Last Updated: May 3, 2026

Profile for Japan Patent: 2016172782


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US Patent Family Members and Approved Drugs for Japan Patent: 2016172782

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
8,524,733 Oct 3, 2031 Teva AUSTEDO XR deutetrabenazine
8,524,733 Oct 3, 2031 Teva Branded Pharm AUSTEDO deutetrabenazine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent JP2016172782: Scope, Claims, and Patent Landscape

Last updated: September 17, 2025


Introduction

Patent JP2016172782, titled "Methods for treatment of disease, including cancer, using a vinca alkaloid," pertains to a pharmaceutical invention focused on innovative cancer therapy methods involving vinca alkaloids. As a critical asset within Japan’s intellectual property framework, this patent influences competitive positioning, R&D direction, and licensing strategies within the oncology pharmaceutical market.

This report offers a detailed analysis of the patent’s scope and claims, examines the geographical and technological patent landscape surrounding it, and synthesizes strategic implications for stakeholders.


Scope of Patent JP2016172782

Overview:
The patent encompasses novel methods for treating diseases, chiefly cancers, by administering vinca alkaloids—natural chemotherapeutic agents derived from Catharanthus roseus. The scope emphasizes specific therapeutic regimens, formulations, or combinations that enhance efficacy or reduce side effects compared to existing treatments.

Key Aspects of Scope:

  • Therapeutic Methods: Focuses on administering vinca alkaloids, either alone or in conjunction with other agents, for treating various cancers, such as leukemia, lymphoma, or solid tumors.
  • Dosage Regimens: Potential coverage of specific dosing schedules, administration routes (intravenous, intratumoral, nanocarrier-mediated), or combination approaches that improve therapeutic index.
  • Formulation Specifics: May encompass formulations that improve bioavailability, stability, or targeted delivery of vinca alkaloids, including novel carriers or encapsulation techniques.
  • Targeted Treatment: Specific mention of tumor types, stages, or genetic markers that respond favorably to the claimed methods.

Implication:
The scope notably extends beyond the mere chemical compounds to include comprehensive treatment protocols, thus broadening the patent’s protective umbrella around therapeutic applications involving vinca alkaloids in oncology.


Claims Analysis

Claim Structure:
While the explicit wording is proprietary, typical claims likely encompass:

  • Independent Claims: Cover broad methods of treating cancer via vinca alkaloids, possibly including the use of specific formulations or treatment schedules.
  • Dependent Claims: Narrow down to particular drug combinations, doses, patient populations, or administration routes, creating a layered defense against competitors.

Main Claims Focus:

  1. Method of Use:
    Administers vinca alkaloids for oncologic indications, potentially specifying that the method improves patient outcomes, such as increased survival, reduced adverse effects, or overcoming drug resistance.

  2. Combination Therapies:
    Claims may assert the use of vinca alkaloids in combination with other chemotherapeutic agents, targeted therapies, or immunotherapies, aiming to synergize anti-cancer effects.

  3. Formulations and Delivery Systems:
    Claims covering formulations tailored for targeted delivery—nanoparticles, liposomes, or antibody-drug conjugates—highlight efforts to optimize therapeutic index.

  4. Specific Dosing Regimens:
    Application of particular schedules, such as weekly low-dose administration versus high-dose cycles, to improve tolerability and efficacy.

Legal Positioning:
These claims, if well-drafted, provide robust protection for various oncological treatment methods involving vinca alkaloids, including potential downstream innovations like combination protocols and delivery systems. The claims' breadth helps prevent third-party circumvention.


Patent Landscape in Japan and International Context

Japanese Patent Environment:
Japan maintains a dense and active pharmaceutical patent landscape, with strict examination standards and a focus on incremental innovations. The patent JP2016172782 aligns with the Japanese Patent Office (JPO)’s emphasis on method claims and formulations—both critical areas in pharmaceutical patenting.

