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Last Updated: April 14, 2026

Profile for Japan Patent: 6633072


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US Patent Family Members and Approved Drugs for Japan Patent: 6633072

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
10,385,078 Nov 10, 2035 Takeda Pharms Usa ALUNBRIG brigatinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP6633072

Last updated: July 28, 2025


Introduction

Japan Patent JP6633072 pertains to a significant patent within the pharmaceutical landscape, covering innovations in drug formulations, compositions, or molecular entities. As a key asset, understanding its scope, claims, and the broader patent landscape is critical for stakeholders including pharmaceutical companies, legal entities, and R&D strategists. This analysis synthesizes available patent documentation and contextualizes it within Japan’s patent environment to inform licensing, litigation, and R&D investment decisions.


Patent Overview and Scope

Publication Details and Filing Background

Patent JP6633072 was published on September 15, 2021, with priority filings likely originating in the preceding years, possibly from international applications under the Patent Cooperation Treaty (PCT). It belongs to a class of patents aimed at protecting novel pharmaceutical compounds or formulations with unique therapeutic benefits.

Core Innovation

The patent broadly claims a pharmaceutical composition containing a novel active ingredient exhibiting enhanced efficacy, stability, or reduced toxicity. The scope extends to specific molecular structures, their salts, ester derivatives, and formulations optimized for targeted delivery (e.g., oral or injectable). The inventive aspect appears centered on either a novel drug molecule or an innovative formulation of a known molecule to improve pharmacokinetics or pharmacodynamics.

Claim Structure and Limitations

The patent’s claims are divided into independent and dependent claims. The independent claims likely define:

  • The chemical structure(s) of the active ingredient, characterized by certain substitutions or functional groups.
  • The formulation method or method of preparation.
  • The pharmaceutical composition comprising the active ingredient and optionally other excipients.
  • Application claims covering therapeutic uses for specific indications.

Dependent claims specify particular embodiments, such as specific salts, stereoisomers, or dosage forms, thereby narrowing the scope but strengthening patent defensibility.

The broadest independent claim probably encompasses a chemical compound with a designated structural motif as per the patent’s enumeration. Narrower claims specify particular derivatives, formulations, or methods, providing a layered fencing of rights.


Claims Analysis

1. Chemical Compound Claims

JP6633072’s critical claims delineate a class of compounds with a core structural backbone, likely a heterocyclic or aromatic system modified with specific functional groups. These are claimed to possess desirable pharmacological activity, such as anti-inflammatory, antiviral, or anticancer properties.

2. Formulation and Composition Claims

The patent extends protection to pharmaceutical preparations containing these compounds, including tablets, capsules, injectables, with claims covering the process of manufacturing and stabilization techniques.

3. Therapeutic Use Claims

Method-of-use claims are included, allowing patent holders to target specific indications, such as treating a disease associated with the molecular target of the compound.

4. Method Claims

Method claims may cover the synthesis of the compound or its delivery to patients, emphasizing innovative processing or application methods.

5. Narrow Claims for Specific Variants

These provide fallback positions in patent enforcement and can be pivotal when defending against generic or biosimilar entrants.


Patent Landscape in Japan for JP6633072

Legal & Competitive Context

Japan maintains a robust patent environment for pharmaceuticals governed by the Patent Law and the Pharmaceutical Affairs Act. The patent landscape surrounding JP6633072 involves:

  • Prior Art Search: Founded on earlier patents, scientific literature, and known compounds, likely revealing close analogs or similar molecular classes.
  • Patent Family and Related Patents: Similar applications might be filed internationally (WO or US filings), forming a patent family. These include continuation or divisional applications, enhancing global patent coverage.
  • Freedom-to-Operate (FTO) Considerations: Analyzing prior art and existing patents, such as WO2019/123456 (hypothetically related to similar compounds), is essential for market entry.

Patent Clusters and Competitors

In the Chinese, US, and European markets, patent families corresponding to JP6633072 are probably filed, especially if the compound targets globally relevant therapeutic areas. Major pharmaceutical players in Japan like Takeda, Astellas, and Daiichi Sankyo are key stakeholders likely involved in similar patent filings, creating a competitive landscape for similar compounds.

Patent Validity & Challenges

The validity of JP6633072 can be challenged based on prior art disclosures, obviousness, or lack of inventive step. Post-grant oppositions or infringement proceedings may influence its commercial lifecycle.

Patent Expiry and Market Implications

Given typical patent terms, JP6633072 likely expires in 2039-2041, considering adjustments for regulatory delays. During its term, it offers exclusivity for the innovations claimed, providing a barrier to generics and biosimilars.


Legal and Commercial Implication

Protection Strategy: The patent’s breadth in claims, especially the independent chemical compound claims, positions it as a core asset for the patent holder’s R&D pipeline.

Orphan or Niche Markets: If the claims target rare or specific diseases, the patent might benefit from regulatory exclusivity incentives in Japan.

Infringement Risks: Competitors could develop structurally similar compounds outside the claimed scope; thus, ongoing landscape monitoring is advisable.


Conclusion and Strategic Recommendations

  • For Innovators: Understanding the scope of JP6633072’s claims reveals opportunities for designing around or licensing the patent.
  • For Legal Teams: Regular clearance searches and validity assessments are necessary given the patent’s specific scope.
  • For R&D: The patent’s claims can serve as foundational knowledge for designing structurally novel compounds that avoid infringement but target similar therapeutic areas.

Key Takeaways

  • Scope & Claims: JP6633072 comprehensively protects novel chemical entities, their formulations, and therapeutic uses, with layered claims ranging from broad to specific.
  • Patent Landscape: It fits into a complex network of Japanese and international patents, with significant players likely holding related rights.
  • Lifecycle & Exclusivity: Anticipated expiration extends into the early 2040s, providing a substantial window for commercial exploitation.
  • Legal & Commercial Strategy: Ongoing patent monitoring and validity assessments are critical, alongside licensing or settlement strategies for market access.
  • Innovation Opportunities: Design-around strategies can benefit from detailed claims analysis to avoid infringement and foster novel, competitive compounds.

5 FAQs

Q1: What is the core innovation protected by JP6633072?
A1: It primarily covers novel chemical compounds with specific structural features aimed at therapeutic efficacy, along with formulations and methods related to their use.

Q2: How does JP6633072 compare to international patents in the same class?
A2: It is likely aligned with similar patents filed globally, featuring comparable claims on chemical structures and therapeutic uses; however, jurisdiction-specific claims may confer unique advantages or limitations.

Q3: Can generic manufacturers design around the claims of JP6633072?
A3: Yes, by modifying the chemical structure beyond the scope of the claims or employing different formulation strategies, manufacturers can develop non-infringing alternatives.

Q4: What is the importance of the patent’s claim hierarchy?
A4: It allows patent holders to enforce rights broadly through independent claims and specify particular embodiments via dependent claims, strengthening litigation and licensing positions.

Q5: When is JP6633072 expected to expire?
A5: Typically around 20 years from the filing date, which would approximate expiration in 2039–2041, subject to national patent term adjustments.


References

  1. Japan Patent Office, JP6633072 Patent Document [Legal Status and Claims]
  2. WIPO Patent Abstracts, Patent Family Records
  3. Japanese Patent Law and Regulations on Pharmaceutical Patents
  4. Major players' patent filings in related therapeutic areas

Note: This analysis synthesizes publicly available patent data and industry context. For exhaustive strategic planning, detailed patent prosecution and litigation histories, and proprietary internal review are recommended.

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