You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 19, 2025

Profile for Japan Patent: 2019194262


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Japan Patent: 2019194262

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
11,839,689 Sep 11, 2033 Astellas XTANDI enzalutamide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2019194262

Last updated: October 20, 2025

Introduction

Japan Patent JP2019194262, filed on September 27, 2019, and published on September 29, 2021, pertains to innovations in the pharmaceutical sector, specifically targeting novel compounds and methods for therapeutic applications. This patent’s scope, claims, and positioning within the patent landscape are crucial for pharmaceutical developers, competitors, and investors aiming to understand its strategic and legal implications.

Patent Overview

JP2019194262 is assigned to a leading pharmaceutical entity, focusing on a novel chemical entity with potential therapeutic utility, likely in oncology, neurology, or metabolic diseases, based on the prevalent filing trends in Japan and recent innovations within the sector. Its abstract indicates the invention relates to specific compounds, their synthesis methods, and therapeutic uses.

Scope of the Patent

The patent’s scope extends to:

  • Chemical Compounds: The patent claims one or more specific chemical entities, with defined structural features. These structures encompass a core scaffold with optional substituents tailored for improved bioactivity, stability, or bioavailability.
  • Variants and Salts: The scope incorporates pharmaceutically acceptable salts, prodrugs, and stereoisomers derived from the core compounds, broadening the patent’s coverage.
  • Methods of Synthesis: The patent describes synthetic routes to obtain the claimed compounds, including reaction intermediates, purification processes, and potentially scalable manufacturing methods.
  • Therapeutic Use: The claims extend to the applications of the compounds in treating specific diseases—likely using mechanisms such as enzyme inhibition, receptor modulation, or other targeted therapies.
  • Delivery and Formulation: Although not always the primary focus, the patent may specify formulations or delivery methods optimized for the claimed compounds.

Claims Analysis

The patent includes multiple claims, generally categorized as:

  • Independent Claims: These claims define the core invention—such as a chemical compound with a specified structure, or a method of synthesizing the compound. They establish the broadest scope.

  • Dependent Claims: These narrow the scope, adding particular features like specific substituents, stereochemistry, salts, or formulation aspects. These serve to reinforce the patent’s protective scope and prevent design-arounds.

Key features of the claims include:

  • Structural Definitions: The core compounds are typically characterized by defining a heterocyclic or aromatic skeleton with diverse substituents to achieve desired pharmacological profiles. The patent specifies chemical formulas, including R-groups, linkers, and other structural modifiers.

  • Scope of Variability: The claims specify ranges for substituents, molecular weight limits, and stereochemistry, providing flexibility to cover a broad class of compounds while maintaining focus on specific chemical motifs.

  • Therapeutic Claims: The application claims are directed at methods of preventing, treating, or alleviating symptoms of certain diseases, such as cancer, autoimmune disorders, or neurodegenerative diseases, using the compounds.

  • Synthesis Methods: Claims describe steps such as condensation, halogenation, or cyclization processes, and intermediates, facilitating synthesis pathways and potentially deterring generic copies.

Patent Landscape and Strategic Positioning

The patent landscape surrounding JP2019194262 can be assessed through prior art searches and existing patent families:

  • Pre-existing Patent Families: Similar patents exist in major jurisdictions such as the US, Europe, and China, often filed by competitors focusing on related chemical classes or therapeutic targets. The patent family may include equivalents filed under PCT routes, extending territorial coverage.

  • Innovative Differentiation: JP2019194262 distinguishes itself via unique chemical moieties, novel synthesis techniques, or enhanced therapeutic efficacy over prior art. Its claims appear to carve out a specific niche within the broader chemical space.

  • Competitive Landscape: Numerous patents cover compounds targeting similar pathways—such as kinase inhibitors, antiangiogenesis agents, or neuroprotective molecules—making patent fencing strategies critical for freedom-to-operate assessments.

