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A Multi-centre, Double-blind, Randomized, Vehicle-controlled Study of Efficacy and Safety of Topical MOB015B in the Treatment of Mild to Moderate Distal Subungual Onychomycosis (DSO)
NCT02859519 · View on ClinicalTrials.gov ↗
Study Summary
The primary objective of this study is to evaluate the efficacy of topical MOB015B in patients with mild to moderate distal subungual onychomycosis (DSO). The secondary objective is to evaluate the safety of topical MOB015B in patients with mild to moderate DSO.
Conditions Studied
Interventions
- DRUG MOB015B
- DRUG MOB015B Vehicle
Study Locations (10)
California
- — Multiple Locations
Florida
- — Multiple Locations
Idaho
- — Multiple Locations
Illinois
- — Rolling Meadows
Minnesota
- — Fridley
New Jersey
- — Multiple Locations
Oregon
- — Multiple Locations
Texas
- — Multiple Locations
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 365 participants |
| Start Date | 2016-10 |
| Est. Completion | 2019-11-13 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02859519
The ClinicalTrials.gov registry entry for NCT02859519 describes a study currently listed as completed. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 365 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Moberg Pharma AB, which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Distal Subungual Onychomycosis appearing as the primary indexed condition, and to 2 interventions — of which MOB015B is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT02859519 reports 10 study locations spanning 10 distinct geographic areas — top geographies include California, Florida, Idaho. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT02859519 about?
NCT02859519 is a clinical study titled "A Multi-centre, Double-blind, Randomized, Vehicle-controlled Study of Efficacy and Safety of Topical MOB015B in the Treatment of Mild to Moderate Distal Subungual Onychomycosis (DSO)". The primary objective of this study is to evaluate the efficacy of topical MOB015B in patients with mild to moderate distal subungual onychomycosis (DSO). The secondary objective is to evaluate the safety of topical MOB015B in patients with mild to moderate DSO.
What is the current status of trial NCT02859519?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 365 participants. The study started on 2016-10. Estimated completion is 2019-11-13.
What conditions does trial NCT02859519 study?
This clinical trial studies the following conditions: Distal Subungual Onychomycosis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT02859519?
The interventions under investigation include: MOB015B (DRUG), MOB015B Vehicle (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT02859519?
This trial is sponsored by Moberg Pharma AB, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT02859519 being conducted?
This trial has 10 study locations across California, Florida, Idaho, Illinois, Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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