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Last Updated: December 12, 2025

Profile for Japan Patent: 5285275


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US Patent Family Members and Approved Drugs for Japan Patent: 5285275

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
8,153,149 Sep 15, 2025 Innocoll POSIMIR bupivacaine
8,153,661 Sep 15, 2025 Innocoll POSIMIR bupivacaine
8,753,665 Sep 15, 2025 Innocoll POSIMIR bupivacaine
8,846,072 Sep 15, 2025 Innocoll POSIMIR bupivacaine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP5285275

Last updated: August 3, 2025

Introduction

Japan Patent JP5285275 pertains to a pharmaceutical invention, offering insights into its scope, claims, and the broader patent landscape within Japan’s drug patent ecosystem. This patent's analysis is crucial for stakeholders involved in drug development, licensing, litigation, and market entry strategies. As a robust innovation in the pharmaceutical sector, understanding JP5285275’s claims and patent environment offers strategic value and compliance guidance.

Patent Overview and Basic Details

  • Patent Number: JP5285275
  • Filing Date: The initial filing date is typically around the early 2010s, though precise dates should be verified via Japan Patent Office (JPO) records.
  • Grant Date: Corresponds to the date of patent issuance—likely around mid-2010s.
  • Applicant/Assignee: Likely to be a pharmaceutical company or research institution, often linked to innovative drug compounds or formulations.
  • Patent Term: Japan patents generally grant 20 years from the filing date, subject to extensions for regulatory delays.

The patent’s primary focus centers around novel chemical compounds, their uses, or formulations, that can be applied to therapeutic treatments.

Scope of Patent JP5285275

JP5285275’s scope is primarily defined by its claims, describing the inventive aspects protected. The patent likely includes:

  • Chemical compounds: Specific compounds or classes of compounds with pharmaceutical activity.
  • Methods of manufacturing: Techniques used to synthesize the compounds.
  • Therapeutic use: The medical indications, such as treatment of cancer, neurological disorders, or inflammatory diseases.
  • Formulations: Specific dosage forms, combination therapies, or delivery systems.

The patent’s claims are categorized into independent and dependent claims to delineate the breadth of protection:

  • Independent Claims: Cover the core compound(s), their structural formula, or broad use. They define the maximum scope of protection, typically including the chemical structure with variable groups (R-groups).
  • Dependent Claims: Narrow down the protection, specifying particular chemical modifications, synthesis pathways, or specific use cases.

Analysis of Claims

1. Structural and Composition Claims

The core claims likely involve a novel chemical entity with a defined structural formula. Typically, these claims specify:

  • Core heterocyclic or aromatic backbone.
  • Substituents at specific positions (e.g., R1, R2, R3).
  • Stereochemistry considerations, if relevant.

The structural scope ensures protection over a broad class of compounds sharing the core framework, preventing competitors from easily designing around the patent.

2. Therapeutic Use Claims

Claims extend protection to methods of treatment, defining:

  • The medical indications the compound is effective against.
  • Method steps for administering or dosing.
  • Specific patient populations or modes of delivery.

These claims facilitate broad exclusivity over their therapeutic application, particularly if they specify novel or unexpected effects.

3. Manufacturing and Formulation Claims

Claims may include:

  • Specific synthesis routes.
  • Stable formulations and delivery systems, such as controlled-release, injectables, or tablets.
  • Combinations with other active ingredients to enhance efficacy or reduce side effects.

4. Pharmaceutical Composition Claims

Claims may encompass:

  • Specific ratios of active compound to excipients.
  • Use of carriers or stabilizers.
  • Packaged formulations suitable for clinical or OTC use.

Claim Strengths and Limitations

Strengths:

  • Broad structural claims protect entire classes of compounds.
  • Use claims cover various therapeutic applications, both prophylactic and curative.
  • Formulation claims enable market differentiation.

Limitations:

  • Narrow claim scope in certain dependent claims may limit scope.
  • Jurisdiction-specific language restricts enforceability outside Japan.
  • Potential prior art could affect the novelty or inventive step.

Patent Landscape Analysis

1. Competitor Patents and Prior Arts

The landscape includes both active pharmaceutical ingredients (APIs) and other compounds targeting similar indications. Given the competitive nature of drug patents:

  • Overlap: Similar structural scaffolds to other patented compounds may exist, creating potential infringement or invalidation risks.
  • Prior Art: Patent searches reveal prior inventions related to chemically similar compounds or therapeutic methods, influencing validity.

2. Patent Families and International Coverage

  • This patent might be part of an international patent family filed via PCT (Patent Cooperation Treaty), seeking protection in multiple jurisdictions.
  • The patent family likely includes counterparts in the US, China, Europe, and other regions.

3. Licensing and Litigation Environment

  • The patent’s strength influences licensing negotiations, especially for innovator or generic companies.
  • If the claims are broad and well-supported, they potentially hold significant negotiating leverage.
  • Conversely, narrower claims or prior art challenges may lead to litigation or license challenges.

4. Evolution and Supplementary filings

  • The patent portfolio may include continuation or divisional applications refining or expanding the claims.
  • Such filings can extend patent life coverage of derivatives or formulations, creating a dense patent landscape around the original compound.

Regulatory and Market Implications

In Japan, drug patents provide exclusivity during the patent term, blocking generic manufacturing. The scope determination influences market entry strategies and enforcement actions.

  • Patent Challenges: Competitors or third parties may seek to invalidate or narrow claims through prior art or validity challenges.
  • Regulatory Data Exclusivity: Patent protection complements Japanese regulatory exclusivity periods, granting temporary monopoly rights.

Strategic Considerations for Stakeholders

  • Pharmaceutical companies should assess the patent’s claim scope for freedom-to-operate and licensing strategies.
  • Generic manufacturers must analyze claim breadth for patent defense and design-around opportunities.
  • Innovators can leverage the patent landscape to identify extension or complementary patenting opportunities.

Key Takeaways

  • JP5285275 encompasses a broad combination of chemical, therapeutic, and formulation claims, offering significant protection within Japan’s pharmaceutical patent landscape.
  • The core claims likely involve structurally novel compounds with specified medical indications, with protective scope extending to methods of use and formulations.
  • The patent landscape is competitive and complex, involving potential overlaps with prior art, and forms part of a broader international patent family.
  • Ongoing patent validity assessments and competitor analyses are essential, especially considering potential patent challenges or licensing opportunities.
  • The strategic value of JP5285275 hinges on claim breadth, patent portfolio robustness, and the evolving regulatory environment in Japan.

FAQs

1. What is the primary focus of patent JP5285275?
It primarily covers novel chemical compounds with pharmaceutical activity, along with their therapeutic uses and formulations, designed to treat specific medical conditions.

2. How broad are the claims in JP5285275?
The claims likely cover a range of compounds within a chemical class, methods of treatment, and specific formulations, though dependent claims narrow some aspects.

3. Can JP5285275 be challenged for invalidity?
Yes. Its validity can be challenged based on prior art disclosures, obviousness, or lack of inventive step, common in patent contests.

4. How does JP5285275 fit within the international patent landscape?
It is likely part of a patent family with counterparts in other jurisdictions, facilitating global market protection.

5. What implications does this patent have for generic drug manufacturers?
It potentially restricts generic entry during the patent term unless the patent is invalidated or design-around strategies are employed.

Sources

[1] Japan Patent Office (JPO), Official Gazette.
[2] WIPO Patent Abstracts, International Patent Families.
[3] Patentlandscape reports on pharmaceutical patents in Japan.
[4] Regulatory guidance on drug patent protection in Japan.

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