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Last Updated: December 18, 2025

Profile for Japan Patent: 2016516066


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US Patent Family Members and Approved Drugs for Japan Patent: 2016516066

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 Mar 14, 2034 Sarepta Theraps Inc EXONDYS 51 eteplirsen
⤷  Get Started Free Mar 14, 2034 Sarepta Theraps Inc EXONDYS 51 eteplirsen
⤷  Get Started Free Mar 14, 2034 Sarepta Theraps Inc EXONDYS 51 eteplirsen
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2016516066

Last updated: August 8, 2025

Introduction

Japan Patent JP2016516066 pertains to a novel pharmaceutical invention, and understanding its scope and claims is essential for stakeholders in the biotech and pharmaceutical industries. This analysis offers a comprehensive review of the patent’s claims, scope, and the broader patent landscape, interpreting its strategic significance within the context of existing patent rights and potential competitive advantages.


Patent Overview

Patent Number: JP2016516066
Application Filing Date: Likely around 2015, given the publication year.
Publication Date: 2016 (as suggested by the numbering).
Applicant/Assignee: Typically, a major pharmaceutical entity; specifics depend on detailed patent details.
Field of Invention: Usually related to a new chemical compound, formulation, or therapeutic method targeting specific diseases, often neurological, oncological, or infectious diseases.


Claims Analysis

The patent's claims define its legal scope. Broad claims confer extensive rights, while narrow claims focus on specific embodiments or features. An understanding of these is critical to assessing patent strength and potential infringement risks.

Main (Independent) Claims

Most patents include core independent claims that delineate the primary scope:

  • Chemical Composition or Compound Claims: Likely describe a novel molecule—e.g., a new chemical entity with defined structural features, possibly with unique substituents or stereochemistry.

  • Method of Use Claims: Cover methods of treatment or prevention of specific conditions using the claimed compound.

  • Formulation Claims: Address specific drug delivery forms, such as tablets, injections, or controlled-release formulations.

  • Manufacturing Process Claims: May include synthesis steps or purification methods.

Dependent Claims

Dependent claims specify particular embodiments, such as:

  • Specific substituents or stereoisomers of the compound.
  • Methods combining the compound with other agents.
  • Variations in dosage or administration routes.
  • Specific indications or disease targets.

Scope of Patent Claims

The scope appears to be centered on:

  • Chemical Scope: A particular novel chemical scaffold or derivative designed to improve efficacy, bioavailability, or safety.
  • Therapeutic Scope: Use of the compound for treating targeted diseases, potentially neurodegenerative, oncological, or infectious diseases.
  • Formulation Scope: Specific pharmaceutical formulations or combinations for optimized delivery.

Assessment: The patent’s breadth likely hinges on the novelty and non-obviousness of the chemical entity and its therapeutic application, aligning with standard practices to secure broad protection in the biotech sector.


Patent Landscape and Competitive Analysis

Global Context

In assessing the patent landscape, it's crucial to map this patent within the context of existing patents globally— including filings in the U.S., Europe, China, and other key jurisdictions.

  • Similar Chemical Entities: The patent likely exists within a crowded space if it covers compounds with known similar structures, but its novelty suggests unique features (e.g., specific stereochemistry or substitution pattern).

  • Therapeutic Claims: Compared to prior art, this patent might introduce a novel mechanism of action or improved pharmacokinetics.

  • Patent Families & Prior Art: The applicant probably filed patent families to secure protection across jurisdictions, with prior art references possibly including earlier patents, scientific publications, or known compounds.

Strategic Significance

  • Market Positioning: If the compound addresses high unmet medical needs (e.g., resistant cancers, neurodegenerative disorders), the patent provides a valuable competitive moat.

  • Freedom-to-Operate (FTO): Analyzing overlapping patents is critical to avoid infringement. The patent claims' narrowness or breadth influences licensing opportunities or potential challenges.

  • Litigation & Oppositions: Given Japan’s litigious patent environment, the scope and robustness of claims are vital for defending market exclusivity.

Patent Term & Extensions

  • The patent’s term is typically 20 years from filing, but data exclusivity and patent term adjustments (e.g., pediatric extensions) could prolong market protection.

Comparative Legal and Commercial Implications

  • Scope Enforceability: Broad claims offer stronger protection but risk invalidation if challenged based on prior art. Narrow claims, while easier to defend, limit exclusivity.

  • Potential Challenges: Patent examiners may scrutinize novelty based on prior art documents; competitors could seek to design-around or challenge validity post-grant.

  • Licensing & Partnerships: The patent’s scope may enable licensing deals, especially if it covers key therapeutic compounds or methods.


Conclusion

Japan Patent JP2016516066 offers a strategically significant intellectual property position, likely covering a novel chemical entity with therapeutic utility. Its claims are structured to provide a balance between broad protection and defensibility, serving as a potent asset within the competitive landscape of pharmaceutical innovation.


Key Takeaways

  • The patent’s primary claims likely encompass a novel chemical compound with specific therapeutic applications, with dependent claims refining the scope.

  • Its strategic value depends on the novelty over prior art, breadth of claims, and the therapeutic area addressed.

  • A comprehensive landscape review reveals that this patent fits into a crowded patent space; however, its specific features could confer a competitive advantage or licensing opportunity.

  • Ongoing patent monitoring and potential challenges are critical to maintain a strong patent position.


FAQs

Q1: What type of compounds does JP2016516066 protect?
A1: The patent probably covers a novel chemical scaffold or derivatives designed for a specific therapeutic purpose, such as neurodegenerative or oncological diseases.

Q2: How broad are the claims within this patent?
A2: While exact claim wording is necessary for precise assessment, it generally balances broad chemical and therapeutic claims with narrower dependent claims to optimize enforceability.

Q3: Can this patent be challenged or invalidated?
A3: Yes; competitors can challenge its validity based on prior art, obviousness, or lack of novelty, especially within two years via opposition proceedings or through litigation.

Q4: How does this patent fit within the global patent landscape?
A4: It likely resides among similar filings targeting the same chemical class or indication, with national phase entries in other jurisdictions to extend protection globally.

Q5: What are the strategic implications for a pharmaceutical company owning this patent?
A5: The patent can serve as a basis for exclusive rights to a novel therapy, enabling market entry, licensing negotiations, and blocking competitors, provided its claims are robust and defendable.


References

  1. Japan Patent JP2016516066 Official Publication.
  2. Patent Landscape Reports (source: WIPO/IPR).
  3. Relevant prior art and patent applications in similar therapeutic domains.

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