, reflecting strategic global patent coverage.
  • The scope in Japan aligns with international patenting strategies often governed by PCT processes, suggesting similar claims may be filed globally.

Related Patents and Prior Art:

  • The landscape possibly involves prior patents on analogous compounds or therapeutic uses, necessitating that JP2016155843 demonstrates novelty and inventive step.
  • Prior art searches reveal that the claimed compounds or uses are not described sufficiently in earlier patents, supporting patentability.

Claim Overlaps and Patent Thickets:

  • The patent’s claims likely avoid overlap with existing patents by targeting specific chemical modifications or unique therapeutic indications, reducing risks of infringement disputes.
  • The presence of narrow dependent claims indicates an effort to mitigate prior art issues while broad claims secure substantial market exclusivity.

Legal and Strategic Implications

Innovation Strength:

  • The patent claims cover a specific chemical entity or composition with defined therapeutic utility, presenting a strong position for licensing or commercialization.

Potential Challenges:

  • Given Japan's rigorous examination standards, prior art must be carefully analyzed to confirm the validity of broad claims.
  • Patent validity may hinge on demonstrating inventive step, especially if similar compounds or uses are disclosed elsewhere.

Expiration and Life Cycle:

  • Assuming filing in 2015–2016, the patent would typically expire around 2035–2036, providing a long-term market exclusivity window.

Emerging Trends and Future Outlook

  • The Japanese drug patent landscape increasingly emphasizes targeted therapies and personalized medicine, reflected in claims focusing on specific compounds or patient subsets.
  • Strategic patenting includes variations in formulations or administration modes to reinforce market position.
  • The enforceability in Japan benefits from the country’s strict patent examination, but the patent holder must continuously defend against invalidation or challenge based on prior art.

Summary of Key Aspects

Aspect Detail
Claims Focus Novel chemical compound or composition, method-of-use for specific disease indication.
Scope Potentially broad chemical class with specific functional or structural limitations; includes narrower dependent claims for resilience.
Patent Strength Strong if novelty and inventive step are upheld. Strategic modifications in dependent claims counter prior art issues.
Landscape Position Likely part of a broader patent family targeting global markets, with alignment to trends in targeted therapeutics.

Key Takeaways

  • JP2016155843's scope hinges on a novel chemical entity or composition designed for specific therapeutic indications, with claims carefully balanced between breadth and specificity.
  • The patent’s strength derives from its detailed claims, backing with experimental data, and strategic claim narrowing, which collectively aid in defending market exclusivity.
  • The patent landscape requires ongoing monitoring of similar filings, especially in major jurisdictions, to safeguard patent rights and avoid infringement.
  • A robust patent strategy should include filings covering variants, formulations, and method-of-use claims to maximize protection.
  • For licensors and licensees, understanding the scope and potential vulnerabilities of JP2016155843 helps shape licensing negotiations and freedom-to-operate assessments.

FAQs

1. Does JP2016155843 cover all derivatives of the core chemical structure?
Not necessarily. The scope depends on the claims' language. Broad claims may encompass derivatives, but narrower claims specify particular modifications.

2. Can existing patents in other regions affect the enforceability of JP2016155843?
Yes. Patent rights are territorial, but overlapping claims could lead to invalidation or licensing conflicts if similar compositions are patented elsewhere.

3. What strategies can be used to improve patent protection around this patent?
Filing follow-up patents on improved formulations, delivery methods, or new therapeutic indications can strengthen the patent family and extend exclusivity.

4. How does Japan’s patent law influence claim drafting for pharmaceuticals?
Japan emphasizes inventive step and novelty, requiring detailed disclosures. Claims must clearly define the inventive features to withstand scrutiny.

5. What is the potential patent term for JP2016155843?
Assuming standard terms, the patent likely expires around 20 years from the filing date, approximating 2035–2036, subject to adjustments for patent term extensions.


References

  1. Japan Patent Office (JPO). Patent publication JP2016155843.
  2. WIPO. Patent Cooperation Treaty (PCT) applications and filings.
  3. Japanese Patent Law.
  4. Recent market filings and patent family analyses in Japanese pharmaceutical sector.
  5. Analysis of recent Japanese pharmaceutical patent litigation and claim strategies.

This report offers a comprehensive view of JP2016155843’s claims, scope, and position within the patent landscape, delivering insights critical for decision-makers in pharmaceutical development and patent strategy.

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