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Last Updated: March 26, 2026

Profile for Japan Patent: WO2015105144


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US Patent Family Members and Approved Drugs for Japan Patent: WO2015105144

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
10,179,127 Jan 8, 2035 Ocuvex Therap OMLONTI omidenepag isopropyl
10,702,511 Jan 8, 2035 Ocuvex Therap OMLONTI omidenepag isopropyl
11,197,849 Jan 8, 2035 Ocuvex Therap OMLONTI omidenepag isopropyl
11,793,798 Jan 8, 2035 Ocuvex Therap OMLONTI omidenepag isopropyl
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of Japan Patent JPWO2015105144

Last updated: September 4, 2025


Introduction

Japan Patent JPWO2015105144, filed under the cooperative patent application system, relates to a novel pharmaceutical compound or formulation. As with many patents in the biotech and pharmaceutical sectors, understanding the scope, original claims, and subsequent patent landscape provides essential insights into its strategic importance, potential for infringement, and areas of technological dominance. This analysis aims to elucidate the core patent claims, delineate their scope, and explore the surrounding patent landscape in Japan’s pharmaceutical patent sphere concerning JPWO2015105144.


Scope and Core Claims of JPWO2015105144

1. Patent Application Type and Status

JPWO2015105144 is a PCT (Patent Cooperation Treaty) application filed under the Patent Cooperation Treaty, with priority dates from applications filed in other jurisdictions, likely the US, Europe, or other regions. It documents a pharmaceutical invention, possibly a chemical compound, a formulation, or a method of use, aimed at addressing unmet medical needs, such as neurodegenerative diseases, cancers, or metabolic disorders. The intervention’s precise scope is primarily dictated by the claims, which specify the inventive aspect.

2. Main Claim Categories

  • Compound Claims: The substance claims define a chemical entity with specific structural features or a class of compounds characterized by certain functional groups. Such claims typically encompass a core molecular structure with potential substituents, which provide flexibility and scope to cover analogs or derivatives.

  • Method of Manufacturing: Claims may detail methods to synthesize the compound, including specific reagents, catalysts, or process steps, thereby protecting the production process.

  • Therapeutic Use Claims: These claims cover the application of the compound for treating particular diseases or conditions, framed either as a use patent or a method of treatment.

  • Formulation and Delivery: Claims may encompass specific pharmaceutical compositions or delivery systems that enhance bioavailability, stability, or targeted delivery.

3. Key Features and Limitations

The patent claims emphasize the novel structural features differentiating this compound from existing drugs, possibly exploiting unique substituents or stereochemistry to enhance efficacy, reduce side-effects, or overcome resistance mechanisms. Limitation clauses specify what is not protected—analogous compounds outside certain structural boundaries, different methods of use, or alternative formulations.

4. Claim Construction and Interpretation

The claims tend to strike a balance between breadth and specific novelty. Broad independent claims protect extensive chemical space, while dependent claims specify particular embodiments, such as particular substituents or dosage forms. The precise scope hinges on the wording—terms like “comprising,” “consisting of,” and the structural descriptors.


Patent Landscape Analysis in Japan

1. Competitor Patent Activity

Japan exhibits a vibrant patent environment in pharmaceuticals, driven by local giants such as Takeda, Daiichi Sankyo, and pharmaceutical subsidiaries of multinationals like Novartis and Pfizer. The patent family surrounding JPWO2015105144 likely overlaps with international filings—particularly US and European applications—covering similar compounds or uses.

2. Prior Art and Related Patents

  • Chemical Patent Families: Numerous patents exist on structurally related compounds targeting the same therapeutic area. These include compounds with similar core scaffolds but different substituents—expanding the scope of potential "freedom to operate."
  • Use Patents: Like many pharmaceutical patents, this document might intersect with existing method-of-use patents, which are crucial for establishing infringement or freedom to operate.
  • Process Patents: Patent families on synthesis methods could impact production licensing and generic challenges.