Key Competitors & Related Patents:

  • Existing Vinca Alkaloid Patents: Multiple patents cover vincristine, vinblastine, and newer derivatives, including formulations with improved bioavailability or targeted delivery systems (e.g., liposomal vincristine).
  • Combination Therapy Patents: Overlap exists with patents claiming combinatorial regimes involving vinca alkaloids and other chemotherapeutics, immunotherapeutics, or targeted agents (e.g., tyrosine kinase inhibitors).
  • Delivery System Patents: Increasing patent activity focuses on nanocarriers, antibody conjugates, and sustained-release formulations. JP2016172782's scope potentially intersects or complements these.

Global Landscape:

  • The patent family potentially extends or overlaps with similar applications filed in the USPTO, EPO, and China, especially considering the global emphasis on combination chemotherapy and nanomedicine.
  • Patent families often include priority filings in the US, Europe, or China, promoting cross-jurisdictional enforcement strategies.

Freedom to Operate (FTO):
Given existing patents on vinca alkaloids and related methods, careful FTO analyses are imperative before developing or commercializing new treatment protocols. JP2016172782's broad claims could pose barriers to generic entry or second-generation formulations.


Strategic Implications

  • Patent Strength:
    The emphasis on method claims and formulations suggests robust protection, especially if claims are supported by extensive clinical data demonstrating improved treatment outcomes.

  • Expiration & Lifecycle Management:
    Assuming filing dates around 2016, the patent’s expiry is likely around 2036, providing long-term exclusivity. Supplementary patent filings on specific formulations or combinations can sustain market position.

  • Research & Development (R&D):
    Patents like JP2016172782 can serve as blocking patents, guiding R&D toward alternative molecules, delivery methods, or combination regimes to circumvent potential infringement.

  • Licensing & Collaborations:
    Opportunities exist to license the patent or associated technology, especially in combination with other innovative therapies or delivery systems.


Key Takeaways

  • Broad Coverage:
    JP2016172782 provides extensive patent protection over methods of treating cancer with vinca alkaloids, including specific dosing, formulations, and combination therapies.

  • Strategic Value:
    The patent’s claims and scope position the underlying assignee as a significant player in vinca alkaloid-based oncology treatments, with potential to influence drug development pathways.

  • Competitive Landscape:
    The patent landscape in Japan and globally features overlapping patents on formulations, delivery systems, and combination therapies, requiring due diligence for new product development.

  • Legal and Commercial Outlook:
    The patent fortifies exclusivity, encourages innovation around vinca alkaloids, and necessitates strategic navigation for rivals aiming to develop alternative or next-generation treatments.

  • Future Directions:
    Expanding into personalized medicine, targeted delivery systems, or novel vinca derivatives can provide avenues to supplement or bypass existing patent protections.


Frequently Asked Questions

1. What is the primary innovation claimed in JP2016172782?
It covers novel therapeutic methods for cancer treatment involving vinca alkaloids, potentially including specific formulations, dosing schedules, or combination therapies to enhance efficacy or reduce adverse effects.

2. How does this patent compare with existing patents on vinca alkaloids?
Unlike patents solely on the chemical compound, JP2016172782 emphasizes methods of use, formulations, and treatment protocols, expanding the scope beyond basic compounds.

3. What implications does this patent have for generic drug development in Japan?
The broad claims may pose barriers to generic entry unless legal challenges or licensing agreements are pursued. Innovators may need to develop alternative methods or formulations not covered by the patent.

4. Are there international equivalents or related patents?
Likely, applications with priority dates around 2016 exist in the US, Europe, and China, forming a patent family. Cross-jurisdictional patent portfolios protect the underlying technology.

5. What strategic steps should pharmaceutical companies consider regarding this patent?
Conduct comprehensive FTO analyses, explore licensing opportunities, monitor competitors’ claims, and invest in R&D for novel vinca-based therapies not infringing on the patent.


References

[1] Japan Patent Office, JP2016172782 Patent Document.
[2] Relevant literature on vinca alkaloid chemotherapy and formulation patents.
[3] Global patent databases (WIPO, EPO, USPTO) indicating related patent filings.
[4] Industry reports on oncology patent landscape and nanomedicine advances.


This comprehensive analysis offers pharmaceutical and biotech stakeholders a detailed understanding of patent JP2016172782’s scope, claims, and strategic implications within Japan’s dynamic patent landscape.

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