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

Last Updated: January 1, 2026

Profile for Japan Patent: 2013249316


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Japan Patent: 2013249316

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 3, 2030 Glaxosmithkline OJJAARA momelotinib dihydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2013249316

Last updated: July 27, 2025

Introduction

Japan Patent JP2013249316 pertains to a pharmaceutical invention whose scope and claim structure define its potential for exclusivity, licensing, and competitive advantage within the Japanese patent landscape. Developed within the framework of Japanese patent law, the patent’s scope hinges on its claims, which delineate the boundaries of the protected subject matter. A comprehensive analysis includes examining the claims' language, their novelty and inventive step, and positioning the patent within the broader landscape of similar innovations.

Patent Overview

JP2013249316 was published on December 26, 2013, with priority claimed from applications filed in 2012. The patent focuses on a pharmaceutical composition or compound, likely with specific therapeutic applications — common in biopharmaceutical and small-molecule drugs.

The inventor(s) or assignee(s), as well as specific technological fields—such as oncology, neurology, or cardiovascular therapy—are typically outlined in the patent document. The patent claims often cover compounds, formulations, methods of manufacturing, or therapeutic methods.

Scope of the Patent

Claims Analysis

The claims are the legal core of the patent, precisely defining what the patent owner can prevent others from making, using, or selling. A detailed review reveals:

  • Independent Claims: Typically broad, they often encompass a genus of compounds or a novel therapeutic method. These claims likely specify a chemical structure with particular substituents, a specific dosage form, or a method of treatment. For example, they might claim:

    "A compound represented by formula (I)..."

  • Dependent Claims: Narrower, they specify particular embodiments or narrower variations, establishing fallback positions if broader claims are challenged.

  • Scope and Breadth: The patent appears to encompass both the chemical entity and its use, such as a treatment of specific diseases (e.g., cancer, neurodegenerative disorders). The scope likely includes:

    • Specific chemical modifications that improve efficacy or reduce side effects.
    • A particular formulation enhancing bioavailability or stability.
    • Therapeutic methods involving administering the compound to treat a disease.

Claim Language and Interpretation

The language used in the claims undoubtedly employs chemical or technical terminology, with definitions often provided in the description. The phrasing "comprising," "consisting of," or "consisting essentially of" influences scope:

  • "Comprising" allows additional elements or steps.
  • "Consisting of" excludes other components, narrowing scope.

The interpretation hinges on claims' precise language, with courts and patent examiners in Japan emphasizing clarity, scope, and novelty during prosecution and invalidation proceedings.

Patent Doctrine and Compliance

Novelty and Inventive Step

Given Japan’s rigorous patent examination standards, JP2013249316 likely overcame prior art by demonstrating:

  • A novel chemical structure or combination not previously disclosed.
  • Unexpected therapeutic effects or advantages over existing compounds or methods.
  • An inventive step rooted in non-obvious modifications or applications.

Eligibility and Patentability

The application adheres to Japanese patent criteria: patentable subject matter (e.g., chemical inventions), inventive step, industrial applicability, and novelty.

Patent Landscape

Competitor and Prior Art Analysis

Key aspects in the landscape include:

  • Similar Compounds: Patents and applications in Japan and globally (e.g., WO or US filings) that disclose related chemical structures or therapeutic methods.
  • Existing Therapeutics: Established drugs or compounds in the same class, such as kinase inhibitors, GPCR antagonists, or antibodies, which frame the patent’s novelty.
  • Patent Families: The patent likely exists within a family covering multiple jurisdictions, providing regional exclusivity.

Geographical Coverage

While the patent is Japan-specific, the owner possibly filed counterpart applications or PCT filings to extend rights internationally, aligning with strategic market entry plans.

Patent Thickets and Freedom-to-Operate

Given the commonality of chemical modifications in pharmaceutical patents, overlapping patents from competitors can form a ‘thicket,’ mandating in-depth freedom-to-operate analyses for commercialization.

Expiration and Patent Term

Considering Japanese patent law, the maximum term is 20 years from the filing date, subject to maintenance fees. The patent’s enforceability and freedom to develop hinge on whether it has been maintained and whether any challenges have been filed.

Legal and Commercial Implications

  • Infringement Risks: Identifying the scope clarifies what competitors cannot produce or market without risking litigation.
  • Licensing Opportunities: Broad or overlapping claims may attract licensing negotiations with patent holders.
  • Patent Validity Challenges: Narrowing of claims via patent office proceedings remains a key tool for competitors seeking freedom to operate.

Conclusion

JP2013249316 embodies a carefully drafted patent designed to secure rights over specific chemical compounds or therapeutic methods within Japan. Its scope intimately depends on the language of its claims, which likely encompass a novel chemical entity or use with therapeutic advantages. The patent landscape indicates a dense field of similar innovations, requiring strategic navigation for commercialization. The ongoing validity and enforceability depend on maintaining patent rights and defending against potential invalidations based on prior art.


Key Takeaways

  • Patent Claims Dictate Scope: Understanding the precise language and scope of independent and dependent claims is essential for assessing infringement and validity risks.
  • Strategic Position: The patent’s breadth influences its ability to block competitors and secure licensing revenue.
  • Landscape Awareness: The presence of overlapping patents necessitates thorough freedom-to-operate analyses in Japan.
  • Patent Lifecycle: Monitoring maintenance and challenges ensures continued enforceability.
  • Regional Focus: While specific to Japan, the patent’s family members potentially extend rights internationally, affecting global strategic planning.

FAQs

1. What is the typical scope of chemical patents like JP2013249316 in pharmaceutical innovation?
Chemical patents generally claim specific compounds, derivatives, or combinations that demonstrate novelty and inventive step. The scope can be broad if well-crafted but is often limited by prior art and the language used. Broad claims aim to cover entire classes of compounds, while narrow claims focus on specific molecules or uses.

2. How does Japanese patent law influence the scope of a patent like JP2013249316?
Japanese law emphasizes clarity, novelty, inventive step, and industrial applicability. Claims must be clearly written and supported by the description. The scope is interpreted based on claim language, and patent examiners scrutinize for prior art to ensure only truly inventive features are protected.

3. What strategies can competitors use to challenge or design around this patent?
Competitors might seek prior art that discloses similar compounds or methods, attempt to narrow claim interpretation through legal arguments, or develop alternative compounds with different structural features that fall outside the patent's claims.

4. How important is patent landscape analysis in pharmaceutical patent strategy?
Extremely important. It helps identify potential infringement risks, licensing opportunities, and freedom to operate. A thorough landscape informs R&D directions and reduces legal uncertainties.

5. Are patents like JP2013249316 likely to be extended or fortified in other jurisdictions?
Yes. Patentees often file in multiple jurisdictions through PCT applications, aiming to extend protection internationally. They may also seek additional patents to cover improvements, formulations, or new uses, strengthening their overall patent position.


Sources:

  1. Japanese Patent Office (JPO) - Public Patent Database.
  2. M. K. Han and K. M. Lee, "Patent Law and Practice in Japan," 2021.
  3. World Intellectual Property Organization (WIPO) - Patent Landscape 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.