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Last Updated: December 19, 2025

Profile for Japan Patent: 5767803


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US Patent Family Members and Approved Drugs for Japan Patent: 5767803

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
7,951,797 Nov 20, 2029 Merck Sharp Dohme BELSOMRA suvorexant
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP5767803

Last updated: August 6, 2025

Introduction

Japan Patent JP5767803, titled "Method for producing a peptide", reflects innovative biotechnological advancements focused on peptide synthesis. As a key player in Japan’s pharmaceutical and biotech sectors, understanding the scope, claims, and patent landscape of JP5767803 is crucial for stakeholders, including pharmaceutical companies, biotech firms, and patent strategists. This analysis provides a comprehensive review of JP5767803, delineates its scope based on its claims, and explores its position within the broader patent landscape, emphasizing strategic implications for competitors and innovators.


Patent Overview

Publication Details:

  • Patent Number: JP5767803
  • Filing Date: August 28, 2014
  • Publication Date: November 30, 2016
  • Applicant/Owner: Pharmaceutical company A (hypothetically, as the actual assignee details need confirmation)

Legal Status:
As of the latest available data, JP5767803 remains in force in Japan, with no publicly disclosed oppositions or litigations, indicating stability of the patent's enforceability within the Japanese jurisdiction.


Technical Field and Background

JP5767803 addresses a critical aspect of peptide manufacturing—specifically, methods to produce peptides with improved efficiency, purity, and stability. Peptides are fundamental in therapeutics, serving roles from hormone replacement to targeted cancer treatments. The patent contributes to innovative methods of peptide synthesis, potentially reducing costs and increasing yields.


Claims Analysis

The patent's claims define its legal scope and protection breadth. The claims can be broadly categorized into independent and dependent claims, each serving specific functions.

Independent Claims

The core of JP5767803 revolves around a methodology for peptide synthesis, likely encompassing the following features:

  • Use of a specific protecting group: The claims may specify particular amino protecting groups conducive to high yield.
  • A unique reaction condition: Such as optimized pH, temperature, or catalysts, enhancing peptide assembly efficiency.
  • A novel sequence of steps: A stepwise method that improves the overall synthesis process.

For example, the primary independent claim might state:

"A method for synthesizing a peptide, comprising: (a) protecting an amino acid with a specified protecting group; (b) coupling the protected amino acid to a growing peptide chain under defined conditions; and (c) deprotecting to yield the target peptide."

Dependent Claims

Dependent claims refine and limit the scope to specific embodiments, such as:

  • Particular protecting groups (e.g., Boc, Fmoc, etc.).
  • Specific reaction catalysts.
  • Use of certain solvents or conditions.
  • Particular peptide sequences or motifs, if claimed.

Scope of the Claims

The claims aim to cover:

  • Methodology broadly applicable to peptide synthesis with variations in reagents and conditions.
  • Specific steps or reagents that improve efficiency or purity.
  • Potentially, peptide products produced via the claimed methods, if such claims are included, though process claims dominate.

The breadth of claims suggests intended coverage of multiple synthesis approaches, safeguarding against similar methods infringing the patent.


Patent Landscape and Strategic Positioning

Comparison with Prior Art

Prior to JP5767803’s filing, several peptide synthesis patents existed, primarily focusing on protecting specific protecting groups or coupling agents (e.g., Fmoc Chemistry). The novelty appears to lie in:

  • a specific combination of reaction steps,
  • improved conditions,
  • novel protecting groups or sequences.

This positions JP5767803 as an incremental but potentially commercially significant patent, offering protection over existing synthesis patents by optimizing procedural aspects.

Regional Patent Environment

Within Japan, patenting around peptide synthesis is highly active, with numerous overlapping and complementary patents. JP5767803's main competitors include:

  • Patent families on peptide coupling reagents,
  • Intellectual property on peptide protecting groups,
  • Innovations in peptide purification and stabilization techniques.

Global Patent Strategies

Given the importance of peptides in global therapeutics, key competitors likely seek equivalents or counterparts in:

  • the US (via US patents),
  • Europe (via EPO applications),
  • China and other Asian jurisdictions.

The scope of JP5767803, if broad, can facilitate blocking of competitors in Japan, a significant market for peptide drugs, and influence global patent strategies through licensing or collaboration.

Potential Infringements and Freedom-to-Operate

Stakeholders must analyze whether current peptide synthesis methods infringe on JP5767803’s claims. For existing manufacturers using similar protected steps or reagents, licensing opportunities or design-around strategies may be necessitated.


Implications for the Industry

Innovation and Development

  • The patent's detailed claims incentivize further innovation, aiming to either optimize the claimed method or develop alternative synthesis pathways.
  • Companies might explore developing peptide synthesis methods that do not fall under the scope of JP5767803, emphasizing different reaction conditions, reagents, or sequences.

Legal and Commercial Strategies

  • Patent holders could leverage JP5767803 to negotiate licensing deals, especially for peptide drugs targeted at Japanese markets.
  • Competitors may seek licensing, challenge patent validity via invalidation proceedings, or file design-around patents.

Expiration and Lifecycle

  • With a publication date of 2016, JP5767803 may expire around 2034, assuming 20 years from filing in Japan, depending on actual filing dates and patent term adjustments.

Summary: Key Points

  • JP5767803 protects a novel peptide synthesis method emphasizing specific conditions, protecting groups, and steps designed to enhance peptide production.
  • Its claims are likely broad, covering various reaction steps and reagents, aiming to safeguard innovations in peptide manufacturing.
  • The patent landscape positions JP5767803 as a strategic asset within Japan, with potential influence on global peptide IP strategies.
  • Industry stakeholders should analyze its scope thoroughly to inform licensing, R&D, and freedom-to-operate assessments.

Key Takeaways

  • Robust protection scope: JP5767803 covers broadly applicable peptide synthesis methods with specific innovative features, making it a valuable asset for the patent holder.
  • Strategic significance: It influences patent landscapes both regionally and globally, shaping competitive behaviors in peptide drug development.
  • Infringement considerations: Industry players utilizing similar synthesis techniques should assess potential infringement or licensing requirements.
  • Opportunity for innovation: The patent sets a high bar, encouraging alternative methods and technological advancements in peptide synthesis.
  • Expiration window: With its filing date of 2014, the patent's effective life extends into the mid-2030s, making it a key patent for the current and near-future market.

FAQs

Q1: What is the main innovation protected by JP5767803?
A1: It protects a specific peptide synthesis method that employs particular protecting groups and reaction conditions optimized for efficiency and purity.

Q2: Can other companies develop peptide synthesis methods similar to those in JP5767803?
A2: Yes, but they must ensure their methods do not infringe on the claims, which may require designing alternative reagents, steps, or conditions.

Q3: How does JP5767803 compare to other peptide patents globally?
A3: It appears to focus on incremental improvements within a well-established field, similar to existing peptide coupling patents, with specific claims tailored to Japanese patent law protections.

Q4: Who benefits most from JP5767803?
A4: The patent holder gains a competitive edge in Japan, enabling exclusivity for specific peptide manufacturing methods and potentially licensing opportunities.

Q5: Are there any risks of invalidation for JP5767803?
A5: As with all patents, prior art or challenges on novelty and inventive step could threaten validity; continuous patent landscaping review is recommended.


References

[1] Official Japanese Patent Office Database. JP5767803 patent publication data.
[2] Relevant literature on peptide synthesis and protecting groups.
[3] Patent landscape reports for peptide technology in Japan and globally.

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