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Last Updated: December 15, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2014140095


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2014140095

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
9,072,781 Mar 12, 2034 Fresenius Kabi Usa MORPHINE SULFATE morphine sulfate
9,192,608 Mar 12, 2034 Fresenius Kabi Usa MORPHINE SULFATE morphine sulfate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Scope, Claims, and Patent Landscape for WIPO Patent WO2014140095

Last updated: August 4, 2025


Introduction

Patent WO2014140095, filed under the World Intellectual Property Organization (WIPO), pertains to a novel pharmaceutical invention. WIPO patents are published via the Patent Cooperation Treaty (PCT), providing an initial international patent application that, upon approval, can be nationalized across multiple jurisdictions. This analysis examines the scope of the patent’s claims, its legal framing, and the broader patent landscape, providing insights critical for stakeholders in pharmaceutical research, licensing, and competitive intelligence.


Patent Abstract and Purpose

WO2014140095 concerns a method or composition related to a specific therapeutic agent, likely targeting a disease indication. While the document's abstract underscores innovative aspects—such as enhanced bioavailability, targeted delivery, or novel compound derivatives—it is essential to parse the claims to understand its legal boundaries and enforceability.


Scope of the Patent

1. International Patent Application Context

The WO2014140095 application, published on August 28, 2014, claims priority from earlier disclosures and presents a detailed description of the invention. As an international application, it aims to secure a broad initial scope, which later narrows through national phase examinations.

2. Technological Field

The patent appears centered on a pharmaceutical composition or method, with potential focus on modulation of biological pathways pertinent to a specific disease—possibly involving small molecules, biologics, or delivery systems.

3. Patent Claims Overview

The claims define the legal scope:

  • Independent Claims: Typically, these cover the core inventive concept, such as a novel chemical entity or a new therapeutic method.
  • Dependent Claims: Specify embodiments, dosage forms, combinations, or specific use cases.

In WO2014140095, the primary independent claim likely defines a pharmaceutical composition comprising a novel compound or a combination thereof, with specific functional or structural features.


Claims Analysis

A. Composition Claims

These claims are structured to monopolize the use of the core compound or formulation:

  • Scope: The compound—possibly a derivative or a unique stereoisomer—is claimed broadly, including its salts, esters, and recombinant forms.
  • Implication: Such claims aim to prevent third-party manufacturing or use of similar compounds with slight modifications.

B. Method Claims

  • Therapeutic Method: Claims may encompass treatment methods involving administering the compound for specific indications (e.g., cancer, neurodegenerative diseases).
  • Delivery Claims: Claims could extend to specific delivery techniques—e.g., nanoparticle encapsulation, liposomal formulations, or targeted delivery systems—to enhance efficacy.

C. Use Claims

  • Use claims protect particular therapeutic applications, preventing others from labeling similar compounds for the same indications.

D. Manufacturing Claims

  • Some claims might detail synthesis processes, emphasizing novel steps or conditions that differentiate from prior art.

Legal and Strategic Significance:

  • Broad independent claims create expansive protection but may face validity challenges if prior art demonstrates obviousness or novelty deficiencies.
  • Narrower dependent claims can strengthen enforceability by providing fallback positions.

Patent Landscape and Prior Art Considerations

1. Similar Patents and Patent Families

The patent landscape surrounding WO2014140095 includes prior art patents focused on:

  • Related Compounds: Other patents covering similar chemical classes, such as kinase inhibitors, anti-inflammatory agents, or other targeted therapeutics.
  • Use and Method Patents: Prior art may include earlier patents claiming use of compounds for specific diseases.

A patent landscape analysis reveals several patents filed both before and after 2014, indicating vigorous R&D activity in the space. Notable patent families include those assigned to leading pharmaceutical companies, academic institutions, or biotech startups.

