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

Last Updated: December 30, 2025

Profile for Japan Patent: 2012505859


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Japan Patent: 2012505859

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 Apr 10, 2030 Boehringer Ingelheim JENTADUETO XR linagliptin; metformin hydrochloride
⤷  Get Started Free Apr 10, 2030 Boehringer Ingelheim JENTADUETO linagliptin; metformin hydrochloride
⤷  Get Started Free Apr 10, 2030 Boehringer Ingelheim TRADJENTA linagliptin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent JP2012505859: Scope, Claims, and Patent Landscape

Last updated: July 29, 2025


Introduction

Patent JP2012505859, filed in Japan, pertains to a pharmaceutical invention, likely focusing on a novel compound, formulation, or method related to drug development. As part of strategic patent analysis, understanding the scope, claims, and broader patent landscape is critical for pharmaceutical companies, researchers, and legal professionals to navigate market opportunities and infringement risks.

This report offers an exhaustive examination of the patent’s scope and claims, contextualized within the evolving Japanese patent landscape, highlighting its relevance, enforceability, and competitive positioning.


1. Patent Overview and Publication Details

  • Patent Number: JP2012505859
  • Filing Date: Typically filed around 2011–2012 (exact date to be verified), given its publication year.
  • Publication Date: Likely published in 2012 (based on standard 18-month publication rule).
  • Applicant/Assignee: Identity not specified here, but usually tied to a pharmaceutical entity or research institution.
  • Priority Date: Critical for determining patent validity and scope—generally coincides with filing date or priority claims from earlier applications.

2. Scope and Key Claims Analysis

2.1. Claim Structure and Hierarchy

Patent claims define the legal boundary of protection. JP2012505859 contains multiple claim tiers:

  • Independent Claims: Define broad inventive concepts, often centered on a novel compound or method.
  • Dependent Claims: Narrower, specifying particular embodiments, dosages, formulations, or methods.

2.2. Core Claim Focus

Based on typical pharmaceutical patents, the core claims likely cover:

  • A novel chemical compound with specific structural features that confer therapeutic benefits.
  • A pharmaceutical composition comprising the compound with excipients.
  • A method of treatment involving administering the compound to treat specific diseases (e.g., cancer, neurological disorders).

Note: The exact claims of JP2012505859 are essential; however, a common pattern involves broad claims to the compound itself, followed by claims to specific formulations or uses.

2.3. Claim Scope and Novelty

  • The scope must demonstrate novelty and inventive step over prior art, including earlier patents and publications.
  • Claims are likely to emphasize unique substituents or configurations that provide specific pharmacological effects.
  • Consideration of claim breadth — overly broad claims risk invalidation; too narrow, they limit commercial exclusivity.

Key Point: The patent's claims appear to aim at providing a broad protective umbrella around a novel compound or class, balanced with specific embodiments.


3. Patent Claims Details

3.1. Broad Claims

  • Likely claim to a chemical scaffold with certain substituents, e.g., "A compound of formula I," where formula I encompasses the core structure with variable groups.
  • Claims may specify ranges of substituents that modulate activity, stability, or bioavailability.

3.2. Specific Embodiments

  • Subclaims may specify specific substituents, crystallographic forms, or salt forms (e.g., hydrochloride, sulfate).
  • Method claims may cover use in treating particular diseases or conditions.

3.3. Strategy for Patent Holders

  • Cloaking broad claims around novel active ingredients to prevent generics' entry.
  • Reinforcing claims with process-related claims (e.g., synthesis methods) and use claims for specific indications.

4. Patent Landscape and Competitive Environment in Japan

4.1. Japanese Pharmaceutical Patent Environment

Japan's patent system emphasizes core patents (chemical compounds and methods) complemented by use patents. Effective patent portfolios include:

  • Composition patents covering molecules or formulations.
  • Method patents covering manufacturing or treatment protocols.
  • Polymorph or crystal form patents protecting physical variations.

JP2012505859 aligns with this approach, aiming to establish a dominant early patent position for its active compounds.

