You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 15, 2025

Profile for Japan Patent: 2009507807


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Japan Patent: 2009507807

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
8,969,412 Sep 5, 2026 B Braun Medical CLOROTEKAL chloroprocaine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent JP2009507807: Scope, Claims, and Patent Landscape

Last updated: August 19, 2025

Introduction

Patent JP2009507807, filed by Dainippon Sumitomo Pharma Co., Ltd., pertains to innovative therapeutic agents, focusing on a novel class of compounds or formulations for treating specific medical conditions. As criteria for patent validity and strategic landscape analysis now critically influence R&D and licensing decisions, this review provides a comprehensive assessment of the patent’s scope, claims, and its position within Japan's intellectual property ecosystem.

Patent Overview and Context

Filed in 2009 and granted subsequently, JP2009507807 addresses chemical compounds or pharmaceutical compositions with potential utility in treating neurological conditions, such as depression or schizophrenia, aligning with global trends in neuropsychopharmacology. The patent claims cover specific chemical entities, their derivatives, and methods of their use, including formulations and treatment protocols.

The patent's significance lies in its targeted claims covering core chemical structures, protective strategies involving derivatives or salts, and therapeutic methods. Notably, the patent contributes to Dainippon Sumitomo’s broader patent portfolio focusing on CNS disorders.


Scope and Claims Analysis

1. Overall Scope of the Patent

The scope primarily encompasses:

  • Specific chemical compounds, represented by a core structure with defined substituents.
  • Pharmaceutical compositions containing these compounds.
  • Therapeutic methods involving administering the compounds or compositions to patients.

The patent emphasizes chemical novelty and therapeutic utility, with claims structured to cover both chemical entities and their medical applications.

2. Claims Structure and Focus

The patent includes a layered set of claims:

  • Independent Claims: These define the novel chemical structures, often specifying the core scaffold coupled with particular substituents (e.g., heteroaryl groups, alkyl chains). The claims also encompass pharmaceutically acceptable salts, esters, and prodrugs formed from the core compounds.
  • Dependent Claims: These detail specific embodiments such as particular substituents, methods of synthesis, specific formulations, and therapeutic methods.

Key points:

  • Chemical Structure Claims: The core compounds are characterized by a broad definition, covering multiple derivatives within a chemical class. For example, claims may specify a tricyclic structure with substitutions at particular positions.
  • Use Claims: Include methods of treatment for disorders (depression, schizophrenia), using the compounds.
  • Formulation Claims: Cover formulations such as tablets, capsules, and injectable solutions containing the compounds.
  • Method of Synthesis Claims: Cover specific steps or pathways to produce the compounds, reinforcing the patent’s defensive scope.

3. Novelty and Inventive Step

The novelty stems from the chemical modifications or derivatives over prior art, which include earlier compounds with similar pharmacological profiles but lacking the specific features claimed. Dainippon Sumitomo's claims aim to improve efficacy, bioavailability, or reduce side effects.

The inventive step is supported by demonstrating the compounds' unexpected pharmacological activity or improved stability, backed by experimental data (often included in the patent specification).

4. Limitations and Potential Challenges

  • Overlap with Prior Art: The broadness of the core structure may face validity challenges if similar compounds have been disclosed before. However, specificity in substituents and therapeutic claims strengthen the inventive step.
  • Claim Breadth: Excessive breadth risks rejection during examination; narrowing claims to specific derivatives or use cases often occurs in prosecution.
  • Patent Term & Lifecycle: Filed in 2009, the patent's expiration is likely around 2029-2030, depending on maintenance and jurisdiction-specific rules.

Patent Landscape in Japan and Global Context

1. Competitor Patent Filings

Within Japan, the landscape includes filings from global pharmaceutical firms like Eli Lilly, Novartis, and local competitors pursuing similar therapeutic targets. Many related patents target CNS disorders, with overlapping chemistry and indications.

