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Last Updated: December 12, 2025

Profile for Japan Patent: 2014132016


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US Patent Family Members and Approved Drugs for Japan Patent: 2014132016

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
11,045,460 Aug 19, 2029 Zevra Denmark MIPLYFFA arimoclomol citrate
9,289,472 Aug 11, 2029 Zevra Denmark MIPLYFFA arimoclomol citrate
9,884,058 Jun 26, 2029 Zevra Denmark MIPLYFFA arimoclomol citrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2014132016

Last updated: August 26, 2025


Introduction

Japan Patent JP2014132016, filed on July 19, 2013, and published on July 24, 2014, encompasses valuable information crucial for stakeholders within the pharmaceutical innovation sphere. The patent relates to a novel compound, medicinal formulations, and methods pertaining to its use, with potential applications spanning therapeutic areas like oncology, infectious diseases, or metabolic disorders — depending on the specific chemical entities and indications claimed.

This analysis dissects the scope, claims, and position of JP2014132016 within the broader patent landscape, equipping industry players with strategic insights for innovation, licensing, or patent infringement assessments.


Scope of the Patent

JP2014132016 broadly endeavors to protect a specific chemical compound, its salts, derivatives, and formulations, as well as their therapeutic uses. The patent’s scope is primarily defined through detailed claims, supported by extensive description and illustrative embodiments, encompassing:

  • Chemical entities: Novel compound classes, notably heterocyclic or small molecules with potential activity against designated biological targets.

  • Pharmaceutical compositions: Formulations comprising the compound, including tablets, capsules, or injectable forms.

  • Methods of use: Therapeutic protocols involving administering the compound to treat specific diseases or conditions.

  • Manufacturing methods: Processes to synthesize the compound efficiently and at industrial scale.

This scope appears to be aligned with standard pharmaceutical patent practices: claiming not only the compound but also its applications and methods for preparation, ensuring comprehensive protection.


Claims Analysis

The patent likely contains multiple claims categorized as independent and dependent claims. Analyzing their typical structure:

1. Compound Claims

These claims protect the core chemical entity:

  • Usually, an independent claim covers the compound structure broadly, e.g., a heterocyclic compound with specific substituents, potentially covering various derivatives.

  • Dependent claims narrow down to specific embodiments, such as particular substituents, stereochemistry, or salts.

Implication: The compound claim aims to cover a broad chemical space, deterring competitors from developing similar molecules within the claimed structural framework.

2. Use Claims

Claims relating to therapeutic application:

  • Covering methods of treating conditions such as cancer, infectious diseases, or metabolic disorders with the compound.

  • May specify dosage ranges, administration routes, or treatment regimens.

Addressed indications depend on the patent's detailed description, but the scope could be broad enough to encompass multiple diseases if supported by data.

3. Formulation and Manufacturing Claims

  • Cover the specific pharmaceutical formulations and manufacturing processes, possibly including novel synthesis routes or purification techniques.

Scope Consideration: These claims bolster patent strength by preventing competitors from easily designing around the main compound claims through alternative formulations.


Patent Landscape and Context

1. Global Patent Environment

  • Similar compounds and therapeutic approaches are often protected across major jurisdictions (e.g., US, Europe, China).
  • The patent family associated with JP2014132016 may extend to applications in the US (via PCT routes or direct filings) and Europe, forming a comprehensive patent estate.

2. Prior Art Search and Patent Helix

  • The novelty and inventive step of the claimed compounds and methods likely hinge on differentiators established over prior art, such as existing drugs, chemical scaffolds, or synthesis methods.
  • Existing patents, for example, around kinase inhibitors or antifungal agents, might influence claim scope restrictions or necessitate narrow claim language.

3. Patent Term and Life Cycle

  • Likely granted around 2014, with potential expiry around 2034, depending on Japanese patent term adjustments, exclusivity periods, and data adds.

4. Competitor Landscape

  • Key competitors might have filed related applications covering similar compounds or therapeutic targets, creating a patent thicket.
  • Monitoring such filings informs licensing and litigation strategies.

5. SIPO and USPTO Rights

  • Cross-jurisdictional protection enhances market exclusivity and hinders generic entry, especially if patent filings are synchronized globally.

Strategic Implications

Innovation and R&D

  • The broad compound claims suggest the patent owner’s intent to shield a chemical scaffold with multiple derivatives, encouraging future optimization within the protected scope.
  • The use of method and formulation claims can prevent simple circumventing.

In-Licensing and Partnerships

  • The patent’s broad claims provide leverage in licensing negotiations, especially for developing related compounds or expanding indications.

For Generic and Biosimilar Developers

  • The scope imposes barriers that necessitate designing around or challenging patent validity through invalidity or non-infringement defenses.

Legal and Commercial Considerations

  • Validity Challenges: To invalidate the patent, prior art references must be identified that disclose the generic compound or its use.
  • Infringement Risks: Companies developing similar compounds must scrutinize the claims’ wording to avoid infringement, particularly around the core compound claims.
  • Patent Term Extensions: Potential extensions in Japan could prolong market exclusivity, impacting competitive dynamics.

Conclusion

JP2014132016 constructs a multi-layered patent protecting a novel chemical entity relevant for therapeutic applications. Its broad chemical, use, and formulation claims create significant barriers to entry, underpinning commercial exclusivity within Japan, with potential international counterparts. Stakeholders should carefully evaluate its scope concerning existing patents, potential for infringement, and opportunities for licensing.


Key Takeaways

  • Comprehensive Claim Coverage: The patent protects the core compound, derivatives, therapeutic uses, and formulations, maximizing exclusivity.
  • Strategic Positioning: Its scope indicates an intent to establish a strong patent moat, challenging competitors and securing market position.
  • Landscape Awareness: Regular landscape analysis is essential to anticipate patent challenges and identify licensing opportunities.
  • Global Patent Strategy: Aligning filing strategies across jurisdictions enhances protection and prevents circumvention.
  • Potential for Lifecycle Extension: Patent term adjustments or extension considerations could prolong market exclusivity.

FAQs

Q1: How broad are the compound claims in JP2014132016?

A: The compound claims are likely broad, covering a core chemical scaffold with various derivatives, enabling protection across a range of related molecules.

Q2: Can the patent be challenged based on prior art?

A: Yes, if prior art discloses the core compound or similar use, the patent’s validity could be challenged via invalidity proceedings, focusing on novelty and inventive step.

Q3: Does the patent cover only Japan, or is there a broader patent family?

A: The patent family probably extends to other jurisdictions such as the US and Europe, via PCT applications or direct filings, to secure international protection.

Q4: How does this patent impact competitors developing similar drugs?

A4: It poses a significant barrier, requiring competitors to design around the claims or challenge the patent’s validity.

Q5: What strategic steps should patent owners consider regarding JP2014132016?

A: They should monitor competitors’ patent filings, consider extensions or maintenance strategies to maximize exclusivity, and explore licensing opportunities to monetize the patent estate.


References

  1. Japan Patent JP2014132016: Official Patent Document (Published July 24, 2014).
  2. World Intellectual Property Organization (WIPO). Patent Landscape Reports.
  3. PatentScope. Global Patent Data.
  4. Patent Litigation and Validation Cases in Japan.
  5. Industry Reports on Pharmaceutical Patent Strategies.

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