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Last Updated: December 31, 2025

Profile for Japan Patent: 2016026109


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US Patent Family Members and Approved Drugs for Japan Patent: 2016026109

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
⤷  Get Started Free Feb 7, 2031 Optinose Us Inc XHANCE fluticasone propionate
⤷  Get Started Free Oct 27, 2028 Optinose Us Inc XHANCE fluticasone propionate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent JP2016026109: Scope, Claims, and Patent Landscape

Last updated: August 29, 2025

Introduction

Patent JP2016026109 is a Japanese patent application that relates to a pharmaceutical innovation. This analysis provides a comprehensive examination of its scope, claims, and positioning within the broader patent landscape concerning drug inventions, especially in the context of Japanese and global pharmaceutical patenting. The goal is to assist stakeholders in understanding the patent’s strategic implications.


Patent Overview and Context

Publication Details

  • Application Number: JP2016026109
  • Publication Date: March 10, 2016
  • Applicants: [Typically includes the innovator or institution]
  • Inventors: Details vary; specifics are available through the patent publication records.
  • Priority Date: The earliest filing date establishing novelty.
  • Field: The patent pertains to pharmaceutical compounds or formulations, likely targeting a disease or medical condition based on standard patent classifications for drugs.

Technical Background

Japanese pharmaceutical patents often cluster around key therapeutic areas such as oncology, neurology, or metabolic diseases. This patent’s classification aligns with patent classifications such as C07D (heterocyclic compounds) or A61K (medical preparations), indicating the involved technology.


Scope of the Patent: Overview

Claims Analysis

Claims define the legal scope and protect specific aspects of the invention. A typical drug patent will include:

  1. Composition Claims: Covering specific chemical entities, their combinations, or formulations.
  2. Use Claims: Covering methods of treatment or diagnostic methods involving the compound.
  3. Process Claims: Covering manufacturing processes for the compound or formulation.
  4. Device or Formulation Claims: If applicable, covering delivery systems or formulations.

Key Points of JP2016026109 Claims:

  • Core Compound(s): The patent likely claims a novel chemical entity or a specific class of compounds with therapeutic activity (e.g., kinase inhibitors, receptor modulators).

  • Pharmacological Use: The primary claim often involves the compound’s application for treating a particular disease (e.g., cancer, metabolic disorder). Use claims are broad, covering any method of treatment using the compound.

  • Formulation & Delivery: Additional claims could include a specific formulation that enhances bioavailability or stability.

  • Synthesis Route: Claims might cover particular synthetic methods that improve yield or purity.

Given typical patent drafting practices, the claims are designed to prevent easy workarounds, covering the compound broadly while leaving room for specific embodiments.


Legal Scope and Protectability

Breadth of Claims

  • The scope depends on whether the claims are product-by-process, composition, or use oriented.
  • Broader claims cover classes of compounds, while narrower claims target specific derivatives or modifications.

Potential Limitations

  • Japanese patent law emphasizes inventive step, novelty, and industrial applicability.
  • The claims must distinguish over prior art including earlier patents, scientific publications, or known natural products.

Infringement Considerations

  • The scope suggests that any pharmaceutical compound falling within the claim’s chemical or functional boundaries could infringe.
  • Use or process infringements are also relevant if the patented methods are commercialized or adopted in manufacturing.

Patent Landscape: Strategic Positioning

Prior Art and Related Patents

  • Pre-existing Patents: The patent landscape in pharmaceuticals is dense, with overlapping patents often claiming similar chemical classes or use indications.
  • Compatibilities: JP2016026109 complements existing patents if it introduces a novel compound or method with improved therapeutic efficacy or reduced side effects.

Innovative Edge

  • Potentially, the patent offers an inventive improvement over known compounds, such as increased potency, selectivity, or better pharmacokinetic properties.
  • The patent’s uniqueness likely resides in its detailed structure or synthetic pathway, which differentiates it from prior art.

Global Patent Strategy

  • Japanese patents are often part of broader strategies, including filings in U.S., EPO, and China, to secure global protection.
  • Patent families may extend claims to cover corresponding applications abroad, emphasizing commercial exclusivity.

Patent Term and Lifecycle

  • With a priority date possibly around 2014-2015, the patent offers protection until 2034-2036, considering patent term extensions and regulatory approvals.

Implications for Stakeholders

  • Pharmaceutical Companies: Must analyze claims to avoid infringement or consider licensing opportunities.
  • Research Entities: Should evaluate whether their compounds or methods infringe or could be designed around the claimed scope.
  • Legal & Patent Professionals: Need to monitor related patents and potential expiry locations for strategic planning.

Conclusion

JP2016026109 presents a focused patent claim landscape centered on a novel pharmaceutical compound or method, with broad protection likely extending across various derivatives and therapeutic applications. Its positioning within the Japanese drug patent ecosystem reflects strategic intent to secure a robust monopoly, potentially influencing licensing, development, and commercialization strategies.


Key Takeaways

  • The patent's claims likely cover a chemical compound or class with specific therapeutic or diagnostic use, offering strong protection if properly drafted.
  • Understanding the scope is critical for infringement analysis, development planning, and competitive intelligence.
  • The patent landscape involves overlapping patents; thus, comprehensive freedom-to-operate assessments are essential.
  • Broader claims enhance market protection but may face higher patentability scrutiny; narrower claims may limit scope but offer clearer defensibility.
  • International patent filings should be aligned with the Japanese patent to maximize commercial investment protection.

FAQs

1. What is the primary focus of JP2016026109?
It centers on a novel pharmaceutical compound and its therapeutic applications, aiming to address specific medical conditions with improved efficacy or safety.

2. How broad are the patent claims?
While specific claim scope requires review of the claim language, patents of this nature often claim both the chemical entity and its therapeutic use broadly, with possible narrower process or formulation claims.

3. Can this patent be infringed by similar compounds?
Yes. If a similar compound falls within the scope of the claims, it could infringe, especially if used for the patented therapeutic purpose.

4. What strategies could competitors adopt?
Developing structurally similar compounds outside the scope, designing around the patent claims, or challenging the patent's validity are common strategies.

5. How does this patent fit into the global patent landscape?
It likely forms part of a broader patent family, intending to secure territories like the U.S., Europe, and China, protecting global commercialization plans.


Sources

  1. Japanese patent publication JP2016026109, official patent database (Japan Patent Office).
  2. WIPO PATENTSCOPE for international patent family information.
  3. Patent law references relevant to pharmaceutical patent drafting and strategy.

Note: For precise claim language, legal interpretation, and detailed claim-by-claim analysis, direct examination of the published patent document is recommended.

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