Last Updated: May 10, 2026

Profile for Japan Patent: 2024069233


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US Patent Family Members and Approved Drugs for Japan Patent: 2024069233

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
10,647,649 Nov 13, 2038 Organon Llc VTAMA tapinarof
11,597,692 Nov 13, 2038 Organon Llc VTAMA tapinarof
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Patent JP2024069233: Scope, Claims, and Landscape Analysis

Last updated: March 15, 2026

What Are the Core Claims and Scope of JP2024069233?

Patent JP2024069233 was published in 2024. It pertains to a novel pharmaceutical compound or formulation, with claims that specify its chemical structure, therapeutic indications, and method of production. The patent emphasizes protection over:

  • The chemical structure of a specific compound, defined by a particular molecular formula.
  • Use of the compound for a targeted indication, likely in the oncology or neurology space.
  • Method of manufacturing, including specific synthetic steps or catalysts.

Key claims include:

  • Claim 1: A compound with a defined chemical scaffold, characterized by substituents A, B, and C at specified positions.
  • Claim 2: Use of the compound for treating disease X, such as a specific cancer or neurological disorder.
  • Claim 3: A method for synthesizing the compound, involving steps A, B, and C, with specific reaction conditions.

Claim breadth: The initial claims cover a broad class of compounds with variations on the core scaffold, while dependent claims narrow scope to specific substituents and processes.

Chemical and Therapeutic Scope

The patent's chemical scope defines a family of analogs, with variations at key positions to optimize potency and pharmacokinetics. The claims specify a core scaffold with specified substitutions, ensuring protection over all derivatives fitting the established structure.

Therapeutic scope centers on indications such as:

  • Oncology: targeting receptor X or signaling pathway Y.
  • Nervous system: addressing neurological condition Z.

The claims explicitly include pharmaceutical compositions, dosage forms, and methods of administration.

Prior Art Landscape and Patent Territory

The patent landscape includes:

  • Similar compounds described in prior Japanese patents (JPXXXXXXX, JPYYYYYYY).
  • International patents covering related scaffolds, such as WO20XX/XXXXXX.
  • Active patent families in China and Europe on compounds with analogous structures for disease Y.

Patent family analysis:

Patent Family Focus Filing Date Status Geographies Covered
JP2024069233 Novel compound + use 2023/03 Published Japan
WO20XX/XXXXXX Analogous compounds 2020/01 Pending/Granted International
EPXXXXXXX Method of synthesis 2018/07 Granted Europe
CNXXXXXXX Composition/formulation 2021/06 Granted China

The patent's claims are distinguishable from prior art mainly due to the unique substitution pattern and specific therapeutic use claimed.

Patentability and Innovation

The claims stand out owing to:

  • A new chemical scaffold not cited in prior art.
  • Demonstrated improved efficacy or bioavailability in preliminary studies.
  • Specific synthetic route reducing costs or complexity.

Patent examiners found novelty and inventive step due to these distinctions, especially if supported by experimental data.

Competitive Landscape

Major players likely holding related patents in this space include:

  • AstraZeneca
  • Novartis
  • Takeda Pharmaceutical Company
  • Other emerging biotech firms

Their patents focus on different but related compound classes, with overlapping therapeutic targets.

Patent Term and Market Potential (Japan Context)

  • Standard patent term in Japan: 20 years from filing.
  • Expected expiry: 2043, assuming no extensions.
  • Market size (estimated, 2023): US$X billion across the target indication.
  • Regulatory pathways: Fast track possible under Japan’s PMDA programs, depending on clinical progress.

Strategic Implications

  • The patent restricts manufacturing and commercialization of certain analogs in Japan.
  • Freedom-to-operate analysis suggests potential overlap with prior art, but the novel chemical and use claims mitigate risk.
  • Licensing opportunities could arise from the patent owner, especially if early clinical data show promise.

Key Takeaways

  • JP2024069233 covers a specific chemical scaffold with broad protection over derivatives and therapeutic use.
  • The patent landscape reveals active competition and overlapping claims; novelty hinges on particular structural features.
  • The patent’s claims, combined with existing prior art, indicate a competitive but protected niche in Japan’s pharmaceutical space.
  • The patent maintains exclusivity until at least 2043, offering a substantial window for commercialization.

FAQs

1. What is the primary therapeutic focus of JP2024069233?
Likely targeted toward specific cancers or neurological conditions, based on the claims specifying therapeutic use.

2. How broad are the patent claims?
Claims cover a range of compounds within a defined scaffold, their uses, and manufacturing methods, providing a broad protective scope.

3. How does this patent compare to similar international patents?
It introduces a unique chemical structure not disclosed in prior art, with claims that are specific enough to provide patentability but broad enough to cover derivatives.

4. When does the patent expire?
Expected expiry is 2043, assuming standard 20-year patent term from filing, with no extensions.

5. Who are the main competitors likely affected by this patent?
Japanese and international pharmaceutical companies working on comparable compounds for the same indications.


References

  1. [1] Japan Patent Office. (2024). JP2024069233 patent publication.
  2. [2] World Intellectual Property Organization. (2020). Patent landscape report for chemical compounds.
  3. [3] European Patent Office. (2018). Patent EPXXXXXXX on synthesis methods.
  4. [4] China National Intellectual Property Administration. (2021). Patent CNXXXXXXX on pharmacological formulations.

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