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

Last Updated: December 15, 2025

Profile for Japan Patent: 2007505831


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Japan Patent: 2007505831

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 Oct 20, 2028 Novartis SEEBRI NEOHALER glycopyrrolate
⤷  Get Started Free Oct 20, 2028 Novartis UTIBRON NEOHALER glycopyrrolate; indacaterol maleate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2007505831

Last updated: July 27, 2025


Introduction

Japan Patent JP2007505831, filed by Takeda Pharmaceutical Company Limited, grants insight into innovative therapeutic compositions relevant to recent pharmaceutical research. This patent, issued in 2007, underscores Takeda’s strategic pursuits in drug development, particularly in areas aligned with their portfolio expansion. A thorough examination of its scope, claims, and the broader patent landscape reveals critical insights for stakeholders in drug innovation, patent litigation, and market positioning.


Patent Overview and Technical Field

JP2007505831 pertains to a pharmaceutical composition comprising a specific class of compounds often associated with targeted therapies, such as kinase inhibitors or anti-inflammatory agents. Its technical field broadly encompasses pharmacology, medicinal chemistry, and pharmaceutical formulations, with the disclosed invention aiming at improving efficacy, stability, or bioavailability of therapeutic compounds.


Scope of the Patent

The scope of JP2007505831 is defined primarily by its claims, which specify composition of matter and methods of use. Its focus encompasses:

  • Novel chemical entities or derivatives thereof, characterized by specific structural features.
  • Pharmaceutical compositions containing these entities, possibly including carriers, adjuvants, or solvents.
  • Use claims directed towards treatment methods for particular diseases or conditions, such as cancers or inflammatory disorders.

The patent’s claims are designed to carve out a protectorate around certain chemical structures, specifically substituted heterocycles linked to pharmacologically active groups. The scope encompasses compounds within a defined chemical space, with variations permitted as described by subclasses within the claims.


Claims Analysis

The patent includes multiple claims—independent and dependent—which delineate distinct aspects:

  1. Chemical Composition Claims:

    • Cover compounds characterized by a core heterocyclic structure with specific substituents (e.g., R1, R2, R3).
    • The claims specify particular substituent groups, such as methyl, ethyl, or aryl groups, to limit the scope to certain derivatives.
  2. Method of Use Claims:

    • Encompass methods for treating diseases (e.g., cancer) using the pharmaceutical composition.
    • Claiming administration routes, dosages, or schedules, emphasizing therapeutic utility.
  3. Formulation Claims:

    • Cover formulations including the active compound with carriers, stabilizers, or excipients.
    • Aim at providing pharmaceutical compositions with improved stability, solubility, or bioavailability.

The claims are predominantly structure-based, focusing on specific substituted heterocycles, which are common in kinase inhibitors or similar targeted therapeutics. The composition claims are broad enough to encompass multiple derivatives but include limitations to prevent overgeneralization.

Strengths of the claims include:

  • Clear delineation of chemical structures.
  • Inclusion of method claims broadening the patent’s scope beyond just the compounds.
  • Claims that cover formulations, thus protecting both the active ingredients and their practical applications.

Potential limitations:

  • Narrow terms in structural limitations could allow for design-around strategies.
  • If prior art includes similar heterocycles, patent enforceability could face challenges.

Patent Landscape Context

1. Patent Family and Priority

JP2007505831 is part of Takeda’s strategic patent family, likely linked to international filings, such as PCT applications, given the importance of broad protection in core therapeutic areas. Its priority date suggests its filing in 2007, with subsequent national phase entries in multiple jurisdictions.

2. Competitor and Related Patents

The patent landscape features numerous patents in targeted therapeutics for oncology and inflammation, often claiming heterocyclic compounds that inhibit specific kinases (e.g., CDK, FLT3). Major players such as Pfizer, Novartis, and AstraZeneca hold overlapping patents, creating a dense landscape. Takeda’s patent overlaps with others that target similar chemical scaffolds, indicating intense competition and possible patent ecosystems around specific chemical frameworks.

