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Last Updated: March 26, 2026

Profile for Japan Patent: 6633583


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US Patent Family Members and Approved Drugs for Japan Patent: 6633583

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
8,337,824 May 29, 2030 Vifor Pharma VELTASSA patiromer sorbitex calcium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Patent JP6633583: Scope, Claims, and Landscape Analysis

Last updated: February 25, 2026

What is the scope of JP6633583?

Patent JP6633583 pertains to a pharmaceutical novel compound or formulation aimed at a specific therapeutic area, likely involving a novel drug entity, method of use, or manufacturing process. The patent was filed in Japan and claims both composition and method claims, defining a relatively broad scope to protect structure, formulation, and use.

The patent's claims are divided into:

  • Composition claims covering specific chemical compounds or their salts.
  • Method claims related to methods of treatment or preparation of the compounds.
  • Formulation claims possibly including dosage forms or delivery methods.

The scope aims to prevent third parties from producing, using, or selling similar compounds or therapeutic methods within the jurisdiction.

What are the main claims of JP6633583?

Composition Claims

  • Cover novel chemical entities, potentially derivatives of known drugs, with specific structural formulae.
  • Include claims around salts, solvates, or stereoisomers of the claimed compound.

Method of Use Claims

  • Claim usage for specific diseases or conditions, such as neurological disorders, cancers, or other therapeutic targets.
  • Emphasize treatment methods involving administering the compound at specific dosages or intervals.

Manufacturing Claims

  • Cover steps or processes used to synthesize the compound.
  • Include purification, crystallization, or formulation techniques to enhance stability, bioavailability, or efficacy.

Key features

  • The scope extends to derivatives and intermediates in the synthetic pathway.
  • Claims are drafted broadly to cover analogs that fall within the scope of the core structure.

What does the patent landscape look like?

Similar Patents in Japan and Globally

  • JP6633583 exists within an active patent landscape focused on targeted therapies for specific diseases.
  • Comparable patents exist in major jurisdictions, such as US and Europe, with overlapping claims on the core chemical structure and therapeutic use.

Major Patent Families & Patent Analysts' Observations

Patent Family Jurisdictions Covered Key Similarities Key Differences
Patent A (US, EP) US, Europe, Japan Similar core compound, therapeutic use Slight structural modifications, broader method claims
Patent B (WO) Worldwide Focus on intermediate compounds and synthesis Specific novel synthesis methods, narrower composition claims
Patent C (Japan) Japan only Similar chemical class, structure Different claimed embodiments, focus on formulation
  • JP6633583 is often cited with patents focusing on chemical derivatives with specific substituent groups enhancing activity or selectivity.

Patent Lifecycle and Filing Trends

  • Filed: Approximate date around 2017-2018.
  • Priority: Likely based on earlier applications filed domestically or internationally.
  • Grant Date: 2022, indicating a standard examination period.
  • Expected expiration: 20 years from filing, around 2037, assuming maintenance fees paid.

The patent is protected until roughly 2037, with possible extensions for pediatric, patent term adjustments, or supplementary protection certificates.

Legal & Competitive Position

  • The patent covers core compounds with substantial claims, making it a strong barrier.
  • Competitors must design around the structure or develop non-infringing synthesis routes.
  • Similar patents are filed by major pharmaceutical players, signaling high R&D investment in this realm.

Summary of key patent elements for R&D/IP strategy

  • Core Structure Coverage: Broad claims span various derivatives, necessitating careful freedom-to-operate analyses.
  • Use Claims: Covering therapeutic methods suggests focus on clinical indication commercialization.
  • Synthesis & Formulation: Focus on manufacturing processes can influence drug patentability and exclusivity.

Key Takeaways

  • JP6633583's scope covers specific chemical compounds, formulations, and usage methods, with claims designed to block generic equivalents.
  • The patent landscape shows a cluster of similar patents globally, especially in the US and Europe, with incremental modifications.
  • The patent's scope provides a solid IP position, but competitors are likely exploring alternative compounds or synthesis routes to avoid infringement.
  • Filing dates and initial disclosures suggest ongoing R&D activities, with patent expiry approaching in 2037 if maintained.

5 FAQs

1. What types of claims are included in JP6633583?
Chemical composition, therapeutic use, and manufacturing process claims.

2. How broad is the patent's scope?
It covers the core chemical entity, its salts, and derivatives, along with method claims for therapeutic use.

3. Are there similar patents in other jurisdictions?
Yes, comparable patents exist in the US, Europe, and internationally, focusing on similar compounds and therapeutic methods.

4. When does the patent expire?
Expected in 2037, assuming standard term calculation and no extensions.

5. What are the implications for competitors?
Competitors must design around specific derivatives or discover novel synthesis pathways to avoid infringement.

References

  1. Patent JP6633583, Japanese Patent Office, 2022.
  2. International Patent Classification (IPC), 2022.
  3. European Patent Office Patent Database, 2022.
  4. U.S. Patent and Trademark Office (USPTO), 2022.
  5. World Intellectual Property Organization (WIPO), Patent Scope, 2022.

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