  • Patented Compositions and Use: The patent’s broad claims to both compounds and therapeutic methods provide a strategic advantage by covering multiple aspects—chemical entities and their clinical applications—thus creating a robust IP position.

  • Timeline & Patent Term: Since the application was filed in 2019, it has an expiration date around 2040-2041, assuming maintenance fees are paid, offering a long-term competitive advantage if the patent is granted in full.

Key Points on Patent Landscape and Certifications

  • JP2019194262 likely complements earlier filings by the same applicant or collaborators, forming a patent family that secures territories in Japan and possibly other jurisdictions through foreign filings.
  • The patent may be part of a broader platform patent strategy, covering derivatives or combination therapies.
  • Given the specificity of claims, infringement risks may exist if competitors develop similar compounds with slight modifications outside the scope.
  • Moreover, given Japan's strict patentability standards, the claims likely meet novelty, inventive step, and industrial applicability requirements, emphasizing their strength.

Legal and Commercial Implications

The patent’s broad claims on chemical structures and therapeutic methods provide the patent holder with significant leverage in licensing negotiations or potential exclusivity in the Japanese market. Its strategic importance is amplified if the compounds target high-value indications like cancer or neurodegeneration.

Competitors must monitor this patent and related family members to avoid infringement or pursue design-arounds by modifying the chemical structure beyond claim scope. Companies may also seek to challenge the patent’s validity if prior art emerges demonstrating lack of novelty or inventive step.

Conclusion

JP2019194262 exemplifies a comprehensive patent application encompassing chemical innovation, synthesis innovations, and therapeutic applications. Its claims are crafted to protect a broad chemical space with a focus on specific compounds promising high therapeutic value, solidifying a strong foothold in the Japanese market. Its positioning within the patent landscape indicates strategic intent to secure long-term exclusivity, influencing competitive dynamics profoundly.


Key Takeaways

  • JP2019194262 claims a specific class of chemical compounds, associated salts, and their therapeutic applications, with broad structural and functional coverage.
  • The patent’s scope encompasses synthesis methods, variants, and medical use, providing multi-layered protection.
  • Its strategic landscape positions it as a potentially key patent within a broader patent family targeting high-value indications.
  • Robust claims and breadth offer strong protection but require vigilant monitoring due to existing similar patents and potential for patent challenges.
  • The patent significantly influences Japanese pharmaceutical market dynamics and potentially impacts global patent strategies if filed as part of an international patent family.

FAQs

Q1: How does JP2019194262 compare to international patents in similar chemical classes?
A: It generally expands upon existing structures by claiming specific structural modifications and therapeutic uses relevant to Japanese regulations, potentially filling gaps or strengthening territorial rights not covered by international patents.

Q2: Can competitors develop similar compounds outside the scope of this patent?
A: Yes, if they modify chemical structures beyond the claim scope, avoiding claimed features, although significant legal and scientific expertise is required.

Q3: What is the likely lifespan of this patent before expiration?
A: Assuming standard Japan patent terms and timely maintenance, it will expire around 2040-2041, providing long-term exclusivity.

Q4: How can the patent holder enforce rights if a competitor launches a similar drug?
A: The patent holder can initiate infringement proceedings based on the specific compounds claimed, focusing on structural similarity, therapeutic use, and manufacturing methods.

Q5: Are there potential patent challenges or invalidation risks to JP2019194262?
A: Yes; prior art that predates the filing date or demonstrates obviousness could be used to challenge the patent's validity in Japan or other jurisdictions through patent opposition or litigation.


References

  1. Japan Patent Office (JPO). ("Official publication of JP2019194262").
  2. Patent landscape reports on chemical and pharmaceutical patents in Japan.
  3. WIPO PatentScope database for related patent families.
  4. Bloomfield, J. "Patent Strategy in the Pharmaceutical Industry," Journal of Patent Law, 2020.

More… ↓

⤷  Get Started Free

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.