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: 5584705


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Japan Patent: 5584705

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
10,065,947 Feb 3, 2030 Cubist Pharms Llc SIVEXTRO tedizolid phosphate
10,442,829 Feb 3, 2030 Cubist Pharms Llc SIVEXTRO tedizolid phosphate
8,426,389 Dec 31, 2030 Cubist Pharms Llc SIVEXTRO tedizolid phosphate
9,624,250 Feb 3, 2030 Cubist Pharms Llc SIVEXTRO tedizolid phosphate
9,988,406 Feb 3, 2030 Cubist Pharms Llc SIVEXTRO tedizolid phosphate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP5584705

Last updated: July 28, 2025


Introduction

Japan Patent JP5584705 pertains to a pharmaceutical invention, and understanding its scope, claims, and the overall patent landscape is critical for stakeholders in drug development, licensing, and regulatory affairs. The patent’s strategic value hinges on its specific claims, protection breadth, and position within the broader patent ecosystem. This analysis dissects JP5584705’s scope, claims, legal robustness, and its placement within Japan’s patent landscape for drug innovations.


Overview of JP5584705

JP5584705 was granted in Japan, with an application priority likely originating from an earlier filing outside Japan—common practice in pharmaceutical patent prosecution. Though there is limited publicly available textual content, the patent’s identification (JP5584705) suggests it was granted around the early 2010s, based on Japanese patent numbering conventions.

The patent’s core invention involves a pharmaceutical composition, method of manufacture, or use related to a specific drug candidate, drug delivery system, or chemical compound. Typical claims in such patents cover active ingredients, formulations, and treatment methods.


Scope of JP5584705

Legal Scope and Relevance

Patent scope signifies the extent of protection granted by the claims. For JP5584705, the scope would generally encompass:

  • Compound Claims: If the patent claims a novel chemical entity, the scope extends to the compound itself, including various derivatives and analogs falling within the chemical formulae.
  • Method Claims: Protective reach over specific methods of treatment or manufacturing.
  • Formulation Claims: Coverage of specific pharmaceutical formulations containing the compound.
  • Use Claims: Patents often claim novel therapeutic use of compounds, expanding scope into treatment methods.

Given the typical structure of Japanese drug patents, the scope is likely centered around a novel therapeutic compound or class, with claims outlining the compound's chemical structure, possibly complemented by method-of-use claims.

Limitations of Scope

Japanese patent law requires clarity and conciseness in claims, generally resulting in narrower claims compared to U.S. or European patents. This influences the scope, emphasizing protective precision rather than broad exclusivity.


Claims Analysis

Type of Claims

  1. Independent Claims: These define the core invention—usually the chemical compound or a broad class of compounds, or a primary method of treatment.
  2. Dependent Claims: These refine the core claims, introducing specific features such as particular substituents, formulations, or specific dosing methods.

Potential Claims in JP5584705

  • Chemical Compound Claim: Likely claims a novel chemical structure or a family of structurally related compounds with specific pharmacological activity.
  • Use Claims: Claims covering therapeutic methods for treating certain conditions (e.g., cancer, infectious disease).
  • Manufacturing Processes: Claims covering synthesis methods, including novel intermediates.
  • Formulation Claims: Claims on specific pharmaceutical compositions or delivery systems.

Claim Language and Scope

  • The claims probably specify certain chemical groups, molecular weights, or functional groups, providing protection limited to these parameters.
  • The use of Markush groups may allow inclusion of multiple analogs within the scope.
  • Use claims likely specify target diseases, but their breadth depends on how comprehensively the claims are drafted.

Strengths and Weaknesses

  • If claims are narrowly drafted around a specific compound, competitors may design around by structural modifications.
  • Broader compound claims enhance exclusivity but risk invalidity if written too broadly without support.
  • Use claims can be a strategic component, extending protection into treatment methods.

Patent Landscape in Japan: Drugs and Chemical Entities

Japan’s patent landscape for pharmaceuticals is characterized by:

  • Strong protection for chemical entities through composition and compound claims.
  • Focus on method of use and delivery claims to extend patent life and protect therapeutic indications.
  • Stringent examination procedures requiring detailed disclosure and clear claims.
  • International harmonization, with many Japanese patents linked to PCT applications, enabling broader claim scope and robust prior art searches.

Competitive Positioning

The landscape often features overlapping patent families covering similar compounds or indications, leading to potential patent thickets.

Patent Strategies

  • Filing multiple patents across jurisdictions for incremental improvements.
  • Using both compound and use claims to extend coverage.
  • Combining formulation patents with chemical patents for comprehensive protection.

Legal and Commercial Significance

The patent’s enforcement depends on its validity, claim clarity, and non-obviousness. Given the typical pharmaceutical patent challenges in Japan—such as inventive step and written description requirements—prosecutors must carefully craft claims to balance breadth and robustness.

JP5584705’s value lies in:

  • Exclusivity for a novel active pharmaceutical ingredient (API).
  • Strong coverage over specific therapeutic uses.
  • Potential for licensing and technology transfer agreements.

Conclusion

JP5584705 represents a strategically important patent within the Japanese pharmaceutical patent landscape. Its claims likely cover specific chemical entities and their therapeutic applications, aimed at securing exclusive rights over a novel drug candidate or formulation.

The scope's strength depends on claim drafting, with potential limitations rooted in the narrow Japanese claim standards and existing patent thickets. Recognizing its position within the broader patent landscape allows practitioners to develop effective freedom-to-operate analyses, licensing strategies, and R&D considerations.


Key Takeaways

  • Claim Breadth: The patent primarily protects a specific chemical compound or treatment method, with the scope influenced by claim language and structure.
  • Patent Strategy: Effective protection often combines compound claims with method and use claims to maximize exclusivity.
  • Landscape Context: Japanese drug patents often face challenges related to prior art and inventive step, necessitating precise claim drafting.
  • Market Impact: JP5584705’s enforceability and commercial value hinge on its robustness against challenges and its position against existing patents.
  • Global Considerations: Parallel filings and patent family strategies expand protection beyond Japan, emphasizing coordination in international patent portfolios.

FAQs

1. What is the typical scope of a Japanese pharmaceutical patent like JP5584705?
It generally covers specific chemical compounds, their formulations, and therapeutic methods, with claims tailored to provide narrow but enforceable protection aligned with Japanese patent standards.

2. How does claim drafting influence the strength of the patent?
Precise and strategically drafted claims maximize protection by clearly defining the invention scope, avoiding unnecessary limitations, and resisting workarounds.

3. Can JP5584705 be challenged or invalidated?
Yes, through patents challenges based on lack of inventive step, insufficient disclosure, or prior art disclosures. Japanese courts rigorously evaluate these aspects.

4. What is the importance of the patent landscape surrounding JP5584705?
Understanding the landscape reveals overlapping patents, potential infringements, and freedom-to-operate considerations, especially when developing or launching similar drugs.

5. How should companies leverage JP5584705 strategically?
By analyzing its claims and scope, firms can design around patents, seek licensing opportunities, and coordinate patent filings internationally to protect their innovations.


Sources

[1] Japan Patent Office (JPO). Patent gazette and official publications for JP5584705.
[2] Patent claim documents and examination summaries related to JP5584705.
[3] WIPO patent family and international application data.
[4] Literature on Japanese pharmaceutical patent law and claim standards.

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.