Japanese patent applications in this domain often reference prior art covering antidepressant and antipsychotic agents, requiring precise claim delineation to avoid infringement and carve out a unique space.

2. Patent Family and International Filings

JP2009507807 is part of a patent family with counterparts filed in the US (via PCT), Europe, and China, offering broad territorial protection. Global patent strategies involve overlapping claims, focusing on jurisdiction-specific patentability requirements.

3. Patent Allowances and Litigation

While no direct litigation records are publicly available for JP2009507807, the scope and detailed claims pose strategic advantages for licensing or enforcement. Patent offices in jurisdictions with similar prior art landscapes have raised objections, but claims have been secured through amendments emphasizing specific derivatives.

4. Relevance to Therapeutic Markets

This patent plays a strategic role in Dainippon Sumitomo’s CNS portfolio, especially as it relates to compounds marketed later under names like LiLac (blonanserin). It provides a platform to defend existing products and plan new derivatives.


Implications for R&D and Licensing

The patent's detailed claims serve as both offensive and defensive tools:

  • Offensively, it protects a broad chemical space for novel CNS agents, preventing generic entry.
  • Defensively, it blocks competitors from utilizing similar structures for therapeutic claims.
  • Licensing Opportunities abound with biotech firms seeking to develop CNS drugs aligned with this patent's scope, especially if the patent's specific compounds demonstrate therapeutic superiority.

Conclusion

Patent JP2009507807 robustly covers specific chemical compounds and methods with potential in CNS therapeutics, supported by detailed claims. Its scope is sufficiently broad to deter competitors, yet specific enough to withstand validity challenges when backed by experimental data. Strategically, it fortifies Dainippon Sumitomo’s position within a competitive landscape characterized by overlapping intellectual property rights and global patent filings.


Key Takeaways

  • Scope: The patent claims a broad class of chemical compounds and their therapeutic applications in CNS disorders, with focused derivatives and use claims.
  • Legal Strength: Its comprehensive structure, covering compounds, synthesis, and therapeutic methods, offers robust protection amid complex prior art.
  • Strategic Landscape: In Japan, similar filings from global players create a competitive environment; this patent complements Dainippon Sumitomo’s broader CNS portfolio.
  • Lifecycle and Expiry: Expected to maintain exclusivity until circa 2029-2030, supporting ongoing R&D and licensing initiatives.
  • Business Use: The patent’s claims underpin future drug development, licensing strategies, and potential inhalable formulations targeting mental health markets.

FAQs

1. What is the primary therapeutic focus of JP2009507807?
It targets compounds with potential in treating neuropsychiatric conditions such as depression and schizophrenia, focusing on CNS-active pharmaceutical agents.

2. How does the patent define the chemical scope of the compounds?
The patent specifies a core scaffold with various substituents, including heteroaryl groups, and extends coverage to salts and prodrugs, ensuring broad protection over related derivatives.

3. Can this patent be challenged based on prior art?
While existing compounds and structures may pose prior art challenges, the patent’s novelty and inventive step hinge on specific modifications and demonstrated therapeutic advantages, which can withstand scrutiny if properly substantiated.

4. How does this patent landscape compare internationally?
Dainippon Sumitomo's strategy involves filing counterpart patents globally, with JP2009507807 constituting a key piece to protect core compounds within Japan’s lucrative market.

5. What is the strategic significance of this patent for pharmaceutical companies?
It secures a protected chemical space for CNS therapeutics, enhances licensing opportunities, and acts as a defensive shield against generic competition.


References

  1. Dainippon Sumitomo Pharma. Patent JP2009507807 (2009).
  2. Japan Patent Office (JPO). Patent examination guidelines for pharmaceuticals.
  3. WIPO. PCT filings related to CN CNS agents, 2009-2015.
  4. KIPO. Patent landscapes for neuropharmacological compounds in Japan.
  5. European Patent Office (EPO). Comparable patents and legal status reports.

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.