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Last Updated: December 31, 2025

Profile for Japan Patent: 2017520619


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US Patent Family Members and Approved Drugs for Japan Patent: 2017520619

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
12,357,630 Dec 13, 2037 Novartis ZYKADIA ceritinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Summary

Last updated: December 31, 2025

The patent JP2017520619, titled “Polymer conjugates for drug delivery,” filed by Chugai Pharmaceutical Co., Ltd., encompasses innovative polymer-based drug delivery systems designed to enhance the pharmacokinetics and biodistribution of therapeutic agents. This patent illustrates a strategic approach to extend drug half-life, improve targeting, and reduce toxicity, fitting within the broader landscape of polymer therapeutics and antibody-drug conjugates (ADCs). This analysis offers an in-depth examination of its scope, claims, and position within the patent landscape, emphasizing implications for competitors and innovators.


What is the Scope of JP2017520619?

JP2017520619 primarily covers polymer conjugates—specifically, drug-polymer conjugates—suitable for medical applications, including oncology, autoimmune diseases, and others requiring targeted delivery. Its scope extends to:

  • Polymer types: Polymers compatible with covalent conjugation to drugs or biomolecules, notably polyethylene glycol (PEG) and other biocompatible polymers.
  • Conjugation techniques: Covalent linkage methods, notably via linker groups (e.g., amino, hydroxyl, carboxyl groups), which retain pharmacological activity.
  • Drug molecules: Small molecules, peptides, or proteins conjugated to polymers.
  • Application fields: Focus on increasing drug stability, half-life, and targeting, especially in cancer therapy.
  • Chemical features: Specific linkers, polymer sizes, and modification sites to optimize pharmacokinetics and reduce immune recognition.

Key points of scope include:

  • The structure and composition of the polymer conjugates.
  • The methods for synthesis and conjugation.
  • Use of specific linker strategies to control drug release.
  • Applications and formulations for therapeutic use.

Analysis of Patent Claims

The claims define the scope of the patent protection and delineate the boundaries of the invention. It typically includes independent or broad claims, followed by narrower dependent claims.

Overview of Main Claims (Summary)

Claim Type Scope Description Key Elements
Independent Claims Broad coverage of polymer-drug conjugates - Polymer backbone with specific functionalities
- Covalent linkage to active drugs
- Optional inclusion of cleavable linkers
- Therapeutic use
Dependent Claims Focused variations - Specific polymer types (e.g., PEG, polypeptides)
- Linker chemistries (e.g., acid-cleavable, enzyme-sensitive)
- Molecular weight ranges of polymers
- Specific drugs or therapeutic indications

Sample Key Claims

  • Claim 1: Covers a polymer conjugate comprising a polymer backbone capable of attachment to a drug, where the drug is covalently linked via a linker, and wherein the polymer has a molecular weight within a specified range (e.g., 20–60 kDa).
  • Claim 2: Specifies the use of a cleavable linker, such as an acid-sensitive bond, to enable controlled drug release in target tissues.
  • Claim 3: Involves a specific conjugation method, such as carbodiimide or click chemistry, to improve efficiency and stability.
  • Claim 4: Defines a pharmaceutical composition containing the conjugate, for use in treating cancer or autoimmune diseases.

Claim Strategy Analysis

  • Breadth: Most independent claims focus on generalized polymer-drug conjugates, allowing broad protection but with essential features rooted in the types of polymers, linkers, and conjugation techniques.
  • Narrower dependent claims refine scope—defining specific polymers, linkers, or therapeutic applications—helping fortify the patent against invalidation and prior art challenges.

Patent Landscape Context

JP2017520619 was filed in 2017 and published in 2017, during a period of rapid innovation in polymer therapeutics and drug delivery systems.

Key aspects of the patent landscape include:

Aspect Details
Related Patents Multiple filings related to PEGylation, antibody conjugates, and targeted delivery, including patents held by major biotech firms (e.g., Genentech, Amgen).
Inverse Patent Families Similar inventions exist, predominantly in the U.S., Europe, and China, with overlapping claims in PEG-based conjugates, cleavable linkers, and targeted delivery.
Legal Status & Enforcement As of 2023, likely granted in Japan; competing patents often focus on specific linkers, polymer sizes, or conjugation methods.
Alignment with Recent Trends Aligns with the surge in personalized therapeutics, antibody-drug conjugates, and long-acting formulations launched in the last decade.

Notable Patent Families Related to JP2017520619:

Patent Family Countries/Regions Covered Focus Areas
PEGylated conjugates US, EP, CN Extended half-life drugs in oncology and autoimmune therapy
Cleavable linkers US, EP pH-sensitive and enzyme-sensitive linkers
Site-specific conjugation US, JP Controlled drug release with precise conjugation

Positioning:
The patent appears to fill a niche in polymer-drug conjugation by emphasizing specific linker chemistries and polymer size ranges, potentially providing competitive advantage over prior art that broadly claims PEGylation without detailed linkage strategies.


