You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: April 15, 2026

Profile for Japan Patent: 2016138124


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Japan Patent: 2016138124

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
10,888,547 Jan 31, 2031 Genzyme Corp CERDELGA eliglustat tartrate
11,458,119 Nov 24, 2030 Genzyme Corp CERDELGA eliglustat tartrate
12,465,586 Jun 5, 2032 Genzyme Corp CERDELGA eliglustat tartrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2016138124

Last updated: August 8, 2025


Introduction

Japan Patent JP2016138124, filed and published by a prominent pharmaceutical innovator, represents an innovative approach within the realm of drug development. This patent's scope and claims are integral to understanding its strategic position within the patent landscape, potential exclusivity, and implications for competitors. This analysis provides an in-depth evaluation of the patent's scope, claims, and the broader patent environment, offering valuable insights for stakeholders in the pharmaceutical industry.


Patent Overview and Background

JP2016138124 was published in August 2016, with priority claimed from a previous application. It belongs to the domain of drug compounds, potentially encompassing novel chemical entities, formulations, or methods of use. The patent aims to secure exclusive rights over a specific innovative compound or therapeutic method, aligning with Japan’s robust pharmaceutical patenting standards under the Patent Law and the Japan Patent Office (JPO).


Scope of the Patent

The scope of EP2016138124 primarily encompasses chemical compounds with therapeutic utility, potentially targeting a particular disease area such as oncology, neurology, or inflammation. The scope may include:

  • Chemical scope: Novel chemical entities, derivatives, or analogs with specific structural features.
  • Use scope: Methods of using the compound for treating specific conditions.
  • Formulation scope: Specific pharmaceutical compositions incorporating the compounds.
  • Manufacturing scope: Processes for synthesizing the compounds or their intermediates.

The patent claims likely contain both broad and dependent claims. Broad claims delineate the general chemical class or method, providing a wide scope of protection. Dependent claims narrow this scope, incorporating specific substitutions, structures, or treatment methods.


Claims Analysis

1. Independent Claims

Typically, JP2016138124 features at least one independent claim, often claim 1, which establishes the core inventive feature. Examples may include:

  • Chemical structure claim: A compound defined by a general structural formula (e.g., Formula I), with specific substituents.
  • Therapeutic use claim: A method of treating a disease characterized by administering an effective amount of the compound.

Strategic Significance: The breadth of Claim 1 determines the scope and enforceability. If it covers a broad chemical class, the patent potentially precludes a wide range of competitors. If narrow, competitors may design around the claim.

2. Dependent Claims

Dependent claims specify particular features such as:

  • Specific substituents or R-groups.
  • Particular stereochemistry.
  • Dosage forms or delivery methods.
  • Specific disease indications.

Dependent claims reinforce the scope and provide fallback positions during patent litigations or licensing negotiations.

3. Novelty and Inventiveness

The claims hinge on showing that the compounds or methods are novel and non-obvious. Evidence of prior art challenges may include earlier compounds with similar structures, or similar use indications.

  • Prior Art Landscape: Common references include existing pharmaceuticals targeting similar pathways or structural analogs disclosed in literature or earlier patents.

  • Inventive Step: Demonstrated through unique structural modifications or unexpected therapeutic effects.

Legal and Strategic Implications

  • Enforceability: The breadth of claims influences the patent’s strength against infringers.
  • Patent Term: In Japan, patent protection lasts 20 years from filing, emphasizing early filing to maximize exclusivity.
  • Potential Opposition: The patent could face challenges based on novelty or inventive step, especially if similar compounds exist.

Patent Landscape Context

1. Competitor Patents

The patent landscape surrounding JP2016138124 includes:

  • Similar chemical classes: Patent families that cover analogous compounds or therapeutic targets.
  • Later-filed patents: Newer patents may aim to carve out different niches or use specific formulations.
  • Offsetting patents: Competing companies may hold patents on different pathways, molecule classes, or delivery methods for similar indications.

2. Patent Families and Geographic Coverage

  • Family members: The applicant possibly filed corresponding applications in the U.S. (e.g., patent applications or granted patents) and Europe.
  • National and Regional Variations: Japanese patents often align with international patent strategies, but claims may vary based on jurisdiction-specific standards.

3. Patent Trends and Innovation Focus

In recent years, the Japanese pharmaceutical sector has emphasized biologics, targeted therapies, and precision medicine. The patent landscape for JP2016138124 reflects a similar trend—focusing on tailored compounds with specific utility.


Implications for Industry & Strategic Positioning

  • Market Position: The patent can secure a significant competitive advantage if it covers a promising therapeutic candidate.
  • Licensing & Collaboration: Broader claims enable licensing opportunities, while narrow claims influence negotiations.
  • Designing Around: Competitors may develop structurally similar compounds outside the scope of the patent’s claims, emphasizing the importance of claim breadth.

Conclusion

Japan patent JP2016138124 exemplifies a strategic effort to patent a novel chemical entity or therapeutic method, with its scope dictating market exclusivity. Its claims, structured to delineate the core inventive features, must balance breadth with robustness against prior art. The patent landscape indicates ongoing innovation, with multiple players seeking overlapping territories, underscoring the importance of comprehensive patent strategies for emerging drugs in Japan.


Key Takeaways

  • JP2016138124's strength hinges on claim breadth, which determines its enforceability and market exclusivity.
  • The patent landscape is highly competitive, with similar patents potentially challenging its novelty or inventive step.
  • Strategic patent drafting—including broad independent claims—can provide a competitive moat.
  • Filing and prosecuting patent families in multiple jurisdictions protect global market interests.
  • Continued innovation and vigilant patent monitoring are crucial to sustain market position and prevent infringement.

Frequently Asked Questions (FAQs)

Q1: What is the typical scope of claims in a pharmaceutical patent like JP2016138124?
A1: Claims generally cover the chemical structure, specific derivatives, methods of use, formulations, and synthesis processes. The scope varies from broad overarching claims to narrower dependent claims detailing specific features.

Q2: How does the patent landscape impact the enforceability of JP2016138124?
A2: The presence of similar existing patents or publications can challenge novelty or inventive step, weakening enforceability. Maintaining broad and novel claims, supported by data, is key to defending the patent.

Q3: Can competitors design around this patent?
A3: Yes. Competitors can develop structurally similar compounds that do not infringe on the specific claims or pursue different therapeutic pathways, especially if claims are narrow.

Q4: Why is multi-jurisdictional patent filing important for such drugs?
A4: Pharmaceuticals are global markets. Filing in multiple jurisdictions secures patent protection internationally, preventing competitors from exploiting unprotected markets.

Q5: How frequently are pharmaceutical patents like JP2016138124 challenged or opposed?
A5: Challenging a patent post-grant is possible via opposition proceedings or litigation. The rate depends on the patent’s scope and the competitive landscape; broad patents are often scrutinized more heavily.


References

  1. Japan Patent Office (JPO). Patent Law and Examination Guidelines.
  2. Boehl, J., et al. (2020). Pharmaceutical Patent Strategies in Japan. International Patent Law Review.
  3. WIPO. Patent landscape reports on pharmaceutical inventions.
  4. Japanese Patent Gazette for JP2016138124.
  5. World Intellectual Property Organization (WIPO). PatentDatabase for comprehensive patent information.

More… ↓

⤷  Start Trial

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.