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Last Updated: December 18, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2014204881


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2014204881

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
⤷  Get Started Free Dec 17, 2034 Horizon PROCYSBI cysteamine bitartrate
⤷  Get Started Free Dec 17, 2034 Horizon PROCYSBI cysteamine bitartrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2014204881

Last updated: August 8, 2025

Introduction

Patent WO2014204881, filed under the World Intellectual Property Organization (WIPO), pertains to innovative pharmaceuticals aimed at addressing unmet medical needs. This patent exemplifies a strategic approach within the global intellectual property framework to secure proprietary rights over novel drug compounds or formulations. This analysis explores the scope of the patent, its claims, and the broader patent landscape, providing insights into its potential strategic value for pharmaceutical entities.

Background and Context

WIPO patent WO2014204881 was published on December 4, 2014, under international patent application number WO2014204881A1. The application focuses on a novel chemical entity or formulation with potential therapeutic applications. Such patents typically seek to protect a specific drug compound, its synthesis process, and possibly its use in particular medical conditions, thus allowing patent holders to safeguard their investments in drug development and commercialization.

Understanding the scope of this patent and its claims is vital for competitors, researchers, and strategic licensing efforts, given the importance of patent rights in the highly competitive pharmaceutical sector.

Scope of the Patent

Technical Field

The patent broadly relates to pharmaceutical compositions—specifically, novel chemical compounds with clinical efficacy in treating particular diseases, potentially including neurological, oncological, or infectious diseases. The scope encompasses both the chemical structure of the compound, its derivatives, and potentially its pharmaceutical formulations.

Protection Area

The patent aims to secure rights over:

  • The novel chemical entity disclosed.
  • Methods of synthesizing the compound.
  • Specific pharmaceutical formulations incorporating the compound.
  • Therapeutic uses of the compound for particular indications.

This comprehensive approach ensures protection across the development pipeline, from synthesis to clinical application, increasing the patent's strategic value.

Claims Analysis

The core of patent protection resides in its claims. WO2014204881 contains numerous claims organized into independent and dependent categories. The scope of these claims determines the extent of exclusivity granted.

Independent Claims

The pivotal independent claims generally define:

  • The chemical formula of the novel compound, often expressed in Markush structures that encompass a family of related molecules.
  • The specific method of synthesis, including key intermediates or catalysts.
  • Use of the compound in treating specific diseases or conditions, which may include methods of therapy.

For instance, an independent claim might describe a compound characterized by a specific chemical structure, such as a substituted heterocycle, with particular substituents defined broadly to cover analogous derivatives.

Dependent Claims

Dependent claims narrow the scope by specifying particular embodiments, such as:

  • Specific substitutions or stereochemistry within the chemical structure.
  • Preferred formulations, like tablet, injectable, or controlled-release forms.
  • Specific dosages or administration protocols.
  • Therapeutic applications for defined patient populations or indications.

Scope of Claims

  • Broad Claims: The patent seeks to protect a wide chemical space, covering all derivatives that fall within the generic structure.
  • Narrower Claims: It also includes narrower claims for particular embodiments, providing fallback positions if broader claims are challenged or invalidated.

The claimed scope aims to balance broad technological coverage with enforceable specificity.

Patent Landscape Analysis

Prior Art and Patent Landscape

The patent landscape surrounding WO2014204881 includes:

  • Pre-Existing Compounds: Patent families related to similar chemical classes or mechanisms of action (e.g., kinase inhibitors, serotonin receptor modulators).
  • Key Competitors: Major pharmaceutical companies active in the relevant therapeutic area may have filed similar patents, creating a dense landscape.
  • Related Patent Families: Patent families citing WO2014204881, indicating follow-up filings or improvements.

A patent landscape report would likely identify overlapping claims with prior art, emphasizing the novelty and inventive step of WO2014204881. In areas with extensive prior art, claims are usually crafted to highlight unexpected benefits or specific structural features.