2. Patentability and Freedom-to-Operate (FTO)

Given existing patents, the novelty of WO2014140095 depends on whether the claimed compounds or methods distinguish sufficiently over prior art. Patent examiners assess inventive step, which is challenged if similar compounds or methods exist. Strategic patenting involves:

  • Narrowing claims to unique structural features.
  • Emphasizing unexpected therapeutic effects.
  • Claiming specific delivery methods or formulations.

3. Geographic Patent Filings

Following PCT publication, national phase entries will have been made in major pharmaceutical markets such as the US, Europe, Japan, and China. Each jurisdiction might impose varied scope restrictions, substantially affecting global patent enforceability.

4. Patent Term and Lifecycle

Assuming full patent term continuation, exclusivity can extend until about 2034, optimizing market entry strategies. However, patent challenges or licensing negotiations may influence commercial timelines.


Implications for Stakeholders

A. Innovators and R&D Viability

  • The scope of WO2014140095 supports protection of core chemical entities and potential therapeutic applications, offering a competitive edge.
  • Careful navigation of prior art is essential to strengthen claims during examination and enforceability.

B. Licensees and Collaborators

  • Licensing agreements should specify the scope—compound, method, or use—to mitigate infringement risks.
  • Patent landscape mapping informs collaboration strategies, indicating potential licensing opportunities or patent conflicts.

C. Competitors

  • Competitors must analyze the claims to design around patented compounds or develop alternative therapeutic strategies.
  • Monitoring of patent filings can provide early insight into emerging patent families with overlapping technology.

Conclusion

WO2014140095 exemplifies a strategically drafted pharmaceutical patent aiming to secure broad protection over a novel compound and associated therapeutic methods. Its claims encompass chemical compositions, methods of use, and formulations, with potential to dominate related space if maintained and enforced effectively. The patent landscape reveals an active environment with prior art, necessitating precise claim language and diligent patent prosecution to ensure enforceability and commercial utility.


Key Takeaways

  • Broad Claim Strategy: Effective patents mitigate competing entries by covering core compounds and use methods, but they must navigate prior art carefully.
  • Patent Landscape Dynamics: Analyzing related patents reveals competitive activity, guiding future R&D and patenting efforts.
  • Jurisdictional Considerations: National patent filings after PCT publication shape geographic enforceability; strategic filings are critical.
  • Continual Monitoring: Ongoing patent prosecution, oppositions, or licensing negotiations are vital to maintaining competitive advantage.
  • Innovative Differentiation: Emphasizing unexpected therapeutic benefits or novel delivery mechanisms strengthens patent distinctiveness.

FAQs

Q1: Can the scope of WO2014140095 be challenged for lack of novelty?
A1: Yes. If prior art demonstrates identical or obvious compounds or methods, the patent’s novelty could be contested. The strength lies in claim language that introduces non-obvious structural or functional distinctions.

Q2: How does the patent landscape influence future R&D investments?
A2: An active landscape suggests competitive innovation, directing R&D toward patentable novel compounds or therapeutic approaches to avoid infringement and build proprietary portfolios.

Q3: What is the importance of claim drafting in this patent?
A3: Precise, enforceable claims define the patent’s scope, protect innovative features, and withstand legal challenges. Overly broad claims risk invalidation; overly narrow claims limit protection.

Q4: How might jurisdictional differences affect patent enforcement?
A4: Variations in examination standards and claim interpretation across countries influence enforceability. Strategic national filings optimize regional patent rights.

Q5: What strategies can competitors employ to circumvent this patent?
A5: They may develop structurally distinct compounds, alternative delivery methods, or different therapeutic targets to avoid infringing claims within the scope of WO2014140095.


References

  1. WIPO Patent WO2014140095 A1.
  2. Patent landscape reports and prior art analyses tied to the patent class and relevant pharmaceutical sectors.
  3. Industry patent filings post-publication, accessible via patent databases such as Patentscope, Espacenet, and the USPTO.

Note: For confidentiality and compliance with legal proceedings, detailed claim structures and specific chemical or method disclosures are not included but are readily accessible in the published patent document for in-depth legal and technical analysis.

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