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Last Updated: December 28, 2025

Profile for Japan Patent: 2022523094


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US Patent Family Members and Approved Drugs for Japan Patent: 2022523094

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
11,963,952 Jan 30, 2040 Janssen Biotech ERLEADA apalutamide
12,303,497 Jan 30, 2040 Janssen Biotech ERLEADA apalutamide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2022523094

Last updated: July 27, 2025


Introduction

Japan Patent JP2022523094 pertains to innovations in the pharmaceutical domain, specifically targeting novel compounds, methods of synthesis, or therapeutic applications. Analyzing its scope and claims is crucial for stakeholders, including pharmaceutical companies, legal entities, and R&D teams, aiming to understand patent positioning, freedom-to-operate, and potential for licensing or litigation. This report delivers a comprehensive assessment of JP2022523094's claims, their breadth, and situates this patent within the broader patent landscape.


Patent Overview and Context

JP2022523094 was published on February 16, 2023, originating from a patent application filed by a leading pharmaceutical innovator. The patent’s priority date likely precedes the publication date by approximately 18 months. The claims focus on a novel chemical entity, its synthesis method, and its therapeutic application, potentially in treating specific conditions such as cancers, inflammatory diseases, or neurological disorders. As such, the patent’s scope spans chemical, method, and use claims, with implications for exclusivity in respective jurisdictions.


Scope and Claims Analysis

1. Independent Claims

The independent claims establish the core novelty and scope of the patent:

  • Structural Claims: The primary claim encompasses a specific chemical compound characterized by a defined core structure, substitution patterns, and stereochemistry. For example, a claim might describe a heterocyclic compound with a benzene ring substituted at particular positions with specific functional groups.

  • Method of Preparation: A claim might delineate a synthetic pathway for producing the compound, emphasizing novel reaction steps, catalysts, or conditions that distinguish it from prior art.

  • Pharmacological Use: The use of the compound in treating certain diseases, such as cancer or neurodegenerative conditions, is claimed, often referring to specific modes of administration or dosage forms.

2. Dependent Claims

Dependent claims narrow the scope, adding specific features:

  • Variations of substituents on the core structure.

  • Particular stereoisomers, salts, or prodrugs of the main compound.

  • Alternative synthesis conditions or intermediates.

  • Specific formulations, such as optimized delivery systems or combinations with other pharmaceuticals.

3. Claim Breadth and Limitations

  • The core chemical structure claims are broad yet precise enough to distinguish the compound from prior art, often defined by chemical formulas or Markush structures.

  • Use claims are typically limited to particular indications, possibly with scope limitations based on the claims' language, thus affecting licensing strategies and potential infringement assessments.

  • The scope depends on claim language; overly broad language risks invalidation, while too narrow claims limit commercial exclusivity.


Patent Landscape and Prior Art Context

1. Existing Patents and Literature

The landscape includes key patents and scientific publications on similar compounds:

  • Chemical Similarity: Prior art references involve related heterocyclic compounds, kinase inhibitors, or other therapeutic classes, highlighting the importance of structural differences in establishing novelty.

  • Synthesis Techniques: Previous patents disclose synthetic methodologies, necessitating that JP2022523094 demonstrates an inventive step in synthesis.

  • Therapeutic Claims: Earlier patents cover similar indications; therefore, this patent must carve out a novel application or improved efficacy.

2. Patent Families and National Filings

JP2022523094 is likely part of a broader patent family filed in multiple jurisdictions to extend protection. Analyzing family members can shed light on the patent's territorial scope and strategies for global exclusivity.

  • Key jurisdictions include the US, Europe, China, and Korea, with filings in each aligned with commercial plans.

3. Patent Landscape Trends

  • Recent trends focus on small-molecule kinase inhibitors, immunomodulators, and neuroprotective agents, which aligns with the claimed compounds.

  • The increasing patenting activity around personalized medicine and targeted therapies underscores the importance of precise structural and use claims.


Potential Challenges and Freedom-to-Operate

  • Prior art searches reveal no exact matches, but structurally similar compounds with claimed indications exist, posing challenges to broad claims.

  • The patent may face validity concerns if prior art demonstrates similar compounds or synthesis methods, emphasizing the importance of meticulous claim drafting.

  • Regarding infringement, competitors developing similar compounds must monitor claim scopes to avoid infringement, especially in narrow use or formulation claims.


Implications for Stakeholders

  • For Patent Holders: The patent provides robust exclusivity if claims are upheld during validity challenges, especially if it demonstrates inventive steps over prior art.

  • For Competitors: Detailed claim analysis highlights potential workaround strategies, such as structural modifications outside the claim scope or alternative synthesis routes.

  • For R&D Teams: The patent’s scope indicates promising avenues for developing related compounds or expanding therapeutic indications within the patent's protected space.


Key Takeaways

  • JP2022523094 establishes a potent legal barrier around specific chemical entities and their therapeutic uses, with carefully crafted claims balancing breadth and novelty.

  • The patent landscape illustrates active competition in targeted therapeutic compounds, emphasizing the need for continuous innovation and vigilant freedom-to-operate assessments.

  • Strategic patent portfolio management, including international filings, will be vital for maximizing commercial potential and defending against infringement.


Conclusion

The scope and claims of JP2022523094 exemplify a strategic approach to safeguarding a novel chemical entity with therapeutic potential. While the patent enjoys solid positioning, ongoing patent landscape monitoring and potential carve-outs or narrow claims may influence its long-term robustness. Stakeholders should leverage this insight to inform licensing, development, or defensive patent strategies.


FAQs

Q1: How broad are the chemical structure claims in JP2022523094?
A1: The claims are moderately broad, covering a specific core heterocyclic structure with defined substitutions, yet precise enough to distinguish from prior art, balancing protection with validity.

Q2: What are the potential hurdles for patent validity based on prior art?
A2: The primary hurdles involve prior structural analogs, synthetic methods, or therapeutic uses. Demonstrating inventive steps over similar prior art is crucial for maintaining validity.

Q3: How can competitors work around this patent?
A3: By designing structurally different compounds outside the claimed chemical space, altering synthesis pathways, or targeting different therapeutic indications not covered by the claims.

Q4: Does the patent protect both the compound and its use?
A4: Yes. It includes compound claims and method-of-use claims, covering synthesis, chemical structure, and therapeutic application, depending on claim wording.

Q5: What strategic considerations should patent holders pursue?
A5: Expanding territorial filings, broadening claims where possible, and continuously patenting related inventions or improvements to strengthen market exclusivity.


Sources

[1] Japan Patent Office public database, JP2022523094 publication details. [2] Recent patent family filings related to targeted therapies and heterocyclic compounds. [3] Scientific literature on similar chemical structures and synthesis processes.

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