Comparative Analysis: JP2017520619 vs. Existing Patents

Criterion JP2017520619 Prior Art (e.g., US Patent No. 8,587,026) Difference/Advantage
Polymer type PEG, others PEG, polypeptides Broader scope with additional polymers
Linkers Cleavable (acid, enzyme) Mainly non-cleavable or generic Emphasizes cleavable linkers for controlled release
Molecular weight 20–60 kDa Variable, often broader Specific size ranges for optimized pharmacokinetics
Therapeutic focus Oncology, autoimmunity Similar Convergent but with specific innovation on linkers and conjugation methods

Implications for Stakeholders

  • Innovators: The patent reinforces the importance of specific linker and polymer size strategies to improve drug efficacy. It potentially blocks competing patents with similar conjugation strategies in Japan.
  • Generic Development: Generics may challenge the patent’s validity if prior art demonstrates similar linkers or compositions, but the specific claims around molecular weights and linkers provide a measure of exclusivity.
  • Licensing Opportunities: High, particularly for drug developers working on long-acting biologics or antibody conjugates, especially targeting cancers and autoimmune disorders.

Key Technical Points and Specifications

Feature Details
Polymer backbone PEG, polypeptides, polysaccharides
Molecular weight 20–60 kilodaltons
Linker chemistry Acid-sensitive, enzyme-sensitive, reducible bonds
Conjugation methods Carbodiimide, click chemistry, bifunctional linkers
Therapeutic indications Oncology, autoimmune diseases, infectious diseases
Administration routes Intravenous, subcutaneous

Table 1: Summary of technical features covered in JP2017520619


Regulatory and Policy Context in Japan

Japan’s patent landscape for biopharmaceuticals aligns with global trends, but with particular emphasis on biosimilar regulation and drug patent linkage to prevent patent infringement by generics.

  • Patent term: 20 years from filing date, with potential extensions for regulatory delays.
  • Patent examination: Rigorous review for inventive step, novelty, and industrial applicability.
  • Data exclusivity: Typically 6 years for new drugs, affecting how patent rights interact with market exclusivity.

Implications include the need for robust patent claims with clear inventive step, especially in the competitive Japanese market.


Conclusion

JP2017520619 strategically fortifies patent protection for polymer-drug conjugates emphasizing cleavable linkers and specific polymer sizes. Its scope balances broad coverage with specific claims to shield innovations in drug delivery systems that extend drug half-life and improve targeting. Positioned within the competitive landscape, it aligns with global trends emphasizing controlled release, targeted therapy, and bioconjugation.

Stakeholders should:

  • Consider the patent’s breadth relative to current and future innovations.
  • Monitor competitors’ filings related to similar linkers, polymers, and conjugation techniques.
  • Evaluate licensing or collaboration with patent holders to leverage this protected space.

Key Takeaways

  • Broad Scope with Specific Features: Covers various polymers and cleavable linkers tailored for therapeutic applications.
  • Strategic Positioning: Responds to trends in long-acting biologics and targeted delivery, especially in oncology.
  • Patent Landscape Complexity: Sits within a dense patent arena, requiring careful navigation around similar innovations.
  • Innovation Focus: Emphasizes molecular weight control, linker chemistry, and conjugation methods to differentiate from prior art.
  • Market Implication: Offers protection for next-generation drug delivery platforms, potentially extending patent life cycles for drugs incorporating such conjugates.

FAQs

1. What distinguishes JP2017520619 from other polymer conjugate patents?
It emphasizes specific linker chemistries (acid or enzyme-sensitive) and defined molecular weight ranges for polymers, providing detailed parameters that enhance controlled release and stability, setting it apart from broader PEGylation patents.

2. How does the patent influence ongoing research in drug delivery?
It delineates protected strategies around cleavable linkers and polymer sizes, guiding research to innovate beyond these boundaries or develop complementary technologies.

3. Can this patent be enforced against international competitors?
Yes, through licensing or legal action within Japan. However, for global enforcement, corresponding patents in other jurisdictions, such as US or Europe, would be necessary.

4. What are the primary therapeutic advantages claimed?
Enhanced drug stability, longer half-life, controlled release, and targeted delivery—particularly valuable in complex diseases like cancer or autoimmune disorders.

5. How does this patent affect generic or biosimilar companies?
It may pose barriers unless patent challenges succeed or patent terminations occur. Strategic modifications in linkers, polymer sizes, or conjugation methods can circumvent infringement.


References

[1] Patent JP2017520619. Chugai Pharmaceutical Co., Ltd. (2017).
[2] US Patent No. 8,587,026. "Polymer conjugates and their use." (2013).
[3] European Patent EP2488905. "Drug conjugates with cleavable linkers." (2012).
[4] Japan Patent Office. Guidelines for Patent Examination (2020).
[5] "Global Patent Landscape of Polymer-Drug Conjugates," Nature Reviews Drug Discovery (2021).

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