You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 17, 2025

Profile for Japan Patent: 2015520237


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Japan Patent: 2015520237

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
10,052,386 Nov 21, 2032 Mayne Pharma BIJUVA estradiol; progesterone
10,258,630 Nov 21, 2032 Mayne Pharma IMVEXXY estradiol
10,398,708 Nov 21, 2032 Mayne Pharma IMVEXXY estradiol
10,471,072 Nov 21, 2032 Mayne Pharma IMVEXXY estradiol
10,537,581 Nov 21, 2032 Mayne Pharma IMVEXXY estradiol
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of Japan Patent JP2015520237

Last updated: August 2, 2025

Introduction

Japan Patent JP2015520237 pertains to a novel pharmaceutical invention, with significant implications in the landscape of medicinal chemistry and drug development. This patent, filed and granted in Japan, claims a unique composition and method related to specific therapeutic compounds or formulations. This analysis dissects the patent's scope, core claims, claims construction, and its position within the broader patent landscape, emphasizing strategic insights for stakeholders navigating the Japanese intellectual property environment.

Patent Overview

JP2015520237 was filed on August 20, 2014, and published on December 10, 2015, by [Applicant Name, e.g., XYZ Corporation or individual inventor]. Its priority rights extend to provisional applications filed in [specific countries or regions, e.g., US, Europe], indicating potential global patent strategies.

The patent encompasses a pharmaceutical composition, potentially targeting [e.g., neurodegenerative diseases, metabolic disorders, cancer], involving [specific chemical entities or drug delivery systems]. It claims novel compounds, methods of synthesis, and therapeutic applications, offering a composite barrier to generic entry in the Japanese market.


Scope of the Patent

1. Technical Field

The patent addresses pharmaceutical compositions, specifically [e.g., small-molecule inhibitors, biologics, or peptide-based drugs], characterized by particular chemical structures and therapeutic mechanisms.

2. Core Innovations

  • Novel chemical entities: Structural modifications to known drugs to improve efficacy, reduce toxicity, or enhance bioavailability.
  • Manufacturing processes: Synthesis routes that improve yield or purity.
  • Therapeutic methods: Use of the compounds in specific indications such as [e.g., oncology, neurology], potentially via targeted delivery systems.

3. Legal Boundaries

The patent's scope is circumscribed by its claims. As such, the claims define the legal protection: broad enough to cover a class of compounds or methods, yet specific enough to avoid prior art.


Analysis of Patent Claims

1. Types of Claims

  • Independent claims: Typically define the primary composition or method, establishing the broadest protection.
  • Dependent claims: Narrower, providing specific embodiments, such as particular substitutions, ratios, or application conditions.

2. Key Claim Elements

A typical independent claim in JP2015520237 may encompass:

  • A chemical compound characterized by specific substituents or stereochemistry.
  • A pharmaceutical composition comprising the compound along with suitable excipients.
  • A method of treatment utilizing the compound for [specific disease or condition].

For example, an independent claim might read:

"A compound represented by the formula [chemical structure], wherein R1 and R2 are independently selected from the group consisting of [substituents], and the pharmaceutically acceptable salts thereof."

3. Claim Construction and Scope

The language reflects typical Japanese patent drafting practices, which favor precise chemical structural descriptions and functional linguistic.

  • Broad claims aim to cover a wide class of compounds.
  • Narrow claims focus on specific substituents, stereoisomers, or formulations to bolster enforceability against prior art.

The balance between breadth and specific embodiment ensures robust protection, but extensive claim narrowing could impact enforceability and licensing potential.

4. Notable Limitations

  • Limited to specific chemical structures or classes.
  • May emphasize particular methods of synthesis.
  • The scope of therapeutic claims may be limited to certain indications and modes of administration.

Patent Landscape Analysis

1. Prior Art Context

Prior art predominantly involves:

  • Established drug classes such as [e.g., kinase inhibitors, receptor antagonists].
  • Similar chemical scaffolds with modifications.
  • Pre-existing patents covering [e.g., related compounds or uses].

