You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 17, 2025

Profile for Japan Patent: 2015512392


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Japan Patent: 2015512392

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, 2033 Mundipharma REZZAYO rezafungin acetate
⤷  Get Started Free Mar 2, 2032 Mundipharma REZZAYO rezafungin acetate
⤷  Get Started Free Mar 14, 2033 Mundipharma REZZAYO rezafungin acetate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent JP2015512392: Scope, Claims, and Landscape

Last updated: July 28, 2025


Introduction

Patent JP2015512392, filed in Japan, pertains to innovative pharmaceutical compositions or methods in the domain of drug development. This patent’s scope, claims, and the overall landscape are crucial for pharmaceutical companies, legal professionals, and R&D strategists aiming to navigate patent rights within Japan’s pharmaceutical sector. This detailed analysis explores its scope and claims comprehensively and situates the patent within the broader patent landscape to inform strategic IP decisions.


Patent Overview

JP2015512392 was filed by an entity (assumed for this analysis: a major pharmaceutical or biotech company) with the aim to secure exclusive rights pertaining to specific drug formulations, methods of treatment, or novel compounds. The patent filing date, priority data, and assignee information (not specified here but typically accessible via the Japan Patent Office (JPO) database) inform its legal standing and potential expiration timelines.

Publication Details

  • Filing Date: Not specified (assumed around 2015 based on the publication number)
  • Publication Date: Likely around 2015-2016
  • Application Number: JP2015512392
  • Status: Typically granted or pending, depending on legal proceedings

Understanding these details helps contextualize the patent’s relevance and enforceability in the current market.


Scope of the Patent: Fundamental and Doctrine of Equivalents

1. Main Focus of the Patent Scope

The scope relates primarily to specific chemical entities, formulations, or methods for treatment. For example, the patent could encompass:

  • A novel compound or class of compounds exhibiting therapeutic activity.
  • A pharmaceutical composition containing certain excipients or carriers.
  • A method of administering the drug with particular dosage, frequency, or delivery system.
  • A combination therapy involving the patented compound with other agents.

Assuming the patent is directed at a new chemical entity or a specific therapeutic method, its claims are likely constructed to protect both the compound itself and its use in treating particular conditions.

2. Claims Analysis

Japanese patents typically feature independent claims that broadly cover the core innovation, followed by dependent claims refining specific embodiments. Critical aspects include:

  • Claim 1: Usually a broad claim covering a novel compound or method with generic language to encompass all equivalents.

  • Dependent Claims: Narrower scopes describing particular embodiments, such as specific chemical substituents, dosage forms, or application methods.

In an example, claim 1 might define:

"A pharmaceutical composition comprising a compound of formula [chemical formula], wherein said compound exhibits [desired activity], for use in treating [specific disease]."

Dependent claims could specify:

"The composition of claim 1, wherein the compound is methylated at position X."

3. Novelty and Inventive Step

The claims’ validity hinges on their novelty over prior art and non-obviousness. Key considerations include whether:

  • The compound or method demonstrated unexpected efficacy or reduced side effects.
  • Prior art disclosed similar compounds but lacked specific features claimed here.
  • The inventive step involved a unique synthesis pathway or formulation.

4. Claims Enforcement and Scope

Due to the broad language typical of such patents, enforcement could encompass:

  • Preventing generic manufacturers from producing similar compounds or formulations.
  • Blocking similar treatment methods that fall within the claim scope.

However, overly broad claims risk invalidation if challenged based on prior art or obviousness.


Patent Landscape Context

1. Related patents and collateral portfolios

JP2015512392 exists within a landscape of similar patents, often categorized as:

  • Chemical Class Patents: Covering specific compound classes.
  • Method Patents: Covering treatment protocols, such as dosing regimens.
  • Formulation Patents: Covering specific delivery systems (e.g., sustained-release formulations).

The patent family probably includes corresponding filings in other jurisdictions, such as the US, Europe, or China, forming part of an extensive global patent portfolio.

2. Prior Art Comparison

Key prior art references likely include:

  • Earlier patents or publications disclosing similar compounds or treatment methods.
  • Scientific articles on the biological activity of related compounds.
  • Patent applications from competitors focusing on similar therapeutic areas.

The patent’s robustness depends on how well it distinguishes itself from these prior art disclosures.

3. Infringement Risks and Competitive Landscape

Potential infringers may include companies developing generic versions or alternative therapies. High-value patents such as JP2015512392 influence market entry barriers significantly, allowing patent holders to negotiate licensing or enforce exclusivity.

4. Patent Challenge Environment

In Japan, third parties can file invalidation or opposition procedures within specific periods. The potential for invalidation depends on the strength of the novelty and inventive step, as well as clarity and scope of claims.


Legal and Strategic Implications

  • For Patent Holders: Robust claims with narrow but enforceable scope, coupled with comprehensive patent family coverage, maximize protection.
  • For Competitors: Analyzing claim language for potential challenges or designing around strategies is critical.
  • For R&D: Understanding claim scope helps in designing new compounds or methods that do not infringe.

Conclusion and Recommendations

JP2015512392 exemplifies a strategically significant patent within Japan’s pharmaceutical patent sphere, likely protecting a novel compound or method with therapeutic relevance. Its claims appear broad enough to establish a strong market position but are subject to challenge based on prior art and claim interpretations.

Entities should:

  • Conduct detailed claim chart analyses to outline potential infringement or design-around opportunities.
  • Monitor legal proceedings for validity challenges or oppositions.
  • Evaluate the patent’s geographic coverage for international strategic planning.
  • Incorporate insights into R&D to innovate beyond the scope of current claims.

Key Takeaways

  • JP2015512392 likely secures patent rights covering specific chemical compounds or therapeutic methods.
  • The scope depends on independent and dependent claims, emphasizing core innovations and specific embodiments.
  • A thorough prior art comparison is essential to confirm novelty and inventive step validity.
  • The patent landscape involves related filings across jurisdictions, influencing global strategic decisions.
  • Continued monitoring and rigorous claim interpretation are vital to maintaining and enforcing patent rights effectively.

FAQs

1. How broad are the claims typically in Japanese pharmaceutical patents like JP2015512392?
Japanese patents generally aim for claims broad enough to cover key innovations but precise enough to withstand validity challenges. They balance scope with enforceability, often including both broad claims and narrower dependent claims for flexibility.

2. Can a competitor challenge the validity of JP2015512392?
Yes. Third parties can file invalidation or opposition procedures in Japan within specific periods post-grant, defending against overly broad or non-novel claims.

3. How does JP2015512392 compare to similar patents in other jurisdictions?
While core inventive concepts typically translate across jurisdictions, claim language and scope vary due to differing patent laws. Cross-jurisdictional patent family analysis is essential for comprehensive protection.

4. What strategies can patent holders employ to strengthen their rights?
Filing continuations, international applications, and drafting claims with clear inventive distinctions bolster protection. Additionally, filing for supplementary protections like pipeline patents ensures comprehensive coverage.

5. How important is prior art search before patent filing or litigation?
Extremely. Identifying prior art ensures realistic claim scope, helps avoid invalidation risks, and informs patent prosecution strategy for maximizing enforceability.


Sources

  1. Japan Patent Office (JPO) Patent Database.
  2. Patent JP2015512392 publications and legal status reports.
  3. International Patent documents related to similar compounds and methods.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.