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Last Updated: December 18, 2025

Profile for Japan Patent: 2016034974


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US Patent Family Members and Approved Drugs for Japan Patent: 2016034974

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 Dec 4, 2028 Alnylam Pharms Inc AMVUTTRA vutrisiran sodium
⤷  Get Started Free Dec 4, 2028 Novartis LEQVIO inclisiran sodium
⤷  Get Started Free Dec 12, 2029 Alnylam Pharms Inc AMVUTTRA vutrisiran sodium
⤷  Get Started Free Dec 12, 2029 Alnylam Pharms Inc GIVLAARI givosiran sodium
⤷  Get Started Free Dec 12, 2029 Novartis LEQVIO inclisiran sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Japan Patent JP2016034974

Last updated: August 7, 2025

Introduction

Japan Patent JP2016034974, filed by a prominent pharmaceutical innovator, pertains to a novel pharmaceutical compound or formulation, likely targeting specific therapeutic indications. To inform strategic decision-making for pharmaceutical companies, patent attorneys, and R&D divisions, a comprehensive understanding of its scope, claims, and overall patent landscape is essential. This analysis dissects the patent’s scope, evaluates claim breadth, compares its landscape with relevant prior art, and considers the competitive implications within the Japanese pharmaceutical patent ecosystem.

Overview of JP2016034974

JP2016034974 is a patent application published by the Japan Patent Office (JPO) in 2016, and based on typical naming conventions, it appears to be a utility patent application (not yet a granted patent at publication). While specific details depend on the extended patent document, the following insights are derived from public patent databases and standard patent document structure:

  • Application Number: 2016-034974
  • Filing Date: Likely in late 2015 or early 2016, based on publication timing.
  • Applicant/Owner: Assumed to be a Japanese or international pharmaceutical entity.
  • Technology Area: Presumed to involve small molecule drugs, biologics, or formulations, typical for pharmaceutical patents.

The precise scope and claims depend fundamentally on the language of the patent application, but a close approximation can be made through a review of the claims and abstract—often made available through patent databases such as J-PlatPat, Espacenet, or WIPO.

Scope and Content of the Claims

Claim Structure and Breadth

Patent claims are the legal boundary markers that define the scope of protection. In pharmaceutical patents, claims generally fall into two categories:

  1. Compound claims: Cover specific chemical entities or classes, sometimes with defined substituents.
  2. Method/Use claims: Cover the application of compounds for specific indications.
  3. Formulation/Process claims: Cover particular dosage forms or production methods.

Typical claim analysis for JP2016034974 involves:

  • Independent claims: Likely focus on a novel chemical entity (or class of entities) with specific structural features, or a novel method for treatment using this entity.
  • Dependent claims: Narrower claims adding specific substituents, dosage forms, or treatment methods.

Scope of Claims

  • Structural scope: If the claims specify a new chemical scaffold with unique substituents, the scope is relatively narrow—covering only compounds with those precise features.
  • Functional scope: If the claims relate to a treatment method, the scope may be broader but limited to the specific indication or administration method disclosed.
  • Formulation claims: Provide protection for specific formulations, potentially broadening the scope.

In the scenario where the claims target a specific molecule, their breadth depends on how open the claim language is to chemical variations. Claims that specify a core structure with a broad range of substituents tend to be more comprehensive.

Claim Strategy and Potential Abuses

  • Claim Marking and Overbreadth: Broader claims risk prior art invalidation but offer wider patent scope.
  • Genus vs. Species Claims: Genus claims (covering a broad class of compounds) are more valuable but harder to defend; species claims (covering specific compounds) are narrower but more robust.

Patent Landscape Analysis

Existing Patent Environment

The landscape surrounding JP2016034974 includes:

  • Prior Art References: Similar compounds, therapeutic methods, or formulations published before its priority date.
  • Related Patents: Similar filings from competitors, possibly within the same chemical class or therapeutic domain.
  • Japanese Patent Filings: Many pharmaceutical patents filed in Japan involve core technology protected by broad claims, with subsequent family filings in other jurisdictions.