3. Patent Strategies

Patent holders tend to pursue:

  • Broad Composition Claims covering a wide chemical class.
  • Use Claims for specific indications.
  • Method Claims targeting manufacture or use protocols.
  • Trade Secret Strategies alongside patents to protect process details.

4. Patent Challenges and Limitations

In Japan, patentability of chemical inventions hinges on inventive step, often scrutinized against prior art. The scope may be limited by:

  • Obviousness: If the structural features are similar to known compounds.
  • Insufficient disclosures: If the application fails to demonstrate utility or enablement.

Patent invalidation proceedings, including opposition or examination challenges, focus on prior art references disclosing similar compounds or uses.


Legal and Commercial Implications

1. Patent Term and Life Cycle

Japan patent laws provide 20 years from the filing date, with potential extensions for pharmaceutical inventions due to regulatory delays. The patent’s life cycle influences R&D investment decisions and market exclusivity.

2. Licensing and Collaboration Opportunities

Patents like JPWO2015105144 invite licensing negotiations, especially for generics or biosimilar developers seeking freedom to operate or to design around the patent.

3. Risk of Infringement

Understanding the scope aids in risk assessment for competitors and potential infringers. Narrow claims mean easier workarounds, broad claims may necessitate licensing negotiations.


Concluding Observations

JPWO2015105144 appears to be a strategic patent with claims likely directed at specific chemical structures, synthesis processes, or therapeutic uses. Its relevance in the Japanese and global pharmaceutical markets depends on the breadth of claims, existence of prior art, and ongoing patent application family developments.

The patent landscape surrounding this application is competitive, with numerous patents targeting similar compounds or indications. Companies operating within this space must conduct detailed freedom-to-operate and validity analyses considering related patents.


Key Takeaways

  • The scope of JPWO2015105144 hinges on its structural, method-of-synthesis, and use claims, with potential for broad protection if claims are well-constructed.
  • The landscape is characterized by extensive prior art, necessitating a strategic approach to patent filing, claim drafting, and enforcement.
  • Broad composition claims in the patent could confer significant market exclusivity, but are vulnerable to obviousness challenges if similar compounds exist.
  • Monitoring international patent filings and related patent families is vital for assessing freedom to operate and designing around.
  • Effective patent strategies include securing claims across chemical, process, and use dimensions, along with considering patent term extensions for lifecycle management.

FAQs

1. What is the primary innovation claimed in JPWO2015105144?
The core innovation revolves around a specific chemical compound or class, designed for therapeutic efficacy, with particular structural features that differentiate it from prior art.

2. How does the Japanese patent landscape influence the enforcement of JPWO2015105144?
Japan’s robust patent system facilitates enforcement but also involves rigorous examination of obviousness. A well-drafted patent with narrow claims may limit enforceability, while broad claims provide better protection but face higher invalidation risk.

3. Can this patent be challenged or bypassed?
Yes, competitors can challenge through invalidation procedures or design around claims by developing structurally or functionally different compounds within the scope of prior art.

4. How does this patent fit into global patent strategies?
Filing in Japan complements international patent families, securing territorial rights and supporting licensing, collaborations, or market entry strategies across key jurisdictions.

5. What are the key considerations for companies aiming to develop similar compounds?
Companies should analyze the exact scope of claims, existing patents, and prior art, and consider alternative chemical structures or methods to avoid infringement while maintaining therapeutic efficacy.


References

  1. Japan Patent Office (JPO). Patent Gazette and Examination Guidelines.
  2. World Intellectual Property Organization (WIPO). PCT Application Data.
  3. PatentScope and espacenet for related patent families and prior art.
  4. Legal analyses of Japanese pharmaceutical patents and patent law practices.
  5. Industry reports on patent strategies in Japanese pharmaceutical sector.

Note: Further detailed claim construction would require access to the full patent document and its claims section.

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