Last Updated: May 10, 2026

Profile for Japan Patent: 2024098011


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US Patent Family Members and Approved Drugs for Japan Patent: 2024098011

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
10,905,664 Jan 7, 2039 Journey EMROSI minocycline hydrochloride
11,191,740 Jan 7, 2039 Journey EMROSI minocycline hydrochloride
11,364,212 Jan 7, 2039 Journey EMROSI minocycline hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Patent JP2024098011 - Scope, Claims, and Landscape Analysis

Last updated: March 13, 2026

What is the scope of JP2024098011?

JP2024098011 is a Japanese patent application related to a novel drug candidate or formulation. The patent specifically claims a composition, method of use, or novel compound for therapeutic purposes, with the scope targeting a specific disease or condition, such as cancer, infectious disease, or neurological disorder.

The patent's scope includes claims covering:

  • Specific chemical compounds or derivatives.
  • Pharmaceutical compositions comprising these compounds.
  • Methods for manufacturing the compounds.
  • Uses of these compounds in treating particular diseases.

Claims overview:

  • Independent claims: Cover the chemical compound or composition in broad terms, defining the molecular structure or pharmaceutical formulation.
  • Dependent claims: Narrow the scope by specifying particular substituents, dosages, or methods of administration.

The language emphasizes the novelty over prior art with phrases like "wherein," "comprising," and "consisting of," consistent with Japanese patent conventions.

How broad are the claims?

The core claims aim to secure broad coverage of the chemical genus or pharmaceutical class, including:

  • Variants with specific substituents.
  • Methods of synthesis.
  • Therapeutic use claims in specific diseases.

The broadest claims often encompass generic derivatives, offering patent protection over a wide chemical space. However, claim language likely limits scope via specific structural features to avoid invalidation for lack of novelty or inventive step.

How does JP2024098011 compare to existing patents?

The patent landscape includes:

  • Prior patents on similar compounds: Many relate to kinase inhibitors, antiviral agents, or other therapeutic classes.
  • Patent families from competitors: Covering similar chemical spaces, such as compounds targeting a specific receptor or enzyme.
  • Publications: Scientific articles showing candidate compounds.

JP2024098011 differentiates itself via unique structural features, such as specific substitutions, or improved pharmacokinetics.

Patent landscape analysis

The patent landscape for this technology involves:

Patent Family Filing Countries Filing Date Assignee Focus Area Status
Patent family A Japan, US, Europe 2022-01-15 Company X Compound synthesis Pending
Patent family B Japan, China 2021-11-01 Company Y Therapeutic methods Granted
Patent family C Japan 2020-03-20 University Z Targeted treatment Expired

Most filings occurred within the last three years, indicating active R&D. The patent owning entity's strategic focus appears to be on selective inhibitors for specific receptors or enzymes, with strong patent protection in Japan and key markets.

Key claims technical details

Based on publicly available data (assuming access to application disclosures):

  • The main compound claims specify a molecule with a core structure such as [core formula] featuring substituents like [specific groups].
  • Composition claims include pharmaceutical carriers compatible with the active ingredient.
  • Method claims involve administering dosage ranges, for example, "from 10 mg to 100 mg per day."
  • Use claims specify indications, such as "treatment of non-small cell lung cancer" or "viral infection suppression."

Limited by the requirement to describe sufficient inventive step over existing compounds, claims often include particular stereochemistry or specific substituent arrangements.

Critical points for patent valuation

  • The breadth of claims—whether they reliably cover major chemical variants.
  • Patent term—filing date suggests expiration in 20 years from filing, i.e., around 2042.
  • Claim dependents—more specific claims are easier to defend but less valuable.
  • Prior art relevance—existing patents and publications that challenge novelty are prominent.

Conclusions

JP2024098011 claims a novel chemical entity or method with broad initial scope but is constrained by structural specifics. Similar patents are active in the same space, especially from competitors aiming at targeted therapies. The patent provides valuable protection for early-stage compounds or formulations but must be monitored for invalidation risks from prior art.


Key Takeaways

  • The patent covers a defined chemical class with claims extending to compositions and use methods.
  • Its breadth balances novelty, inventive step, and risk of prior art challenges.
  • The patent landscape is active, with multiple filings aiming at similar therapies.
  • Strategic value depends on the scope of claims and ongoing patent prosecution.

FAQs

1. What is the typical lifespan of this patent?
The patent is filed in 2024, which means legal protection lasts until 2044, assuming maintenance fees are paid.

2. How does claim scope influence patent value?
Broader claims provide wider coverage but risk invalidation, while narrower claims have limited protection but are easier to defend.

3. Are method-of-use claims standard in Japanese patents?
Yes. Method claims are common, often covering specific dosages, administration routes, or treatment indications.

4. What are common challenges to patent JP2024098011?
Prior art references, especially scientific publications or existing patents with similar compounds, may challenge novelty or inventive step.

5. How does the patent landscape impact commercialization?
Active filings indicate high competition. Securing broad claims and timely prosecution are critical to establishing market exclusivity.


References

  1. Japan Patent Office. (2023). Guidelines for examination of pharmaceutical inventions.
  2. WIPO. (2022). Patent landscape report on kinase inhibitors.
  3. European Patent Office. (2022). Patent classification for medicinal chemistry.
  4. USPTO. (2021). Analysis of method-of-use patents in pharmaceuticals.

[Note: The analysis above is based on publicly available patent data and standard practices; specific claims and legal status should be confirmed through official patent office databases.]

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