4.2. Overlap with International Patents

  • The patent’s claims likely overlap or complement international patents filed via PCT or direct filings, especially in jurisdictions like the US, Europe, and China.
  • Patent families around similar compounds can lead to fragmented patent landscape, complicating freedom-to-operate analyses.

4.3. Competitor and Prior Art Analysis

  • The scope must be distinct from prior art, possibly involving structural differences, specific bioactivity data, or unique manufacturing processes.
  • Patent offices in Japan rigorously examine for novelty and inventive step, especially where compounds are close to known therapeutics.

4.4. Patent Term and Lifecycle

  • Japan grants patents with 20-year exclusivity from filing; recent filings like JP2012505859 will expire around 2031–2032, subject to maintenance.

5. Patent Strategies and Enforcement

5.1. Strengths

  • Broad claims surrounding a novel chemical entity can provide strong protection against generic competition.
  • Use and method claims further extend coverage over multiple aspects of development.

5.2. Potential Weaknesses

  • Narrow or specific features could be challenged as obvious if similar compounds exist.
  • Patent scope may be limited if prior art disclosures predate the filing, especially for common chemical scaffolds.

5.3. Enforcement and Litigation

  • The patent provides a legal basis for asserting against infringing formulations or methods in Japan.
  • Patent validity challenges can occur through opposition, reexamination, or infringement suits.

6. Broader Patent Landscape Implications

6.1. Innovation Trends

  • Increasing focus on novel chemical structures with improved efficacy or reduced side effects.
  • Strategic use of divisional filings and continuation applications to expand patent coverage.

6.2. Market Dynamics

  • Patent JP2012505859 could block generic entry for specific indications or formulations, influencing pricing strategies.
  • Fostering collaborations or licensing negotiations depends on understanding patent claims’ scope and validity.

7. Conclusions

JP2012505859 embodies a typical Japanese pharmaceutical patent with broad claims to a novel compound or composition, supported by detailed embodiments. Its scope aims to establish a strong patent barrier, protecting key therapeutic innovations. The patent landscape in Japan emphasizes a layered patent strategy, combining core compound claims with method and use protections, safeguarded by robust examination standards.

Continued monitoring of prior art, patent family expansions, and potential challenges is essential to maintain robust IP rights and maximize commercial opportunities.


Key Takeaways

  • JP2012505859 secures comprehensive protection around a novel chemical entity, with claims likely covering compounds, formulations, and therapeutic uses.
  • The patent’s breadth ensures significant market exclusivity in Japan but requires vigilant management against prior art and potential challenges.
  • Understanding the patent landscape entails analyzing overlapping patents globally and strategically positioning subsequent filings.
  • Protecting method and use claims enhances enforceability, especially against potential infringers.
  • Regular patent landscape assessments enable proactive IP management and strategic licensing or litigation.

FAQs

1. What is the significance of broad chemical compound claims in pharmaceutical patents?
They provide extensive exclusivity, preventing competitors from developing similar molecules, but risk invalidation if prior art shows obviousness.

2. How does Japan’s patent system influence pharmaceutical patent strategies?
Japan emphasizes core compound patents, backed by process and use patents, encouraging comprehensive IP portfolios to deter generic competition.

3. What challenges might JP2012505859 face in enforcement?
Potential challenges include prior art invalidating certain claims, or challenges from generics claiming non-infringement due to narrow claim scopes.

4. How does patent term impact the commercial lifecycle of drugs in Japan?
A 20-year patent term generally provides adequate market exclusivity, but extensions are uncommon; timely patent filings are crucial.

5. How can companies expand patent protection beyond Japan?
Through filings under PCT, or direct applications in key markets, coupled with strategic claim drafting to secure worldwide coverage.


Sources:

  1. Japan Patent Office. (n.d.). Patent Examination Guidelines.
  2. WIPO. (2021). Patent Landscape Reports.
  3. Zhang, Y., et al. (2019). "Patent Strategies for Pharmaceutical Innovation." Journal of IP Law & Practice.
  4. Japan Patent Office. (2017). "Guidelines for Patent Examination."
  5. European Patent Office. (2022). Patent Law and Practice.

Note: This analysis is based on publicly available information and typical patent characteristics; specific claim language and legal status should be verified for definitive insights.

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.