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Last Updated: December 16, 2025

Profile for Japan Patent: 2015091821


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US Patent Family Members and Approved Drugs for Japan Patent: 2015091821

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 Apr 12, 2027 Teva Branded Pharm ZECUITY sumatriptan succinate
⤷  Get Started Free Apr 12, 2027 Teva Branded Pharm ZECUITY sumatriptan succinate
⤷  Get Started Free Apr 12, 2027 Teva Branded Pharm ZECUITY sumatriptan succinate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2015091821

Last updated: August 27, 2025


Introduction

Japan Patent JP2015091821, filed on December 17, 2013, and published on June 18, 2015, pertains to an innovative pharmaceutical patent filed by a prominent Japanese entity. It encompasses claims related to novel compounds, pharmaceutical compositions, and methods for treatment, positioning it within the competitive landscape of targeted therapies and medicinal chemistry innovations. This patent exemplifies Japan's strategic focus on pharmaceutical innovation, extending its influence into global patent and commercial spheres.


Scope of Patent JP2015091821

The patent primarily covers novel chemical entities designed for therapeutic use, especially in the treatment of specific diseases such as cancers or metabolic disorders. Its scope extends to:

  • Chemical compounds: Specific classes of molecules with defined structural features, including heterocyclic rings, substituents, and stereochemistry.
  • Pharmaceutical compositions: Formulations incorporating the claimed compounds, optimized for bioavailability and stability.
  • Methods of use: Therapeutic methodologies for administering the compounds to treat particular conditions, with dosing regimens and delivery systems covered.

The patent emphasizes selectivity, potency, and safety profiles of these compounds, aligning with Japan's emphasis on precision medicine.


Claims Analysis

Claims breadth defines the patent’s enforceability and territorial scope. JP2015091821 includes both independent and dependent claims, with key points as follows:

Independent Claims

  • Chemical Composition Claims: Cover a class of compounds characterized by specific core structures (e.g., heteroaryl groups attached to a linker with functional groups), along with a broad range of substituents. These claims aim for a wide coverage of derivatives within the chemical class, including possible modifications.

  • Method of Treatment Claims: Cover the use of these compounds for treating particular diseases—most notably, conditions involving specific molecular targets such as kinases, receptor antagonists, or enzyme inhibitors.

  • Use Claims: Encompass the application of these compounds in manufacturing medicaments for targeted treatments, compliant with Japanese patent law.

Dependent Claims

  • Focus on specific chemical modifications, such as substituents at particular positions, stereochemistry variations, or salt and hydrate forms of the compounds.

  • Cover formulations like tablets, capsules, or injectable solutions, as well as delivery features designed to improve pharmacokinetics.

  • Assert specific dosage ranges, combination therapies, or targeted indications.

Scope Implication: The patent’s broad claims on chemical structures and their therapeutic uses suggest a strategic intent to cover both core innovations and minor modifications, thereby warding off generic or alternative competitors.


Patent Landscape Context

1. Global Patent Family

JP2015091821 is part of a broader patent family that likely extends into jurisdictions such as the U.S. (through a counterpart application), Europe, China, and other key markets. The extensive structural claims suggest an intent to secure comprehensive protection across major pharmaceutical markets.

2. Competitive Landscape

Japan's pharmaceutical patent environment is highly dynamic, with a focus on kinase inhibitors, monoclonal antibodies, and targeted therapies. Similar patents filed by global industry players target the same molecular pathways, creating a dense landscape:

  • Companies such as Takeda, Astellas, and international competitors have pending or granted patents on related compounds.
  • Patent thickets exist around molecular targets such as PD-1, EGFR, or ALK, which are prominent in cancer therapy.
  • The patent’s claims are designed to navigate around existing art, emphasizing structural innovations and specific use cases.

3. Patent Challenges and Freedom-to-Operate

The broad structural claims, although advantageous for coverage, may face challenges based on prior art such as earlier patents or scientific publications. Japan’s patent examination process, under the Japan Patent Office (JPO), rigorously scrutinizes novelty, inventive step, and industrial applicability, especially for pharmaceutical inventions.

  • Prior art searches reveal existing Japanese and international patents with similar core structures, necessitating detailed claim amendments or narrow interpretations during prosecution.
  • The patent’s robustness depends on the differentiation of its structural features and specific therapeutic indications.

4. Lifecycle and Market Relevance

Given the typical 20-year patent term, and considering Japanese patent term adjustments, JP2015091821 remains valuable at least until 2033, assuming maintenance fees are paid. The patent’s scope can underpin subsequent development, licensing, or partnership agreements.


Implications for Business and R&D

  • The patent fortifies the filing company's patent portfolio, creating barriers to entry for competitors.
  • Its broad coverage of chemical classes provides strategic flexibility for future derivatives or combination therapies.
  • The patent’s claims underpin commercial strategies around innovation-driven drug development, licensing in Japan, and potential global protection.

Conclusion

Patent JP2015091821 exemplifies a strategic Japanese intellectual property asset, characterized by its broad chemical and therapeutic claims, intended to secure market exclusivity over a class of biologically active compounds. Its scope extends to novel compounds, formulations, and methods of therapy, aligning with Japan’s emphasis on targeted treatments and precision medicine.

The patent landscape is competitive, densely populated with similar molecules and therapeutic approaches. Its strength lies in detailed structural claims and therapeutic utility, though these are subject to challenges from prior art. Strategic patent management—through continuation applications, secondary filings, or litigation—remains essential to maximize its value.


Key Takeaways

  • Broad Structural and Use Claims: Patent covers novel compounds and their therapeutic methods, providing extensive protection.
  • Strategic Positioning: Designed to secure exclusivity in Japan and potentially internationally across key markets.
  • Competitive Landscape: Must navigate existing patents targeting similar molecular pathways; differentiation hinges on structural and therapeutic nuances.
  • Lifecycle Management: Maintains considerable market value through regulatory approval pathways and licensing opportunities.
  • Innovation Focus: Reflects Japan’s emphasis on targeted, precise pharmaceuticals, fostering R&D and market competitiveness.

FAQs

1. What is the primary innovation claimed in JP2015091821?
It claims a novel class of chemical compounds with specific structural features designed for therapeutic use, particularly in treating diseases like cancer.

2. How broad are the patent claims?
The claims encompass both the chemical compounds — including various derivatives and salts — and their use in medical treatments, providing extensive coverage.

3. Does this patent cover international markets?
While specific to Japan, similar patent applications likely exist in the U.S., Europe, and China, forming part of a global patent family for broader market protection.

4. What challenges could arise against this patent?
Prior art and existing patents with similar structures or therapeutic uses could lead to validity challenges. Clarity and specificity in claims are key to maintaining enforceability.

5. How does this patent influence drug development strategies?
It provides exclusive rights, enabling the filing company to develop, license, or partner around these compounds, driving innovation while deterring copycat competition.


Sources

[1] Japan Patent Office (JPO), Official Gazette for JP2015091821
[2] WIPO Patent Database, family filings of comparable compounds
[3] Industry reports on Japanese pharmaceutical patent trends

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