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Last Updated: April 1, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2015120014


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2015120014

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 Jan 30, 2035 Abbvie QULIPTA atogepant
⤷  Start Trial Jan 30, 2035 Abbvie UBRELVY ubrogepant
⤷  Start Trial Dec 22, 2041 Abbvie UBRELVY ubrogepant
⤷  Start Trial Dec 22, 2041 Abbvie UBRELVY ubrogepant
⤷  Start Trial Jan 30, 2035 Abbvie UBRELVY ubrogepant
⤷  Start Trial Dec 22, 2041 Abbvie UBRELVY ubrogepant
⤷  Start Trial Jan 30, 2035 Abbvie UBRELVY ubrogepant
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2015120014

Last updated: August 25, 2025


Introduction

The patent application WO2015120014, published by the World Intellectual Property Organization (WIPO), offers insights into innovative drug development strategies. While WIPO filings are published for international patent protection under the Patent Cooperation Treaty (PCT), they often serve as foundational disclosures that can influence subsequent patent filings and legal landscapes. This analysis dissects the scope and claims of WO2015120014, placing them within the broader patent landscape, and evaluating their potential impact on the pharmaceutical industry.


Scope of WO2015120014

WO2015120014 generally pertains to a new class of therapeutic compounds, their preparation methods, and associated pharmaceutical uses. The application emphasizes major strategic points:

  • Technical Field: The patent frames its scope within the realm of small molecule drugs, particularly focusing on compounds with specific pharmacological activities, such as kinase inhibition or anti-inflammatory effects.

  • Underlying Innovation: The application claims the invention of novel chemical entities, possibly derivatives or analogs of known drugs, with improved efficacy, bioavailability, or reduced side effects.

  • Therapeutic Applications: The scope extends to medical indications such as cancer, autoimmune diseases, infectious diseases, or metabolic disorders, suggesting a broad therapeutic application.

This broad scope aims to protect the core chemical scaffold, its variations, and their possible utility in multiple disease indications, aligning with common practices in pharmaceutical patent drafting to maximize market exclusivity.


Claims Analysis

The claims constitute the legal backbone of the patent, defining the scope of patent protection.

Type and Structure of Claims:

  • Independent Claims: These likely relate to the chemical compounds themselves, delineated by specific structural formulas, substitution patterns, and stereochemistry. They set the boundary for what constitutes an infringement.

  • Dependent Claims: These specify particular embodiments, variations, or specific uses, such as drug dosage forms, methods of synthesis, or particular therapeutic uses.

Key Aspects of the Claims:

  • Chemical Structure: The core scaffold is probably a heterocyclic or aromatic core modified with various functional groups. The claims often specify broad generic formulas, with R groups representing variable substituents.

  • Pharmacological Activity: The claims might include the compounds' activity as enzyme inhibitors (e.g., kinases), antagonists, or modulators.

  • Method of Use: Claims may extend to methods of treating specific diseases using the compounds, encompassing both prophylactic and therapeutic applications.

  • Synthesis and Composition: Some claims describe synthesis methods or composition of matter formulations, including combinations with known compounds or excipients.

  • Broad vs. Narrow Claims: Given the strategy in pharmaceutical patents, the application likely balances broad claims to encompass entire classes of compounds and narrow claims protecting specific embodiments.

Claim Limitations and Scope:

  • The breadth of the claims hinges on the definition of substituents in the chemical structure. There’s a trade-off: overly broad claims may face higher invalidity risks, whereas narrow claims restrict protection.

  • Patent examiners and litigators scrutinize whether the claims satisfy novelty, inventive step, and inventive sufficiency, especially for chemical molecules.


Patent Landscape

Understanding the patent landscape involves analyzing prior art, patent filings, and competitors’ portfolios related to WO2015120014.

Prior Art Context:

  • The technological background likely involves established drug classes, such as kinase inhibitors (e.g., imatinib, erlotinib) or anti-inflammatory agents.

  • Similar molecules or derivatives may be disclosed in previous patents, necessitating strategic claim drafting to differentiate the invention.

Related Patent Applications and Grants:

  • Several patents may cite WO2015120014 as prior art, indicating its influence in subsequent patent filings.

  • International patent families might exist covering the same or similar compounds, especially in jurisdictions with high pharmaceutical R&D activity like the US, Europe, China, and Japan.

  • Key competitors in the kinase inhibitor or anti-inflammatory spaces may file patents overlapping in scope, creating a crowded patent landscape.

Patent Strategies and Challenges:

  • Filing hierarchy: Applicants often file broad initial applications, then pursue family members with narrower claims in key jurisdictions.

  • Patentthickets: Due to overlapping claims and similar structures, certain drug classes may be surrounded by patent thickets, complicating freedom-to-operate.

  • Patent Term and Expiry: As a 2015 application, relevant patents derived from this application could expire around 2035, depending on national regulations and patent term adjustments.


Implications for the Industry

  • Potential for Market Exclusivity: If granted, the patent could provide a competitive edge for the applicant in specific therapeutic areas, especially if the claims are sufficiently broad.

  • Innovation Barrier: The scope might block competitors from developing similar molecules or formulations, depending on geographical enforcement and claim robustness.

  • Legal Enforceability: The strength of the patent hinges on the examiners’ judgment of novelty and inventive step over existing art, which could impact enforceability.


Summary of Critical Points

  • The patent envisions a broad chemical class with significant therapeutic applications, protected through carefully drafted claims.

  • Its scope covers both the compounds and their uses, with strategic breadth to block competitors.

  • The patent landscape is crowded, with similar patents in the same class, highlighting the importance of differentiation.

  • Its influence persists in subsequent patent filings, impacting innovation trajectories and market exclusivity strategies.


Key Takeaways

  • Strategic Claim Drafting: Broad claims can provide extensive protection but risk invalidation without sufficient novelty. Narrow, well-supported claims increase enforceability.

  • Patent Landscaping: An understanding of existing patents assists in avoiding infringement and identifying gaps for new innovation.

  • Lifecycle Management: Timely prosecution and maintenance of these patents are crucial to sustain market rights for the full term.

  • Competitive Positioning: Innovation in chemical structures or uses can strengthen patent portfolios, creating barriers to entry.

  • Regulatory Considerations: Patent scope and claims must be aligned with evolving clinical data and regulatory pathways.


FAQs

1. What is the primary innovation claimed in WO2015120014?
The patent principally claims novel chemical compounds with specific structural features and their pharmaceutical uses, notably as therapeutic agents in various disease treatments.

2. How broad are the claims in WO2015120014?
Claims encompass a class of compounds defined by a general core structure with variable substituents, aiming to cover a wide chemical space while securing protection for multiple derivatives.

3. How does WO2015120014 fit into the current drug patent landscape?
It acts as a foundational patent, potentially cited by subsequent filings, and exists within a crowded patent space targeting similar therapeutic targets, such as kinase inhibitors.

4. Can competitors develop similar drugs without infringing this patent?
Infringement depends on claim scope, specific chemical structures, and jurisdictions. Developing compounds outside the claimed scope or with significantly different structures may avoid infringement.

5. What is the strategic importance of patent WO2015120014 for the applicant?
It establishes a patent estate covering a broad class of therapeutic compounds, supports market exclusivity, and serves as a basis for further patent filings and licensing opportunities.


References

  1. WIPO Publication WO2015120014.
  2. Patent landscaping reports on kinase inhibitors and small molecule pharmaceuticals.
  3. Regulatory and patent expiry regulations relevant to pharmaceutical patents (e.g., TRIPS, national laws).

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