An Open,Single-centre Pilot Study of Efficacy and Safety of Topical MOB015B in the Treatment of Distal Subungual Onychomycosis (DSO)
NCT01814020 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL
Last updated 2014-09-22
Summary
Assess efficacy and safety of topical MOB015B, applied daily during 48 weeks, in adults with fungal nail infection.
Conditions
- Distal Subungual Onychomycosis
Interventions
- DRUG
-
MOB015B
Sponsors & Collaborators
-
Moberg Pharma AB
lead INDUSTRY
Eligibility
- Min Age
- 18 Years
- Max Age
- 70 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2012-12-31
- Primary Completion
- 2014-07-31
- Completion
- 2014-07-31
Countries
- Sweden
Study Locations
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