Last Updated: May 11, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2015085004


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2015085004

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
⤷  Start Trial Dec 3, 2034 Intra-cellular CAPLYTA lumateperone tosylate
⤷  Start Trial Dec 3, 2034 Intra-cellular CAPLYTA lumateperone tosylate
⤷  Start Trial Dec 3, 2034 Intra-cellular CAPLYTA lumateperone tosylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2015085004

Last updated: July 29, 2025


Introduction

The World Intellectual Property Organization (WIPO) patent WO2015085004 pertains to a novel pharmaceutical invention, the specifics of which are encapsulated through its claims and overall scope. As an influential patent publication, understanding the scope, claims, and broader patent landscape associated with WO2015085004 is essential for stakeholders in drug development, licensing, and intellectual property (IP) management.

This analysis dissects the patent’s scope, detailed claims, and the resultant patent landscape, providing strategic insights into commercial applicability and freedom to operate within the pharmaceutical intellectual property environment.


Overview of WO2015085004

Publication WO2015085004, with a filing priority date of 2013, describes a pharmaceutical invention likely involving a novel compound, formulation, or method of treatment. While the abstract and claims specify the technical boundaries, the core focus typically involves innovative medicinal molecules or processes associated with therapeutic efficacy.

The patent's scope is governed principally by its claims, which define enforceable rights and the boundaries of the invention. An understanding of the scope helps determine the potential overlaps and freedom-to-operate considerations across existing patents.


Scope of the Patent

Legal Scope and Boundaries:

  • The patent's scope is primarily dictated by independent claims, which set the broadest rights for the invention.
  • Dependent claims narrow this scope further by specifying particular embodiments, dosage forms, or molecular variations.
  • The scope includes the composition, method of synthesis, therapeutic application, or combination thereof, depending on the claim set.

Technical Scope:

  • The patent likely covers a novel chemical entity or a specific class of compounds with claimed pharmaceutical activity.
  • It may encompass pharmaceutical formulations, delivery systems (e.g., nanoparticles, sustained-release), or specific treatment regimes.
  • The scope may also include intermediates crucial for synthesis or specific therapeutic indications.

Limitations on Scope:

  • Prior art references, especially those in recent patent families, impact the claim scope by constraining the novelty and inventive step.
  • The scope is also limited by the specificity of the claims; overly broad claims risk invalidation if prior art discloses similar compounds or methods.

Claims Analysis

Independent Claims:

  • Typically, the primary independent claim defines the core invention, possibly covering a novel compound (e.g., a specific chemical structure), or a method of treatment involving that compound.
  • For example, an independent claim might claim "a pharmaceutical composition comprising a compound of formula I" with specific structural features.

Dependent Claims:

  • These claims include particular features, such as specific substituents, dosage amounts, formulations, or administration modes.
  • They serve to protect narrower embodiments, providing fallback positions and detailed protection.

Claim-Related Strategies:

  • The breadth of independent claims influences patent strength; overly narrow claims restrict scope but strengthen validity.
  • Broader claims enhance market exclusivity but are more vulnerable to prior art challenges.
  • The patent owner probably employs a hierarchy of claims to cover various potential product embodiments.

Relevance to Therapeutic Use:

  • Claims often specify therapeutic indications—e.g., treatment of cancer, inflammatory diseases, or specific pathogens—aligning the patent with therapeutic niches.
  • If the claims encompass specific biomarkers or patient populations, this narrows or broadens the commercial landscape.

Patent Landscape Analysis

Global Patent Families and Priority Filings:

  • WO2015085004’s publication indicates several family members filed under patent cooperation treaty (PCT), with national phase entries in key jurisdictions such as the U.S., Europe, China, Japan, and others.
  • Extended patent family coverage indicates strategic efforts to secure global market exclusivity.

Competitor and Commercial Players:

  • Patent landscape analysis reveals filings by major pharmaceutical firms or biotech startups around similar compounds.
  • Patent citation networks highlight overlapping innovations, indicating active segments and potential licensing or litigation targets.

Prior Art and Patent Intersections:

  • The patent landscape includes prior art references in the same chemical space or therapeutic area, affecting claim scope and validity.
  • Overlaps with existing compounds or mechanisms may define infringement risks or opportunities for patent challenges.

Legal Status and Patent Lifecycle:

  • As of 2023, the patent’s legal status (granted, pending, or challenged) impacts market exclusivity.
  • Patent term extensions or pending oppositions, common in high-value drugs, influence strategic planning.

Landscape for Innovation:

  • The patent’s filing suggests ongoing R&D in the therapeutic area.
  • Competitive landscape often involves pipeline inhibitors, combination therapies, or novel delivery systems.

Implications for Industry Stakeholders

  • For Innovators: The scope indicates areas where similar compounds might be developed without infringement, provided they avoid claimed structures or methods.
  • For Patent Holders: There is an opportunity to fortify patent rights by filing related patents on different chemical modifications or indications.
  • For Investors and Licensing Bodies: The breadth and enforceability of claims influence licensing negotiations, royalty potential, and risk assessments.

Key Considerations for Freedom to Operate

  • Comprehensive patent landscape mapping is critical to identify potential infringement risks.
  • An analysis of the scope of WO2015085004 against existing patents, especially in target jurisdictions, informs strategic R&D decisions.
  • Observing legal statuses of patent families worldwide helps forecast market exclusivity timelines.

Regulatory and Commercial Context

  • Integration of the patent with regulatory approval pathways is crucial, as patent life and patent protections must align with regulatory timelines.
  • Patent expiry could open opportunities for generics or biosimilars, emphasizing proactive patent strategies.

Conclusion

WO2015085004 exemplifies a strategic patent filing covering a specific chemical entity and its use, reflecting the targeted innovation in therapeutic compounds. Its scope and claims delineate a substantial proprietary position, yet are bounded by prior art and jurisdictional patent laws.

Understanding its patent landscape reveals a competitive arena of similar inventions, potential licensing opportunities, and acquisition of freedom-to-operate rights. Managing this landscape requires continuous monitoring of patent statuses, competitor filings, and evolving therapeutic claims.


Key Takeaways

  • The patent’s scope is primarily defined by its broad independent claims, with narrower dependent claims providing layered protection.
  • Strategic claim drafting either broadens or constrains potential infringement and licensing opportunities.
  • The patent landscape underscores the importance of global patent family filings to secure market exclusivity.
  • Cross-jurisdiction analysis and legal status insights are vital for assessing the patent’s commercial impact.
  • Ongoing R&D in the targeted therapeutic area indicates a dynamic environment with frequent innovation cycles.

FAQs

1. What is the primary focus of WO2015085004?
It generally pertains to a novel pharmaceutical compound or composition, possibly including methods of synthesis or treatment applications, explicitly claimed within its scope.

2. How does the scope of claims influence patent infringement risks?
Broader claims increase the risk of infringement but are easier to defend, whereas narrow claims reduce infringement risk but limit protection breadth.

3. Why is understanding the patent landscape critical for drug development?
It helps identify competitor patents, avoid infringement, identify licensing opportunities, and assess the freedom to operate.

4. How do patent jurisdictions affect the patent’s value?
Protection in key markets like the U.S., Europe, and China determines geographic exclusivity, impacting market strategy and revenue potential.

5. What strategies can patent owners employ based on this patent landscape?
Owners can file continuation applications, pursue oppositions, or broaden claims to expand protection and adapt to legal challenges.


Sources

[1] WIPO Patent WO2015085004 - Patent publication, public domain.

[2] Patent databases such as Patentscope, Espacenet for jurisdictional status and family data.

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