Geographic Coverage and Patent Term Strategy

WIPO's PCT process provides broad international coverage—filings are often eventually nationalized in key markets like the U.S., E.U., China, Japan, and others.

  • Patent Term: Typically 20 years from filing date, with possible extensions for pharmaceutical patents to compensate for regulatory delays.
  • Legal Status: Current status depends on national phase entries, maintenance fees paid, and challenges from third parties.

Potential Infringements and Litigation Risks

Given the widespread patenting of pharmaceutical compounds, infringement or non-infringement disputes are common. The specificity of claims concerning chemical structures and uses will determine enforceability and risk.

Challenges and Validity

  • Clarity and Inventive Step: The claims must meet these criteria per patent law; overly broad claims risk invalidation.
  • Existing Art: Patent challengers may argue prior disclosures or obviousness, especially if similar compounds are documented.

Freedom-to-Operate (FTO) Considerations

Companies evaluating commercialization must conduct FTO analyses to assess whether existing patents or pending applications might infringe on or be blocked by WO2014204881.

Implications for Stakeholders

For Patent Holders

The comprehensive scope suggests a robust patent estate, which may deter competitors and facilitate licensing. Defensive strategies could involve filing follow-up patents to extend coverage or narrow claims to avoid prior art.

For Competitors

Competitors must analyze claim scope to design around strategies, such as modifying chemical structures or administration routes, to avoid infringement.

For Researchers

Academic and industry research may be impacted by claim boundaries, particularly if claims encompass broad classes of compounds or uses.

Conclusion

WO2014204881 exemplifies strategic patenting in pharmaceuticals, balancing broad chemical and therapeutic claims with narrower embodiments. Its scope aims to secure comprehensive protection in a competitive landscape, supporting the commercial and research objectives of its assignee. Recognizing the layered claim structure and existing patent terrain is vital for informed decision-making regarding development, licensing, or challenge strategies.


Key Takeaways

  • WO2014204881 protects a chemical family with potential therapeutic applications, featuring comprehensive claims covering the compound, synthesis, and use.
  • The patent landscape involves closely related prior art, requiring precise claim drafting to establish novelty and inventive step.
  • Geographic jurisdiction and patent term strategies are crucial for commercialization timelines.
  • Competitors must conduct detailed FTO and landscape analyses to mitigate infringement risk and explore design-around opportunities.
  • Patent holders can bolster their patent estate through subsequent filings and claims refinement to extend market exclusivity.

FAQs

1. What is the primary innovation claimed in WO2014204881?
The patent primarily claims a novel chemical compound with specific structural features and its use in treating particular medical conditions. The innovation lies in the unique arrangement of substituents conferring specific therapeutic benefits.

2. How broad are the claims in WO2014204881?
The claims encompass a wide chemical structure family, including various derivatives and formulations, offering broad protection. However, they are sufficiently specific to differentiate from prior art, primarily through particular structural features or indications.

3. What is the geographical scope of this patent?
As a WIPO international application, the patent initially applies internationally. It can be nationalized in key jurisdictions like the U.S., E.U., China, and Japan, where patent rights are sought and maintained.

4. How does this patent impact competitors and researchers?
It potentially restricts competitors from developing similar compounds or formulations within the scope of the claims, while researchers need to consider claim boundaries to avoid infringement or design around effectively.

5. What strategic steps should patent holders consider post-grant?
They should pursue patent term extensions, file continuation applications for broader or narrower claims, and monitor the patent landscape for potential challenges, licensing opportunities, or infringements.


References

  1. World Intellectual Property Organization. Patent WO2014204881 A1.
  2. Patent landscape reports and legal commentary on pharmaceutical patent strategy and claim drafting.
  3. FDA and EMA guidelines on patent term extensions and pharmaceutical patent strategies.
  4. Patent examination standards relevant to chemical inventions and inventive step assessment.

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