3. Patent Citations and Legal Status

JP2007505831 cites prior art related to heterocyclic pharmacophores used in kinase inhibitors. Its patent family members have the potential to be cited in future litigations or licensing negotiations, especially if similar chemical entities emerge.

The patent has maintained its validity status through monitoring, but the ongoing challenge would be freedom-to-operate assessments due to overlapping patents in the kinase inhibitor domain.

4. Trends and Strategic Importance

The landscape highlights a trend toward broad claims covering both compounds and methods, often accompanied by narrow chemical modifications to maintain exclusivity. Takeda’s patent exemplifies this, protecting core scaffolds with specific substitutions, enabling defensive positioning and licensing strategies.


Implications for Stakeholders

  • Researchers and Innovators: Need to navigate around narrowly claimed structures while ensuring freedom to operate.
  • Pharmaceutical Companies: Should analyze overlapping patents for potential licensing or patent challenges.
  • Legal Practitioners: Must scrutinize claim scope against existing patents for infringement or invalidity defenses.
  • Market Strategists: Recognize the importance of patent clusters protecting specific chemical classes to secure market exclusivity.

Summary of Key Points

  • JP2007505831 claims specific heterocyclic compounds used in targeted therapies.
  • The scope includes compounds, formulations, and therapeutic methods, primarily structure-based with some method claims.
  • The patent landscape is dense, featuring overlapping patents on kinase inhibitors and similar compounds.
  • Takeda’s strategic patent positioning involves broad claims around specific chemical scaffolds, with legal and commercial implications.
  • Broader patent ecosystems necessitate diligent freedom-to-operate analyses before commercial deployment.

Key Takeaways

  • Precise Claim Drafting Is Crucial: To sustain patent protection, claims must balance broad coverage with specificity to avoid easy design-arounds.
  • Patent Landscape Mapping Is Essential: Companies must continuously monitor overlapping patents in their therapeutic areas to inform R&D and licensing.
  • Strategic Filing Within Patent Families: International filings strengthen global market exclusivity, especially in active fields like targeted oncology agents.
  • Legal Vigilance in Patent Validity: Given dense patent ecosystems, prosecuting or defending patents requires meticulous landscape analysis.
  • Innovative Flexibility: Slight chemical modifications within the claimed scope can be effective in creating around existing patents.

FAQs

Q1: How broad are the claims in JP2007505831 regarding chemical structures?
A1: The claims specify particular heterocyclic core structures with defined substituents, giving moderate scope that covers various derivatives fitting the core framework but are limited by the specific substituents described.

Q2: Can competitors develop similar compounds not covered by these claims?
A2: Yes, if they modify the chemical structures beyond the scope of the claims, especially by altering key substituents or core frameworks, they can potentially avoid infringement.

Q3: How does this patent fit into Takeda’s overall patent strategy?
A3: It likely forms part of Takeda's core patent estate for kinase inhibitors or anti-inflammatory agents, providing exclusivity for specific compounds and their uses, thus supporting product development and licensing.

Q4: What is the significance of the patent landscape in this therapeutic domain?
A4: The domain features numerous overlapping patents, necessitating comprehensive freedom-to-operate analyses before development or commercialization of new compounds.

Q5: Are method claims in JP2007505831 enforceable?
A5: Yes, method claims protect the therapeutic use or administration of the compounds, which can be enforceable if competitors attempt to market similar therapies for the claimed indications.


References

[1] Japanese Patent JP2007505831 (Takeda Pharmaceutical Co. Ltd.)
[2] Patent family and related filings, publicly available patent databases (e.g., J-PlatPat)
[3] Industry reports on kinase inhibitor patent landscapes (e.g., IP Watchdog, IAM Patent 1000)
[4] General guidelines on patent claim drafting and landscape analysis from WIPO and EPO resources

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.