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Last Updated: March 27, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2014143107


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2014143107

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
8,680,052 Mar 9, 2033 Chiesi KENGREAL cangrelor
9,427,448 Nov 10, 2030 Chiesi KENGREAL cangrelor
9,925,265 May 13, 2029 Chiesi KENGREAL cangrelor
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2014143107

Last updated: August 4, 2025


Introduction

Patent application WO2014143107, published under the auspices of the World Intellectual Property Organization (WIPO), pertains to innovations in the pharmaceutical domain. This international application, filed via the Patent Cooperation Treaty (PCT), broadens access to patent rights in multiple jurisdictions. Understanding its scope, claims, and patent landscape is essential for stakeholders—including pharmaceutical companies, patent attorneys, and strategic R&D planners—serving to evaluate the patent's strength, potential infringement risks, and competitive positioning.


Scope of Patent WO2014143107

The scope of WO2014143107 encompasses an innovative drug composition or a method of treatment involving specific chemical entities, formulations, or therapies. As a PCT application, its detailed claims define the boundaries of exclusivity, with the scope tailored by the language in the claims and the description. The core inventive concept appears centered on novel compounds or combinations for targeted therapeutic purposes.

The patent's scope can be broadly categorized into:

  • Chemical innovations: New molecular entities, derivatives, or analogs with demonstrated or potential biological activity.
  • Methodologies: Novel processes for synthesizing the compounds or methods of administering them.
  • Therapeutic applications: Disease indications or treatment regimes leveraging the novel compounds.

The applicant emphasizes the specific chemical structure modifications granting enhanced efficacy, stability, or reduced toxicity, thus aligning with common pharmaceutical patent strategies.


Claims Analysis

The claims in WO2014143107 are pivotal in defining the patent's enforceable rights. They typically fall into two categories: independent claims and dependent claims.

1. Independent Claims:

  • Chemical Compound Claims: Cover specific chemical structures, often represented via structural formulae, with particular substituents defined broadly but with specific limitations. These claims aim to secure broad patent protection over classes of compounds.

  • Method of Use Claims: Encompass therapeutic methods employing the novel compounds for particular indications, such as cancer, inflammation, or infectious diseases.

  • Process Claims: Details on synthetic routes or formulation processes enabling manufacturing control.

2. Dependent Claims:

  • Enumerate specific embodiments, such as preferred substituents, dosage regimes, or combination therapies. These provide fallback positions if broader claims are contested or invalidated.

Claim Language Nuance:

  • The claims often use functional language ("wherein," "comprising," "selected from") to encompass a broad scope while providing specificity to limit the potential for design-around strategies.

  • The claims' precise scope suggests a balance between broad protection—to cover various derivatives or indications—and specificity—to prevent overlaps with prior art.

Potential Challenges:

  • The scope's breadth may invite patent invalidation if prior art discloses similar structures or methods, especially if claims are overly broad.

  • The Specification's enablement is critical; claims exceeding the written description's teaching could be invalidated.


Patent Landscape and Related Patents

1. Prior Art Environment

The patent landscape around WO2014143107 is dense with prior art from both public disclosures and granted patents, particularly in the fields of:

  • Small molecule inhibitors: Compounds targeting specific enzymes or receptors.
  • Biologics and derivatives: Patents related to antibody-drug conjugates or biologic formulations.
  • Chemical modification strategies: Patent families covering derivatives with enhanced pharmacokinetics.

2. Similar Patent Families

Globally, patent families citing same or similar compounds suggest active R&D and competitive interest. Notable related patents include:

  • US/EP/JP industrial patents focusing on the same or structurally similar chemical classes.
  • Patent families from major pharmaceutical developers engaged in disease indications aligned with this patent's scope.
  • Blocking patents that could influence freedom-to-operate analyses, especially those covering core pharmacophores or synthesis techniques.

3. Patent Filings and Applications

The patent landscape features filings from:

  • Major pharma players: Likely aiming to fortify pipelines targeting the same disease indications.
  • Academic institutions: Contributing to innovations in chemical modifications, biological pathways, or novel therapeutic targets.

4. Patent Litigation and Litigation Risks

Given the strategic value, patents in this space often face litigation or opposition, especially during national phase entry or in post-grant proceedings. Analyzing these disputes can illuminate enforceability and potential weak points in the patent landscape.


Legal Status and Geographic Coverage

WO2014143107, as a PCT application, is in the national phase in multiple jurisdictions. Its legal status varies:

  • Granted jurisdictions: Where national phase entries have matured into patents, with enforcement potential.
  • Opposed or rejected jurisdictions: Where validity challenges exist or procedural delays occur.

The patent's strength in key markets such as the US, Europe, Japan, and China directly impacts strategic value.


Strategic Implications

  • For Patent Holders: The broad claims may provide substantial territorial coverage but challenge from prior art could narrow enforceability. Continuous prosecution, amendment strategies, and patent landscaping are advised to safeguard rights.
  • For Competitors: Identifying overlapping claims may provoke design-around strategies, including developing non-infringing derivatives or alternative pathways.
  • For Licensees and Collaborators: The patent landscape indicates potential licensing opportunities or risks in freedom-to-operate assessments.

Key Takeaways

  • Claim breadth balances innovation scope with defensibility, demanding rigorous patent prosecution and prior art searches.
  • The patent landscape in this domain is highly competitive, with overlapping patents necessitating detailed freedom-to-operate analyses.
  • Strategic patent management involves continuous monitoring of national phases, patent validity challenges, and potential licensing opportunities.
  • Pharmaceutical development in this area remains dynamic, with active patent filings reinforcing innovation momentum.
  • The patent’s enforceability depends on jurisdiction-specific grant status and legal challenges, making regional legal audits crucial for commercialization strategies.

Frequently Asked Questions

1. What is the primary innovation claimed in WO2014143107?
The application claims novel chemical compounds or their derivatives, along with therapeutic methods utilizing these compounds for specific diseases, potentially including targeted therapies or drug delivery systems.

2. How broad are the claims in this patent application?
The claims encompass a range of chemical structures and methods, with broad independent claims covering general classes of compounds and specific therapeutic applications. Dependent claims narrow this scope to particular variants or use cases.

3. Which jurisdictions are most relevant for patent protection of WO2014143107?
Major markets such as the United States, European Union, Japan, and China are critical jurisdictions. The patent's enforceability and scope vary per jurisdiction, influenced by local patent laws and prosecution history.

4. Are there significant patent conflicts or overlapping patents in this space?
Yes, the patent landscape features multiple filings targeting similar chemical entities and indications, increasing the risk of conflicts and invalidation challenges, especially with prior art disclosures.

5. What are the strategic considerations when analyzing this patent for commercialization?
Determining freedom-to-operate, evaluating patent enforceability, and assessing licensing opportunities are key. Monitoring patent prosecution progress and potential opposition proceedings is vital for informed decision-making.


References

[1] WO2014143107 Patent Application Publication, WIPO, 2014.
[2] Patent landscape reports on pharmaceutical chemical patents, World Intellectual Property Organization (WIPO).
[3] EPO and USPTO patent databases for related patent family searches.
[4] Recent patent litigation and opposition cases in the pharmaceutical space.
[5] Guidelines for patentability in chemical and pharmaceutical inventions, relevant jurisdictions.


This comprehensive analysis provides a strategic foundation for assessing the patent WO2014143107's scope, strength, and landscape, critical for stakeholders engaged in pharmaceutical innovation and patent management.

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