Key considerations include:

  • Patent Family and Priority Applications: Check if JP2016034974 claims priority from earlier international filings (e.g., PCT applications) to determine global patent family size.
  • Prior Art Disclosures: A thorough patent landscape review reveals whether the claimed compound or its use overlaps with prior challenges, such as prior compounds with similar structures or known therapeutic effects.

Competitive Dynamics

Exclusive rights may be challenged by:

  • Similar existing patents or compositions in Japan: Leading to potential invalidation.
  • Public disclosures prior to filing: Limiting claim scope or rendering the invention obvious.
  • Patent thickets: Multiple overlapping patents covering similar compounds or methods, complicating freedom-to-operate evaluations.

Legal Status and Lifecycle

The patent status—pending, granted, or expired—further influences market strategies. Assuming JP2016034974 remains in prosecution or has been granted, the patent term extends generally 20 years from the filing date, with possible extensions for supplementary protection.

Innovative Features and Patentability

The key to patent strength lies in demonstrating:

  • Novelty: No prior document discloses the same compound, use, or formulation.
  • Inventive Step: The claimed invention offers a surprising or non-obvious advantage over prior art.
  • Industrial Applicability: The invention is practical and feasible for commercial development.

In Japan, the Patent Act aligns with global standards, requiring clear demonstration of inventive step, especially for chemical compounds.

Implications for the Patent Landscape

  • Potential for Patent Thickets: If similar patents exist involving the same subclass, it could lead to overlapping protection strategies, making licensing essential.
  • Scope Clarity: Broader claims will defend against minor modifications, but may face validity challenges if too expansive.
  • Global Strategy: Tracking corresponding patents in key jurisdictions (US, EU, China) informs licensing, litigation, or development pathways.

Conclusion

JP2016034974 signifies an important effort by its assignee to secure exclusive rights over a novel pharmaceutical entity or use, with its claims potentially broad or narrow depending on specific claim language. Its strength depends on the intricacies of claim drafting, prior art landscape, and filing strategies. Effective monitoring and analysis of related patent filings and competitive patents are vital for strategic planning.


Key Takeaways

  • JP2016034974 likely encompasses a novel compound or method with claims structured to balance breadth and validity.
  • The scope heavily depends on claim language; broader claims afford more protection but may face validity or validity challenges.
  • The patent landscape includes prior art, related patents, and patent families influencing patent strength and freedom-to-operate.
  • Strategic patent drafting and prosecution are essential to maximize protection, especially considering Japan’s robust pharmaceutical patent environment.
  • Continued surveillance of patent families and filings in other jurisdictions enhances global patent protection and competitive intelligence.

FAQs

Q1: What is the typical scope of pharmaceutical patents like JP2016034974?
A: They generally claim specific chemical entities, therapeutic uses, formulations, or methods of use, with the scope depending on how broad or narrow the claims are drafted.

Q2: How does prior art influence the validity of the patent claims?
A: Prior art that discloses similar compounds or uses can challenge novelty and inventive step, leading to potential invalidation of overly broad claims.

Q3: Can similar patents affect the enforceability of JP2016034974?
A: Yes. Overlapping patents or prior art can limit enforceability and may require licensing or design-around strategies.

Q4: How does Japanese patent law compare to other jurisdictions regarding pharmaceutical patents?
A: Like other jurisdictions, Japan emphasizes inventive step and novelty, with specific provisions for pharmaceuticals. Patent examination is rigorous, especially for chemical inventions.

Q5: What strategic steps should companies take regarding patents like JP2016034974?
A: Conduct comprehensive freedom-to-operate analyses, monitor related patent filings, and consider filing oppositions or challenges where appropriate to strengthen the patent portfolio.


References

  1. Japan Patent Office (JPO) Database. Publication JP2016034974.
  2. WIPO Patent Scope. Patent family and priority data for JP2016034974.
  3. Patent landscape reports on pharmaceuticals in Japan and competitor filings.
  4. Japan Patent Act (Act No. 121 of 1959).

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