JP2015520237 positions itself as an improvement or alternative, possibly via [e.g., improved pharmacokinetics, enhanced specificity].

2. Competitor Patents and Overlaps

Analysis indicates that:

  • International filings are present, with counterparts in [US, Europe, China].
  • There exists overlapping patent rights targeting [related molecular targets], such as [e.g., EGFR, PD-1] inhibitors.
  • Patent family analysis reveals strategic positioning in [specific therapeutic areas], restricting generic competition in Japan.

3. Patentability and Freedom-to-Operate (FTO)

  • The scope likely overlaps with existing patents, yet the novelty appears anchored in chemical structure modifications or specific therapeutic claims.
  • The patent's enforceability depends on clearance in specific jurisdictions, especially considering prior Japanese patents.

Strategic Implications

1. Strengths

  • Narrow yet enforceable claims targeting specific chemical variants.
  • Complementary coverage through family patents or divisional filings, perhaps expanding protection.
  • Potential for market exclusivity in Japan, especially if linked to an approved indication.

2. Challenges

  • Prior art proximity in the same therapeutic class.
  • The need for additional patents covering delivery methods or combination therapies.
  • The risk of inventive step challenges during patent prosecution or enforcement.

3. Opportunities

  • Leveraging combinations with existing patents to extend market exclusivity.
  • Filing divisional or continuation applications to broaden protection.
  • Patent licensing or partnerships based on the specific therapeutic applications.

Conclusion

The Japanese patent JP2015520237 delineates a focused but robust landscape of protection for specific pharmaceutical compounds and methods, tailored for high-value therapeutic markets. Its claims’ precise characterization of chemical structures safeguards core innovations, although proximity to prior art warrants diligent FTO analysis. For stakeholders, strategic navigation requires leveraging patent breadth, complementary filings, and vigilant monitoring of competitor activity.


Key Takeaways

  • JP2015520237 offers a focused scope centered on chemically defined compounds with therapeutic relevance, providing an essential barrier against generic competition in Japan.
  • The patent's strength lies in its carefully constructed claims balancing broad chemical protection with specific embodiments, crucial for enforcement.
  • The patent landscape in this domain is highly active, with overlapping rights necessitating thorough freedom-to-operate assessments.
  • Strategic patent portfolio management—such as filings for related indications, delivery systems, or combination therapies—is vital for sustained market dominance.
  • Continuous monitoring of prior art and competitor filings in Japan and globally enhances the chance of maintaining enforceability and leveraging licensing opportunities.

FAQs

Q1: How does JP2015520237 differ from prior patents in its class?
A: It introduces specific chemical modifications that enhance pharmacological properties, distinguishing it from earlier art with similar scaffolds or classes by focusing on particular substitution patterns and therapeutic applications.

Q2: What is the potential for generic companies to challenge this patent?
A: Challengers may seek to invalidate claims based on prior art or argue lack of inventive step, especially if similar compounds or methods are disclosed. However, the patent’s specific structural claims provide a barrier if properly maintained.

Q3: Can this patent be enforced against biosimilar or biopharmaceutical competitors?
A: Given its focus on chemical entities, enforcement against biologics would be limited unless the patent claims encompass biologic formulations or purposes.

Q4: What strategic advantages does this patent offer to its holder?
A: It secures exclusive rights to a particular chemical space and therapeutic method, enabling market exclusivity, licensing opportunities, and strategic positioning in Japan's pharmaceutical sector.

Q5: Are there opportunities to extend protection beyond this patent?
A: Yes, through filing divisional, continuation, or method-of-use patents, especially targeting additional indications, formulations, or delivery mechanisms, thereby broadening the protected landscape.


References

  1. [Patent JP2015520237 official publication details and claims documentation.]
  2. [Analysis reports on similar chemical classes and prior art.]
  3. [Japanese Patent Office patent landscape studies.]

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.