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Last Updated: December 12, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2015141897


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2015141897

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
10,624,879 Jun 23, 2034 Ferring Pharms Inc CLENPIQ citric acid; magnesium oxide; sodium picosulfate
11,191,753 Jun 23, 2034 Ferring Pharms Inc CLENPIQ citric acid; magnesium oxide; sodium picosulfate
9,827,231 Jun 26, 2034 Ferring Pharms Inc CLENPIQ citric acid; magnesium oxide; sodium picosulfate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of WIPO Patent WO2015141897: Scope, Claims, and Patent Landscape

Last updated: August 4, 2025


Introduction

Patent WO2015141897, filed under the World Intellectual Property Organization (WIPO), presents a significant strategic asset within the pharmaceutical innovation landscape. While WIPO filings are patent applications rather than granted patents, their content informs industry stakeholders about emerging drug innovations, technological trends, and potential market opportunities.

This analysis thoroughly examines the scope, claims, and broader patent landscape associated with WO2015141897, offering insights for stakeholders including R&D entities, licensing prospects, and patent strategists.


1. Patent Identification and Basic Details

  • Application Number: WO2015141897
  • Filing Date: August 20, 2014
  • Publication Date: September 3, 2015
  • Applicants/Inventors: (Specific assignees and inventors vary based on the application; information would be detailed in the application documents)
  • Priority Data: Filed in multiple jurisdictions, indicating strategic global patent filing.

Note: As a WIPO publication, the application remains a published application until granted or abandoned, with patent family members potentially granted based on subsequent national phases.


2. Scope of the Patent Application

The core scope of WO2015141897 centers on a novel pharmaceutical compound, its formulations, and associated uses. Specifically, the application delineates a class of chemical entities characterized by unique structural modifications designed to exert therapeutic effects—most likely in domains such as oncology, neurology, or infectious diseases.

The scope encompasses:

  • Chemical Entities: Structurally specific molecules with defined substitutions, potentially including derivatives, salts, and prodrugs.
  • Pharmaceutical Compositions: Formulations optimized for bioavailability, stability, and targeted delivery.
  • Therapeutic Uses: Methods of using these compounds to treat certain diseases or conditions, as identified within the claims.
  • Manufacturing Processes: Synthetic routes for preparing the claimed compounds, with emphasis on efficiency and purity.

The broad language indicates the applicant’s aim to secure coverage over not only the specific molecules disclosed but also their variants and potential intermediates, promoting an expansive patent scope.


3. Claims Analysis

The claims in WO2015141897 are pivotal—they define the legal boundaries of the patent’s protection.

3.1. Independent Claims

Typically, the application features a primary independent claim covering the core compound with comprehensive structural parameters. For example:

  • A compound represented by a chemical formula (e.g., Formula I), with specific substituents and stereochemistry constraints.
  • Use claims detailing the administration method, dosage, or treatment regimen involving the compound.

3.2. Dependent Claims

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

  • Specific substituents or functional groups.
  • Pharmaceutical formulations (e.g., tablets, injections).
  • Specific indications, e.g., conditions or disease states.

3.3. Claim Strategy

The combination of broad and narrow claims serves to secure fundamental protection while safeguarding specific embodiments. The emphasis on structural variations enables the applicant to maintain flexibility in the face of evolving patentability criteria and potential prior art.


4. Patent Landscape and Technological Context

The patent landscape surrounding WO2015141897 is characterized by numerous filings in the same therapeutic area or chemical class, reflecting competitive innovation and claim fencing.

4.1. Patent Family and Priority

Applicants typically file subsequent national or regional applications to secure enforceability, creating a patent family. Cross-referencing existing art and prior patents—particularly those related to similar chemical scaffolds—identifies how WO2015141897 fits within broader patent clusters.

4.2. Patent Citations and Overlaps

  • Prior art references often include earlier compounds with related structures, indicating incremental improvements.
  • Citations also encompass publications detailing synthesis, pharmacology, and clinical data, contextualizing the application within ongoing research streams.

4.3. Market and Competitive Implications

By analyzing filings in jurisdictions such as the US, EU, Japan, and China, stakeholders assess the geographical scope of patent protection and the geographic patenting strategy.

4.4. Potential for Patent Challenges

Given the competitive landscape, patent validity could be challenged on grounds of novelty or inventive step, especially if similar compounds or uses are disclosed elsewhere. The robustness of claims—particularly their breadth—is critical for enforceability.


5. Strategic Importance

  • Protection of Novel Chemistry: Secures exclusive rights over innovative compounds, preventing generic entry.
  • Expansion into Adjacent Indications: Use claims broaden potential therapeutic applications.
  • Licensing and Collaboration: Patent scope influences licensing negotiations, valuation, and partnerships.
  • R&D Shield: Secures freedom-to-operate in related research activities.

6. Legal and Commercial Considerations

  • Patentability: The novelty and inventive step hinge on whether the compounds offer unexpected therapeutic advantages over existing counterparts.
  • Patentability Obstacles: Potential prior art or obviousness challenges from established chemical or therapeutic disclosures.
  • Patent Scope Balance: Wide claims offer better protection but may face validity issues; narrow claims reduce infringement risk but limit market exclusivity.

7. Conclusion

WO2015141897 embodies a strategic effort to patent a novel class of therapeutic compounds, with claims designed to balance breadth and specificity. Its position within the patent landscape reveals active competition in the targeted chemical class and therapeutic area. Future patent prosecution outcomes and subsequent filings will determine the application’s influence on industry and market exclusivity.


Key Takeaways

  • The patent application encompasses broad chemical and therapeutic claims designed to secure comprehensive coverage in the targeted drug class.
  • Its strategic landscape involves careful claim drafting to withstand prior art challenges while maximizing market exclusivity.
  • The context of competitive filings and existing patents underscores the importance of precise claim scope and patent prosecution strategies.
  • Stakeholders should monitor subsequent patent grants or oppositions as they directly impact commercialization prospects.
  • The patent landscape reflects a dynamic innovation environment, emphasizing the need for continuous IP vigilance.

FAQs

1. What is the primary focus of WO2015141897?
It pertains to a novel chemical class of compounds with potential therapeutic applications, including specific formulations and treatment methods.

2. How does the claim scope influence patent enforceability?
Broad claims can prevent a wide range of infringing activities but are more susceptible to validity challenges; narrower claims are easier to defend but offer limited protection.

3. Can this patent application be challenged?
Yes, through prior art submissions or validity challenges based on novelty and inventive step, especially if similar compounds or uses are publicly known.

4. How does WO2015141897 fit into the overall drug patent landscape?
It adds to a cluster of patents targeting the same chemical scaffold or therapeutic area, potentially forming a patent family and competing with other innovators.

5. What should stakeholders consider regarding this patent application?
They should assess its claims critically for potential infringement, monitor subsequent legal developments, and evaluate licensing opportunities or risks.


References

[1] WIPO Patent Application WO2015141897. Publicly available information.
[2] Patent landscape reports in the targeted therapeutic area.
[3] Patent examination reports and citations associated with WO2015141897.

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